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UTeach Dallas Students Show They are Class Acts, Secure K-12 Jobs – University of Texas at Dallas

When the COVID-19 pandemic closed K-12 schools in North Texas, three University of Texas at Dallas seniors in the UTeach Dallas program took the initiative to help their mentor teachers in area school districts transition to online learning. Now each has been hired at the same school where they performed their student teaching.

Tommy Fabyan

Tommy Fabyan, who earned a bachelors degree in interdisciplinary studies and a mathematics certificate, will teach math at Trent Middle School in the Frisco Independent School District. Neuroscience senior Aaly Hussain has landed a job teaching science at Skyline High School in Dallas ISD, while David Le, who graduated with a Bachelor of Science degree in biology, will be a science teacher at North Garland High School in Garland ISD.

Students in the UTeach Dallas program earn undergraduate degrees, primarily in STEM fields science, technology, engineering and math concurrently with teacher training and certification.The program is housed in the Department of Science/Mathematics Education in the School of Natural Sciences and Mathematics.

Fabyan, Hussain and Le are among the 26 UTeach Dallas students who have graduated or will graduate this year by August. Four more students have been hired as teachers at Dallas, Houston and Amarillo schools. Two more have completed the Master of Arts in Teaching program and will go on to share their expertise with area students.

UTeach Dallas is the gift that keeps giving to the University, because our graduates are teaching STEM subjects to younger students in the area, many of whom will go on to enroll at UTDallas. Its a long-term investment that pays off.

Katie Donaldson, assistant director of UTeach Dallas

Many UTeach Dallas graduates receive multiple job offers because of their subject expertise and experience in the classroom, said Katie Donaldson, assistant director of UTeach Dallas and master teacher.

Were getting calls daily from employers. Our students have a deep, rich content knowledge coming in to professional teaching. We put them in schools their first semester, helping teachers with fourth- or fifth-grade science or math. Before they ever start their student teaching, they have had 18 to 20 hours in the classroom, Donaldson said.

All of them were student teaching when COVID-19 hit, she added. We told them to jump in and help their teachers wherever they could.

Fabyan had several challenges as he was completing his student teaching. His close-knit family had come to the U.S. from Ghana when he was 13. When his mother also a teacher had to undergo medical treatment last fall, Fabyan dropped out of student teaching to help care for her. After she stabilized, he returned to teaching this spring.

As the COVID-19 pandemic prompted teachers to transition completely to online learning for middle school math classes, Fabyan took charge of digital instruction for kids who did not respond particularly well to lectures. He set up Zoom tutorial sessions, videos and math games to target the areas where students needed help.

To get them even an inch closer to the aha! moment was amazing, Fabyan said.

He credited his mentor teacher for helping him overcome obstacles and even land a job at the school.

Being able to finally cross that finish line in my student teaching was really great. My mentor teacher has been my biggest cheerleader from the day I met her. She told me to invite the principal to watch me teach, so when it came to hiring someone, they already knew what I was capable of in the classroom, Fabyan said.

Aaly Hussain

At Skyline High School, Hussain was able to combine her love of the sciences and teaching, working with two different mentors to teach anatomy, physiology and pre-Advanced Placement chemistry. She decided to pursue teaching after working as a tutor in high school, where students told her she explained things nicely.

By the time COVID-19 hit, Hussain had already been using the online platform Google Classroom to upload assignments and videos that allowed students to do their projects online and receive feedback quickly.

It was perfect, Hussain said of the transition to online learning. I think its easier for my generation because we grew up with it. I had a good exchange with my mentors and set up Google pages for classes and internships.

Hussain, who is also a pre-med student, hopes to go to medical school and become a faculty member after gaining more teaching experience. The teaching aspect of it is what intrigues me, Hussain said.

David Le

Le, who will teach either chemistry or physics at North Garland High School this fall, also helped his mentors quickly formulate plans for online learning using interactive platforms to upload PowerPoint presentations, worksheets and videos with questions for students to answer.

When he learned he was going to be hired at the school, Le was thrilled and a little surprised. I slapped myself to see if I was awake, he said.

