Category Archives: Embryonic Stem Cells


Research and Markets – Global Human Embryonic Stem Cells … – Markets Insider

DUBLIN, May 1, 2017 /PRNewswire/ --

Research and Markets has announced the addition of the "Human Embryonic Stem Cells (hESC) Market Analysis By Application (Regenerative Medicines, Stem Cell Biology Research, Tissue Engineering, Toxicology Testing), By Country (U.S., UK, Germany, Japan, China), And Segment Forecasts, 2014 - 2025" report to their offering.

The global human embryonic stem cells (hESCs) market is anticipated to reach USD 1.06 billion by 2025

Application of hESCs as a promising donor source for cellular transplantation therapies is anticipated to bolster progress through to 2025. hESCs technology tends to be useful for tissue engineering in humans due to high histocompatibility between host and graft.

Maintenance of developmental potential for contribution of derivatives of all three germ layers is an important feature of these cells. This ability remains consistent even after clonal derivation or prolonged undifferentiated proliferation, thus pronouncing its accelerated uptake.

In addition, these are capable in expressing high level of alkaline phosphatase, key transcription factors, and telomerase. These factors are found to be of great importance in the maintenance of the inner cellular mass pluripotency.

Furthermore, hESCs can be easily differentiated into defined neurons, neural lineages, oligodendrocytes, and astrocytes. Aforementioned characteristic makes it useful in studying the sequence of events that take place during early neurodevelopment.

However, use of stem cells derived from viable embryos is fraught with ethical issues, prompting scientists to explore other methods to generate ESCs. The other methods include derivation of embryonic germ cells, stem cells from dead embryos, and other techniques.

Further Key Findings from the Report Suggest:

Key Topics Covered:

1 Research Methodology

2 Executive Summary

3 Human Embryonic Stem Cells Market Variables, Trends & Scope 3.1 Market Segmentation & Scope 3.1.1 Market Driver Analysis 3.1.1.1 Technological advancement involving stem cells therapy 3.1.1.2 Rising demand for regenerative medicines 3.1.1.3 R&D in toxicology testing 3.1.1.4 Technological advanvcements for the production of embryonic stem cells through alternative methods 3.1.1.5 Increasing prevalence of genetic disorders 3.1.2 Market Restraint Analysis 3.1.2.1 Ethical concern related to stem cell research 3.2 Penetration & Growth Prospect Mapping for Application, 2015 3.3 Human embryonic stem cells -Swot Analysis, By Factor (Political & Legal, Economic And Technological) 3.4 Industry Analysis - Porter's

4 Human Embryonic Stem Cells Market: Application Estimates & Trend Analysis 4.1 Global Human Embryonic Stem Cells Market: Application Movement Analysis 4.2 Regenerative Medicine 4.3 Stem Cell Biology Research 4.4 Tissue Engineering 4.5 Toxicology Testing

5 Human Embryonic Stem Cells Market: Regional Estimates & Trend Analysis, by Application

6 Competitive Landscape 6.1 Strategy Framework 6.2 Market Participation Categorization 6.3 Company Profiles

For more information about this report visit http://www.researchandmarkets.com/research/cnx9vb/human_embryonic

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Human Embryonic Stem Cells (HESC) Market Analysis and Growth Forecast by Applications, Types and Competitors to … – DailyNewsKs

Human Embryonic Stem Cells (HESC) Market research report is a professional and in-depth study on the current state. The Human Embryonic Stem Cells (HESC) Industry analysis is provided for the international market including development history, competitive landscape analysis, and major regional development status.

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Next part of the Human Embryonic Stem Cells (HESC) Market sheds light on the production, production plants, their capacities, global production and revenue are studied. Also, the Human Embryonic Stem Cells (HESC) Market growth in various regions and R&D status are also covered.

Human Embryonic Stem Cells (HESC) Market report key players-Astellas Pharma Inc/ Ocata Therapeutics, STEMCELL Technologies, BIOTIME, INC, Thermo Fisher Scientific, CellGenix, ESI BIO, PromoCell, Lonza, Kite Pharma, Cynata, Sumanas, LifeCell, Geron And Many Others

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Further in the report, Human Embryonic Stem Cells (HESC) Market is examined for price, cost and gross revenue. These three points are analysed for types, companies and regions. In prolongation with this data sale price for various types, applications and region is also included.

Human Embryonic Stem Cells (HESC) Market split by Product Type-Adult Sources, Fetal Sources Human Embryonic Stem Cells (HESC) Market split by Application Regenerative Medicine, Stem Cell Biology Research, Tissue Engineering, Toxicology Testing Human Embryonic Stem Cells (HESC) Market Segment by Regions-North America, China, Europe, Southeast Asia, Japan, India

With the help of supply and consumption data, gap between these two is also explained. To provide information on competitive landscape, this report includes detailed profiles of Human Embryonic Stem Cells (HESC) Market key players.

