Page 1,667«..1020..1,6661,6671,6681,669..1,6801,690..»

Category Archives: Transhuman News

Startling revelation of how Christianity was in already in Africa before colonization – GhanaWeb

Posted: July 5, 2017 at 8:48 am

Feature Article of Tuesday, 4 July 2017

Columnist: King David Dzirasah

It cannot be said that Christianity is a colonial relic or symbolism of slavery

Jerusalem long lost or not, Christianity is Afro-orient, not European. Christianity was thriving in the horn of Africa in the 1st century before this religion had really taken root anywhere in Europe. Akinyi Princess of KOrinda Yimbo.

Most often both academic and non-intellectuals based on historical understanding conclude that Europeans brought or introduced Christianity to Africa. It is often said that missionaries from Europe during the colonial days came down from Europe to Africa in their quest of spreading Christianity on a dark continent that is heading towards hell. However, there is ample evidence suggesting that Christianity was already on the continent before the advent of colonization and the coming of European missionaries.

The Coptic orthodox church of Alexandria is an oriental orthodox Christian church in Egypt, northeast Africa and Middle East. The Egyptian church is traditionally believed to be founded by Saint Mark at around AD 42. Christianity spread throughout Egypt within half a century of Saint Marks arrival. Christianity being introduced to the horn of Africa clearly is not as a result of missionary work of Europeans. Even though Christianity was able to spread from the northern part of Africa to the eastern part (Ethiopia), the complete spread of the religion to all part of the continent was made impossible due to the advancement of Islam in the northern part of the continent.

It is recognizable that historically Christianity came to Sub-Sahara Africa in the 15th century but that cannot over shadow the fact that Christianity was already on the continent before the coming of colonial imperialist. As of the 7th to 8th century, African warriors were fighting in Europe under the banner of the lion and the half-moon in order to bring the truth faith, Christianity or Islam, to Europe.

Europeans at the time were in the majority heathen and did everything in their power to remain heathen. Because Christ came from their corner of the world, Africans had embraced Christianity at a time when the religion was struggling to take root in Greece and Rome. Princess of Korinda-Yimbo. Historically Jesus was actually taken to the northern part of Africa (Egypt) as a child. With that link to that part of the continent, the people were accommodating to the missionary work of Saint Mark.

The biblical Ark of the Covenant is now believed to be kept in St Mary of Zions Church in Axum, Ethiopia. With the knowledge in mind that Africans actually play a crucial role in the expansion of the religion in Europe, one cannot make the assertion that Europeans actually introduced Africans to the religion. It cannot be said that Christianity is a colonial relic or symbolism of slavery since evidentially the existence of the religion precede colonization.

Go here to read the rest:
Startling revelation of how Christianity was in already in Africa before colonization - GhanaWeb

Posted in Moon Colonization | Comments Off on Startling revelation of how Christianity was in already in Africa before colonization – GhanaWeb

‘Woolly’ Breathes New Life Into A Scientific Saga – NPR

Posted: at 8:48 am

In the winter of 1990, George Church and Ting Wu he resplendent in his bushy beard, she wearing a skirt, which she rarely did rode their bicycles to city hall in Cambridge, Mass., to be wed. For years they kept their marriage an open secret, and that relationship would have ramifications, both positive and otherwise, for their careers: They worked together in a Harvard lab, trying to unlock the secrets of DNA.

Ben Mezrich's new book, Woolly, is about science's attempt in recent years to use genetic engineering to revive the extinct woolly mammoth. But as with his previous bestselling works of narrative nonfiction such as Bringing Down the House, the basis of the film 21, and The Accidental Billionaires, the basis of the film The Social Network Woolly dwells on close-ups before zooming out to the big picture.

Church and Wu are two of the main characters in Mezrich's taut yet detailed dramatization. Theirs is a synergistic relationship, and while it would be an overreach to call Woolly a love story at heart, the couple's dynamic is one of the essential threads of Mezrich's story. By all accounts geniuses, the two form the nucleus of a group of Harvard scientists whose revolutionary research leads them to a staggering conclusion: They must use their knowledge and abilities to manipulate the genome of Mammuthus primigenius, the hairy pachyderm that perished from the face of the earth over 3,000 years ago.

Their reasons, as Mezrich spells out, are more than academic. By pioneering the methods it would take to clone a mammoth and gestate the fetus successfully in the womb of an elephant, Church, Wu, and crew would open the door to further efforts to revive extinct species and, through the impact these reintroduced species would have on the environment, to help reverse the damages that modern civilization has had on Earth's ecosystem and climate.

The Harvard group isn't the only one working toward this end. In Russia, the father-son team of Sergey and Nikita Zimov launch Pleistocene Park, a wildlife preserve on the steppes of Siberia, where the mammoth once freely roamed and where they could possibly roam once more.

It all sounds very Jurassic Park, of course, and Mezrich doesn't hesitate to draw that parallel. The hubris of such scientific endeavors, as well as the ethical issues involved, crop up in Woolly, although it's clear the author's sympathies lie with his subjects. Anecdotes like the wedding of Church and Wu form the backbone of the book, rather than serving as ornament. Mezrich's eye for characterization is as sharp as his ability to break down scientific jargon into easily digestible chunks.