A first-generation college student, Le credited UTeach Dallas for stimulating his interest in STEM education. Being placed in a classroom early in his college career helped him realize that he enjoyed class preparation and interacting with students.

After being in the classroom, I was in love. UTeach pushed me when I needed it most. The energy and passion of the master teachers was out of this world. It was contagious, Le said.

Since 2008, UTeach Dallas has graduated almost 200 students with science or mathematics certification. All faculty instructors are award-winning master teachers with years of expertise.

UTeach Dallas is the gift that keeps giving to the University, because our graduates are teaching STEM subjects to younger students in the area, many of whom will go on to enroll at UTDallas. Its a long-term investment that pays off, Donaldson said.

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UTeach Dallas Students Show They are Class Acts, Secure K-12 Jobs - University of Texas at Dallas

What near-death experiences can tell scientists about how the brain works – Boing Boing

Floating out of your body and looking down on it. The story of your life flashing by before your eyes. Seeing a bright light at the end of a dark tunnel. These are just two of the most common experiences that people report after a near-death experience (NDE). For some people, NDEs are a transformative spiritual or mystical experience. But what's the source of the phenomena? That's a question that fascinates Dr. Christof Koch is president and chief scientist of the Allen Institute for Brain Science who studies the neuroscience of consciousness. In Scientific American, Koch surveys the science of near-death experiences and what they can tell us about how our brains work under extreme duress. From Scientific American:

Modern death requires irreversible loss of brain function. When the brain is starved of blood flow (ischemia) and oxygen (anoxia), the patient faints in a fraction of a minute and his or her electroencephalogram, or EEG, becomes isoelectricin other words, flat. This implies that large-scale, spatially distributed electrical activity within the cortex, the outermost layer of the brain, has broken down. Like a town that loses power one neighborhood at a time, local regions of the brain go offline one after another. The mind, whose substrate is whichever neurons remain capable of generating electrical activity, does what it always does: it tells a story shaped by the persons experience, memory and cultural expectations.

Given these power outages, this experience may produce the rather strange and idiosyncratic stories that make up the corpus of NDE reports. To the person undergoing it, the NDE is as real as anything the mind produces during normal waking. When the entire brain has shut down because of complete power loss, the mind is extinguished, along with consciousness. If and when oxygen and blood flow are restored, the brain boots up, and the narrative flow of experience resumes.[...]

Why the mind should experience the struggle to sustain its operations in the face of loss of blood flow and oxygen as positive and blissful rather than as panic-inducing remains mysterious. It is intriguing, though, that the outer limit of the spectrum of human experience encompasses other occasions in which reduced oxygen causes pleasurable feelings of jauntiness, light-headedness and heightened arousaldeepwater diving, high-altitude climbing, flying, the choking or fainting game, and sexual asphyxiation.

"What Near-Death Experiences Reveal about the Brain" (SciAm)

image: detail of "Ascent of the Blessed" by Hieronymus Bosch

Repeating the word fuck actually can reduce your experience of pain, according to a new study by Keele University researchers. The psychologists ran an experiment in which subjects underwent a cold pressor test, a common method to pain threshold and tolerance by immersing your hand in freezing cold water for a minute. (See above video []

I enjoy the fun science stunts on ScienceBobs YouTube Channel.

The Lancet says Trumps letter contains factually incorrect details.

Weve all been cooped up in the house for way too long. Even though were all trying to be more health-conscious these days, the confinement is likely doing a number on both the physical and psychological health of millions. Young or old, male or female, its time for many to take some proactive steps toward []

At some point in the future, global communications networks will likely reach one standardized protocol that everyone uses. If you look back over the past few decades, theres a decent chance that when the story of digital networking is finally settled once and for all, its Cisco and Cisco-based systems that the globe will be []

Weve all grown accustomed to the new world order. And until we can go out and experience the world again like we used to, well settle for the next best thing: bringing the world to our door. And if ever there was a time for wine (and lots of it), its now. So even if []

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What near-death experiences can tell scientists about how the brain works - Boing Boing

DNA May Not Be the Blueprint for Life Just a Scrambled List of Ingredients – SciTechDaily

DNA may not be lifes instruction book, but just a jumbled list of ingredients.

