All posts by student

Life Science Reference – Biology Online

Biology-Online.org is run by enthusiasts from all around the world and visited by over 25,000 people every day. Please help us grow our content! Submit your own articles, tutorials, essays, reports or any other biology related work and we will publish it online in the appropriate section.

World's largest and most comprehensive biology discussion board, made up of sections on Cell Biology, Molecular Biology, Zoology, Evolution, Microbiology, Bioinformatics, Human Biology, Botany, Genetics, Physiology, Ecology and others. Go to Forum.

Trending discussion:

Our editable Wiki Dictionary provides explanations for thousands of terms with links to relevant tutorials. Help us make this dictionary more comprehensive by editing its content. All changes are monitored by moderators. Go to Wiki Dictionary.

Quick Wiki Dictionary Links: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9 OTHER

This section contains hand picked articles in Agriculture, Astrobiology, Biochemistry, Bioengineering, Biophysics, Health and Medicine and many other topics. Our administrators add new articles daily. Submit your own work including articles, essays, assignments, PHD research or anything else related to biology, and help us grow this section. Go to Articles.

The biology tutorials aim to give an introductory to intermediate understanding of various biological concepts and disciplines, split up into sections for ease of use. Within each tutorial are references to the biology dictionary, intending to give an easy reference to the terminology used. Read tutorials.

Browse through our extensive book catalogue which covers all aspects of biological sciences. Read expert and consumer reviews and ratings. Go to Books.

Use this directory to find external links and resources to a broad range of Earth and Life Science websites. The sites are split up categorically to help you pinpoint the web page that discusses the subject you are interested in. Go to the Directory.

Go here to read the rest:
Life Science Reference - Biology Online

Spinal Arterial Anatomy | neuroangio.org

Development this abbreviated, important sectionprecedsdiscussion of adult anatomy. A more complete discussion is found in the dedicated section of neurovascular embryology.

The basicarrangementof the spinal system consists of ametameric grid of trasversely oriented segmental vessels, connected by various longitudinal channels. This simple bit of knowledge goes a long way in understanding spinal anatomy. Millions of years of speciation have taken place upon a basic building block of the organism the metameric segment. Just like the fly and the worm, the human body consists of metameric segments, with ecto-, meso-, and endodermal elements. Each vertebral body, its ribs, muscle, nerves, and dermatome, correspond to one level or segment. It is perhaps easiest to appreciate this concept at the thoracic level, where each rib, vertebral body, and other elements constitute the prototyical segment. In the early human embryo, the neural tube is first supplied by simple diffusion. When its limits are reached (200 micrometers perhaps), a primitive vascular system consisting of paired dorsal and ventral aortae (longitudinal vessels) and transversely oriented segmental arteries come into play to vascularize the developing tissue of the embryo.

As the tissue of spinal cord continues to enlarge, new longitudinal connections form between the transverse segmental arteries, most likely to facilitate distribution of blood within the vascular system. This pattern is seen throughout the body, but is somewhat easier to recognize in the vertebrospinal arterial system, where it gives rise to adult anterior spinal artery and numerous extradural longitudinal segmental connections which will be discussed below.

Gradual establishment of dominant longitudinal vessels leads to regression of most transverse segmental arteries, except at some levels where such vessels persist in supplying the longitudinal artery.

This process, in terms of the spinal cord, gives rise to the familiar adult appearanec of the anterior spinal artery and its remaining radiculomedullary feeders, while most segmental arteriespreviouslyconnected to it in early fetal life are limited to supply of the nerve root and adjacent tissues in the adult.

The same pattern of development takes place in the extra-axial, paravertebral space, where longitudinal connections between segmental arteries form a multitude of adult vessels, such as the vertebral, pre-vertebral, pre-transverse, deep cervical, lateral spinal, and other arteries, as will be illustrated below.

Adult Vertebrospinal Arterial Anatomy

The basic arterial vertebrospinal vascular unit consists of two segmental vessels, left and right, arising from the dorsal surface of the aorta. The vessel curves posterolaterally in front of the vertebral body, and sends small branches into its marrow. In front of the transverse process, the segmental artery bifurcates into a dorsal branch and an intrercostal branch. The intercostal segment supplies the rib and adjacent muscle and other tissues. The dorsal branch feeds the posterior elements and, via the neural foramen, sends branches to supply the local epidural and dural elements, as well as a radicular artery to nourish the nerve root. At some levels, the radicular artery is enlarged because, instead of supplying local neural elements, it maintained its embryonic access to the anterior spinal artery. At this level, the artery is called radiculomedullary because it also supplies a large segment of the spinal cord. Various other arrangements are seen, for example when radicular artery supplies portions of the dorsal spinal cord, a discontinuous network which is often misrepresented in venerable anatomical texts as a continuous system of two posterior spinal arteries. This is the basic arrangement of spinal supply.

The system varies in the cervical, upper thoracic, and sacral segments (i.e. exceptions are greater than the rule) but the basic principle of segmental dural and radicular vessels supplying neural tube elements is a very useful guide. Variation comes chiefly in form of segmental vessel origin whereas descending aorta serves this puprose for most thoracic and lumbar segments, the vertebral artery, subclavian branches (costocervical trunk for example), supreme intercostal artery, and median sacral artery (effectively a diminuitive continuation of the aorta below the iliac bifurcation) play this role at the appropriate segments. These vessels of origin are part of the gridline of longitudinal channels which form to connect embryonic segmental vessels. For example, the vertebral artery represents a confluence of discontinuous embryonic channels termed the longitudinal neural system into a single trunk. This, in part, explains multiple variations and duplications encountered in the vertebral territory.