The true protagonists of Mezrich's saga, though, are the great mammoths themselves. Through his fluid use of close perspective, poetic license, and present-tense recreations of past events not to mention his occasional speculation into the future the author dramatically illustrates his tale. It's paced like a thriller, with the frustrating politics of the research industry bleeding over into the maneuverings of capitalists who see dollar signs in investing in widespread genetic engineering. Mezrich also frequently reconstructs dialogue between the plot's players, which at times feels overly contrived and distracting.

Thankfully it's not enough to inhibit the intimate look into the lives of the men and women who are humbly and at time not so humbly hoping to put the power of creation at their fingertips. With all the passion and vision of the scientists seeking to bring the mammoth back to life, Woolly reanimates history and breathes new life into the narrative of nature.

Jason Heller is a senior writer at The A.V. Club, a Hugo Award-winning editor and author of the novel Taft 2012.

More here:
'Woolly' Breathes New Life Into A Scientific Saga - NPR

Posted in Genetic Engineering | Comments Off on ‘Woolly’ Breathes New Life Into A Scientific Saga – NPR

$10 million gift launches joint Harvard, Children’s Hospital brain center – The Boston Globe

Posted: at 8:47 am

By Felice J. Freyer Globe Staff July 04, 2017

How did the human brain develop skills far beyond those of any other primate? Which genes enabled language, science, and art?

Those are some of the central questions facing the newly created Allen Discovery Center for Human Brain Evolution, a joint initiative of Boston Childrens Hospital and Harvard Medical School.

Advertisement

The Paul G. Allen Frontiers Group , a Seattle-based funder of scientific research, announced Wednesday that it is awarding $10 million over four years to launch the center.

The Allen Discovery Center will bring together researchers in neuronal molecular biology, human evolution, genetics, and genomics to figure out what exactly makes humans unique which genes were involved, when they came into play, and how they were affected by experience and environment.

Get Fast Forward in your inbox:

Forget yesterday's news. Get what you need today in this early-morning email.

Its just amazing to try to contemplate how humans developed with all the unique capacities that we have, said Dr. Christopher A. Walsh, chief of the Division of Genetics and Genomics at Boston Childrens Hospital and the centers leader.

The grant, he said, forces interactions between people doing very good work in their own separate areas.

For example, Walshs team at Childrens identified the genetic cause of a rare condition that results in babies born with tiny brains. The condition occurs when a certain gene is disabled. Could that gene have been responsible for the development of humans larger brains? Maybe nature boosted its function as a way of making the brains of our human ancestors get bigger, he said.

Advertisement

The Allen Discovery Center will make it easier for Walsh to answer that question by teaming up with center co-leader David E. Reich, a Harvard Medical School genetics professor, who studies the evolution of populations.

Michael Greenberg, a Harvard neurobiologist and also a center co-leader, said in a statement that the Allen grant would enable three laboratories that have been working independently to come together and study the genetic, molecular, and evolutionary forces that have given rise to the spectacular capacities of the human brain.

Originally posted here:
$10 million gift launches joint Harvard, Children's Hospital brain center - The Boston Globe

Posted in Human Genetics | Comments Off on $10 million gift launches joint Harvard, Children’s Hospital brain center – The Boston Globe

Genetics causing arthritis possibly helped humans survive Ice Age – The Indian Express

Posted: at 8:47 am

By: IANS | New York | Published:July 4, 2017 10:51 pm Mutations in the gene called GDF5 resulted in shorter bones that led to a compact body structure while reducing the risk of bone fracture from falling. Thus, it also favoured early humans to better withstand frostbite. (Source: File photo)

A genetic change associated with shorter stature and increased risk of arthritis might have helped our ancestors survive the Ice Age, a study has showed. The findings showed that mutations in the gene called GDF5 resulted in shorter bones that led to a compact body structure while reducing the risk of bone fracture from falling. Thus, it also favoured early humans to better withstand frostbite as well as helped them migrate from Africa to colder northern climates between 50,000 and 100,000 years ago.

These advantages in dealing with chilly temperatures and icy surfaces may have outweighed the threat of osteoarthritis, which usually occurs after a prime reproductive age, the researchers said. The variant that decreases height is lowering the activity of GDF5 in the growth plates of the bone.

Interestingly, the region that harbours this variant is closely linked to other mutations that affect GDF5 activity in the joints, increasing the risk of osteoarthritis in the knee and hip, said Terence Capellini, Associate Professor at the Harvard University. For the study, published in the journal Nature, the team examined gene GDF5 first linked to skeletal growth in the early 1990s to learn more about how the DNA sequences surrounding GDF5 might affect the genes expression.

They identified a single nucleotide change that is highly prevalent in Europeans and Asians but rarely occurs in Africans. Introducing this nucleotide change into laboratory mice revealed that it decreased the activity of GDF5 in the growth plates of the long bones of foetal mice. The potential medical impact of the finding is very interesting because so many people are affected, said David Kingsley, Professor at the Stanford University.