University of Maryland researcher develops potentially revolutionary framework for heredity and evolution in which inheritable information is stored outside the genome.

The common view of heredity is that all information passed down from one generation to the next is stored in an organisms DNA. But Antony Jose, associate professor of cell biology and molecular genetics at the University of Maryland, disagrees.

In two new papers, Jose argues that DNA is just the ingredient list, not the set of instructions used to build and maintain a living organism. The instructions, he says, are much more complicated, and theyre stored in the molecules that regulate a cells DNA and other functioning systems.

Jose outlined a new theoretical framework for heredity, which was developed through 20 years of research on genetics and epigenetics, in peer-reviewed papers in the Journal of the Royal Society Interface and the journal BioEssays. Both papers were published on April 22, 2020.

Joses argument suggests that scientists may be overlooking important avenues for studying and treating hereditary diseases, and current beliefs about evolution may be overly focused on the role of the genome, which contains all of an organisms DNA.

DNA cannot be seen as the blueprint for life, Jose said. It is at best an overlapping and potentially scrambled list of ingredients that is used differently by different cells at different times.

For example, the gene for eye color exists in every cell of the body, but the process that produces the protein for eye color only occurs during a specific stage of development and only in the cells that constitute the colored portion of the eyes. That information is not stored in the DNA.

In addition, scientists are unable to determine the complex shape of an organ such as an eye, or that a creature will have eyes at all, by reading the creatures DNA. These fundamental aspects of anatomy are dictated by something outside of the DNA.

Jose argues that these aspects of development, which enable a fertilized egg to grow from a single cell into a complex organism, must be seen as an integral part of heredity. Joses new framework recasts heredity as a complex, networked information system in which all the regulatory molecules that help the cell to function can constitute a store of hereditary information.

Michael Levin, a professor of biology and director of the Tufts Center for Regenerative and Developmental Biology and the Allen Discovery Center at Tufts University, believes Joses approach could help answer many questions not addressed by the current genome-centric view of biology. Levin was not involved with either of the published papers.

Understanding the transmission, storage and encoding of biological information is a critical goal, not only for basic science but also for transformative advances in regenerative medicine, Levin said. In these two papers, Antony Jose masterfully applies a computer science approach to provide an overview and a quantitative analysis of possible molecular dynamics that could serve as a medium for heritable information.

Jose proposes that instructions not coded in the DNA are contained in the arrangement of the molecules within cells and their interactions with one another. This arrangement of molecules is preserved and passed down from one generation to the next.

In his papers, Joses framework recasts inheritance as the combined effects of three components: entities, sensors and properties.

Entities include the genome and all the other molecules within a cell that are needed to build an organism. Entities can change over time, but they are recreated with their original structure, arrangement and interactions at the start of each generation.

That aspect of heredity, that the arrangement of molecules is similar across generations, is deeply underappreciated, and it leads to all sorts of misunderstandings of how heredity works, Jose said.

Sensors are specific entities that interact with and respond to other entities or to their environment. Sensors respond to certain properties, such as the arrangement of a molecule, its concentration in the cell or its proximity to another molecule.

Together, entities, sensors and properties enable a living organism to sense or know things about itself and its environment. Some of this knowledge is used along with the genome in every generation to build an organism.

This framework is built on years of experimental research in many labs, including ours, on epigenetics and multi-generational gene silencing combined with our growing interest in theoretical biology, Jose said. Given how two people who contract the same disease do not necessarily show the same symptoms, we really need to understand all the places where two people can be differentnot just their genomes.

The folly of maintaining a genome-centric view of heredity, according to Jose, is that scientists may be missing opportunities to combat heritable diseases and to understand the secrets of evolution.

In medicine, for instance, research into why hereditary diseases affect individuals differently focuses on genetic differences and on chemical or physical differences in entities. But this new framework suggests researchers should be looking for non-genetic differences in the cells of individuals with hereditary diseases, such as the arrangement of molecules and their interactions. Scientists dont currently have methods to measure some of these things, so this work points to potentially important new avenues for research.

