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FDA OKs Pfizer drug for rare, fast-killing type of leukemia – New Jersey Herald

Posted: August 24, 2017 at 5:44 am

Posted: Aug. 17, 2017 8:00 am Updated: Aug. 17, 2017 5:35 pm

TRENTON, N.J. (AP) The Food and Drug Administration has approved a new medicine for use against a rare, rapidly progressing blood cancer after other treatments have failed.

The agency approved Pfizer Inc.'s Besponsa for patients with a type of advanced acute lymphoblastic leukemia. By then, life expectancy is low.

"These patients have few treatments available and today's approval provides a new, targeted treatment option," Dr. Richard Pazdur, the FDA's director for cancer drugs, said in a statement.

This year an estimated 5,970 Americans will be diagnosed and 1,440 will die from the cancer, according to the National Cancer Institute.

The drug will cost $168,300 without insurance for the typical nine-week treatment course.

In testing that included 218 patients, 36 percent given Besponsa had their cancer vanish for eight months on average; 17 percent of those given chemotherapy had complete remission for a median five months.

Besponsa is believed to work by blocking the growth of cancerous cells by binding to their surface.

The powerful injected drug, known chemically as inotuzumab ozogamicin, comes with the FDA's most-stringent warning because it can cause severe liver disease, including blocking veins in the liver. It also carries an increased risk of death in patients who have received a certain type of stem cell transplant.

Besponsa also can cause a decrease in blood-cell and platelet production, infusion-related reactions and problems with the heart's electrical pulses. Women who are pregnant or breastfeeding should not take Besponsa because it may harm a developing fetus or a newborn baby, the FDA warned.

More-common side effects include fatigue, severe bleeding, fever, nausea and headaches.

___

Follow Linda A. Johnson at http://www.twitter.com/LindaJ_onPharma

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FDA OKs Pfizer drug for rare, fast-killing type of leukemia - New Jersey Herald

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Shoulder Stem Cell and Platelet Treatments – Vermont …

Posted: August 23, 2017 at 4:48 am

Shoulder Stem Cell and Platelet TreatmentsVermont Regenerative Medicine2017-08-07T18:22:31+00:00Shoulder Stem Cell Therapy and PRP / Platelet Rich Plasma Procedures for Shoulder & Rotator Cuff Injuries and Arthritis

Regenexx Shoulder Stem Cell Therapy and PRP Procedures for Rotator Cuff Injuries offer the most advanced, non-surgical treatments for people suffering from shoulder arthritis, torn rotator cuff, shoulder bursitis, tendonitis and other common injuries. These minimally invasive procedures offer a viable treatment alternative for individuals considering elective shoulder surgery or shoulder replacement surgery.

The shoulder is an incredibly complex joint, making all types of shoulder surgery difficult, with unpredictable outcomes. Shoulder surgery recovery can require months of painful rehabilitation to help rebuild strength and range of motion in the shoulder joint.

Alternatively, the Regenexx procedures may help heal and alleviate shoulder problems with a same-day stem cell or platelet rich plasma injection procedure. Regenexx patients typically experience little to no down time from the procedure and avoid the wide range of problems that often follow surgery.

This outcome information summarizes the 2014 registry data for shoulders treated with the Regenexx Stem Cell Procedure using the patients own stem cells. It was comprised of a mix of patients with rotator cuff tears, arthritis, labral tears, and instability. Rotator cuff tear patients are doing the best in this group.

View This Shoulder / Rotator Cuff Outcome Data

Stem Cells are in all of us and they are responsible for healing injured bone, ligaments, tendons and tissues. They are the key component behind the Regenexx Procedures. As we get older or injured, we sometimes cannot get enough of these cells into the area in need. The Regenexx Procedures help solve that problem by precisely delivering a high concentration of stem cells and growth factors into the injured area, aiding your bodys ability to heal naturally. Regenexx patients experience little or no down-time from the procedure and typically avoid the long, painful rehabilitation periods to restore joint strength and mobility following invasive surgeries.

If you are suffering from a shoulder injury or degenerative condition like osteoarthritis, you may be a good candidate for these ground-breaking stem cell and blood platelet treatments. Please complete the Procedure Candidate Form below and we will immediately email you more information.

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Shoulder Stem Cell and Platelet Treatments - Vermont ...

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S Muoio & Company Has Raised Its Clarcor (CLC) Position; Biolife Solutions (BLFS) Shorts Raised By 7.43% – HuronReport

Posted: August 23, 2017 at 4:47 am

August 18, 2017 - By Hazel Jackson

Biolife Solutions Incorporated (NASDAQ:BLFS) had an increase of 7.43% in short interest. BLFSs SI was 245,800 shares in August as released by FINRA. Its up 7.43% from 228,800 shares previously. With 22,800 avg volume, 11 days are for Biolife Solutions Incorporated (NASDAQ:BLFS)s short sellers to cover BLFSs short positions. The SI to Biolife Solutions Incorporateds float is 3.89%. The stock decreased 5.23% or $0.24 on August 18, reaching $4.35. About 168,018 shares traded or 15.97% up from the average. BioLife Solutions Inc (NASDAQ:BLFS) has risen 37.27% since August 18, 2016 and is uptrending. It has outperformed by 20.57% the S&P500.

S Muoio & Company increased Clarcor Inc (CLC) stake by 38.27% reported in 2016Q4 SEC filing. S Muoio & Company acquired 4,000 shares as Clarcor Inc (CLC)s stock 0.00%. The S Muoio & Company holds 14,452 shares with $1.19 million value, up from 10,452 last quarter. Clarcor Inc now has $4.06B valuation. It is 0.00% or $0 reaching $0 per share. It is down 0.00% since August 18, 2016 and is . It has underperformed by 16.70% the S&P500.

Investors sentiment increased to 2.33 in 2016 Q4. Its up 0.83, from 1.5 in 2016Q3. It is positive, as 3 investors sold BioLife Solutions Inc shares while 0 reduced holdings. 5 funds opened positions while 2 raised stakes. 267,289 shares or 5.47% less from 282,746 shares in 2016Q3 were reported. Blackrock Fund Advsrs has 0% invested in BioLife Solutions Inc (NASDAQ:BLFS) for 2,526 shares. Community Financial Bank Na stated it has 0% in BioLife Solutions Inc (NASDAQ:BLFS). Deutsche National Bank & Trust Ag reported 1 shares. Retail Bank Of America De holds 0% in BioLife Solutions Inc (NASDAQ:BLFS) or 1 shares. Tower Cap Limited Liability (Trc) invested in 0% or 862 shares. Price T Rowe Assoc Incorporated Md has invested 0% in BioLife Solutions Inc (NASDAQ:BLFS). Citadel Advsrs Ltd Liability Company accumulated 16,710 shares. Creative Planning holds 143 shares. Hudock Group Limited Liability Company reported 43 shares. Pnc Financial Group holds 0% or 10,000 shares in its portfolio. The California-based Wells Fargo & Mn has invested 0% in BioLife Solutions Inc (NASDAQ:BLFS). 2,500 are owned by Ancora Limited Liability Company. Vanguard Gru has invested 0% in BioLife Solutions Inc (NASDAQ:BLFS). Blackrock Institutional Na holds 0% of its portfolio in BioLife Solutions Inc (NASDAQ:BLFS) for 33,039 shares. Perkins holds 10,000 shares or 0.02% of its portfolio.