This is an incredibly prevalent, and ancient, variant. Many people think of osteoarthritis as a kind of wear-and-tear disease, but theres clearly a genetic component at work here as well. Now weve shown that positive evolutionary selection has given rise to one of the most common height variants and arthritis risk factors known in human populations, Kingsley said.

For all the latest Lifestyle News, download Indian Express App

Visit link:
Genetics causing arthritis possibly helped humans survive Ice Age - The Indian Express

Posted in Human Genetics | Comments Off on Genetics causing arthritis possibly helped humans survive Ice Age – The Indian Express

Getting Serious About Race – Stratfor Worldview (press release) (subscription) (blog)

Posted: at 8:47 am

Approaches to Unity

Over the millennia, people have found many different ways to solve coordination problems. Broadly speaking, there was a shift from a more cooperative hunter-gatherer toward a more coercive world after the agricultural revolution (which began around 9500 B.C. in the Middle East) followed by a shift back toward more cooperative versions in the last few hundred years. Between about 1000 B.C. and A.D. 1500, most people in the world lived in empires in which a small elite monopolizing military, administrative, religious and sometimes commercial functions used state power to integrate the activities of vast numbers of people in villages and towns. The Roman and Han Chinese empires coordinated tens of millions of subjects; the Song, Ming and Qing dynasties in China ruled over 100 million.

These empires tried to lower the costs of obtaining their subjects' obedience by promoting shared identities, but local, kin-based loyalties typically retained more appeal than the center. This became a fatal flaw when, in the last 200 years, empires had to compete with nation-states, which fused politics and ethnicity by insisting that the citizens of each state all shared a common ethnicity. Nation-states were, on the whole, much better than empires at persuading their citizens to make sacrifices for the common good, and the strains of competing against nation-states brought about the collapse of all the great traditional empires between 1911 (Qing China) and 1922 (Ottoman Turkey).

In reality, of course, the populations of nation-states were anything but homogeneous, and so their leaders always had to struggle to find ways to override genetic imperatives and make different people feel similar. We might range their responses along a spectrum from the illiberal to the liberal. Illiberal responses aimed to create homogeneity by destroying difference, in extreme cases by expelling or killing people who did not conform to the ideal. Communist Russia and China defined the ideal in terms of class and killed tens of millions of non-proletarians; fascist Germany defined it in terms of race and killed six million Jews.

Liberal responses, by contrast, aimed to create homogeneity by arguing that difference just did not matter. Two hundred years ago, even the most liberal societies excluded the bulk of their populations from full membership on the basis of race, sex, class, religion or some other variable. Since then, legislation and changing attitudes have steadily rolled back the exclusions. Thanks particularly to the defeat of fascism in World War II and Soviet communism in the Cold War, the illiberal vision of the nation-state was broadly discredited in the West, and for seventy years its democracies not only leaned toward liberal solutions but even pursued equality of outcome through aggressive programs of affirmative action.

For a good fifty years, anyone such as Barry Goldwater in the United States in 1964 and Enoch Powell in Britain in 1968 who emphasized racial differences between citizens courted political suicide. But that is now changing. Enough of the liberal consensus survives that politicians still have to treat race carefully, but in 2016 almost half of American voters supported a presidential candidate who promised to spend between $4 billion (his own lowest estimate) and $21.6 billion (the Department of Homeland Security's estimate) to build a wall to keep out Mexicans, and slightly more than half of the British electorate said it was ready to accept the major economic costs of leaving the European single market in order to limit immigration to 100,000 people per year. Something important is happening in politics.

Something important is happening in the scientific study of race too. In June 2000, in a speech celebrating the completion of the first survey of the entire human genome, President Bill Clinton announced that "one of the great truths to emerge from this triumphant expedition inside the human genome is that in genetic terms, all human beings, regardless of race, are more than 99.9 percent the same." This remains true; however, it is also true that humans and chimpanzees are genetically more than 98.8 percent the same. The 1.2 percent, however, makes all the difference in the world; and as they map genetic distributions in increasing detail, scientists have increasingly asked whether the 0.1 percent difference separating human genomes might not also matter.

As yet there is no clear answer to this question, as I learned in June at a conference at the Institute for Advanced Study in Toulouse. There, a group of distinguished economists, biologists, evolutionary anthropologists and psychologists debated the causes of institutional change, and several of the speakers discussed cross-country correlations between genetic differences and institutional differences. This is controversial stuff; any scientist who raises the possibility that genetic distance might have institutional and cultural consequences runs the risk of being dismissed as a Goldwater/Powell kind of crank, not fit for civilized company. However, at a time when racial arguments seem to be on the rise in Western politics, there can surely be few questions more important than this, and I was delighted to learn that scholars of this caliber were willing to take the risks.