In evolution, Joses framework suggests that organisms could evolve through changes in the arrangement of molecules without changes in their DNA sequence. And in conservation science, this work suggests that attempts to preserve endangered species through DNA banks alone are missing critical information stored in non-DNA molecules.

Jose acknowledged that there will be much debate about these ideas, and experiments are needed to test his hypotheses. But, he said, preliminary feedback from scientists like Levin and other colleagues has been positive.

Antony Joses generalization of memory and encoding via the entity-sensor-property framework sheds novel insights into evolution and biological complexity and suggests important revisions to existing paradigms in genetics, epigenetics and development, Levin said.

###

References:

A framework for parsing heritable information by Antony M. Jose, 22 April 2020, Journal of the Royal Society Interface.DOI: 10.1098/rsif.2020.0154

Heritable Epigenetic Changes Alter Transgenerational Waveforms Maintained by Cycling Stores of Information by Antony M. Jose, 22 April 2020, BioEssays.DOI: 10.1002/bies.201900254

Research in Antony Joses laboratory is supported by the National Institutes of Health (Award Nos. R01GM111457 and R01GM124356). The content of this article does not necessarily reflect the view of this organization.

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DNA May Not Be the Blueprint for Life Just a Scrambled List of Ingredients - SciTechDaily

Watch Out Why Life Science Reagent Market Thriving Worldwide over the Forecasted Period 2020-2027 | Trends, Scope, Segmentation, Competitors Analysis,…

Life Science Reagent Market is analyzed with industry experts in mind to maximize return on investment by providing clear information needed for informed business decisions. This research will help both established and new entrants to identify and analyze market needs, market size, and competition. It explains the supply and demand situation, the competitive scenario, and the challenges for market growth, market opportunities, and the threats faced by key players.

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Nikon Instruments Announces Judging Panel For The 46th Nikon Small World Competition – PRNewswire

Dylan Burnette, Ph.D., Assistant Professor of Cell and Developmental Biology at Vanderbilt University, Christophe Leterrier, Ph.D., group leader at CNRS and Aix-Marseille University, Samantha Clarke, Photo Editor at National Geographic, Sean Greene, Data and Science journalist at The Los Angeles Times, and Ariel Waldman, Antarctic explorer and NASA advisor will make up the 2020 judging panel choosing this year's winning imagery.

For 46 years, Nikon Small World has been recognized as a leading forum to celebrate excellency in microscopy in the form of photos and videos. The competition will honor the top 20 photography and top 5 video winners in addition to awarding Honorable Mentions and Images of Distinction. Winning submissions will be recognized for their exceptional ability to capture visually stunning and scientifically significant moments under the microscope. To celebrate the 10th anniversary of Nikon Small World in Motion, this year's top prize winners of both the video and photo competitions will receive a trip to Japan for themselves and a loved one in addition to the yearly cash prize.

From its beginning, Nikon Small World has aimed to share science, the unseen world, and artistic accomplishments in a vast range of scientific and artistic disciplines with the public at large. Recent past winners have ranged from a turtle embryo to flowers, to frozen water, amino acids, and espresso beans.

The meticulously selected expert judging panel are instrumental in selecting the images and videos that best blend science and artistry. Meet this year's panel:

"Nikon Small World strives to educate, entertain, and share stunning visuals and scientific discoveries with the world at large," said Eric Flem, Communications Manager at Nikon Instruments. "While this year is no doubt different because we are judging remotely, we're excited to come together with an impressive panel of judges whose expertise in art, science, and visualizations will guide us in picking the best microscopy the science community has to offer."

The Nikon Small World in Motion video winners and the winners of the Small World photomicrography competition will be released in the Fall.

For additional information, please visit http://www.nikonsmallworld.com. To get an inside look at the judging process and experience, follow the hashtag #NikonSmallWorld and conversation on Facebook, Twitter (@NikonSmallWorld) and Instagram (@nikoninstruments).