BioLife Solutions, Inc. is engaged in the developing, manufacturing and marketing a portfolio of biopreservation tools and services for cells, tissues and organs, including clinical grade cell and tissue hypothermic storage and cryopreservation freeze media and a related cloud hosted biologistics cold chain management application for shippers. The company has market cap of $57.54 million. The Companys product offerings include hypothermic storage and cryopreservation freeze media products for cells, tissues, and organs; generic blood stem cell freezing and cell thawing media products; custom product formulation and custom packaging services; cold chain logistics services incorporating precision thermal packaging products and cloud-hosted Web applications, and contract aseptic manufacturing formulation, fill and finish services of liquid media products. It currently has negative earnings.

Among 2 analysts covering BioLife Solutions (NASDAQ:BLFS), 2 have Buy rating, 0 Sell and 0 Hold. Therefore 100% are positive. BioLife Solutions had 4 analyst reports since June 14, 2017 according to SRatingsIntel. The company was maintained on Friday, August 11 by Maxim Group. The stock of BioLife Solutions Inc (NASDAQ:BLFS) earned Buy rating by Maxim Group on Monday, July 31. The company was upgraded on Wednesday, July 5 by Janney Capital. The stock of BioLife Solutions Inc (NASDAQ:BLFS) has Buy rating given on Wednesday, June 14 by Maxim Group.

Investors sentiment decreased to 0.84 in Q4 2016. Its down 0.29, from 1.13 in 2016Q3. It worsened, as 30 investors sold CLC shares while 92 reduced holdings. 42 funds opened positions while 61 raised stakes. 41.40 million shares or 3.54% less from 42.91 million shares in 2016Q3 were reported. Rhumbline Advisers has invested 0.02% of its portfolio in CLARCOR Inc. (NYSE:CLC). Champlain Prns Limited Co owns 2.01 million shares. Qs Invsts Limited Liability Company owns 0% invested in CLARCOR Inc. (NYSE:CLC) for 6 shares. Tower Rech Capital Lc (Trc) stated it has 0.02% in CLARCOR Inc. (NYSE:CLC). Tcw Grp holds 12,484 shares or 0.01% of its portfolio. Metropolitan Life Ins New York owns 77,248 shares or 0.05% of their US portfolio. Kcg Incorporated holds 0.01% of its portfolio in CLARCOR Inc. (NYSE:CLC) for 5,211 shares. Pillar Pacific Cap Mgmt Limited Liability invested in 0.07% or 5,800 shares. Barclays Public Llc invested 0% of its portfolio in CLARCOR Inc. (NYSE:CLC). Gabelli Funds Ltd Limited Liability Company has invested 0.43% in CLARCOR Inc. (NYSE:CLC). Gardner Lewis Asset Mgmt Limited Partnership holds 0.43% or 67,851 shares. Tru Communications Of Vermont reported 4,389 shares. Swiss Bankshares stated it has 80,200 shares. 7,300 were reported by Weik Invest Services. Teachers Retirement Of The State Of Kentucky accumulated 10,300 shares.

S Muoio & Company decreased Frontier Communications Corp Ser B (NASDAQ:FTR) stake by 500,000 shares to 299,192 valued at $1.01M in 2016Q4. It also reduced Gannett Co Inc stake by 52,523 shares and now owns 47,058 shares. Amc Networks Inc (NASDAQ:AMCX) was reduced too.

Among 4 analysts covering CLARCOR (NYSE:CLC), 0 have Buy rating, 2 Sell and 2 Hold. Therefore 0 are positive. CLARCOR had 8 analyst reports since August 12, 2015 according to SRatingsIntel. The stock of CLARCOR Inc. (NYSE:CLC) earned Hold rating by Zacks on Tuesday, August 18. The stock has Sell rating by Zacks on Wednesday, August 12. The firm has Sell rating by Gabelli given on Friday, December 2. On Monday, August 31 the stock rating was upgraded by Zacks to Sell. Robert W. Baird downgraded CLARCOR Inc. (NYSE:CLC) rating on Friday, September 18. Robert W. Baird has Neutral rating and $53 target. The firm has Sell rating given on Tuesday, September 22 by Zacks. The firm earned Hold rating on Tuesday, September 22 by TheStreet. The stock of CLARCOR Inc. (NYSE:CLC) has Neutral rating given on Friday, September 16 by Robert W. Baird.

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S Muoio & Company Has Raised Its Clarcor (CLC) Position; Biolife Solutions (BLFS) Shorts Raised By 7.43% - HuronReport

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Stronger, smarter, happier – what if a drug could make you a better version of yourself? – CBC.ca

Posted: August 23, 2017 at 4:46 am

Thursday August 10, 2017

If there werea pill that made yousmarter without studying, stronger without exercising, and happier without trying, would you take it?

That's the premiseof the 2011movie, Limitless,in which actor BradleyCooper plays astruggling writer who is offered a drug that promises him access to the full capacities of his brain.

Soon enough Cooper's character hasfinished writinghis book, acquired a wide range of newof skills, and is on his way to becoming one of the richest and most powerfulpeople in the country.

The fictitious scenario isfarfetched, but the idea of using drugs for self-enhancement is completely grounded in reality and it's possible you're participating in self-enhancement without even knowing it.

When thinking about LSD, your mind probably conjuresup images of the Beatles oruntethered hallucinations.

But there are also people some of them prestigious jobs with high stakeswho are using LSD to boost their performance at work.Microdosinginvolves taking small doses of LSD far less than you would use to have a full on hallucinatory trip in order to boost productivity and focus.

PJVogt, host of the hitpodcastReply All, and show producer PhiaBennindecided to put microdosing to the test, all while hiding their social experiment from their colleagues to see whether anyone would notice.

Thetales of the paranoia, accidental 'macrodosing,' and the very mixed results that ensued are all documented in a hilarious Reply All episode thatyou can listen to here.