However, not everyone is ready to do so. From Toulouse, I went directly to a conference at the British Academy in London, where another distinguished gathering, this time of historians, sociologists and experts in cultural studies were debating the concept of the "Anglosphere." This is a new name for the old idea that something vitally important connects Britain, the United States, Canada, Australia and New Zealand. In a famous book, Winston Churchill called this group The English-Speaking Peoples; other scholars since the late 19th century have preferred to speak of the Anglo-Saxon Race.

The newest term, "Anglosphere," leaves the question of whether we are investigating a racial or a linguistic category deliberately ambiguous. Speakers who thought "Anglosphere" was a useful concept tended to emphasize linguistic ties, arguing that these had created cultural and institutional similarities, which, in the wake of Brexit, should be deepened. Some even argued for that the time is ripe for a formal political union of Canzuk (Canada, Australia, New Zealand and the United Kingdom). Other speakers, however, insisted that the "Anglosphere" is a deeply racist idea, designed merely to legitimate White Anglo-Saxon Protestant oppression of minorities within these countries.

Continued here:
Getting Serious About Race - Stratfor Worldview (press release) (subscription) (blog)

Posted in Human Genetics | Comments Off on Getting Serious About Race – Stratfor Worldview (press release) (subscription) (blog)

Bladder control: Is there a genetic treatment for urinary incontinence? – Genetic Literacy Project

Posted: at 8:47 am

For many women particularly those who are older, pregnant or overweighta sudden sneeze or laugh can trigger a squirt of urine. And forget about jumping jacks.

Thanks to a genome-wide association study (GWAS) that identifies a gene that may contribute to stress urinary incontinence (the sneezing kind) or even the less common urge incontinence(aka overactive bladder), women may be able to add a re-purposed drug or two to the list of gadgets, medications, and procedures that can lower leak frequency.

The best way to minimize stress incontinence, is to do Kegel exercises, which contract the pelvic floor muscles. Also helpful is the bridge pose in Pilates (head and feet down, abdomen up). Wearing absorbent pads may work, as can losing weight and avoiding foods and drinks that promote peeing.

Of course, there are appsfor leaks. iDry, BladderPal, and Kegel Kat chart trips to the bathroom, schedule Kegel reminders,or, in one app that Charmin sponsors, locate the nearest restroom.

Devices to treat urinary incontinence are held in the vagina to keep things in place, and resemble certain sexual aids that somewhat rhyme with mildew. Advertisements for one FDA-approved product that signals the bladder not to spasm proclaims itselfa trip to the gym for your pelvic floor.

Clinicaltrials.gov, my go-to site for upcoming treatments, lists suchinterventionsas a rectal balloon, a hydrogel shot into the urethra, electrical stimulation, and various single-incision devices. I was excited to see one study coaxing human induced pluripotent stem cells to become skeletal muscle progenitor cells, which presumably can be implanted into the muscles failing at supporting the offending organ.

Related approaches to treat urinary incontinence are already available: Electrodesin the vagina or rectum. Various meshes, slings, hammocks, tapes, and ribbons Drugs(the old antidepressant imipramine, estrogen gel, anticholinergics, and antimuscarinics) Designer vagina surgery that in one unfortunate woman triggered a lasting sensation akin to an internal invasion of fire ants

The non-surgical Nu-Vseemed promising until I noticed the spelling errors on the website, at the literary level of a Trump tweet.

At the recent European Society of Human Genetics annual meeting in Copenhagen, Rufus Cartwright,a visiting researcher at Imperial College, London, reported that his team genotyped 8,979 women, consulted six additional studies, and sampled bladder cells in some participants to identify expressed genes.

The idea behind a GWAS is to narrow down parts of the genome that include specific gene variants that are found nearly exclusively among people with a particular condition in this case, urinary incontinence. Complementing that analysis is cataloguing which genes are active in those with incontinence but not others the transcriptome.

Three genes of interest emerged:

CHRM3 encodes a cholinergic receptor. Its already the main drug target for urge incontinence. SULF2 encodes a signaling enzyme and Im not sure how its connected to incontinence. Maybe the published paper will eventually explain it. EDN1 specifies endothelin 1, a protein produced on the interior surfaces of blood vessels that is the most potent smooth muscle vasoconstrictor known. Its expressed differently in bladders of women with stress incontinence. Bingo!

Implicating endothelin 1 is exciting, because drugs that target its pathway are already used to treat pulmonary hypertensionand Raynauds syndrome, both of which arise from constricted blood vessels.

Cartwright described the work:

Previous studies had failed to confirm any genetic causes for incontinence. Although I was always hopeful that we would find something significant, there were major challenges involved in finding enough women to participate, and then collecting the information about incontinence. It has taken more than five years of work, and has only been possible thanks to the existence of high quality cohort studies with participants who were keen to help. Clearly this will need further debate and an analysis, not just of the cost to healthcare systems, but also of the benefit to women who may be spared the distress of urinary incontinence.

Finding a gene variant that could be behind urinary incontinence is more than a possible route to a repurposed new treatment. It is also a shout-out to the value of basic biomedical research something threatened in the proposed federal budget.