Figure 1: Somatotopic organization of the vertebrospinal arterial vasculature, highlighting segmental vascular organization of the vertebrospinal axis and homologous longitudinal anastomoses along its entire length.

As you can see, numerous longitudinal vessels exist throughout the vertebrospinal axis, often with the same vessel going by several different names, for historical reasons. For example, see above for homology between the lateral spinal, pre-transverse, and deep cervical arteries. The segmental arrangement is particularly modified in the cervical region, where longitudinal vessels are dominant most obviously the vertebral arteries. It is important however to recognize the existence of segmental vessels connecting the three dominant cervical longitudinal arteries (ascending cervical, vertebral, and deep cervical) in terms of their anastomotic potential and its implications for both collateral revascularization and inadvertent embolization during interventional procedures.

The following diagrams provide a basic view of relevant arterial anatomy of the spinal elements, serving as a guide for interpretation of subsequent catheter angiography illustrations.

A aorta; B segmental artery; Ba intersegmental arterial anastomosis; C prevertebral anastomotic network; D direct vertebral body feeding arteries; E dorsal spinal artery; F intercostal/muscular artery; G pretransverse anastomotic network; H dorsal division of the dorsal spinal artery; I post-transverse anastomotic network; J muscular branches of the post-transverse anastomotic network; K ventral division of the dorsal spinal artery; Ka radicular artery; La ventral epidural arcade; Lb dorsal epidural arcade; M nerve root sleeve dural branch of the ventral division dorsal spinal artery; N dural branch of the ventral division dorsal spinal artery; O radiculopial artery; P radiculomedullary artery; Q anterior spinal artery; R mesh-like pial arterial network; S, T posterior spinal artery; U, V pial arterial network (a.k.a. vasocorona) anastomoses between anterior and posterior spinal arterial systems, W sulco-commissural artery, X rami perforantes of the peripheral (centripetal) system, Y central (centrifugal) system of sulcal arteries, originating from pial network of the cord; altogether, the pial network and rami perforantes (R+Y) are called the vasocorona or corona vasorum; Z rami cruciantes (a.k.a. crux vasculosa, a.k.a. rami anastomotici arcuati)

In the following examples, nomenclature using the above letters will be used for correlation.

Aorta and segmental vessels. Many spinal angiogramsstart with imaging the biggest vessel in the body. Some are surprised to discover that these segmental lumbar and intercostal arteries (red)are actually not that small (between 1 and 2 mm diameter typically) most can be easily engaged (and occluded) with a 5F catheter. The aortic injection gives a roadmap, may identify a particularly large fistula, and show which levels may have missing segmental arteries, thereby obviating a frustrating search. In this angiogram of a patient with a dural fistula, a congested spinal cord vein (light blue) can be seen in the venous phase (dark blue). Celiac trunk (orange) and renal arteries (yellow) are also labeled.

Typical Lumbar artery (segmental artery) injection. During spinal angiography, the segmental artery is selected with an appropriate 4F or 5F catheter (RDC, SAS). Injection rates are 1-2 cc/sec for as long as you think you need it, typically 2-4 seconds. Frame rates vary from 1-3 per second, and should not exceed 3 unless particularly necessary (to visualize microanatomy of a high flow fistula, for example). When dural or other fistula is suspected, multiple levels may need to be interrogated. One can easily go through 300 ml or more of contrast, so be aware. For metastatic disease, the search may be more focused. It is helpful to view the angiogram in both subtracted and native views to appreciate both fine vascular detail and bony landmarks.

The lumbar artery (purple, B)is relatively selectively injected, with trace opacification of hte contralateral left L3 lumbar artery due to proximity of the left and right orifices to each other. Since there is no rib, the artery does not have a prominent intercostal component. The arteries of the dorsal branch (red, H, J) supply the lamina and adjacent tissues, with anastomosis to the spinal process arterial arcade (yellow, I). You can see continuation of this arcade inferiorly, NOT to be mistaken for the anterior spinal artery or other spinal artery. The anterior spinal artery is straighter and has a characteristic radiculomedullary hairpin turn (see below). A large paravertebral anastomotic branch (green, G) is present, which opacifes ipsilateral L4 level dorsal branches (blue, H, J). No radiculomedullary artery is seen at this level.

Common lumbar trunk: Especially in the lower spine, single left and right lumbar artery origins are common. Absent levels are also common, usually supplied via paravertebral and prevertebral anasomoses.

Paravertebral anastomotic network typically, this is the dominant longitudinal anastomotic connection between adjacent segmental arteries.It is particularly well visualized in young, normotensive patients. Technical considerations are also important having the catheter well-wedged into the ostium of the segmental artery, as well as longer, higher volume injections (within reason, of course), are key to opacifying all kinds of collaterals.The paravertebral network is located along the lateral aspect of the vertebral body, adjacent to the sympathetic chain, for example. A well developedparavertebral network (blue, G) is present. The catheter (red) is engaged in a lumbar artery (brown, B) and via this network opacifies thelumbar atery of the level immediately above (purple) and immediately below (pink). Notice the spinous process arcade again (black, I). This network ensures virtual impunity for atherosclerotic or iatrogenic occlusion ofa proximal segmental artery. More care should be excersized at radiculomedullary artery levels.

Multiple longtitudinal anastomotic networks prevertebral, paravertebral, spinous process

In this patient, all three networks are demonstrated stereoscopy is very helpful to decide which is which. Also notice prevertebral transverse and retrocorporeal networks at same level.