About Nikon Small World Photomicrography CompetitionThe Nikon Small World Photomicrography Competition is open to anyone with an interest in photography or video. Participants may get details and upload digital images and videos directly at http://www.nikonsmallworld.com. For additional information, contact Nikon Small World, Nikon Instruments Inc., 1300 Walt Whitman Road, Melville, NY 11747, USA, or email us at [emailprotected]

About Nikon Instruments Inc. Nikon Instruments Inc. is the US microscopy arm of Nikon Healthcare, a world leader in the development and manufacture of optical and digital imaging technology for biomedical applications. For more information, visit https://www.microscope.healthcare.nikon.com/ or contact us at 1-800-52-NIKON.

SOURCE Nikon Instruments Inc.

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Lab Mice Shed Fat and Build Muscle with Gene Therapy – The Great Courses Daily News

By Jonny Lupsha, News Writer

According to the Fierce Biotech article, the mice who underwent the new gene therapy were injected with a gene that makes the protein follistatin, which in turn blocks a protein called myostatin. Myostatin regulates muscle growth. The therapy caused a significant buildup of muscle mass in the mice while also preventing obesity, the article said. The mice didnt just build muscle; they also nearly doubled their strength without exercising any more than they usually did. Despite being fed a high-fat diet, they had fewer metabolic issues and stronger hearts than did animals that did not receive the follistatin gene.

Scientists have been developing gene therapy for many years. It can change our bodies in many ways, and has potential serving as a treatment for cancer and muscular dystrophy.

The procedure that the mice underwent encapsulates what gene therapy isalthough scientists generally focus on people.

I define [gene therapy] as the addition of genes to humans for medical purposes, said Dr. David Sadava, Adjunct Professor of Cancer Cell Biology at the City of Hope Medical Center.

Dr. Sadava said gene therapy is based on four assumptions. First, whoever is doing the gene therapy has to know the gene thats involved in whichever problem needs to be treated. Second, they must have a normal, healthy copy of that gene available in the lab. Third, they must know where and when the gene is normally expressed. Finally, they have to be fairly certain what will happen when the gene is expressed normally.

Additionally, gene therapy must do several things in order to be considered successful.

First, gene therapy must get the gene into the appropriate cells, Dr. Sadava said. Second, gene therapy must get the gene expressed in those cells. Third, we have to get the gene integrated into the genome of the target cells so itll be there permanently. And fourth, you better not have any bad side effects to gene therapy, like any therapy in medicine.

According to Dr. Sadava, one kind of gene therapy is referred to as gene augmentation, and it comes into play when the functional product of a gene has been lost and no longer gets produced normally. By injecting a gene into someone, healthy copies of a protein product will be made and function restored.

We could hypothetically think of muscular dystrophy as a good target for gene therapy, he said. We know that muscles lack the protein dystrophinits an organizing proteinso well put in the good gene for good dystrophin.

Another kind of gene therapy is called target cell killing. Dr. Sadava said it uses a gene that either produces a poison that kills certain types of cells or it stimulates the immune system to do so. Target cell killing can be applied to cancer.

A gene is put into cancer cells that allows them to produce a protein that will make a toxic drug from a harmless chemical, Dr. Sadava said. So the idea is we inject a harmless chemical into the body, it goes all over the body and when it enters a tumor cell, its converted into a poison by the gene product of the gene that weve put in for gene therapy. So we might put in a gene that will cause a protein to be made that attracts killer T cells so the tumor will stick up its hand and say Come kill me now.'

Gene therapy is an exciting field in science and medicine with a lot of potential for humans. For now, it may seem like its just helping some overweight mice get a confidence boost, but the practical applications should shore up within our lifetime.

Dr. David Sadava contributed to this article. Dr. Sadava is Adjunct Professor of Cancer Cell Biology at the City of Hope Medical Center in Duarte, CA, and the Pritzker Family Foundation Professor of Biology, Emeritus, at The Claremont Colleges. Professor Sadava graduated from Carleton University with a B.S. with first-class honors in biology and chemistry. He earned a Ph.D. in Biology from the University of California, San Diego.