The awkwardly-acronymed genome-wide association study GWAS was at first more or less a fishing expedition, directing attention to a vast swath of genomic territory that might harbor a gene that could explain why a bunch of people with the same trait or condition share it significantly more often than do others. The roots of the technique go back to the earliest days of human genome sequencing, as researchers identified single nucleotide polymorphisms (SNPs) single DNA base differences in a population at specific sites among the 3.2 billion A, T, G, and C nitrogenous bases.

A GWAS is especially helpful to understand the causes of more common conditions, the ones that arise from interactions of more than one gene and the environment and that dont exhibit the simple inheritance patterns of rare, single-gene diseases. A GWAS result can often be articulated in just a sentence or two, but it represents an incredible amount of work.

Now, with so many human genome sequences annotated since thefirst GWASwas published a dozen years ago, the technologys time has truly come. Find enough participants, and a GWAS can zero in on important, possibly causative, genes. The evolution of GWAS is a little like that of Google maps, from imaging a town to highlighting a specific house.

The idea for a GWAS was hatched long before genome analysis became fast enough and deep enough to reveal enough information to dissect the molecular underpinnings of common conditions like incontinence. A short-sighted federal budget that slashes funding for the type of basic research that led to this and other biotechnologies is not in anyones best interest.

Ricki Lewis is a long-time science writer with a PhD in genetics. She writes the DNA Science blog at PLOS and contributes regularly to Rare Disease Report and Medscape Medical News. Ricki is the author of the textbook Human Genetics: Concepts and Applications (McGraw-Hill, 12thedition out late summer); The Forever Fix: Gene Therapy and the Boy Who Saved It (St. Martins Press, 2013) and the just-published second edition of Human Genetics: The Basics (Routledge Press, 2017). She teaches Genethics online for the Alden March Bioethics Institute at Albany Medical College and is a genetic counselor at CareNet Medical Group in Schenectady, NY. You can find her at her website or on Twitter at @rickilewis

Read the rest here:
Bladder control: Is there a genetic treatment for urinary incontinence? - Genetic Literacy Project

Posted in Human Genetics | Comments Off on Bladder control: Is there a genetic treatment for urinary incontinence? – Genetic Literacy Project

In Neanderthal DNA, Signs of a Mysterious Human Migration – New York Times

Posted: at 8:46 am

The mystery only deepened in 2013. Another team of researchers retrieved mitochondrial DNA from a Neanderthal-like fossil at Sima de los Huesos, dating back 430,000 years.

The researchers had expected the DNA to resemble that of later Neanderthals in Europe. Instead, the mitochondrial DNA looked like it belonged to Denisovans even though the Denisova cave was 4,000 miles away in Siberia.

Last year, the researchers announced they had gathered a small fraction of the nuclear DNA from the same Sima de los Huesos fossil. That genetic material looked like it belonged to a Neanderthal, not a Denisovan.

Dr. Krause and his colleagues have now discovered new Neanderthal DNA that they believe can solve the mystery of this genetic mismatch.

In 2013, one of Dr. Krauses graduate students, Cosimo Posth, examined a Neanderthal fossil from a German cave called Hohlenstein-Stadel. He was able to reconstruct all of its mitochondrial DNA.

Dr. Posth estimated that the Neanderthal fossil was 120,000 years old and, more important, that it belonged to a branch of the Neanderthal family tree with a long history. He and his colleagues determined that all known Neanderthals inherited their mitochondrial DNA from an ancestor who lived 270,000 years ago.

All the data pointed to a sequence of events that could solve the puzzle that had bedeviled Dr. Krause for so long.

The common ancestors of Neanderthals and Denisovans spread across Europe and Asia over half a million years ago. Gradually the eastern and western populations parted ways, genetically speaking.

In the east, they became Denisovans. In the west, they became Neanderthals. The 430,000-year-old fossils at Sima de los Huesos Neanderthals with Denisovanlike genes capture the early stage of that split.

At some point before 270,000 years ago, African humans closely related to us moved into Europe and interbred with Neanderthals. Their DNA entered the Neanderthal gene pool.

Over many generations, most of that new DNA disappeared. But the mitochondrial DNA survived, passed down from mothers to their children. In fact, eventually all the Neanderthals inherited it, for some reason discarding the mitochondrial DNA that the species once had.

Dr. Posth said it was possible that early members of our own species moved from North Africa into Europe. Supporting this idea was the discovery reported last month of fossils of Homo sapiens in Morocco dating back 300,000 years.

But Dr. Posth said it was too soon to rule out another possibility: that these migrants belonged to another species in Africa closely related to us that scientists have yet to document.

I feel uncomfortable to give a name to these humans, Dr. Posth said.

Adam C. Siepel, a geneticist at Cold Spring Harbor Laboratory on Long Island who was not involved in the new study, said the hypothesis fit the evidence. I think thats absolutely possible, he said.

The new study raises a host of tantalizing implications about human history.

It is not possible to know just how many times these early Africans interbred with Neanderthals. But somewhere in prehistory, at least one female human from Africa must have carried the child of a male Neanderthal.

Now you have this hybrid child, which is probably pretty unusual-looking, Dr. Siepel said. One way or another, this hybrid individual was absorbed into Neanderthal society.