Caffeine has been shown to boost athletic performance. (Unsplash/Kyle Meck)

Of course, regular LSD doses, however small, may not be everyone's cup of tea.

But there's also a legal, relatively safe drug that has been proven to make athletes perform better. It can also make you more alert and focused,and there's a pretty good chance some of it is already in your system right now.

If you haven't guessed yet it's caffeine.

Terry Graham,professor emeritusat the University of Guelph, spent years studying the effects of caffeine. After Canadian sprinter Ben Johnson was disqualified fordoping at the 1988 Olympic games in Seoul, Graham asked for funding to study whether caffeineaffects athletic performance with the hypothesis that its positive effects would be inconsequential.

"I was absolutely, 100 per cent wrong," he said. "Caffeine was a tremendous stimulant to exercise endurance and performance."

The boost provided by caffeine occurs within the muscle itself. Muscles are made up of motor units groups of muscle cells that contract all at once. When caffeine is present, each of those units produces a little more tension than usual, making the entiremuscle contractionstronger.

"Many of the substances that athletes can use to promote a better performance only act within acertain window, it could be strength, sprinting, or a prolonged activity. Butcaffeine seems to be able to influence all of these types of activities, so it's quite universal," he explained.

If tiny doses ofLSD, and big doses of coffee don't appeal to you as means of self-enhancement, there's always transhumanism abroad movement that aims to overcome our human limitations.

People involved with transhumanism believe that humans can be improved through things like smart drugs and gene editing. The three major strands aresuperintelligence, superlongevity, and superhappiness.

As explained by David Pearce, a philosopher and prominent figure in the transhumanist movement, this re-alignment of the basic human conditionshinges on something called the hedonistic imperative.

"Each of us has this approximate hedonic set point, some people are very, by today's standards, fortunate. They're pretty cheerful and they vacillate with a relatively high hedonic set point. Other people are more depressive and gloomy, and seem to fluctuate around gradients of ill-being."

"Nature didn't intend us to be happy, at least permanently happy, And we're just starting to decipher the particular genes and alleles associated with having either a high or low hedonic set point. Iwouldvery much hope that every future civilization would be based on everyone enjoying a high hedonic set point."

If you're trying to figure out your hedonic set point, Pearcesays toimagine a time in your life where you were happier than usual then imagine if you could feel that way all the time.

"If suffering were a recipe for nobility of character perhaps there would be some kind of case for obtaining it, but ... typically prolonged suffering tends to embitter. So we can argue what it actually means to be human. If we abolish suffering, would it have taken away our essential humanity?"

"Nature is exceptionally miserly with pleasure, an I see the challenge ahead isdelivering an extremely rich quality of life for everyone, but doing so in ways that don't compromise social responsibility or intellectual progress."

To subscribe to the podcastand hear more episodes of CBC On Drugs, follow the linkhere.

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Stronger, smarter, happier - what if a drug could make you a better version of yourself? - CBC.ca

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Genetics, Not Laziness, Might Be Why You Hate Exercising – Medical Daily

Posted: August 23, 2017 at 4:45 am

For some, the hardest part of hitting the gym is lacing up their shoes. But for others, its the actual exercise that makes working out so excruciating. The labored breathing, sore muscles, and sweat dripping into your eyes can be a high or just one step above torture depending on which type of person you are. A new study aimed to determine what accounts for these differences, and it turns out your genetics might be to blame for how much you dread going for a run.

The British Psychological Societys Research Digest reports on a study at the Vrije Universiteit Amsterdam in the Netherlands, which enlisted 115 pairs of identical twins, 111 pairs of non-identical twins, 35 siblings related to the twins and 6 sibling pairs not from families with twins. Everyone rode an exercise bike for 20 minutes and completed a 20-minute run, both at a comfortable pace. Researchers monitored breathing to ensure the workouts were low intensity, and a warm up and cool down accompanied the routines. Subjects also completed a second short ride on the exercise bike that was more vigorous.

The siblings completed assessments while exercising, answering how they felt while working out, how much effort they put in, and whether they were energetic, lively, jittery or tense. Additionally, participants were interviewed about how often they exercised and to what intensity. Using the responses, researchers determined the participants psychological state during physical activity.

Then, scientists looked at the data to determine whether identical twins, who also have identical genes, had similar responses to exercising compared to fraternal twins and non-twin siblings. This allowed them to theorizehow much genetics actually played a role in someone's mental state during physical fitness. They concluded that genetics could account for up to 37 percent of the differences in the way people experienced exercise. Unsurprisingly, people who enjoyed fitness were prone to doing it more. However, its important to note that the study doesnt show a cause and effect relationship.

While this new research indicates that somemay not be born to love fitness, theres no denying that we should still do it. Aside from helping maintain weight, working out can lift your mood, reduce stress and anxiety, strengthen bones and and reduce risk of certain diseases.

Thankfully, it is possible to actually enjoy physical activity. Health reports that the most important thing is to take up an activity you actually like (and yes, there is bound to be something). "Too often I see people who sign up to do something like running, even though they know they hate running," Shavise Glascoe, exercise physiologist at the Johns Hopkins Weight Management Center, explained to the magazine. Even non-vigorous activities like walking your dog or dancing in your room count as exercise.

Finding a workout buddy is an easy way to instantly make jogging, walking or lifting weights more interesting. A study from 2013 found that people who worked out with a spouse, friend or family member reported more enjoyment than doing it alone. If the activity took place around nature, people reported even more enjoyment and better moods. So, stop reading this, grab a buddy and hit your nearest walking trail.

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Genetics, Not Laziness, Might Be Why You Hate Exercising - Medical Daily

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Using Genetics to Uncover Human History – JD Supra (press release)

Posted: August 23, 2017 at 4:45 am

Human history is often something modern man only sees as through a glass, darkly. This is particularly the case when that history did not occur in the Mediterranean, the Nile Valley, India, or China, or when there is no written record on which scholars can rely. Exacerbating the disrupting effects of time on history can be when that history occurs in a region where extensive migration has disrupted whatever temporarily stable civilization happened to have taken root at that place at any particular time.

But humans leave traces of themselves in their history and a variety of such traces have been the source of reconstructions outside conventional sources. Luigi Cavalli-Sforza began the study of human population genetics as a way to understand this history in 1971 in The Genetics of Human Populations, and later extended these studies to include language and how it influences gene flow between human populations. More recent efforts to use genetics to reconstruct history include Deep Ancestry: The Landmark DNA Quest to Decipher Our Distant Past by Spencer Wells (National Geographic: 2006), and The Seven Daughters of Eve: The Science that Reveals our Genetic Ancestry by Brian Sykes (Carrol & Graf: 2002). And even more recently, genetic studies have illuminated the "fine structure" of human populations in England (see "Fine-structure Genetic Mapping of Human Population in Britain").

