Category Archives: Genetics

You and Your Doppelganger Might Have More in Common Than Just Looks – Gizmodo

Some of the lookalike pairs who were studied in the current research.Photo: Joshi, et al/Cell Reports

It turns out that unrelated doppelgangers may have quite a bit in common beyond just twin faces. New research suggests that lookalikes with incredibly similar faces tend to share many genetic variantsvariants that dont just seem to shape their appearance but general aspects of their life. At the same time, other important influences, such as the microbiome, appear to contribute little to their symmetry.

Study author Manel Esteller, a geneticist and director of the Josep Carreras Leukemia Research Institute (IJC) in Barcelona, Spain, is interested in what makes people the way they are. In 2005, he and his colleagues published research showing that identical twins werent as identical as they appear at first glance. While they had the same basic genetic patterns, they differed noticeably in their epigenetics: changes in how our genes express themselves, which are caused by environmental or behavioral factors, such as smoking or age.

In their new research, published Tuesday in Cell Reports, Estellers team wanted to look at the other side of the coinpeople who look so similar that they could be twins but arent actually related. To do this, they turned to the work of Canadian photographer Franois Brunelle, who has been documenting doppelgangers around the world as a long-running project. With his help, they were able to get in touch with 32 pairs of lookalikes who were willing to offer their time and a spit sample so that the researchers could take a peek at their DNA and other inner workings, such as the community of microbes living in their mouth.

Brunelles project relies on a subjective interpretation of peoples similarity. So to find the most identical non-identical people, Estellers team ran peoples photos through three different facial algorithms. Out of the original 32, 16 pairs were deemed to completely match by all three programs, and the researchers focused the bulk of their study on them.

In general, these pairs shared many single nucleotide polymorphisms (SNPs), which are the most common type of genetic variation in humans. Nine of the 16 were so genetically in-sync that they were considered ultra lookalikes. By contrast, however, the pairs epigenetics and oral microbiomes had relatively little in common.

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The results were that these lookalike humans had similar genetic sequences and are therefore like virtual twins, while their epigenetic and microorganism flora profiles differentiate them, Esteller said in an email to Gizmodo. Interestingly, he added, this genetic similarity didnt stop at facial appearance. Compared to non-lookalike pairs, for instance, doppelgangers were more likely to have similar levels of education, height, weight, and even smoking history.

The researchers took pains to make sure that the doppelgangers werent unknowingly closely related. While the pairs did tend to share the same country of origin or self-described ethnic background, they werent any more related to each other than pairs randomly selected from the same population, the team determined. Only one pair was suspected to possibly have had a common ancestor in the last several hundred years, while some pairs were living on wholly different continents.

Thus, we think that the generation of some genetic similarities between these couples occurred by random chance, Esteller said. There are so many people on the planet that the system is repeating itselfthe combinations of the genome are no longer infinite.

It may make sense that facial doppelgangers would have many genetic similarities, but the findings could offer new insights on the ever-running debate of nature versus nurture, Esteller noted. While our genetics seem to play a leading role in shaping our face and other aspects of who we are, both this study and Estellers earlier work indicates that genes arent the be-all, end-all.

Thus, nature is very strong, but nurture tunes up the genome a little bit, he said.

There may be other far-reaching implications of this and similar research. If its true that our genes are so influential to facial appearance, then it could very well be possible to someday accurately reconstruct the unknown face of a criminal though DNA left at a crime scene, the team argues. Health-wise, it could also be possible that a persons face would be able to provide clues about their genetics, including the presence of high-risk variants for diseases like diabetes or dementia.

These are two goals that Esteller and his team are interested in pursuing further. They also hope to expand their project to document more lookalikes and to study other factors that influence our lives, such as the transcriptome (how our RNA is expressed) and the proteome (the proteins that our cells actually make based on their genetic instructions).

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You and Your Doppelganger Might Have More in Common Than Just Looks - Gizmodo

Genetics May Play a Role in Taste Preferences, Study Finds – Prevention Magazine

Whether youre someone who adds hot sauce to everything you eat or someone who requests mild sauce on the side, its clear that we all have different taste preferences. And though its frustrating when you have to tame a dish for a dinner guest or request a not-so-spicy option when ordering at a restaurant, new research may explain our taste preferences. The reason people love certain foods and dislike others is based off of than your culture, taste buds, or exposure to food as a childscience says its actually linked to our genetics.