Dr. Siepel warned that the hypothesis hinges on the new DNA found in the Hohlenstein-Stadel fossil. Dr. Krause and his colleagues are now trying to retrieve nuclear DNA from the fossil.

The research at Sima de los Huesos shows just how far back in time scientists can now search for genes. The most revealing DNA might come from the mountains of Morocco.

There, scientists may be able to find genes from the earliest Homo sapiens, which they can then compare to Neanderthals.

These are things that I never thought possible five years ago, Dr. Krause said.

See the original post here:
In Neanderthal DNA, Signs of a Mysterious Human Migration - New York Times

Posted in DNA | Comments Off on In Neanderthal DNA, Signs of a Mysterious Human Migration – New York Times

A French Choreographer Who Plays With the DNA of Dance – New York Times

Posted: at 8:46 am

Mr. Charmatz said the idea for 10000 Gestures came to him while watching one of his own pieces, Leve des Conflits Extended, at the Museum of Modern Art in New York in 2013. The idea of Leve was that it was based on limited gestures, so you were constantly circling through the sequence, like a living sculpture changing shape, he said. I thought, what if you flip that, and have a piece where none of the dancers ever repeat a gesture or do the same one as anyone else?

How do you create 10,000 completely different gestures? Over many, many hours working in a group on various themes, Mr. Charmatz explained. The themes included: doing nothing, microscopic movements (raising an eyebrow, flicking fingers), violence, eroticism, dance history, obscenity, and politics a Brexit means Brexit gesture made by Theresa May is even in there.

Each person has a different idea about what an erotic or a violent gesture might be, Mr. Charmatz said, so you get 25 variations on these ideas all happening together.

All the themes come in a specific order and last for a predetermined amount of time, he explained, although the number of dancers onstage and the groupings they create vary constantly. When it was pointed out that structuring the work through changing configurations might verge on good choreography, he laughed. Of course I want it to be compelling to watch, he said. Im bringing all my skills, even the ones I dont have, to this piece.

A major name in the European contemporary dance world, Mr. Charmatz has never followed a traditional path. He made his name when still quite young: In 1993, at 19, he choreographed Bras le Corps with Dimitri Chamblas, a friend from the Conservatoire de Lyon, where both had trained after defecting from the Paris Opera Ballet school to pursue a more contemporary dance orientation. The simplicity, physicality and direct attack of Bras le Corps, performed in a boxing ring with spectators seated on all sides, was a salutary shock in the highly theatricalized world of 1990s French dance.

Mr. Charmatz continued on an iconoclastic path. He did not form his own ensemble or accept commissions for companies. He danced with various troupes and collaborated with fellow choreographers while creating relatively few pieces, which were often more like installation works than conventional dance performances. From 2002 to 2004, he ran a nomadic school for 15 students; he has written a book about contemporary dance and is a co-author of two others.

When he was appointed, in 2009, to lead the National Choreographic Center in Rennes, his first decision was to change its name to the Muse de la Danse. Unlike most of the choreographers who head regional centers in France, Mr. Charmatz has no permanent company, and works on a project-to-project basis. (His term in Rennes ends in 2018.)

Boris brings movement and ideas together in space in extraordinary ways, said John McGrath, the director of the Manchester International Festival, who added that he was keen to make dance an increasingly important part of the biennial event. How do ideas manifest in art? The ambition of this work, the largest he has ever made, and the ambition of the idea felt like something we could really embrace.

The experience of creating 10000 Gestures has been grueling but exhilarating, said Mr. Chamblas, who still dances Bras le Corps with Mr. Charmatz and is performing in 10000 Gestures. It is all entirely fixed choreographically, and you have to be very precise, and switch from one parameter to another extremely fast, he said.

He gave a quick run-down: At the beginning of the piece are the gestures of doing nothing, but very fast, 25 of them; then 15 movements going backwards, then 55 crazy movements, then five rest positions. All of that is about a minute.

Mr. Charmatz said that an important early decision was to perform almost everything at high speed. Whats interesting is to create a storm, like snowflakes coming at you in the light, he said. Its as if we keep running, the piece will hold together. Or like the idea that when you are dying, your life flashes before you. It plays also with the idea, which people are always saying, that dance is ephemeral, that no two moments are ever the same.

The underlying idea of death, he added, felt important, and also the idea of being fully present. Referring to the recent suicide bombing at an Ariana Grande concert, he said: We are in Manchester, with everything that happened here, so I have used Mozarts Requiem in the piece. And not to be too political, but its easy to feel, especially in France, like you cant move for problems migrants, unemployment, Brexit. In some ways this is also about moving on. Every moment says now.

A version of this article appears in print on July 5, 2017, on Page C2 of the New York edition with the headline: Breaking Down the DNA of Dance.