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Distribution of human tumor mutations more similar to that of chimpanzees, gorillas – News-Medical.net

Reviewed by Emily Henderson, B.Sc.May 21 2020

A new study by researchers from the Institute of Evolutionary Biology (IBE), a joint center of UPF and the Spanish National Research Council (CSIC), shows that, surprisingly, the distribution of mutations in human tumors is more similar to that of chimpanzees and gorillas than that of humans.

The article, which analyses cancer from the evolutionary point of view, is published today, 19 May, in Nature Communications. It was led by Arcadi Navarro and David Juan and involved the researchers Txema Heredia-Genestar and Toms Marqus-Bonet.

Mutations are changes that occur in DNA. They are not distributed throughout the genome evenly, but some regions accumulate more and others less. Although mutations are common in healthy human cells, cancer cells display a greater number of genetic changes. During the development of cancer, tumors rapidly accumulate a large number of mutations. In previous studies, however, it had been observed that surprisingly tumors accumulate mutations in very different regions of the genome from those normally observed in humans.

Now, thanks to the data from the project PanCancer, a research team from the IBE has compared the regions of the genome that accumulate more and less mutations in tumor processes, in the recent history of the human population, and in the history of other primates. The results of this new study reveal that the distribution of mutations in tumors is more like that in chimpanzees and gorillas than in humans.

To date, it was thought that the genetic differences we find when we compare tumors and healthy humans could be caused by the 'abnormal' way tumors have of accumulating mutations. In fact, we know that tumors rapidly accumulate a large number of mutations and that many of their genome repair mechanisms do not work well. But now, we have discovered that many of these genetic differences have to do with our evolutionary history".

Txema Heredia-Genestar, first author of the study who recently completed his Ph.D. at the IBE

When an individual's genome is sequenced, it is observed to have a small number of new mutations -- some 60-- compared to their parents, those of their parents with respect to their grandparents, and so on with each previous generation. Therefore, in a person, approximately three million mutations can be seen that represent the evolutionary history of the mutations accumulated over hundreds of thousands of years. Of these, a few are recent and most are very old.

However, when tumor mutations are analyzed, what is seen are just the mutations that have taken place during the tumor process, since the analysis does not take into account the information on populational history.

"We have seen that the distribution of mutations in the human genome is skewed because of human evolutionary history", Heredia-Genestar details. The manner in which a tumor accumulates mutations is the same as a human cell has of accumulating mutations. "But, we do not see this in the human genome because we have had such a complicated history that has made our distributions of mutations change, and this has deleted the signals we should have", he adds.

Throughout history, the human population has suffered drastic declines and has even repeatedly been on the verge of extinction. This phenomenon is known as a bottleneck, and it causes humans as a species to have very little diversity and fewer mutations: they are very similar to each other. In fact, chimpanzees are four times more genetically diverse than humans.

Therefore, the global way for a cell to accumulate mutations can be observed in chimpanzees because they have not undergone these population events. The study concludes that to understand how mutations accumulate in human cells, which is important for studying tumors, it is more useful to look at how they accumulate in other primates rather than looking at it in human populations , whose signal was destroyed by population events.

"Cancers, like chimpanzees and gorillas, only show the complete mutation landscape of a normal human cell. It is we humans, with our turbulent distant past, who display a distorted distribution of mutations", adds Arcadi Navarro, ICREA research professor at the IBE, full professor at UPF and co-leader of the study.

The research suggests that the conservation and study of the great apes could be highly relevant to understanding human health. David Juan, co-leader of the study, concludes that "in the particular case of the development of tumors, other primates have proved to be a better model for understanding how tumors develop at genetic level than humans themselves. In the future, our closest relatives could shed light on many other human diseases".

Source:

Journal reference:

Heredia-Genestar, J.M., et al. (2020) Extreme differences between human germline and tumor mutation densities are driven by ancestral human-specific deviations. Nature Communications. doi.org/10.1038/s41467-020-16296-4.

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New analytic tool designed to help guide precision oncology discovery and treatments – Newswise

Newswise ANN ARBOR, Michigan Recent large-scale efforts to categorize the molecular data of multiple cancer types has yielded so much information that researchers now have a new question: How to turn all this data into meaningful information that guides cancer research and patient care.