The study, published in the journal Nature Communications, discovered hundreds of genetic variations that are linked to specific foods, including ones that can make you like or dislike foods like oily fish, avocados, chiles, and more.

In the large genetic study of food preferences, researchers from the University of Edinburgh looked at responses from more than 160,000 participants from the UK Biobank about the likes and dislikes of 139 different foods and beverages using a nine-point scale. Participants responded to questionnaires and researchers used genetic information to find if food groups or flavors were influenced by specific genetic traits.

Scientists found 401 genetic variations, many of which impacted multiple food-liking or disliking traits. Based on the results, the researchers created a food map that outlined three clusters of food tied to genetics: highly palatable, low caloric, and acquired foods.

These include genetic components that made people lean toward high-calorie (highly palatable) foods, like meat, dairy, and sweets. Another genetic component was linked to those who liked strong-tasting foods (acquired ) like alcohol and pungent vegetables. The third group of genetics is linked to people who are drawn to fruits and vegetables (low caloric).

Researchers noted that those who had genetics tying them to one category of food also shared genetics for specific health traits. For example, people who typically enjoyed highly palatable foods also carried gene variants connected to increased risk for obesity and lower activity levels. Whereas people who enjoyed strong-tasting foods often were genetically predisposed to lower cholesterol levels and higher physical activity, but a higher chance of high alcohol intake or smoking. And, those who leaned toward fruits and vegetables were genetically predisposed to perform more physical activity.

The research did indicate that those who were genetically predisposed to like vegetables didnt necessarily like all vegetables. Scientists found a weaker link to enjoying salad vegetables, cooked vegetables, and some stronger-tasting vegetables, like spinach and asparagus. Additionally, researchers indicated those who were predisposed to turn to higher-calorie, more palatable foods may have more going on than just genetics. They hypothesize after MRI scans that this may be more likely linked to the part of the brain involved in pleasure processing, according to the news release.

Our food preferences arent always within our control. This research may at some point aid in discovering ways to help people change their diet to achieve specific health goals, but in the meantime, its a great excuse to use when your taste preferences get in the way. After all, your genes tell you that you have to have some sriracha on top of your scrambled eggs.

Arielle Weg is the associate editor at Prevention and loves to share her favorite wellness and nutrition obsessions. She previously managed content at The Vitamin Shoppe, and her work has also appeared in Womens Health, Mens Health, Cooking Light, MyRecipes, and more. You can usually find her taking an online workout class or making a mess in the kitchen, creating something delicious she found in her cookbook collection or saved on Instagram.

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Genetics May Play a Role in Taste Preferences, Study Finds - Prevention Magazine

A legal defense grounded in genetics: Is DNA testing the magic wand to winning (or losing) a negligence case? – Genetic Literacy Project

Among the four elements required to establish liability for the tort of negligence is causation. In addition to proving that the defendant was careless or otherwise breached the legal standard of care, the plaintiff must establish that the wrongful conduct caused the harm the plaintiff suffers. This 1941 New Hampshire Supreme Court decision explains:

Necessary elements of a cause of action based on negligence are the causal negligence of the defendant plus the resultant harm to the plaintiff. Putting it another way, there must be negligence and harm and they must have a causal connection.

At the height of asbestos litigation, mesothelioma, a cancer of the lining of the pleural (lung) cavity or the abdominal cavity (peritoneal mesothelioma) was believed to be pathognomonic of asbestos exposure, meaning that the disease was a signal cancer of asbestos exposure, and only asbestos exposure. A diagnosis of the disease was tantamount to legal recovery (and virtually certain and swift death). No longer.

Today, it is recognized that mesothelioma has other causes, including erionite, another naturally occurring mineral used in pet litter, soil conditioners, animal feed, wastewater treatment, and gas absorbents. Radiation is also a recognized cause of mesothelioma, either from employment-related exposures, or older therapeutic uses which are now known to cause disease. And then there are causes we dont even yet know about as well as those arising spontaneously. These are known as idiopathic causes.

Asbestos exposure significantly declined beginning in the 1970s when the first OSHA asbestos laws were enacted. However, the incidence of mesothelioma, even with its notoriously long latency or delay period, is increasing in women, and has remaining constant overall. This lends credence to the fact that mesotheliomas arises from causes other than asbestos or even arises spontaneously, meaning the body needs no help from asbestos or anything else in generating them.