Excerpt from:
A French Choreographer Who Plays With the DNA of Dance - New York Times

Posted in DNA | Comments Off on A French Choreographer Who Plays With the DNA of Dance – New York Times

Is running ability down to effort or DNA? And can it be proved? – The Guardian (blog)

Posted: at 8:46 am

From long-distance running to sprinting is ability down to DNA or effort or both. Composite: Getty Images

Growing up, I was always the dumpy, unsporty one. Matt, my older brother, was the skinny one who did the running, jumping and anything requiring quickness and coordination. He seemed to excel with ease while I laboured away on a sluggish course towards sub-mediocrity. This pattern lasted until our late teens when Matt, being older, beat me to booze. While he was away on a year-long, round-the-world bender, I took up running with a vengeance. It was time to turn the tables.

By the time Matt got back, Id joined the local running club and was training every day. It turned out that becoming a competent runner didnt require special talent, just lots of miles driven on by the sense I was outrunning my former, slouchy self. Matt, visibly shaken by my transformation, threw himself into training to catch up stymied by his three-kilo beer belly.

'The biggest shock is my aerobic potential, rated "low". OK, I'm no Mo Farah, but but surely my aerobic capacity is at least middling'

Well skip the gory details the dozens of races where I beat Matt with ease and fast-forward to 2012. I had been training consistently for six years by now. Matt was swiftly catching up, but I still had a clear edge in any race of more than10 miles, so I decided to step up to the marathon. After putting in the hardest three months training of my life, I came away with a shiny new PB of 2hr 28 min 46 sec.

The point is not to revel in my glory. My time was decent club standard but hardly impressive against proper British marathoners, let alone African elites. The point is, it was amazing for me, given my widely presumed lack of ability. If only I had realised sooner that I had the potential

Imagine someone had tested my genes as a podgy kid and told me: dont worry, youre an athlete inside, its only your Sherbet Dip Dab habit holding you back. What wonderful reassurance and motivation that would have been. But wait. What if they had looked at my results and said: sorry, its not through lack of effort that you are sub-mediocre its down to your DNA. What then?

I was intrigued to find companies offering to do just that test my DNA to determine my sporting potential. Could it really work? I decided to find out.

I got in touch with DNAFit, the leading provider, and asked if they would blind-test my DNA plus a few other samples. To my surprise, they said yes. A call to some friends with connections in elite sport secured a sample from a multi-Olympian and world champion runner (on condition I wouldnt reveal his identity) lets call him Mr Swift and another from pro cyclist James McLaughlin. If their results tallied with their achievements, I figured, DNA testing would be worth taking notice of.

A few weeks later the results were in. Swifts read as follows: Aerobic potential: medium, which qualified as an intermediate VO2max tendency. Yet according to his physiologist, Swifts VO2max is above 77 quite definitely not an intermediate score. Furthermore, the report deems his power/endurance profile as favouring power over endurance by a ratio of 70/30. Swift is one of the greatest endurance runners in the history of the sport. His injury risk, marked medium, is also at odds with the actual evidence. He has had many, many injuries, his physiologist confides. Id say his injury risk is untypically high.

McLaughlins results are similarly at odds with his track record: his aerobic potential is rated medium, with a slight tendency towards power over endurance. It doesnt ring true at all, McLaughlin tells me. My VO2max is very high, nearly 82, and Im a pure endurance rider I fare far better in long, sustained efforts than in sprints.

My own results also suggest a predisposition towards power rather than endurance, 56/47. This flies in the face of my running experience: I am hopeless at shorter, power-based events; the longer the race, the better I do (relative to others). The biggest shock is my aerobic potential, rated low. OK, Im no Mo Farah, but surely my aerobic capacity is at least middling, or how could I have run a sub-2hr 30min marathon?

I owe it to DNAFit to give them a chance to explain after all, they have been generous in blind-testing samples, opening themselves up to journalistic scrutiny. The companys head of sport science is the former Olympic sprinter Craig Pickering, to whom I reveal the disparities between our results and our sporting track records.

You almost certainly cant use genes to tell who will be a good athlete or not a good athlete, he responds. There is no talent identification use in this.

Fair enough, but our world-class marathon runner was rated as having medium aerobic potential.

Thats a great example of how you cant use genetics to tell you what sport youll be good at.

OK, fine, so what can genetic testing tell us?

What the tests and reports do is give you information on which to base your training, to have a better informed programme.

Citing one DNAFit-supported study on a small group of athletes, Pickering says that the results provide enough information to guide training, either towards power (short, sharp) or endurance (longer, slower) sessions. This insight, he says, relates to genetically determined trainability rate of fitness gain rather than aptitude. Yet this wasnt the impression I had been given by the reports, covered as they are with the word potential.

I stress my concern to Pickering that, had I received my apparently bleak results as a newcomer to running, my athletic ambitions might have been crushed. But he thinks I am missing the subtleties. Because you have a low aerobic potential we have options, we can fine-tune and target other areas like movement economy and efficiency.

Low aerobic potential? We know that marathoners rely on their aerobic capacity, so surely this implies that my prospects were limited. No, that isnt what it means, he replies. I accept that potential does imply that. The title should be changed. I often call it your aerobic trainability.