C prevertebral anastomotic network; G paravertebral anastomotic network (can opacify adjacent levels with strong injection, or supply adjacent level in case of intercostal artery hypoplasia/aquired stenosis);I spinous process branch and associated anastomotic network connecting spinous processes; Blue precorporeal anastomotic network (not shown in diagram); blue retrocorporeal anastomotic network (pink color vessels in diagram, and see section below); light blue left L1 segmental artery; brown left T12 segmental artery; dark green right T12 segmental artery; pink radiculopial artery.

Another demonstration of multiple longitudinal anastomoses:

Lumbar segmental artery injection, demonstrating a well-developed post-transverse anastomotic network (I) visualized through the ventral division (H) of the segmental artery (B), with its muscular branches (J), as well as the pre-transverse anastomosis (G), both contributing to collateral visualization of the adjacent cranial segmental artery (B). F muscular artery, homolog of the intercostal artery.

Retrocorporeal arterial network

This characteristic diamond-shaped network behind the vertebral body (in the epidural space dorsal to the posterior vertebral body cortex, also known as anterior [with respect to the spinal cord] epidural space) marked with L on the diagrams above, constitutes the primary anastomotic connection between left and right segmental arteries of the same level. Like everything, else it is variable in prominence based on developmental and other considerations. A good injection can usually opacify parts of the network, but it becomes quite obvious once the diamond-shaped configuration corresponding to left and right superior and inferior contributors to the diamond are revealed. One way to improve visualization of the network is via an injection adjacent to a dissected segmental artery.

More retrocorporeal arcade images, demonstrated to great advantage in a young patient

T12 segmental artery injection of a young, normotensive slender patient, providing exquisite visualization of the various trans-segmental anastomoses, demonstrating a hexagon-shaped multilevel anterior epidural arcade (La), and prevertebral anastomoses (G). Notice developmental hypoplasia of the right T11 segmental artery (single white arrow, one level above the catheter), with a corresponding small intercostal artery caudal to its normal position (double white arrow). Both radiculomedullary (P) and radiculopial (O) arteries are present, the former demonstrating its characteristic midline course.

Another injection, which happens to preferentially opacify the retrocorporeal network

The median sacral artery continuation of the aorta, the median sacral artery usually comes off the carotid bifurcation, and can be most easily engaged via some kind of recurved catheter (It is the artery to the tail of countless species which happen to have one). As a homolog of the aorta, it gives origin to segmental vessels of the sacrum. Thus median sacral artery injection is in fact a sacral aortogram opacifying multiple segmental sacral branches. It is a must see artery when looking for a fistula. Here, the median sacral artery (red) originates from the left L4 branch (blue and yellow). Lumbar segmental vessels seen on the aortogram are shown in green.

Median Sacral Artery andLateral Sacral Arteries -- the lateral sacral arteries are longitudinal vessels wich are homologous to the paravertebral (pre-transverse) anastomoses in the thoracolumbar segments and to the vertebral artery in the cervical spine. They arise from proximal internal iliac arteries, and can be seen from either internal iliac or median sacral injections, as well-demonstrated below:

Inferior lumbar and sacral anatomy. A stereo pair, B native image, C legends: Selective catheterization of a common L5 segmental trunk (white arrow), also giving rise to the median sacral artery (normally arising from the region of aortoiliac bifurcation). The injection opacifies bilateral L5 and sacral segmental arteries (B), and the prevertebral anastomotic network (G), which is homologous with lateral sacral arteries. A stereo pair; B native image; C Labels.

Here is an injection of the lateral sacral artery (center) with adjacent images of bilateral internal iliac injections, demonstrating existence of extensive collateralization between the internal iliac and median sacral systems by opacifying the same arteries which are labeled with the same color arrows. The purple and red arrows point to the lateral spinal artery seen from both median sacral and internal iliac injections. Green arrows outline the remainder of the lateral sacral system, best seen from medial sacral in this case.

Median sacral artery (purple) giving rise to multiple sacral segmental arteries (red) and to a lumbar artery (yellow)

In this example, median sacral artery arises from a common L5 trunk.

Below the aortic bifurcation, segmental arteries can be visualized by injection of the median sacral artery (above) and internal iliac arteries, via the lateral sacral artery (see figure 1 above) The importance of iliac artery investigation cannot be overstated. The patient whose images are shown below underwent two spinal angiograms for investigation of suspected dural fistula, based on classic MRI appearance of cord congestion and serpiginous vessels in setting of progressive neurologic decline. Only on third time around was the left internal iliac artery interrogated, easily disclosing a dural fistula, supplied by a segmental artery (purple) and collateral probably dural artery (orange) with fistula point (red) and draining into a radicular vein (light blue) connected to the spinal venous network (above, not shown).

ANTERIOR SPINAL ARTERY (ASA): Cervical, thoracic, lumbar, and conus regions.