Two recent reports illustrate how genetics can inform history: the first, in the American Journal of Human Genetics entitled "Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome Sequences"; and a second in the Proceedings of the National Academy of Sciences USA, entitled "Genomic landscape of human diversity across Madagascar." In the first study, authors* from The Wellcome Trust Sanger Institute, University of Cambridge, University of Zurich, University of Otago, Bournemouth University, Lebanese American University, and Harvard University found evidence of genetic admixture over 5,000 years of a Canaanite population that has persisted in Lebanese populations into the modern era. This population is interesting for historians in view of the central location of the ancestral home of the Canaanites, the Levant, in the Fertile Crescent that ran from Egypt through Mesopotamia. The Canaanites also inhabited the Levant during the Bronze Age and provide a critical link between the Neolithic transition from hunter gatherer societies to agriculture. This group (known to the ancient Greeks as the Phoenicians) is also a link to the great early societies recognized through their historical writings and civilizations (including the Egyptians, Assyrians, Babylonians, Persians, Greeks, and Romans); if the Canaanites had any such texts or other writings they have not survived. In addition, the type of genetic analyses that have been done for European populations has not been done for descendants of inhabitants of the Levant from this historical period. This paper uses genetic comparisons between 99 modern day residents of Lebanon (specifically, from Sidon and the Lebanese interior) and ancient DNA (aDNA) from ~3,700 year old genomes from petrous bone of individuals interred in gravesites in Sidon. For aDNA, these analyses yielded 0.4-2.3-fold genomic DNA coverage and 53-264-fold mitochondrial DNA coverage, and also compared Y chromosome sequences with present-day Lebanese, two Canaanite males and samples from the 1000 Genomes Project. Over one million single nucleotide polymorphisms (SNPs) were used for comparison.

These results indicated that the Canaanite ancestry was an admixture of local Neolithic populations and migrants from Chalcolithic (Copper Age) Iran. The authors estimate from these linkage disequilibrium studies that this admixture occurred between 6,600 and 3,550 years ago, a date that is consistent with recorded mass migrations in the region during that time. Perhaps surprisingly, their results also show that the majority of the present-day Lebanese population has inherited most of their genomic DNA from these Canaanite ancestors. These researchers also found traces of Eurasian ancestry consistent with conquests by outside populations during the period from 3,750-2,170 years ago, as well as the expansion of Phoenician maritime trade network that extended during historical time to the Iberian Peninsula.

The second paper arose from genetic studies of an Asian/African admixture population on Mozambique. This group** from the University of Toulouse, INSERM, the University of Bordeaux, University of Indonesia, the Max Plank Institute for Evolutionary Anthropology, Institut genomique, Centre Nacional de Genotypage, University of Melbourne, and the Universite de la Rochelle, showed geographic stratification between ancestral African (mostly Bantu) and Asian (Austronesean) ancestors. Cultural, historical, linguistic, ethnographic, archeological, and genetic studies supports the conclusion that Madagascar residents have traits from both populations but the effects of settlement history are termed "contentious" by these authors. Various competing putative "founder" populations (including Arabic, Indian, Papuan, and/or Jewish populations as well as first settlers found only in legend, under names like "Vazimba," "Kimosy," and "Gola") have been posited as initial settlers. These researchers report an attempt to illuminate the ancestry of the Malagasy by a study of human genetics.

These results showed common Bantu and Austronesian descent for the population with what the authors termed "limited" paternal contributions from Europe and Middle Eastern populations. The admixture of African and Austronesian populations occurred "recently" (i.e., over the past millennium) but was gender-biased and heterogeneous, which reflected for these researchers independent colonization by the two groups. The results also indicated that detectable genetic structure can be imposed on human populations over a relatively brief time (~ a few centuries).

Using a "grid-based approach" the researchers performed a high-resolution genetic diversity study that included maternal and paternal lineages as well as genome-wide data from 257 villages and over 2,700 Malagasy individuals. Maternal inheritance patterns were interrogated using mitochondrial DNA and patterns of paternity assayed using Y chromosomal sequences. Non-gender specific relationships were assessed through 2.5 million SNPs. Mitochondrial DNA analyses showed maternal inheritance from either African or East Asian origins (with one unique Madagascar variant termed M23) in roughly equal amounts, with no evidence of maternal gene flow from Europe or the Middle East. The M23 variant shows evidence of recent (within 900-1500 years) origin. Y chromosomal sequences, in contrast are much more prevalent from African origins (70.7% Africa:20.7% East Asia); the authors hypothesize that the remainder may reflect Muslim influences, with evidence of but little European ancestry.

Admixture assessments support Southeast Asian (Indonesian) and East African source populations for the Malagasy admixture. These results provide the frequency of the African component to be ~59%, the Asian component frequency to be ~37%, and the Western European component to have a frequency of about 4% (albeit with considerable variation, e.g., African ancestry can range from ~26% to almost 93%). Similar results were obtained when the frequency of chromosomal fragments shared with other populations were compared to the Malagasy population (finding the closest link to Asian populations from south Borneo, and excluding Indian, Somali, and Ethiopian populations, although the analysis was sensitive in one individual to detect French Basque ancestry). The split with ancestral Asian populations either occurred ~2,500 years ago or by slower divergence between ~2,000-3,000 years ago, while divergence with Bantu populations occurred more recently (~1,500 years ago).

There were also significant differences in geographic distribution between descendants of these ancestral populations. Maternal African lineages were found predominantly in north Madagascar, with material Asian lineages found in central and southern Madagascar (from mtDNA analyses). Paternal lineages were generally much lower overall for Asian descendants (~30% in central Madagascar) based on Y chromosome analyses. Genome-wide analyses showed "highlanders" had predominantly Asian ancestry (~65%) while coastal inhabitants had predominantly (~65%) African ancestry; these results depended greatly on the method of performing the analyses which affected the granularity of the geographic correlates. Finally, assessing admixture patterns indicated that the genetic results are consistent with single intermixing event (500-900 years ago) for all but one geographic area, which may have seen a first event 28 generations ago and a second one only 4 generations ago. These researchers also found evidence of at least one population bottleneck, where the number of individuals dropped to a few hundred people about 1,000-800 years ago.

These results are represented pictorially in the paper:

In view of the current political climate, the eloquent opening of the paper deserves attention:

Ancient long-distance voyaging between continents stimulates the imagination, raises questions about the circumstances surrounding such voyages, and reminds us that globalization is not a recent phenomenon. Moreover, populations which thereby come into contact can exchange genes, goods, ideas and technologies.