Of course, spontaneously does not mean magically or out of the blue. Rather, of the estimates that perhaps twenty to fifty percent of mesotheliomas dont arise from asbestos, it appears some are attributable to genetic misfirings, or mutations, that arise over time, some occurring as we age, and our defenses or repair mechanisms are no longer functioning optimally. (Think how slow your older computer worked compared to the new one you bought when old-trusty melted down.)

These genetic mutations are not necessarily inherited (although some are), but rather occur in clusters - or more rarely, singly due to natural causes or DNA breakage. The mutations can cause mesothelioma, either alone or by increasing susceptibility to minute exposures. The difference in the causal mechanism, however, has a huge impact on legal liability. And so it is that attention to genetics is now finding its way into the courtroom.

Courts are becoming more attentive to the need to establish that a potential carcinogen is responsible for causing the disease in a particular person, rather than based on its statistical or historical significance for a general population. Recently, in toxic tort cases, some courts are requiring a two-stage level of proof:

Specific causation requires showing that the plaintiff was exposed to a sufficient dose which is capable of causing the disease in that person. The application of this requirement is derailing some talc-mesothelioma cases.

But attention to the plaintiffs burden of proving specific causation is not the only monkey-wrench appearing in toxic tort cases these days. And not all courts are requiring specific quantification of plaintiffs exposure to prove causal-negligence, i.e, that the defendants asbestos caused the particular plaintiffs disease.

This situation invites another option for defense lawyers to protect their clients: genetics. And so we find defense lawyers turning to genetics to establish the defense that it wasnt exposure to asbestos per se, that caused the plaintiffs mesothelioma. Rather it was something else notably, something in their genes.

The genetic defense has found itself into other types of cases as well. And as we learn more about the genetic components of disease, we can expect to find its use burgeoning. Take the case of Bowen v. EI Dupont, in which the plaintiff alleged her retarded fetal growth and birth defects were caused by exposure to the fungicide Benlate during her gestation, when her mother was spraying houseplants.

The defendant obtained a court order to genetically test the plaintiff for a specific genetic variation (CHD7) that causes a specific condition (the CHARGE syndrome, a rare condition that causes birth defects), that resembled the plaintiffs condition. The defense argued that the mutated CHD7 was the sole and proximate cause of the plaintiffs condition a CHARGE syndrome-driven birth defect, a theory with substantial support in the record and substantiated in peer-reviewed literature. After the testing and finding the mutation present, the court dismissed the case.

In a similar case, Naomi Guzman v. ExxonMobil Corp, the plaintiff claimed that she was exposed to radioactive material as a bystander to her fathers work as an oil pipe cleaner. The court granted the defendants request for genetic testing of plaintiffs preserved thyroid tissue.

Genetic tests revealed both that the plaintiff did not have the genetic signature for radiation-induced cancer. It also revealed that plaintiff had several hereditary gene mutations predisposing her to thyroid cancer, leading the defenses expert-toxicologist to conclude her thyroid cancer was caused by her genetic predisposition and not exposure to her fathers drilling pipe. The jury agreed and sided with the defense.

Genetic defenses, however, must be used with care. In some cases, exposure to a chemical overwhelms multiple natural genetic repair mechanisms, leading to the cancer or disease. In those cases, the genetic defense may not work.

Thus, the failure of a genetic-defense mechanism to activate (or activation of a susceptibility gene) may not absolve the defendant, since it was the impact of exposure (to their asbestos or whatever chemical) that caused these genes to malfunction, and which in turn began the chain-reaction leading to the disease.

Instead, focusing on point mutations, where cancers occur as the direct result of a consequential change in a particular genetic set of alleles (subparts of a gene responsible for expression of a particular trait), independent of exposure, present the genetic alterations generating the most success in legal cases.

So far, two genes have been implicated as causally-related to mesothelioma in the absence of asbestos exposure. One, is a mutation on the AKL gene. While the discovery may not help plaintiffs in a legal setting, such discoveries do bode well for enhanced therapeutics and treatment.