Overview: the anterior spinal artery (Q) develops as a longitudinal vessels connecting transversely oriented segmental arteries, as discussed at length above. It is located on the ventral surface of the cord, adjacent to the ventral median fissure of the spinal cord. It varies in size, more or less based on the amount of gray matter at the given segment. As such, its size is substantially larger in the cervical and lumbar segments (might be500-750 micrometersin diameter), as compared with slender mid-thoracic size. As such, one end of the ASA has limited to no capacity to support the other should its dominant radiculomedullary supply fail. The arterial supply to the ASA consists of radiculomedullary arteries (P), which represent persistence of embyronic segmental connections between the aorta and the developing ASA. Their number varies, perhaps being 6-10 in the human. Some are quite small and, as such, below resolution of in vivo spinal angiography. The larger cervical and lumbar ASA segments are associated with larger radiculomedullary arteries to supply them the famous artery of lumbar enlargement (Adamkiewicz), and the less well known (radiculomedullary) artery of the cervical enlargement, known to some neurovacular anatomists as the artery of Lazorthes. The Lazorthes most commonly arises from lower cervical vertebral artery, though not infrequently from deep cervical or supreme intercostal vessels also. The Adamkiewicz comes off between T9 and T12 in 75% of cases,more commonlyon the left (which means, to me, that 1/4 of the time, its somewhere else). Not infrequently, there are two relatively smaller radiculomedullary arteries at the lower thoracic spine, instead of one big Adamkiewicz. At the bottom of the cord, the anterior spinal atery is typically connected to posterior spinal arteries (T) via what paired arteries (Z) which go by many names (such as rami cruciantes), forming a kind ofarterial basket (see above diagram, and below for angio images). Visualization of this basket is critical if you wish to call a spinal angiogram complete.

Cervical ASA:

Bilateral vertebral artery study in anterior spinal artery supply. Sometimes, in intracranial work, it becomes important to know the location of the anterior spinal artery with respect to the cervical spine. For example, vertebral artery dissection may be treated differently depending on whether it involves ASA origin. Vertebral artery sacrifice should not be undertaken until the location of the ASA has been considered. For example, closing a vert immediately distal to radiculomedullary ASA contribution, without other runoff branches, risks possibility of the vert stump thrombosing back and closing this ASA segment. Collaterals are often insufficient to maintain cord viability.

Just seeing one radiculomedullary ASA contributor may not be enough in some cases to truly define full anatomy one must opacify the entire ASA system. If a given radiculomedullary artery only shows the ASA inferior to its level, then one must keep looking for additional rostral sourses. For example, if one sees an ASA from C5 down in a case where ascending or deep cervical embolization is required, it would be advisable to find the source of superior cervical supply before concluding that ASA territory is safe. In this case, the upper cervical cord segment is supplied from the left C5/6 level, while the inferior cervical cord from the right C4/5 segment.

Left vertebral (top) and right vertebral (bottom) set of images from the same patient, demonstrating full length of cervical anterior cerebral artery supply from the vertebral system. The lower portion of the cervical ASA (red, Q) is fed via the left C5/6 radiculomedullary contributor (yellow, P), which also happens to supply the posterior spinal artery network (purple, S, T). The upper ASA segment is fed by the right C4/5 radiculomedullary artery (yellow, P) seen on the image below. The radicular portion is labeled in yellow. ASA=red; Posterior spinal arteries = purple

Another view of cervical radiculomedullary artery (of Lazorthes) arising from inferior vertebral (C6 segment). This kind of dominant supply is seen less frequently for the cervical spinal cord than it is for the thoracolumbar enlargement in case of the artery of Adamkiewicz.

A, B Frontal and C lateral stereo pair projection digital subtraction and native angiographic views of right vertebral artery injection, visualizing a dominant cervical radiculomedullary artery (P, artery of Lazores) and the anterior spinal artery (Q), anastomosing with its basilar homolog (long white arrowhead). Very faint posterior spinal artery (T) is best seen in stereo, as well as the lateral spinal artery (short white arrow).

Another view of the cervical cord, this one also displaying the posterior spinal (brown) axis and the pial vessels (yellow) which connect the anterior and posterior axes on the pial surface of the cord. Visualizaton of the pial network of the thoracolumbar cord is limited by the body habitus of the patient, which works against resolving small vessels even under conditions of perfect paralysis and apnea. The situation is much better in the cervical spine. Notice the discontiguous nature of the posterior spinal network, in contrast to the straight anterior spinal artery.

Although balanced supply to the cervical cord is more common, and most of the time it comes from the cervical vert, occasionally the typically small distal intracranial vertebral artery supply is dominant, as in this case. It is important to pay attention to this when flow diversion methods are used in the distal vertebral artery.

Lateral view of the same, in stereo

Deep Cervical origin of the radiculomedullary artery second most common after the vert. At our institution, all cases of posterior fossa subarachnoid hemorrhage with no intracranial cause REQUIRE indentification of the anterior spinal artery, as in ~10% of cases (in-house experience) the pathology turns out to be in the cervical spine.

Anterior spinal artery (Q) origin from deep cervical artery, P= radiculomedullary artery; notice collateral opacification of the vertebral artery (long white arrow) via the C2 segmental artery (short white arrow).

Another deep cervical origin any longitudinal system can give origin to the radiculomedullary artery in this case the radiculomedullar artery (orange) originates from the deep cervical branch (red). Notice also injection of supreme intercostal artery (pink, lower two images)with extensive deep servical artery anastomoses (yellow) through which the anterior spinal artery can be inadvertently embolized. The catheter, barely engaged in the supreme intercostal,is labeled in blue.

Same patient, contralateral side, demonstrating tumor blush (hemangiopericytoma) from the right subclavian injection supplied by costocervical (purple) and thyrocervical (orange) branches. An ipsilateral supreme interconstal (red) injection demonstrates extensive additional tumor, which is not apparent from the subclavian injection. The vert is labeled in light blue.