* Marc Haber, Claude Doumet-Serhal, Christiana Scheib, Yali Xue, Petr Danecek, Massimo Mezzavilla, Sonia Youhanna, Rui Martiniano, Javier Prado-Martinez, Micha Szpak, Elizabeth Matisoo-Smith, Holger Schutkowski, Richard Mikulski, Pierre Zalloua, Toomas Kivisild, Chris Tyler-Smith

** Denis Pierrona, Margit Heiskea, Harilanto Razafindrazakaa, Ignace Rakotob, Nelly Rabetokotanyb, Bodo Ravololomangab, Lucien M.-A. Rakotozafyb, Mireille Mialy Rakotomalalab, Michel Razafiarivonyb, Bako Rasoarifetrab, Miakabola Andriamampianina Raharijesyb, Lolona Razafindralambob, Ramilisoninab, Fulgence Fanonyb, Sendra Lejamblec, Olivier Thomasc, Ahmed Mohamed Abdallahc, Christophe Rocherc,, Amal Arachichec, Laure Tonasoa, Veronica Pereda-lotha, Stphanie Schiavinatoa, Nicolas Brucatoa, Francois-Xavier Ricauta, Pradiptajati Kusumaa,d,e, Herawati Sudoyod,e, Shengyu Nif, Anne Bolandg, Jean-Francois Deleuzeg, Philippe Beaujardh, Philippe Grangei, Sander Adelaarj, Mark Stonekingf, Jean-Aim Rakotoarisoab, Chantal Radimilahy, and Thierry Letelliera

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Using Genetics to Uncover Human History - JD Supra (press release)

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Hendrix Genetics is an economic ‘win-win’ for GI – Grand Island Independent

Posted: August 23, 2017 at 4:45 am

The opening of Hendrix Genetics in Grand Island on Aug. 15 is an excellent example of the power of markets supplemented by appropriate government policy.

Feeding a growing world population now estimated to be 7.5 billion provides both a challenge and an opportunity as food producers endeavor to meet the growing demand for food. For Hendrix Genetics this demand represents opportunity as it is a world leader in turkey, layer and trout breeding as well as a major player in swine, salmon and guinea fowl production.

The numbers connected with Hendrix Genetics are impressive. They currently have 25 percent of the United States egg hatchery market and the new hatchery in Grand Island will serve 10 percent of the U.S. market. With good science and management, poultry production is an excellent way to provide quality food for both domestic and world markets.

Hendrix Genetics was willing and able to create the Grand Island plant because essential markets were available to meet their needs. After a nationwide search they determined that Grand Island was an excellent location. It provided needed isolation that was essential for the required biosecurity. In our area they found infrastructure for transportation needs, access to willing, affordable and capable labor and area producers to build and manage outlying barns as well as to provide feed.

For each component in the production process, prices, profits and wages had to be sufficient to bring together all the resources necessary to open and operate the plant.

Government policies had to align with needs of Hendrix Genetics and our community gave them an excellent invitation to grow our economy. The work of the Grand Island Area Economic Development Corporation was very important and we would add necessary and effective. Government and private enterprise had an effective partnership.

Also to be noted is that Hendrix Genetics is based in Holland and joins other industries in our community that are based in other countries such as New Holland-Italy and JBS-Brazil. Global interdependence is a reality and a plus for all those ready and willing to participate in the global economy.

America first may be effective political rhetoric in some parts of our country, but it is not good long term economic policy. Free trade and open borders will serve us better, particularly the food producers in the Midwest who are willing and able to feed the growing world population and rely on world markets.

This confluence of markets has added an $18 million investment to the city of Grand Island, more than 40 permanent jobs and an economic infusion estimated at $40 million.

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How white supremacists respond when their DNA says they’re not … – PBS NewsHour

Posted: August 23, 2017 at 4:45 am

A white supremacist wears a shirt with the slogan European Brotherhood at a rally in Charlottesville, Virginia, U.S., August 12, 2017. Photo by Joshua Roberts/Reuters

Whether youre a white supremacist, a white nationalist or a member of the alt-right, much of your ideology centers around a simple principle: being white. The creation of a white ethnostate, populated and controlled by pure descendants of white Europeans, ranks high on your priority list.

Yet, when confronted with genetic evidence suggesting someone isnt pure blood, as white supremacists put it, they do not cast the person out of online communities. They bargain.

A new study from UCLA found when genetic ancestry tests like 23andMe spot mixed ancestry among white supremacists, most respond in three ways to discount the results and keep members with impure genealogy in their clan. Their reactions range from challenging the basic math behind the tests to accusing Jewish conspirators of sabotage.

Some argued their family history was all the proof they needed. Or they looked in the mirror and clung to the notion that race and ethnicity are directly visible, which is false.

But the real takeaway centers on a new, nuanced pattern within white supremacist groups to redefine and solidify their ranks through genetic ancestry testing, said Aaron Panofsky, a UCLA sociologist who co-led the study presented Monday at the American Sociological Associations 112th annual meeting in Montreal.

Once they start to see that a lot of members of their community are not going to fit the all-white criteria, they start to say, Well, do we have to think about what percentage [of white European genealogy] could define membership? said Aaron Panofsky, a UCLA sociologist who co-led the study presented Monday at the American Sociological Associations 112th annual meeting in Montreal.

And this co-opting of science raises an important reminder: The best way to counter white supremacists may not be to fight their alternative facts with logical ones, according to people who rehabilitate far-right extremists.

To catalog white supremacists reactions to genetic ancestry results, this study logged onto the website Stormfront. Launched in 1995, Stormfront was an original forum of white supremacy views on the internet. The website resembles a Reddit-style social network, filled with chat forums and users posting under anonymous nicknames. By housing nearly one million archived threads and over twelve million posts by 325,000 or more members, Stormfront serves as a living history of the white nationalist movement.

Over the course of two years, Panofsky and fellow UCLA sociologist Joan Donovan combed through this online community and found 153 posts where users volunteered the results of genetic ancestry tests. They then read through the subsequent discussion threads 2,341 posts wherein the community faced their collective identities.

No surprise, but white supremacists celebrate the test results that suggest full European ancestry. One example:

67% British isles18% Balkan15% Scandinavian100% white! HURRAY!

On the flip side, Panofsky and Donovan found that bad news was rarely met with expulsion from the group.

So sometimes, someone says, Yeah, this makes you not white. Go kill yourself,' Panofsky said. Much more of the responses are what we call repair responses where theyre saying, OK, this is bad news. Lets think about how you should interpret this news to make it to make it right.'