Other studies have identified mutations on the BAP1 gene, discoveries that again bode well for possible treatment, although not necessarily for success in the legal setting. The BAPI gene is also related to several other cancers, including melanoma, so the causal connection is not one-on-one. But the BAP1 gene also has an additional effect- not only has it been related to direct causation of mesothelioma, it is also known to enhance susceptibility to prior exposures to asbestos. And that poses a legal problem.

The published findings do not establish a synergistic gene/environment interaction as a causal factor for the development of mesothelioma [and Bap1].,,, At present, it is estimated that between 1 and 8 percent of all spontaneous mesothelioma cases involve BAP1 germline mutations.

Bernier et al.

In law, the defendant is said to take the plaintiff as one finds him/her. That means if a plaintiff, by virtue of his or her individual make-up, is unusually susceptible to a condition, the defendant is still liable for all incident harms of their negligence. These include even those that might not have happened if the same wrongdoing was inflicted on a hardier plaintiff. (The term got its name from a case about running over a plaintiff with a skull as thin as an eggshell).

That maxim makes finding a BAP1 gene problematic. In some cases, the gene will render the plaintiff unusually susceptible to a small amount of exposure; in others it can cause mesothelioma, outright. Where the gene acts as a susceptibility gene, the defendant is still liable. Where it causes the disease outright, the plaintiffs case fails.

At the end of the day, the answer becomes a matter of fact for the jury to decide after listening to a battle of experts. But recent research shows that up to one-third of all cancers are produced by the bodys own mutation errors, and not by environmental causes. The complete genetic-cause defense would likely work best in cases of teenagers or women who were unlikely to have been exposed to significant levels of exposure.

To maintain a genetic defense, the plaintiff would have to petition the court to compel genetic tests of the plaintiff and sometimes the family to show a hereditary defect. Courts usually direct the plaintiff to submit to genetic testing (via blood test or tissue swipe), if the requested tests are particularized enough, although they will often reject requests to compel family-testing.

Is this forced test legal? Yes. First because such tests are not usually invasive; and second, by bringing the lawsuit, the plaintiff has put his condition into controversy and hence waives some rights.

To date, a few dozen personal injury cases have involved court-ordered genetic testing. Most courts have allowed it, especially as the tests are not painful, protracted, or intrusive. (Although, when the genetic tests are to be used for prospective or predictive purposes, such as medical monitoring or gauging the likelihood of future disease severity or longevity, the courts may not agree. In these cases courts often conclude that DNA tests are more speculative in prediction than identifying causal genes in those already suffering a disease).

Most important, however, a defendant who wants to compel a test must seekprecise information or evidence. In other words, like in any litigation discovery procedure, neither party is given largesse to go on a fishing expedition, for example by seeking reems of data, hoping to uncover an unanticipated smoking gun.

This objection wouldnt be typical in the asbestos cases, since specific and responsible genetic culprits have been identified. But we can see the abuse in other cases, notably birth-related negligence cases which often result in a surfeit of issues, such as brain damage, developmental issues, and physical disabilities. To be sure, such conditions can be caused by environmental exposures, poor pre-natal care, or even the birth process itself, especially if negligently performed.

In one birth-related negligence case, Fisher for XSF v. Winding Waters Clinic, the defendant sought a court order compelling the plaintiff to submit to genetic testing to confirm whether their impairments are more likely than not the result of a genetic condition unrelated to prenatal care

The problem was that the defendants had no specific condition in mind. They sought a WES (Whole Exome Sequencing) array meaning they wanted to look through the plaintiffs entire genomic vocabulary in the hopes of finding one or more errors to explain the condition. The court rejected the request.

Recognizing that overbroad requests promote the possibilities for abuse, including privacy violations or the potential to uncover genetic predispositions to numerous unrelated conditions, the court noted that the defendants request was particularly troubling.

Nevertheless, we can expect an onslaught of compelled genetic testing arising out of litigation to continue. As to where the results take us, thats an interesting and open- question. Perhaps the most curious case is the pending matter of Lohmann v. Aaon Inc. There, the defendants experts sought evidence of the BAP-1 disorder. Not only did they want to use it for the litigation, they wanted it for their own research purposes, as well.

Seems the value of these tests is greater than we might imagine. No word yet, on the legal resolution. But Id bet the judge denies the request.