Supreme Intercostal Origin of Cervical Spinal Artery occasionally seen as well, and important to know. The supreme intercostal and upper thoracic arteries can be difficult to catheterize sometimes, especially in patients with capacious dilated atherosclerotic aortas. We use a 4F or 5F RDC (which can be too small for the upper thoracic spine); if that does not work, one can try an appropriately-sized Cobra, or perhaps a Simmons 1. Sometimes, hand-shaping an RDC to produce a bigger curve (so as to push against the contralateral aortic wall) is more helpful than another catheter. In this case, the supereme intercostal was visualized via the T4 segmenal injection through a prominent paraspinal anastomosis (I)

stereo pair, supreme intercostal arteyr origin ofthe anterior spinal artery (same legends as above), visualized via T4 injection through a prominent post-transverse anastomosis (I). Notice transient contrast reflux into a cervical radiculomedullary branch (P); another longitudinal anastomosis (white arrow) between adjacent T3, T4, and T5 segmental arteries

Supreme intercostal artery (redP origin from the vertebral artery another example of homology between various longitudinal anastomoses. Notice multiple intercostal arteries (yellow)

Stereo pairs, demonstrating posterior course of the supreme intercostal artery at the level of dorsal ribs

Thoracic region: The artery of thoracic enlargement (Adamkiewicz) usually comes of T9 throughT12 region. There is often a region of thoracic cord (mid-lower, depending on the Adamkiewitz origin, which is rather small in caliber, relative to the more well-developed cervical region vessel. A watershed of sorts (yellow) therefore exists which occasionally may correspond to cord infarction in states of hypotension. This double catheter injection (done for evaluation of cord infarction in the region of the basket, below the watershed) demonstrates the slender size of mid-to-lower thoracic ASA. Red=ASA; Purple=radiculomedullary arteries

The artery of Adamkiewicz. Typical appearance. Another patient, with stereo views of the radiculomedullary artery.The radiculomedullary artery (pink) often demonstrates a small segment of narrowing at the point where itpierces the dura(white arrow). The intradural segment (blue) opacifies the anterior spinal artery (red). RDC (catheter) is labeled in green.

Radiculomedullopial artery. By definition, the radiculomedullary artery is a radicular artery which supplies the ASA (red). A radiculopial artery is one which supplies the pial (posterior spinal) system (yellow). When one does both (orange), it is called radiculomedullopial. So there

Figure 9 A-D: A early arterial, B late arterial, C native, and D venous phase images. The artery of Adamkiewicz (Ka), originating at left L1 level, opacifies the anterior spinal artery (Q). The force of contrast injection transiently reverses flow in a smaller radiculomedullary contributor (Ka) sephalad of the Adamkiewicz. A faint radiculopial artery (O) from contralateral right L1 level is visualized through the anterior epidural arcade (La). Notice subtle caliber change where the radiculopial artery pierces the dura (short black arrow). D- venous phase image demonstrating expected visualization of spinal vein (e, either anterior or posterior), and the Great Radicular Vein (j), the venous homolog of the Adamkiewicz.

The main contributor to the anterior spinal axis (Adamkiewicz, ) arises from the left T11 level. The tumor can still be embolized from the right T8 level as long as the Adamkiewicz can adequately reconstitute the anterior spinal axis at the level supplied by the right T8 segment. This can be determined by Balloon Test Occlusion of the right T8 radiculomedullary artery while injecting the level of the Adamkiewicz. The decision is made on angiographic basis as the patient is asleep and, in my opinion, the exam is too unreliable in the time span of the BTO. If the patient passes BTO, the right T8 radiculomedullary artery is closed (very tightly) with coils, and the tumor can then be embolized (particles). So, below is an injection of the left T11 Adamkiewicz (pink) with balloon inflated in the right T8 ventral division (black). Notice amazing visualization of the anterior spinal axis (white), with contrast reflux into the radiculomedullary arteries at the right T8 level (light blue) and left T10 levels (dark blue). Also extremely well seen are long contiguous segments of the posterior spinal artery on the right and somewhat shorter but still quite extensive for the posterior spinal system segment on the left (purple arrows), The PSAs are opacified via the well-seen vasocorona (pial) networks (green), retrogradely visualizing radiculopial contributing vessels (orange). The left T10 level supplies both anterior and posterior spinal arteries, and therefore would be technically radiculomedullopial.

This kind of anatomy is best seen in stereo:

Variant high origin of thoracic ASA. The Adamkiewicz can occasionally (25% of the time) come off unusually high or low. In these cases, there is often variation in terms of posterior cerebral artery anatomy as well. In this patient, a large Left T5 level radiculomedullary artery supplies the ASA (white) of entire thoracic spine. Patients like these are at a somewhat higher risk of cord infarction, having little in the way of collateral radiculomedullary ASA supply. An unusually prominent posterior spinal artery (red) is present also.

See the rest here:
Spinal Arterial Anatomy | neuroangio.org

Biochemistry Department: Graduate Program

The Biochemistry and Molecular Biology Graduate Program, which confers both M.S. and Ph.D. degrees, prepares graduate students for a career in science by expanding knowledge of biochemistry and molecular biology, and by developing the student's abilities in critical thought and creativity. The academic program emphasizes an in-depth study of the field with considerable flexibility to individually tailor course selection with regard to academic interests and area of specialization in the student's field of research.

A diversity of research programs is available for students. Areas of research specialization include molecular biology, physical biochemistry, molecular endocrinology, plant biochemistry and molecular biology, signal transduction, and biomedical research. Each program bestows a strong preparation for an academic research and teaching career, or a biochemical research career at both the pure and applied levels in private, governmental or industrial laboratories.