These repair responses fell into two categories.

Reject! One coping mechanism involved the outright rejection of genetic tests validity. Some argued their family history was all the proof they needed. Or they looked in the mirror and clung to the notion that race and ethnicity are directly visible, which is false, University of Chicago population geneticist John Novembre told NewsHour.

Genetically, the idea of white European as a single homogenous group does not hold up.

Though the genetics of whiteness are not completely understood, the gene variants known to influence skin color are more diluted across the globe than any random spot in the human genome. That is to say, humans appear, based on our skin pigmentation, to be much more different from each other than we actually are on a genomic level, Novembre said.

Others accused the ancestry companies of being run and manipulated by Jews, in an attempt to thwart white nationalism, but even other Stormfront users pointed out the inaccuracy of this idea.

Reinterpret:The biggest proportion of responses 1,260 posts tried to rationalize the result by offering an educational or scientific explanation for the genetic ancestry results. Many in the online community played a numbers game. If a genetic ancestry test stated someone was 95 percent white European, they would merely count the remaining 5 percent as a statistical error.

Many adapted this line of thinking to make exceptions for those with mixed ancestry. Nearly 500 posts made appeals by misapplying theories of genetics or by saying whiteness is a culture, not just biology an apparent contradiction to the mission of forming a pure ethnostate. This trend led some white supremacists to debate the boundaries of their ethnostate, Panofsky said.

They start to think about the genetic signs and markers of white nationalism that might be useful for our community, Panofsky said. [They say] maybe there are going to be lots of different white nations, each with slightly different rules for nationalism? Or an overlapping set of nations, that are genetically defined in their own ways?

But these arguments are moot, because these genetic ancestry boundaries are inherently built on shaky ground.

If it seems white supremacists are making arbitrary decisions about their ancestry tests, its hard to blame them. Direct-to-consumer ancestry testing is a slippery, secretive industry, built largely upon arbitrary scientific definitions.

Its black box because its corporate, said Jonathan Marks, biological anthropologist at the University of North Carolina at Charlotte. The way these answers are generated depends strongly on the sampling, the laboratory work that you do and the algorithm that you use to analyze the information. All of this stuff is intellectual property. We cant really evaluate it.

White nationalists carry torches on the grounds of the University of Virginia, on the eve of a planned Unite The Right rally in Charlottesville, Virginia, U.S. August 11, 2017. Picture taken August 11, 2017. Photo by Alejandro Alvarez/News2Share via REUTERS

Genetic ancestry companies assess a persons geographic heritage by analyzing DNA markers in their autosomal DNA (for individual variation), mitochondrial DNA (for maternal history) or their Y chromosome (for paternal history). The latter two sources of DNA remain unchanged from parent to child to grandchild, aside from a relatively small number of mutations that occur naturally during life. These mutations can serve as branch points in the trees of human ancestry, Panofsky and Donovan wrote, and as DNA markers specific to different regions around the world.

When genetic anthropologists examine the full scope of humans, they find that historical patterns in DNA markers make the case that everyone in the world came from a common ancestor who was born in East Africa within the last 100,000 to 200,000 years. Plus, groups intermingled so much over the course of history that genetic diversity is a continuum both within American and Europe, through to Asia and Africa, Novembre of the University of Chicago said.

WATCH: Years after transatlantic slavery, DNA tests give clarity

Genetically, the idea of white European as a single homogenous group does not hold up. The classic geographic boundaries of the Mediterranean, Caucasus, and Urals that have shaped human movement and contact are all permeable barriers, said Novembre. Most of the genetic variants you or I carry, we share with other people all across the globeIf you are in some ethnic group, there are not single genetic variants that you definitely have and everyone outside the group does not.

Commercial ancestry companies know these truths, but bend them to draw arbitrary conclusions about peoples ancestry, researchers say. They compare DNA from a customer to the genomes of people or reference groups whose ancestries they claim to already know.

23andMe, for instance, uses reference dataset that include genomes from 10,418 people who were carefully chosen to reflect populations that existed before transcontinental travel and migration were common (at least 500 years ago). To build these geographic groups, they select individuals who say all four of their grandparents were born in the same country, and then remove outliers whose DNA markers do not match well within the group.

These choices willfully bias the genetic definitions for both geography and time. They claim that a relatively small group of modern people can reveal the past makeup of Europe, Africa and Asia and the ancestral histories for millions of customers. But their reference groups skew toward the present and overpromise on the details of where people came from.

While 23andMe denounces the use of their services to justify hateful ideologies, they do not actively ban known white supremacists from their DNA testing.

A study by 23andMe reported that with their definition of European ancestry, there is an average of 98.6 percent European ancestry among self-reported European-Americans. But given all Ive said, we should digest this with caution, Novembre said. An individual with 100 percent European ancestry tests is simply someone who looks very much like the European reference samples being used.

Though ancestry companies cite research that claims genetic tests can pinpoint someone within 100 miles of their European ancestral home, thats not always the case. Marks offered the recent example of three blond triplets who took an ancestry test for the TV show The Doctors. The test said the triplets were 99 percent European. But one sister had more English and Irish ancestry, while another had more French and German. Did we mention they are identical triplets?

That shows you just how much slop there is in these kinds of of ancestry estimates, Marks said.

Marks described commercial ancestry testing as recreational science because its proprietary nature lacks public, academic oversight, but uses scientific practices to validate stereotypical notions of race and ethnicity.

While 23andMe denounces the use of their services to justify hateful ideologies, they do not actively ban known white supremacists from their DNA testing, BuzzFeed reported.

But white supremacists arent the only ones to buy into these wayward notions when genetic ancestry tests support their self-prescribed identities or reject the science when things dont pan out as expected. African-Americans do it too, as Columbia University sociologist Alondra Nelson found in 2008.

Consumers have what I call genealogical aspiration, Nelson told NewsHour. They often make choices among dozens of companies based on the kind of information theyre seeking. If youre interested in finding whether or not youre a member of the small group that has, for example, some trace of Neanderthal DNA, then youre going to go to a company that focuses on that.

She said Panofsky and Donovans study shows that white nationalists will engage in a process of psychic and symbolic negotiation when genetic ancestry results fail to satisfy their impossible idea for racial purity.

But Panofsky, who doesnt support or sympathize with white nationalists, believes these negotiations are not a reason to dismiss white nationalists as ignorant and stupid.

I think that is actually a dangerous view, Panofsky said. Our study reveals that these white nationalists are often engaging with genetic information in extraordinarily sophisticated ways.

Many white supremacists are dealing with toxic shame, a perpetual subconscious belief system where their sense of identity is negative.