Dr. Barbara Pfeffer Billauer, JD MA (Occ. Health) Ph.D. is Professor of Law and Bioethics in the International Program in Bioethics of the University of Porto and Research Professor of Scientific Statecraft at the Institute ofWorld Politics in Washington DC. Find Barbara on Twitter@BBillauer

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A legal defense grounded in genetics: Is DNA testing the magic wand to winning (or losing) a negligence case? - Genetic Literacy Project

A genetics startup wants to bring the Tasmanian tiger back from extinction – Popular Science

It looks like the thylacines (aka the Tasmanian tiger) turn to enter the debate on whether or not scientists can or should bring species back from extinction.Colossal Biosciences & Laboratories, announced yesterday that it plans to resurrect the extinct marsupial. The self-titled de-extinction company based in Dallas first made headlines last September when with its plans to de-extinct the Wooly Mammoth.

[ Related: This CRISPR startup thinks that mammoths can save the Arctic. Is it right? ]

The Tasmanian tiger was a dog-sized carnivorous marsupial with sharp claws, that was native to New Guinea, the Australian mainland, and Tasmania for four million years. Sporting yellowish to gray fur and distinctive tiger stripes covering its body, it first disappeared from the mainland about 2,000 years ago. The National Australia Museum speculates multiple factors, including over hunting and the introduction of the dingo led to this first wave of extinction.

By the late 19th and early 20th centuries, Europeans began to colonize the island of Tasmaniaan island about 150 miles south of Australia. They incorrectly blamed the marsupials for killing their chickens and sheep and thylacines were slaughtered by the thousands, with the government even offering bounties for thylacine pelts. Throw in the same fight for dominance with dingoes and the Tasmanian tiger was doomed. In 1936, the last known living Tasmanian tiger died at Beaumaris Zoo in Hobart, Tasmania.

Colossal plans to use CRISPR gene-editing technology to bring back the southern marsupial. While the Jurassic Park-esque science isnt quite here yet, the company founded by tech entrepreneur Ben Lamm and Harvard geneticist George Church, laid out a 10 step plan to re-introduce a Tasmanian tiger like animal back into the wild. They are partnering with and investing in the University of Melbournes Thylacine Integrated Genetic Restoration Research Lab (TIGRR). TIGRR is currently led by marsupial evolutionary biologist and Tasmanian tiger expert Andrew Pask and has already performed the crucial first step of sequencing most of the animals genome.

The team is comparingthe sequenced thylacine genome with the fat-tailed dunnart, a marsupial from the dasyurid family that looks more like a common mouse than a dog. This species of dunnart will provide the living cells and genetic map thats theoretically needed to theoretically create both a Tasmanian tiger genome that can create life and potentially a complete specimen.

Not everyone in the marsupial conservation community is confident that this de-extinction strategy will work. In an interview with Scientific American, Australian Museum mammal expert Kris Helgen said that the dunnart DNA and thylacine DNA are far too different from one another and separated by too many millions of years of evolution to create an animal that even resembles to Tasmanian tiger. Helgen was on the team that sequenced the thylacines mitochondrial genome in 2009.

In an interview with the Sydney Morning Herald, Jeremy Austin from the Australian Centre for Ancient DNA de-extinction fairytale science, and claimed that efforts to bring back the thylacine or the mammoth are more about media attention than the actual science. In the same interview, marsupial DNA expert Dr. Mike Westerman from La Trobe University added that he is not convinced that it can be done with our current knowledge. Where on earth would a self-sustaining population be maintained?

Colossal did not announce a timeline for this de-extinction project to be completed.

Australia is no stranger to seeing its species vanish and is currently in the midst of a major biodiversity crisis. It has seen years of severe drought, historic bushfires, record-breaking floods, and six mass bleaching events on the Great Barrier Reef. A 2022 State of the Environment report commissioned by the Australian government found or reiterated that 19 ecosystems are on the brink of collapse, that there are more non-native plant species in Australia versus native ones, and that the continent has lost more species to extinction than any other. The report underscores the need for a better framework for preserving biodiversity in the region to prevent further catastrophe.

Editors Disclosure:Matt Sechrest, the managing partner ofPopular Sciences parent company, North Equity, is an investor in Colossal. He was not involved in the assigning, writing, or editing of this story.