Students who have earned a bachelor's degree in physical, chemical, biological, or agricultural sciences at an accredited college or university are eligible to apply.

Students should prepare with the following courses prior to beginning graduate study in biochemistry:

See the article here:
Biochemistry Department: Graduate Program

American Physiological Society > Physiology – the APS

Physiology publishes invited review articles written by leaders in their fields. These articles are peer reviewed and highlight major advances in the broadly defined field of physiology. The journal also publishes shorter articles that either present important emerging topics and technologies or differing points of view. Finally, the journal highlights and briefly summarizes some of the most exciting new papers in physiology. With a new format that is both exciting and attractive, the journal is a valuable tool for researchers, educators, and students.

Read the rest here:
American Physiological Society > Physiology - the APS

Acland’s Video Atlas of Human Anatomy | Home

Acland's Video Atlas of Human Anatomy contains nearly 330 videos of real human anatomic specimens in their natural colors, including 5 new, groundbreaking videos of the inner ear. Dr. Robert Acland presents moving structuresmuscles, tendons, and jointsmaking the same movements that they make in life. The videos show complex structures step by stepfrom bone to surface anatomyto provide a foundation for understanding anatomical structure and function. The entire series was digitally re-mastered producing clearer, brighter, and more detailed videos than seen in previous versions.

Presents a 360-degree view of specimens accompanied by clear narration and labeled structures.

Ideal for preparation and review in human/gross anatomy courses and labs.

Searchable and accessible on all platforms and optimized for mobile devices.

See the original post:
Acland's Video Atlas of Human Anatomy | Home

Biochemistry 2017 | Dubai | UAE | Worldwide Events | Asia …

Session/Tracks

Conferences Series LLCinvites all the participants from all over the world to attend the 2ndInternational Conference onBiochemistry during September 28-29, 2017 at Dubai, UAE which includes prompt keynote presentations, Oral talks, Poster presentations and Exhibitions.

Biochemistryis a multidisciplinary field with research interests covering all aspects of modern molecular and cellular biochemistry. Biochemistry is often considered as a tool to investigate and to studymolecular biology. It deals with the structure, function and interactions amongst biological macromolecules.

The theme of the conference "Exploring the facets of Biochemistry", will focus on the study of the molecular mechanisms by which genetic information present on DNA is able to result in the processes of life.Biochemistryhas its applications in various fields. The findings of biochemistry are applied primarily in medicine, nutrition, and agriculture. In medicine, biochemists investigate the cause and cure for the disease.In nutrition, it leads to maintain health and effects of deficiency of nutrients. In agriculture, biochemists investigate soil and fertilizers, and try to discover ways to improve crop cultivation, storage and pest control.

For more conferences kindly go throughconference seriesweb page.

Track 1:Clinical Biochemistry

The fieldClinical biochemistryis the study of biochemical mechanisms in the body in relation to disease condition, through the testing of body fluids such as urine or blood or saliva. Many diseases tend to show significant changes in their chemical composition of body fluids like the increased levels ofblood enzymesdue to their release from heart muscles soon after a heart attack or also elevated blood sugar levels indiabetes mellitusthat occurs due to less or nil of insulin. Biochemical tests are aimed to detect these modifications either qualitatively or quantitatively in comparison to results from nutritious people. Clinical biochemistry uses a wide range of analytical techniques with its applications mostly inclinical chemistry, molecular biology, therapeutic drug monitoring, toxicology,laboratory immunology& medicine used for diagnosis, prognosis, therapy and management of disease.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 2:Structural Biochemistry

Structural Biochemistry is a sub-division ofbiochemistrythat mainly focuses on the structural characteristics of the molecules within cells and other made up of living organisms. The main area is focused on structural basis of fundamental biological processes. It involves the study of the structure of macro molecules. It includes methods for structure determination and huge data of structural information. Few of the tools will be used to study some class of structures such as membrane, regulatory proteins, structural proteins. These structuralmacromoleculeswill provide the framework for discussion on domains, motifs, structural homology, etc., as well as addressing as to how specific biological problems can be solved at the atomic level.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 3:Molecular Biochemistry

A major branch of Biochemistry deals with the varied aspects of macromolecules at the structural and functional levels. It also deals with the interactions amongst different cell components including macromolecules likenucleic acids, proteins, lipids, amino acids andcarbohydrates. Molecular Biochemistry has grown widely to capture the array of chemistry, physics, medicine and biology. It is one of the most important aspects of molecular biology to discover the chemical properties of the molecules. The processes that occur within the cell are responsible for their structure, reproduction and response to stimuli.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 4:Cell Signaling

Cell signalingis part of a complex system of communication that governs basic cellular activities and coordinates cell actions. The ability of cells to perceive and correctly respond to their microenvironment is the basis of development, tissue repair, and immunity as well as normal tissue homeostasis. Errors in cellular information processing are responsible for diseases such as cancer, autoimmunity, and diabetes. By understanding cell signaling, diseases may be treated effectively and, theoretically, artificial tissues may be created. The principle ofcell signalingis hinged on the fact that cellular communication frequently involves converting signals that carry information from one form to another. During cell communication, the signaling cell releases a particular signaling molecule that is then detected by the target cell. Most animal cells send and receive signals and as such act as both signaling and target cells. Animal cells can communicate through direct contact or by secreting local regulators such as growth factors or neurotransmitters.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 5:Analytical biochemistry