White supremacists are trying to deal with the issue of identity as an intellectual problem, said Tony McAleer, the co-founder and board chair of Life After Hate, a counseling organization that rehabs white supremacists. But he said the rehab of white nationalist views doesnt start with challenging their mental gymnastics with data.

We need to deal with the emotional drivers first, McAleer said. University of Maryland did a study of violent extremists and what they found was the number one correlated factor with someone joining a violent extremist group was childhood trauma.

But McAleer continued that the emotional trauma fueling white supremacy extends past physical and sexual abuse. Many white supremacists are dealing with toxic shame, a perpetual subconscious belief system where their sense of identity is negative.

The person feels at a subconscious level theyre not good enough, McAleer said. One way to react to that is to perpetually spend all of your efforts to prove to the world that you are a winner.

So, Life After Hates antidote to this shame is compassion and empathy, he said. Rather than toss statistics about how Muslims arent flooding the country and do not lead to spikes in crime, they will take a white supremacist to an Islamic center and have them sit down and spend time there.

A personal connection is a much more powerful way to change the dynamics within a person, than it is to re-educate the dataset thats in their head, McAleer said.

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Antonio Silva is on a troubling career trajectory, and there’s no one who can stop him – MMAjunkie.com

Posted: August 23, 2017 at 4:45 am

Heres what Antonio Silvas career looks like over the past two years: Win (TKO), loss (TKO), loss (KO), loss (KO), loss (decision), loss (KO).

Hes been stopped by strikes in seven of his past 10 bouts. He has just two victories since 2012 one over Soa Palelei, and one over Alistair Overeem, who was beating him soundly until a sudden third-round comeback by Silva.

If you do some combat sports math on the 37-year-old Bigfoot, what you see is a fighter on a dangerous trajectory. That path took him out of the UFC and into two fights for smaller Russian promotions, both of which he lost. His last knockout loss was two months ago.

So why did Silva (19-12-1 MMA)just sign on for a kickboxing bout against GLORY heavyweight champion Rico Verhoeven (51-10-1 kickboxing)in China this October?

Obviously, its not a good fight for Bigfoot, Silvas longtime manager Alex Davis told MMAjunkie. Jumping right into (GLORY) to go against the current champ, whos a murderer? Yeah, we get it.

But Silvas doing it anyway, and for reasons that are as old as the fight game.

For one, he thinks he can win. According to Davis, Bigfoot is back on testosterone-replacement therapy, which he used somewhat controversially for a time in the UFC, before the practice was effectively banned.

Now, fighting in places like Russia and China, and for organizations whose anti-doping policies are notably less stringent, hes free to resume the use of synthetic testosterone, which makes a huge difference for him, Davis said.

And also he needs money, Davis said. He cant turn down fights at the moment for that reason. If it was up to me, he would not take this fight. But at the end of the day, my job is to inform him, give him my advice, and the one who has to make the final decision is him.

Here we get into a persistent problem for fighters and fight sports. No one can tell Silva to stop. They can suggest and argue and recommend. Promoters can cut him and trainers could refuse to train him. Even Davis, a longtime friend, could stop managing him.

But as long as Silva can find someone willing to pay for his name and his willingness to walk face-first into someone elses fists, he gets to keep going.

It was the same with Gary Goodridge, another MMA fighter who turned to kickboxing later in his career. He lost about twice as many kickboxing bouts as he won, but his appeal for promoters was that, when you booked Big Daddy, you knew someone would get knocked out even if the someone was usually him.

For Goodridge, those years of damage contributed to brain trauma that eventually left him unable to remember conversations moments after theyd ended. By the evening, he couldnt tell you what hed done during the afternoon.

But Goodridge also needed the money. Even when he knew he shouldnt fight anymore, he was a man in his forties with no real work history outside of cages and rings. What else was he supposed to do?

According to Davis, Silvas brain health has been closely monitored with testing done at the Cleveland Clinics Lou Ruvo Center for Brain Health in Las Vegas.

Physically, Bigfoot has no problems whatsoever, Davis said. He has no brain damage. Weve done extensive research and testing, even before he left the UFC. So hes OK on that end.

But then, some signs of degenerative brain diseases like CTE (chronic traumatic encephalopathy), which researchers have found in the brains of deceased fighters and football players, are sometimes not apparent until years after the actual trauma.

And clearly, Silva is doing himself no favors. He went less than five months between knockout losses in 2016. Youd have to go back to 2010 to find a single calendar year in which he didnt suffer at least one knockout.

This fight against Verhoeven doesnt promise to be any easier on his brain. Verhoeven is younger, faster, and riding a winning streak thats about as good as Silvas losing streak is bad. If anything, the kickboxing rules will likely only lead to Silva absorbing more punishment than he would in an MMA bout. And then what?

Soon the paycheck will be spent and Silva will face the same questions about his future that he faces now. So far, he only seems to know one answer.

Ill be very sincere and tell you, I cant defend a man from himself, Davis said. If he fights and doesnt manage his money, hell go looking for the next fight. This is a very common problem with many fighters, not just Bigfoot. Thats what creates situations like Gary Goodridge.

As for Goodridge, he also had people telling him he should stop. Then he had people telling him that there was something troubling happening to him. The damage sneaks up on you, he said later. When he finally realized the full extent of it, it was too late to stop it.

I had no idea it was coming, Goodridge said in 2012. You dont know. Everyone around you tells you its happening, but you dont notice it yourself.

For more on the upcoming MMA schedule, check out the MMA Rumors section of the site.

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‘There is no contradiction to being a vegan and eating GMO foods’ – Genetic Literacy Project

Posted: August 23, 2017 at 4:44 am

My names Diana Pea, and I am a yoga-loving, bicycle-riding, palm oil-avoiding. environmentalist, ingredient list-reading vegan. I get 92.4 percent of my monthly calories from simple foods: rice, beans, tofu, and soybean oil (yes, I calculated it). I calculated the ecological impact of the rice I eat assuming it came from California vs. Arkansas. Essentially, Im a walking stereotype.

The reason why I state these things about myself is because I want to make it clear that I share the same concerns as the rest of the vegan population, particularly an adherence to the central tenant of the vegan philosophy: an optimization of agriculture to minimize suffering and pain of sentient beings. However, regardless of my stereotypically vegan behavior, I, unlike many vegans, am in favor of biotechnology, particularly GMOs, in agriculture, and I think that all vegans should be.