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A genetics startup wants to bring the Tasmanian tiger back from extinction - Popular Science

Some types of itches are genetic related: Expert – Telangana Today

Published: Published Date - 07:05 PM, Mon - 22 August 22

Hyderabad: Severe itching is usually associated with allergies, immunity disorders, parasitic insects and even fungal infections. However, there are instances wherein severe itching is also linked to genetics.

Sometimes, itching could be a condition that has been passed down from parents to children and in some cases it could congenital in nature.

Such rare forms of itching and links to genetics were showcased by Prof. Geoff Woods, human geneticist from Cambridge Institute for Medical Research, UK, while delivering a talk on With ExtremePhenotypes, think of Genetics, even with Itch, organised by Hyderabad-based Genome Foundation.

Dr Woods explained how genetics of a few rare diseases lead to the deciphering biological pathways. He also presented case-studies of ultra-rare diseases like congenital itch inherited in families. The geneticist in his presentation said that itch from birth in both males and females could be severe and unrelenting.

Senior officerbears from Genome Foundation including its Chairman, Dr. KPC Gandhi, Dean (Research), Prof.V.R.Rao, Director, Aparna Kaja and senior dermatologist, Dr V Anand Kumar were present.

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Some types of itches are genetic related: Expert - Telangana Today

Genetic variants cause different reactions to psychedelic therapy – The Well : The Well – The Well

When all else fails, some patients trying to overcome alcoholism, severe depression or anxiety, and even cluster headaches, turn to psychedelic drugs, which clinical research has shown can help treat individuals with these conditions, sometimes with dramatically positive results.

But sometimes, as with any therapy, the psychedelic treatment does not work. It just takes a patient on a long strange trip.

Now, UNC School of Medicine researchers led by Dr. Bryan Roth, the Michael Hooker Distinguished Professor of Pharmacology, report that one reason for treatment disparity could be common genetic variations in one serotonin receptor.

Dr. Bryan L. Roth

Published in the journal ACS Chemical Neuroscience, the lab research in cells shows that seven variants uniquely and differentially impact the receptors response to four psychedelic drugs psilocin, LSD, 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT) and mescaline.

Based on our study, we expect that patients with different genetic variations will react differently to psychedelic-assisted treatments, said Roth, who leads the NIH Psychotropic Drug Screening Program. We think physicians should consider the genetics of a patients serotonin receptors to identify which psychedelic compound is likely to be the most effective treatment in future clinical trials.

After decades of taboo regarding potential therapeutic benefit of psychotropic drugs, there has been renewed interest and research in using such compounds to treat neuropsychiatric disorders, such as major depression disorder, because the drugs stimulate serotonin receptors in the brain. These receptors bind the neurotransmitter serotonin and other similar amine-containing molecules, helping regulate peoples mood and emotions, as well as their appetite. In particular, the 5-hydroxytryptamine receptor known as 5-HT2A is responsible for mediating how a person reacts to psychedelic drugs. However, there are several naturally occurring, random genetic variations, known as single nucleotide polymorphisms, or SNPs, that can affect the function and structure of the 5-HT2A receptor.

Site of the 5-HT2A serotonin receptor.

Roth and colleagues wanted to explore how variation in this one serotonin receptor changes the activity of four psychedelic therapies.

Graduate student Gavin Schmitz and postdoctoral researchers Manish Jain and Samuel Slocum used a series of experimental assays to measure the effect that seven different SNPs had onin vitro binding and signaling of the 5-HT2A serotonin receptor when in the presence of one of the four drugs. Their results indicated that some gene variations even ones far from the exact location where the drug binds to the receptor alter the way that the receptor interacts with the psychedelic drugs.

For example, the SNP Ala230Th had decreased response to one of the four drugs (psilocin the active metabolite of psilocybin) while the Ala447Val mutation showed only reduced effects to two of the drugs.

This is another piece of the puzzle we must know when deciding to prescribe any therapeutic with such dramatic effect aside from the therapeutic effect, Roth said. Further research will help us continue to find the best ways to help individual patients.

The National Institutes of Health and the Defense Advanced Research Projects Agency (DARPA) funded this research.

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Genetic variants cause different reactions to psychedelic therapy - The Well : The Well - The Well

AgriGold to debut 15 Corn Hybrids and 35 Soybean Varieties for 2023 – Farm Progress

AgriGold will bring 15 new corn hybrids with 21 new trait additions on new and proven hybrids as well as 35 new soybean varieties to the market in 2023. Its latest soybean lineup features 14 new XtendFlexproducts, 13 new Enlist E3soybeans and a new conventional line of eight agronomically sound and versatile varieties.