A new analytic tool developed by University of Michigan Rogel Cancer Center researchers combines multiple data sets to help sift the signal from the noise.

Our idea was to combine three sources of data sets molecular data from both cancer cell lines and patients and drug profiling data to understand proper preclinical models that are most representative of these tumors, says Veerabhadran Baladandayuthapani, Ph.D., professor of biostatistics at the University of Michigan School of Public Health and senior author of a paper published in the Journal of Clinical Oncology Clinical Cancer Informatics that describes this new tool.

The tool, called TransPRECISE, uses data from 7,714 patient samples across 31 cancer types, collected as part of the Cancer Proteome Atlas. This is combined with 640 cancer cell lines from the MD Anderson Cell Lines Project and drug sensitivity data representing 481 drugs from the Genomics of Drug Sensitivity in Cancer model system.

The good thing is this is a very dynamic process. We can have this whole system set up in a computer. As new patients come in or new data comes in, you can keep adding it, says Rupam Bhattacharrya, M.Stat., a doctoral student and first author on the paper.

The tool builds on an earlier model the team had created, which they called PRECISE. With an eye toward precision medicine, they created a model to look at what changes occur to the molecular structure of individual patients individual tumors. TransPRECISE adds in data from cell lines and drug sensitivity, which will be helpful for researchers translating cancer cell biology into drug discovery.

Now that we have tens of thousands of tumors on these patients we can evaluate what might be the potential therapeutic efficiency of these drugs. The key idea was to develop an analytic tool to do that, says Baladandayuthapani, who is also director of the Rogel Cancer Centers cancer data science shared resource.

In the JCO Clinical Cancer Informatics paper, researchers validated the tool by comparing known drug responses and clinical outcomes in patient data. TransPRECISE identified the differences in proteins among individual tumors and accurately tied it back to actual patient outcomes. In addition, they looked at several pathways to predict potential drug targets. This yielded results that mirrored current treatment recommendations or targets being tested in clinical trials, such as ibruutinib for BRCA-positive breast cancer, and lapatinib for colon cancer.

We have so much data, how do we drill it down to make it more informative so an oncologist can understand? Our work would potentially help oncologists or researchers develop concrete hypotheses based on which mechanism is working, potentially bringing to the top drugs that might warrant more evaluation, Baladandayuthapani says.

The researchers have made publicly available a comprehensive database and visualization of the findings at https://bayesrx.shinyapps.io/TransPRECISE.

Additional authors: Min Jin Ha, Qingzhi Liu, Rehan Akbani, Han Liang

Funding: National Institutes of Health grants R21 CA220299-01A1, U54 CA224065, 3P50 CA070907-20S1, R01 CA160736, R01 CA194391, P30 CA46592, R01 CA1745486, U24 CA209851, U01 CA217842, P30 CA016672; Leukemia and Lymphoma Society, Cancer Prevention and Research Institute of Texas, National Science Foundation, University of Michigan Rogel Cancer Center, University of Michigan School of Public Health

Disclosure: None

Reference: Journal of Clinical Oncology Clinical Cancer Informatics, doi:10.1200/CCI.19.00140, published May 6, 2020

Resources:

University of Michigan Rogel Cancer Center, http://www.rogelcancercenter.org

Michigan Health Lab, http://www.MichiganHealthLab.org

Michigan Medicine Cancer AnswerLine, 800-865-1125

# # #

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New analytic tool designed to help guide precision oncology discovery and treatments - Newswise

The Anatomy Of A Thunderstorm – WTHITV.com

TERRE HAUTE, Ind. (WTHI) -The warm months across the Midwest bring a common sightthunderstorms.

Since we all like to get outside when the temperature gets warmer, we need to know how to spot a thunderstorm.

These are usually formed with big clouds.

At the front of the storm, on the bottom, you may see what we call a shelf cloud.

It sticks out from the bottom of the storm, as one long cloud.

On the front part of the storm at the top is what we call the mammatus.

This looks like a much bigger shelf angling out ahead of the top of the storm.