Lets take one simple example first: genetically-engineered wheat and other staples or seeds to produce omega-3 fatty acids. Crops like these could very well be an excellent replacement of fish for omega-3 fatty acids, taking away any excuse for people to continue eating fish. This would reduce the suffering within aquatic ecosystems, and it could be implemented if we got burdensome governments out of the way of innovation. There is no plausible mechanism of harm to such an idea. We know that the staples we eat are safe and that omega-3 fatty acids are safe. Thus, a staple that is engineered to produce omega-3 wouldnt be dangerous.

One might argue that we can simply use flaxseeds instead of GE foods; however, this isnt a very practical idea. First of all, staples are already widely eaten, making it much easier to get people to switch from fish to a staple with GEO-derived oils than to flaxseeds. Additionally, 96 percent of the US flaxseeds are grown in North Dakota. This isnt a coincidence. This is because of the fact that different places have varying soil conditions, climates, and other factors that lead to different yields of different crops.

Farmers want to optimize yields, which is why farmers in Idaho grow lots of potatoes, while those in Arkansas grow lots of rice. If we were to decide to suddenly eat more flaxseed as a nation, then not only would many farmers have to switch to growing these seeds, but yields wouldnt be optimal everywhere. This would mean more land being devoted to agriculture, which would hurt natural ecosystems. These practical limitations make GE staples a much better substitute source for omega-3 than flax seeds.

A vegans view of GE innovations

Many of my fellow vegans might argue whether such an innovation will be vegan at all. They might say that they dont want fish genes in their wheat, ignoring the fact that fish genes dont exist (All humans share many genes in common with fish: are they human genes or fish genes?). There is no need to use genes from an actual fish in the first place. Modern technology, being as cool as it is today, gave us DNA synthesizers that enable the construction of synthetic genes from known genomic templates, making an actual fish totally unnecessary in the process of genetically engineering staple crops to make omega-3. Besides, even if we did need the fish, there would be no need to kill one to get DNA. Youd simply need one cell sample, and you could then use PCR (polymerase chain reaction) to make thousands of copies of the gene in question for R&D. Lets not make the perfect the enemy of the good here. Nonetheless, the genes in question would come from algae since fish dont have them, so the entire debate is moot. Although the point still stands for any crops modified with genes originally found in animals.

Furthermore, yield-preserving traits like Bt and Roundup-Ready allow for crops to beat pests like insects and weeds in a safe, effective way, and there are hundreds of independent studies to prove it. This means less land for agriculture being needed, allowing for more habitats for animals around the world. On top of that, Simplots Innate Potato resists browning and bruising and allows for long-term storage, with a future generation model resisting late blight fungus, all with the FDA seal of approval.

These traits mean fewer fungicides used, less food waste (on the field, in the store, and at home), less land needed to grow the same amount of potatoes, and more affordable crops. All of these traits are good for optimizing agriculture for the environment and consumers, and are just a few examples of traits that could be and are being utilized as we speak. Imagine what more could be done if we stopped hampering this amazing technology with burdensome regulations. We could do a lot of good for the world of agriculture with such beneficial innovation.

Additionally, biotechnology could generate synthetic animal products. We already use genetically engineered yeast and bacteria to produce all sorts of valuable substances, from insulin to the vitamins in the tablets I personally use in place of many foods. They are also used in making many common foods, such as almost all of the hard cheese made in the world, and many beersalthough many GMO labeling laws exempt these foods. The rennet used in the cheese-making process used to come from calves, making GE microorganisms a more humane source. There is no reason why we cant use this same biotechnology to produce milk proteins to make cheese free of cows or to accelerate growth in cell cultures to make synthetic meats.

In fact, many groups are working on these sorts of projects, and some dont involve genetic engineering at all. Memphis Meats, New Wave Foods, and many other groups are doing the admirable work of taking animals out of agriculture, while feeding the world more efficiently in the process. Its extremely unfortunate that many of those getting in the way of such goals are vegans, but would rather let their naturalist ideology and dogma supersede their opposition to animal exploitation

Harmless biopsies allow for the collection of cells from donor animals, and these cells can be used to make tons of meat to make millions of burgers. Yes, you read that right. Even if this technology involved the deaths of a few animals to harvest the substrate medium and scaffolding structure for the cultured beef, that doesnt change the fact that this is a net benefit to preventing animal deaths. This technology could lower the death toll from the current unimaginable number (go ahead and try to imagine 10,000,000,000 per year of anything; its literally unimaginable) to a much smaller amount that is a net benefit to livestock. Once again, lets not make the perfect the enemy of the good here. Being purists will only hurt animals.

Other technologies such as induced-pluripotent stem cells (regular cells turned into stem cells) can take what little animal involvement that takes place in cellular agriculture and reduce it even further to almost nothing Scientists are already developing gel-based scaffolding methods to replace the collagen used normally, along with growth media free from fetal bovine serum. Cellular agriculture is progressively lessening its reliance on animals to produce food to feed the world. Its important for vegans to come together to support this technology to back research that could improve it even more. I cannot stress enough the point that being purists will only hurt our cause; we can make cellular agriculture rely as little on animals as possible, which is a net benefit to animals.

Call for vegan action

Unfortunately, people arent choosing to adopt a vegan diet. The reasons are irrelevant, as the end result is still the same: less than 2 percent of the population consists of vegans at any given time. We are never going to convince the large majority of people to adopt a collective vegan diet. Attempting to do so is admirable, but its not working. As unfortunate as that is, we can still do a lot more good for livestock animals with the aforementioned technology. There is no good reason to eschew it and stand in the way of perfectly good solutions through fear mongering and obstruction.

I became a vegan as an extension of my pacifist and environmentalist leanings. Because of this, I would hate to see fellow vegans stand in the way of protecting our fellow earthlings for baseless ideological reasons. Vegans could come together through finances, promotional manpower, and even by becoming researchers and educators to create a new generation of scientists to work on cellular agriculture.

With that being said, I think we should all remember the following: The best argument against the outreach method is a five-minute conversation with the average meat eater.

Im sorry to say that, but its true. People view the animal rights movement negatively, and extremist organizations like PETA have only hardened stereotypes. Organizations like Mercy for Animals utilize proven, effective methods of advocacy, but, while commendable, is not enough.

My goal is the same as that of many ethical vegans: sending the animal-based food industry as close to obsolescence as is practically possible. Im going to side with the winning team to make that goal a reality, and I truly hope that fellow vegans will side with me on that front in principle, participation, and finances. Our fellow earthlings demand it. Please dont let them down.

Diana Pea is an ethical/ecological vegan at Brooklyn College training to educate people about science. A long-time advocate, she promotes biotechnology and other evidence-based agricultural solutions to optimize food production and distribution, feed the world and to finally put an end to animal agriculture. Follow her on Twitter @Inorganic_Vegan.

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