Analytical biochemistryis the study of biochemical components found in a cell or other biological sample. This scientific discipline uses a broad range of techniques for separation, identification, quantification and functional characterization ofbiological moleculeslike nucleic acids, enzymes, proteins, pigments, carbohydrates and more. The major methods involved in analytical biochemistry to separate the biological components are Spectroscopic techniques, Chromatographic Techniques, Protein Estimation & Purification Techniques and Immunological Techniques.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 6:Nutritional Biochemistry

Nutritional biochemistrymaintains with the perception of mechanism by which diet influences human health & disease condition. It mainly contributes with the properties of nutrients, other dietary substitutes & the study of their physiological, metabolic, biochemical &epigenetic functions. Nutritional biochemistry is a combined form of science as it incorporates physiology,pharmacology, medicine, biology, microbiology & chemistry & implements these sciences specifically to study of disease conditions, health, nutrition, & the connections that exist between them.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 7:Bioenergetics

Bioenergeticsis the part of biochemistry concerned with the energy involved in making and breaking of chemical bonds in the molecules found inbiological organisms. It can also be defined as the study of energy relationships and energy transformations in living organisms. It spans applications of structural biology, molecular modeling, spectroscopy and biophysics in these systems, throughbioenergeticaspects of mitochondrial biology including biomedicine aspects of energy metabolism in mitochondrial disorders, neurodegenerative diseases like Parkinson's and Alzheimer's, aging, diabetes and even cancer. Bioenergetics is at higher echelons that enhance the intelligence and information dissemination on topics closely related to study ofbiomembranes, molecular mechanism of photosynthesis, mitochondrial and bacterial respiration, motility and transport, fossil fuels,biothermodynamics, fish bioenergetics, environmental microbiology, bio process engineering, cellular respiration, mitochondrial disease, electronic coupling fluctuations, electron-transfer proteins, molecular recognition and signal transduction.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 8:Medical Biochemistry

Medical Biochemistryis that branch of medicine concerned with the biochemistry and metabolism of human health and disease. The medical biochemist is trained in the operation and management of clinicalbiochemistrylaboratories, and acts as a consultant in all aspects of their use. The medical biochemist directs clinical laboratories, consults, diagnoses and treats patients with a variety of metabolic disorders and biochemical abnormalities. Medical biochemistry addresses the functioning of normal and diseased organisms from a biochemical point of view. Through modules in neurodegeneration, cardiovascular disease andimmunology, one will develop a strong understanding of the implications of biochemistry within medicine alongside the research and experimental skills.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 9:Bioengineering

Bioengineeringis usually defined as the biological or medical application of engineering principles or engineering equipment to create modified versions of organisms or enhance the populations and products, it is also termed asbiomedical engineering. Bioengineering is implemented in fermentation industry, in production of biomass, biofuel. Through various r-DNA techniques and analytical techniques manybiomoleculesare produced and purified. Protein & Antibody Engineering is one of the recent branches in Bioengineering that has advanced throughBioprocessand Systems Engineering

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 10:Nano Biochemistry

The science of Nano scale structures deals with the investigation as well as utilization of components or systems that are 109times smaller than the standard size of components. Biochemistry deals with various metabolic andbiochemicalprocesses within the living creatures. Amalgamation of these two technologies resulted in beginning of Nano biochemistry. This interdisciplinary combination of nanotechnology & biochemistry can create numerous innovative tools. Application ofnanotechnologyto biological sciences indicates creation of materials and devices designed to interact within the body with high degree specificity. This could be possibly used to target cellular and tissue-specific clinical applications that are directed at maximal therapeutic effects with no adverse-effects. Nanotechnology Application to biomedical sciences will present many revolutionary chances in the fight against most sorts ofcancers,cardiac,neurodegenerative disorders, infection and diseases.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 11:Pharmaceutical Biochemistry

PharmaceuticalBiochemistry consist the knowledge of biochemistry & chemistry & applies to the production of many useful drugs.It mainly concerns with the science of drugs, their clinical uses and the study of their adverse effects on living organisms. It provides a complete understanding of all chemical processes occurring and associated with living cells at the molecular level that is related to drug action. It also helps to acquire knowledge on theadverse effects,molecular targets, & characterization of drugs or other chemical substance within the living cells & organisms.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 12:Inflammatory Diseases

Inflammation is the body's attempt at self-protection that aim to remove harmful stimuli, including damaged cells, irritants, pathogens begin the healing process. Researchers distinguish inflammation as a key component of the major diseases disturbing human health. Inflammation contributes todiseaseby damaging the tissues & it has advanced to protect. Apparently unrelated disorders such as asthma,Alzheimer, multiple sclerosis, inflammatory bowel diseases and rheumatoid arthritis all have common inflammatory features that underlie the disease process.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 13:Biochemistry of Multimolecular Complexes

Biological systems depend on multimolecular complexes to accomplish the tasks. While these complexes can be large and may comprise several tens of components, the present imaging techniques are limited to imaging only two or three independent components of amolecularcomplexthat can be 8-10 nm in diameter. Isolation of multimolecular complexes while retaining their supramolecular interactions has been critical to the study of mitochondrial respiratory supercomplexes.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 14:Systems Biology and Proteomics

The vital goal of a systemsbiologyapproach is to illustrate & predict the vigorous properties of the biological network. Whereas microarray data was most amenable for systems modeling, & ongoing advances in MS-based quantitative proteomics are yielding a developing number of datasets suitable for systems biology applications.Proteomicdatasets are obviously essential for building network models with precise predictive power.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Track 15:Cell Signaling, Kinase and Chemotherapy