One of those exciting new traits is SmartStaxPRO, which is geared toward fighting corn rootworm. It utilizes RNAi technology, providing a third mode of action against corn rootworm and tripling root node protection compared with Qromeproducts.

We take pride in selling versatile products that offer consistent results and allow farmers solutions for their unique challenges, says Whitney Monin, AgriGold national agronomy manager. The 2023 additions expand AgriGolds diverse portfolio to 80 proven corn hybrids and 74 soybean varieties, better enabling us to meet farmers needs. Thats powerful.

Related: Farm Progress America, August 23, 2022

AgriGold Field GXsimplifies decisionsAgriGolds standout hybrid categories combine world-class genetics with farmer fields.AgriGolds Field GXclassifies every hybrid into five genetic families based on genetic background and agronomic characteristics. Knowing a hybrids genetic family helps simplify management, reduce risk, and maximize results in farmers fields.

Standout new corn hybridsThe new lineup of corn hybrids aligns with AgriGolds mission of moving genetics forward, says John Brien, AgriGold eastern agronomy manager. He details, The 2023 offerings with relative maturities (RM) ranging from 89 to 120 days averaged an impressive 5.8 bushel per acre genetic gain compared with last years lineup.

Just a few of the hybrids expected to make waves in 2023 include the following:

Related: Country star, equipment company enter new collaboration

The hybrid profile is an important component of AgriGolds story. To better relay that story to the farmer, the seed company has improved its ear flex categorization. It now categorizes products based on ear length, ear girth and kernel flex, telling a more complete story that farmers can leverage.

This is the biggest change weve made in years, and its a shift aimed at telling farmers a lot more about the hybrids they are purchasing and how they fit their ground, management style and goals, Brien explains.

Soybean offerings expandOur soybean portfolio is bigger and more diverse than it has ever been before, Western Agronomy Manager Steve Schany says, referencing the companys 74 different soybean varieties with maturities spanning from 0.3 to a 6.4 determinant soybean. Our 2023 soybean platform is the most offensive we have offered to date, he says, adding Weve been able to maintain an outstanding 2.44 bushel per acre annual genetic gain in this new launch class.

The following are some standouts from the class of 2023:

AgriGold will also simplify its seed treatment options with the 2023 lineup to ensure adequate supplies while still providing the flexibility for farmers to select a value or premium option. Schany explains, Weve upgraded two major ingredients in our AgriShieldMAX with Saltroseed treatment. We have replaced metalaxyl with a mefenoxam for improvedPythiumcontrol. Were also stepping upRhizoctoniacontrol with the addition of the brand new, industry-leading sedaxane.

Robust AgriGold lineup gives farmers more freedom to chooseAgriGolds large and diverse portfolio of corn and soybean products deliver freedom. Our farmer customers have the freedom to choose the trait thats best for their farm, their management style and their yield goals thanks to our robust product offerings, Monin says.

Source: AgriGold,who is solely responsible for the information provided and is wholly owned by the source. Informa Business Media and all itssubsidiaries are not responsible for any of the content contained in this information asset.

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AgriGold to debut 15 Corn Hybrids and 35 Soybean Varieties for 2023 - Farm Progress

Before Serena Williams Shock Defeat, Floyd Mayweather Made Genetics Revelation That Likened Him to Tennis Legend – EssentiallySports

Floyd Mayweather and Serena Williams are both icons in their respective sports. It can be argued that the pair are the greatest athletes of their generation, if not the best ever. Mayweather walked away from the sport with a perfect record of 50-0 while Williams has 23-Grand Slam titles under her belt.

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Moreover, Money certainly thought that he and Williams were similar in many aspects. Back in 2015, before his fight against Andre Berto, Mayweather came out in support of the tennis ace. Williams was also set to face off Roberta Vinci in the US Open Semifinals. This was an important match for her as she was on her way to becoming the first player since 1998 to hold all four major titles in a single year.

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In an interview leading up to his fight, Mayweather admitted he wanted to see Williams break this record and supported her endeavors, They say records are made to be broken.