By by this point, I have to admit, I am erring towards unconvinced. My scepticism deepens when I read the Athlome Projects consensus statement on direct-to-consumer (DTC) DNA tests:

The information provided by DTC is virtually meaningless for prediction and/or optimisation of sport performance. There is currently no evidence that existing genetic tests provide information that is useful regarding either predisposition for a particular sport, prediction of the training response likely to occur to a particular training programme, or predisposition to exercise-related injury.

Athlomes founder, Professor Yannis Pitsiladis, is even more damning: These results are pointless, throw them away. There are no grounds for any of it.

According to Pitsiladis, although there is vast, exciting scope for genetics-guided training, the science has a very long way to go: Were beginning to understand that performance is determined by hundreds, possibly even thousands of interacting genes. Even once they are known, we may not be able to make predictions with clinical significance; we will need to take into account the environmental factors as well.

Countering the criticism from Pitsiladis and his Athlome colleagues, Pickering alleges sour grapes: Theyre annoyed that weve done it before them and thats why theyre causing these problems. Their main goal was to sell genetic tests to people, in my opinion. They are frustrated that were one or two years ahead of them.

Pitsiladis doesnt deny having commercial interests in genetic testing but insists he is involved only in areas with demonstrable utility, such as using genetics to create improved anti-doping tests. He draws a sharp distinction between genetically testing elite athletes to assess their shared traits and testing amateurs who are almost as diverse a group as the general population.

Parents whove failed as athletes go buy this stuff, desperate for their kids to succeed Selling direct to consumers is the problem.

That is precisely my concern, too. Cant Pickering appreciate that for people such as myself, starting out as the unsporty sibling with every reason to doubt my genetic potential, my gloomy test results could have snuffed out my marathon dreams before I had even tried a 5k run?

I share your concern, he replies. Its something that, as a company, we try to communicate. Our reports use the word potential, and that needs to change We have to do a better job, and well continue to try.

Make no mistake, talent matters. Athletes such as McLaughlin and Swift are prodigiously genetically blessed. My older brother, too, is a natural. He overtook me and became a far superior athlete, as I always suspected he would. But being the best you can be isnt about biology, it is art as much as science. Talent isnt destiny decipherable from DNA; it waits to be realised through hard work, like a sculpture inside a boulder. So dont let anyone put you off get hammering.

Originally posted here:
Is running ability down to effort or DNA? And can it be proved? - The Guardian (blog)

Posted in DNA | Comments Off on Is running ability down to effort or DNA? And can it be proved? – The Guardian (blog)

New DNA identified in AMIA Jewish center bombing points to suicide attack – Jewish Telegraphic Agency

Posted: at 8:46 am

BUENOS AIRES (JTA) A new set of DNA has been identified among the 85 victims of the AMIA Buenos Aires Jewish Center attack, strengthening the hypothesis that the 1994 attack was carried out by a suicide bomber.

The discovery was announced on Monday by the AMIA Special Investigation Unit of the General Prosecution, two weeks before the 23rd anniversary of the bombing that also injured hundreds. The final report after two years of investigation by a forensics team, reveals for first time the existence of a genetic profile among the reserved remains in the laboratory of the Federal Police that doesnt belong to any known victims.

With this information the prosecutors in charge of the special unit are working on the hypothesis of the suicide bomber and have already taken steps in the field of international cooperation to try to match the profile obtained with that of samples of relatives of the suspected individual. The suspected individual isnt mentioned in thereport released to the publicbut is part of a previous report by the special unit, where he is named asIbrahim Hussein Berro, a Lebanese citizen and an alleged member of the terrorist group Hezbollah.

In May 2016, U.S. Attorney General Loretta Lynch and FBI director James Comeymet in Washington, D.C., with Argentine Justice Minister Germn Garavano and offered to extendtechnical help to the Argentinean Justice Department regarding the AMIA attack and the death of special prosecutor Alberto Nisman.

The body of a possible suicide terrorist was never found or identified until now. Five Iranians are on the Interpol international police agencys most wanted list in connection with the AMIA 1994 attack, however.

ProsecutorsSabrina Namer, Roberto Salum and Leonardo Filippini have led the AMIA Special Investigatory Unit since their predecessor, Alberto Nisman, who was discovered shot dead in his apartment in January 2015 hours before he had been scheduled to appear in Congress to present allegations that then-President Cristina Fernandez de Kirchner orchestrated a secret deal to cover up Iranian officials alleged role in the AMIA bombing. Fernandez denied the allegations and judges threw out the case; it was reopened one year ago, though no conclusions have yet been announced.

The two years work on the DNA analysis was conducted by the Argentine Forensic Anthropology Team, the Forensic Medical Body and the University of Buenos Aires.The same team one year ago identified victim number 85 of the AMIA attack.

Visit link:
New DNA identified in AMIA Jewish center bombing points to suicide attack - Jewish Telegraphic Agency

Posted in DNA | Comments Off on New DNA identified in AMIA Jewish center bombing points to suicide attack – Jewish Telegraphic Agency

Page 1,667«..1020..1,6661,6671,6681,669..1,6801,690..»