Kinase-mediated signaling plays vital roles in cell growth, differentiation & homeostasis. Kinases signal by switching between on & off conformational states, and many inputs regulate the activity of all specific kinase. Abnormal kinase activity, frequently the result ofmutation, is associated with numerous cancers, and kinase inhibitors have become a highly successful and growing course of anti-cancer agents.Biochemistry2017 will focus on emerging insights into the molecular mechanisms by which kinase activity is regulated and how these insights are influencing strategies to target kinase activity in cancer.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

2ndInternationalConference on Biochemistry, Sep 28-29 2017, Dubai, UAE; InternationalConference on Enzymology, March 20-21, 2017 Rome, Italy; 8thInternational Conference andExhibition on Metabolomics, May 11-13, 2017 Singapore; 9thInternational Conference andExpo on Proteomics, October 23-25, 2017 Paris, France; 8thInternationalConference on ProteomicsandBioinformatics, May 22-24, 2017 Osaka, Japan; InternationalConference on BiochemistryandBiotechnology, Dec 24-25, 2017, Dubai UAE; InternationalConference on BiophysicsandBiochemistry, Nov 24-25, 2017, Dubai UAE; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Biochemical Society;Belgian Society of Biochemistry and Molecular Biology;American Society for Biochemistry and Molecular Biology;American Chemical Society - Division of Biological Chemistry.

Track 16:Medical Genetics

The science ofMedical Geneticsis concerned with the physical and chemical characteristics of genes and their expression that controls the development & maintenance of the organism.The field of medical genetics is quite new & currently used to describe the cause of severalinherited diseases. The disease typically results in generation of unreliable proteins such as in cases of hemophilia A then more than 200 'inborn errors' of metabolism are recognized in animals, disease conditions such as mannosidosis & galactosemia occur due to lack of a specific protein/enzyme that prohibits metabolism of carbohydrates, proteins, fats & thus shows clinical signs.

Relevant Biochemistry Conferences | Biochemistry Events | Biochemistry Meetings

3rdGlycobiology World Congress, June 26-28, 2017 London, UK; 2ndInternationalConference on Nucleic Acids, Molecular Biology & Biologics, August 31-September 01, 2017, Philadelphia, USA; 9thInternationalConference on Structural Biology, September 18-19, 2017 Zurich, Switzerland; 3rdInternationalConference on Transcriptomics, October 30 - November 01, 2017 Bangkok, Thailand; 9thInternationalConference on Bioinformatics, October 23-24, 2017 Paris, France; InternationalConference on Biochemistryand Microphotonics, Oct 17-18, 2017, Dubai UAE; InternationalConference on Microbial Biochemistry, Mar 29-30, 2017, Singapore, SG; InternationalConference on ChemistryandBiochemistry, Sep 28-29, 2018, New Delhi, India; InternationalConference on BiochemistryandMicrophotonics, Aug 24-25, 2018, Boston, USA; InternationalConference on Molecular ChemistryandBiochemistry, May 28-29, 2018, Tokyo, Japan;Croatian Society of Medical Biochemistry and Laboratory;Federation of European Biochemical Societies;International Union of Biochemistry and Molecular Biology.

Read the rest here:
Biochemistry 2017 | Dubai | UAE | Worldwide Events | Asia ...

Peer Reviewed Biochemistry Journals | Impact Factors Rankings

Biochemistry emphasis on the study of chemical processes occurring in the living organisms. It is the branch of science that helps to explore the various chemical processes occurring within and related to the living matter and studies these mechanisms by using chemical knowledge and techniques to understand and solve biological problems. Biochemistry deals with the structures, functions and interactions of biological macromolecules, such as proteins, nucleic acids, carbohydrates and lipids, which provide the structure of cells and perform many of the functions associated with life.

Link:
Peer Reviewed Biochemistry Journals | Impact Factors Rankings

Biochemistry – Macalester College

Biochemistry at Macalester

Students in the Biochemistry Program at Macalester receive a broad-based and robust grounding in the molecular structures and chemical reactions of biology.

Biochemistry students work alongside faculty with expertise spanning biology and chemistry, using state-of-the art equipment.

After graduation, biochemistry students have gone on to graduate study, medical school, and a variety of positions in industry.

Poster sessions bring together student and faculty researchers from various disciplines.

Here is the original post:
Biochemistry - Macalester College

Home | UIC Department of Biochemistry and Molecular Genetics

Welcome

The Department of Biochemistry and Molecular Genetics is one of five Basic Science Departments in the College of Medicine at UIC.

"During the last several decades there have been a series of dramatic advances in the way basic biomedical research is carried out. We are now able to produce large quantities of single proteins and determine their structures at atomic resolution, we can mutate these proteins and modify their properties... [ READ MORE + ]

Follow this link:
Home | UIC Department of Biochemistry and Molecular Genetics

Search neuroscience | Quizlet

Types of axoplasmic transport, what is

Antegrade

Retrograde (terminal to axon)

Localization of smell receptors

- Antegrade (orthograde)... - Retrograde

Fast: 400mm/day, metabolic imp. subst. , using ATP, done by k

175 mm/day. dynein action, viruses/toxins, endocytosis, trans

- olfactory epithelium 2,5mm2

Types of axoplasmic transport, what is

- Antegrade (orthograde)... - Retrograde

Antegrade

Fast: 400mm/day, metabolic imp. subst. , using ATP, done by k

Read the original post:
Search neuroscience | Quizlet