Im just very proud of her and what shes done during her career. Shes done some amazing things in her career. Its just marvelous what she did. Im behind her 100% He said

Moreover he claimed that he and Williams shared similar genetics and had an undeterred dedication to their craft. Genetics. I think that the older you get, the harder you have to work, Thats what Ive done. The older I get, the harder I work. He added.

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Mayweather would go on to beat Berto to secure his 49th win in the sport. However, things would not turn out great for Williams as she lost to Vinic in one of tenniss biggest upsets.

Retiring with a perfect record is a feat that has only been managed by a few greats. Mayweather is one of those greats. The time and effort Money has put into becoming one of the best is unmatched. Unlike several other top boxers, he relies on his defensive prowess, using his footwork and head movement to frustrate his opponents into making mistakes.

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His skills can be attributed to the countless hours he had to put in the training, especially as he got older.

Mayweather has described his mantra as hard work and dedication which has evolved into a crowd chant. He gets the crowd involved by having them say half of it and he says the other half.

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Do you think Mayweather and Williams are alike? Let us know in the comments.

Watch This Story:Hardest Shots Landed on Floyd Mayweather

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Before Serena Williams Shock Defeat, Floyd Mayweather Made Genetics Revelation That Likened Him to Tennis Legend - EssentiallySports

Genetics and management drive lamb weights to record level – Sheep Central

NATIONAL lamb carcase weights reached record highs in the last financial year, the release of Australian Bureau of Statistics data has revealed.

Meat & Livestock Australias market information manager Stephen Bignell said lamb slaughter for Q2 in FY2022 was recorded at 5.44 million, an increase of 9.5 percent on the previous quarter and 1.1pc higher than the June 2021 quarter.

For the full financial year, lamb slaughter nationally stood at 20.8m lambs.

The fact that lamb slaughter for Q2 2022 (October to December 2021) was not within in the historical top 20 lamb slaughter volumes, but was the third highest level of production, shows the benefits of increasing carcase weights, he said.

The implementation of new genetics, well managed on-farm production and above average rainfall patterns have ensured national lamb carcase weights achieved record highs in Q2 2022.

At 25.8kg/head, this was a 0.6pc increase year-on-year levels, demonstrating that genetic improvement and management is driving increased efficiencies and production for the national lamb flock, Mr Bignell said.

New South Wales lambs weighed 26.8kg/head on average, leading the trend for heavier lambs nationally, followed by South Australian lambs at 26.7kg/head.

The value of lambs and sheep slaughtered in FY2022 was $5.13 billion, 14.5pc above the value of sheep and lambs slaughtered in FY2021.

The second quarter in FY2022 (October to December 2021) recorded the highest value of sheep and slaughtered ever, MLA said. The average price for a finished lamb/sheep in FY22 was $189.39, up 10.5pc on 2021.

In Q2 of 2022, lamb production was 140,165 tonnes, the third highest quarterly volume on record, behind Q2 2018 and Q4 2016. The quarterly total of 140,165 tonnes was a 12.5pc increase on Q1 2022 levels and 1.8pc higher than the same quarter in 2021, MLA said.

MLA said unlike lambs and cattle, sheep slaughter fell in Q2 2022, reducing by 13.2pc or 209,600 head. However, according to Mr Bignell, a drop in slaughter in the June quarter is common as producers are retaining ewes for lambing during this period.

Encouragingly, when compared to the corresponding June period in 2021, mutton slaughter is up 27pc or close to 300,000 head.

This would suggest the flock rebuild is maturing and in line with MLAs most recent June sheep projections, he said.

MLA said production of mutton was recorded at 35,091 tonnes in Q2 2022, a 11.3pc reduction on the previous quarter, but 25pc higher than 2021 levels. As mutton production fell by less than the fall in slaughter, carcase weights climbed, MLA said.

National sheep carcase weights for Q2 2022 were recorded at 25.5kg/head, a 500g increase on Q1 2022 levels, but well below the 2.2kg/head below the highs recorded in December 2021.

Interestingly, the average carcase weights for sheep are below that of lambs on a national level.

Sheep in New South Wales are the heaviest weighting 27.3kg, while sheep in Tasmania are the lightest weighing 19.5kg/head, Mr Bignell said.

Source: MLA.

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Genetics and management drive lamb weights to record level - Sheep Central