After a storm passes through, the back side has some specific characteristics as well.

On the bottom is what looks like the shelf cloud, except it is more compact.

This is what we call the wall cloud.

The wall cloud can also be the start of a tornado developing.

On the back side of the storm is called the flanking line.

This is what we see as the storm goes away, and these clouds look more scattered out, and not as full.

Finally the last two parts may be the most important.

This first line is called a spiraling updraft.

This is the warm air that fuels the storm.

Once it makes it to the top of the storm, we get a downdraft.

This is where wind, hail, and rain are formed as they make their way to the ground.

Now something else we usually associate with a thunderstorm is lightning.

So next time Ill be talking about heat lightning, and whether or not its actually real.

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The Anatomy Of A Thunderstorm - WTHITV.com

Anatomy of a Book – The New Yorker

In D. W. Youngs lighthearted, lexical short film A Body of Language, a bookdealer shows off one of the antiquarian book worlds favorite prints: a caricature of a bedraggled, elderly bibliophile standing in a muddle of books, as if he has risen from them. His hair is slightly mussed, eyes obscured behind spectacles, and he wears a suit with a pocket square. Titled Anatomy of an Antiquarian Bookseller, the posters provenance makes it something that dealers of rare tomes especially appreciate: only fifty lithographs of the design, by the artist Ronald Searle, were produced, as a commission for the centenary of a Scottish book-trading firm. Searle labelled the portrait with terms drawn from the vernacular of book-dealing that apply equally to the settling and slumping of a body, which, once in fine condition, is now merely fair: dog-eared; mottled calf; joints badly worn; spine cracked.

The obscure and fanciful language of the book worldparticularly the bodily lingois the focus of the above film, and the two dozen or so booksellers interviewed on camera describe with relish their favorite terms. I love the words, one dealer says. The way that they resonate within a kind of closed system is so beautiful, and the way that they relate to humansthe head of the spine, the foot of the spine, the spine. Dentelles, another tells us, as he ever so gently traces a finger down a frilly gilt border, is the name for the golden edging on the inside of a cover; the word is drawn from the French dentelle, which means lace, and which itself comes from the Middle French for little tooth.

It is often fascinating to hear experts discuss their craft, because the demonstration of extreme competence and precision is powerfully appealing: there is a name for every part and every production method, and particularly for every malady. The specialized language is all in the service of diagnosis and correction. When a book has been read too much or loved too roughly, its thumb-soiled (deliciously icky-sounding). If the spine tilts just a bit to the side, its slightly cocked. (A little juvenile, dont you think? one book dealer exclaims.) When paper is browning from age or moisture, its foxed. Some things sound bad but are not so: stab holes might show that a book has been bound from side-stitched installments that were published separately. And that mottled calf from the poster isnt a sign of decayits only the name for a method of using dribbles of acid to make young leather look more interesting. Accordingly, and comfortingly, the language of cures for booky ills is also expansive. The film tells us about wormholes in the binding, showing spines chawed to dust by pests, but it also reassures us about the existence of rembotage: the procedure for swapping covers if you have one volume with marvellous innards but a ragged cover, and another that is gorgeously packaged but drab inside. And a look through the ABC for Book Collectorsthe antiquarians bible, compiled by John Carter and Nicolas Barkerreveals that, while books can be chipped, creased, tired, and disbound, they can also be re-cased, pressed, re-hinged, and guarded. (If only healing the cockled or faded body were so easy.)

If all professions are conspiracies against the laityas one bookseller jokes, quoting George Bernard Shawthen sometimes the rest of us want to be in the congregation, guided by someone who can offer us the language to describe our parts. The professionals, positively glowing with their expertise, reassure us that someone has already seen and recognized the details, and has a word for the state of things and how they are likely to change over time. Whats more, someone has already devised a fix for our troubles. Searles scribbly and just a bit soiled librarian does not need to be a rare survivalan astonishingly well-preserved and scarce piece. His appeal comes from his dictionary of imperfections, and because the cataloguing of exacting terms is its own kind of delight.

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Anatomy of a Book - The New Yorker