Have any query? Ask our expert @ http://www.360marketupdates.com/enquiry/pre-order-enquiry/10613660

Other Major Topics Covered in Human Embryonic Stem Cells (HESC) market report are as follows:

Marketing Strategy Analysis, Distributors/Traders: Marketing Channel, Direct Marketing, Indirect Marketing, Marketing Channel Development Trend, Market Positioning, Pricing Strategy, Brand Strategy, Target Client, Distributors/Traders List. Market Effect Factors Analysis: Technology Progress/Risk; Substitutes Threat; Technology Progress in Related Industry; Consumer Needs/Customer; reference Change; Economic/Political Environmental Change. Global Human Embryonic Stem Cells (HESC) Market Forecast 2017-2021: Global Human Embryonic Stem Cells (HESC) Capacity, Production, Revenue Forecast 2017-2021; Global Human Embryonic Stem Cells (HESC) Production, Consumption Forecast by Regions 2017-2021; Global Human Embryonic Stem Cells (HESC) Production Forecast by Type 2017-2021; Global Human Embryonic Stem Cells (HESC) Consumption Forecast by Application 2017-2021; Human Embryonic Stem Cells (HESC) Price Forecast 2017-2021.

In this Human Embryonic Stem Cells (HESC) Market analysis, traders and distributors analysis is given along with contact details. For material and equipment suppliers also, contact details are given. New investment feasibility analysis is included in the report.

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Human Embryonic Stem Cells (HESC) Market Analysis and Growth Forecast by Applications, Types and Competitors to ... - DailyNewsKs

Stem cells were one of the biggest controversies of 2001. Where are they now? – Vox

Remember stem cells? They were one of the biggest scientific controversies during the early years of George W. Bushs presidency.

At the time, scientists had realized thatembryonic stem cells had the incredible capacity to transform into virtually any cell in the human body and so could potentially lead to new treatments or cures for a multitude of illnesses. On the other hand, extracting these stem cells required destroying human embryos, an action opposed by some pro-life individuals.

EMBRYONIC stem-cell THERAPIES ARE GETTING TESTED IN ACTUAL PATIENTS

The stem-cell debate got really heated. But then ... it just sort of fizzled out from public view. So whatever happened to stem cells?

A couple of things helped lessen the controversy. By the late 2000s, researchers discovered other ways to createcells similar to embryonic stem cells without destroying human embryos, a promising advance that helped defuse the culture-war aspect. Then, in 2009, Obama somewhat loosened the Bush-era restrictions on federal funding for stem-cell research and thecompromise seemed to quiet both sides down a fair amount.

So, lately, scientists have been patiently continuing their stem-cell research in a less noisy atmosphere. And that work has actually led to a few advances like restoring some sight in 10 patients with vision diseases. But the stem-cell controversy is far from dead. Researchers still might need cells from embryos to create certain treatments. If it turns out that non-embryonic stem cells aren't good enough, that could re-ignite the culture wars. So here's a guide to the debate:

Shinya Yamanaka (right) receiving flowers from Sweden's ambassador to Japan in 2012, after it was announced that Yamanaka won a Nobel Prize in medicine. (Jiji Press/AFP/Getty Images)

Embryonic stem cells attracted scientific attention because they have the potential to grow into virtually any cell in the human body say, insulin-producing cells for people with diabetes, brain cells for people with Parkinsons, or even wholenew organs to replace faulty ones.

But for many people, there was one huge ethical problem: creating them required destroying an embryo. That's why, in 2001,George W. Bush decided to limit federal funding of research to a list of 60 pre-existing embryonic stem-cell lines (so as to discourage the destruction of any more embryos). Many scientists viewed the rules as too strict. Hence the controversy.

Obama SOMEWHAT relaxed Bushs restrictions on embryonic stem cells

But then in 2007, Japanese scientistShinya Yamanaka and his colleagues managed to coax cells from adult humans into embryo-like flexibility. In other words, they were able to create cells that seemed to resemble embryonic stem cells but that didn't require destroying an embryo. (These new cells were named induced pluripotent stem cells, IPSCs.) Other researchers began finding that adult stem cells have similar, but more limited, properties, too.

Meanwhile, the politics shifted. In 2009, Barack Obama came into office and signed anexecutive order that somewhat relaxed Bushs restrictions on embryonic stem cells. Under the new rules, the federal government would fund work on new stem-cell lines, but only if they had been made from leftover embryos from fertility clinics andwith non-federal money. That compromise seemed tohelp thecontroversy settledown.

A figure of visual ability after an embryonic-stem-cell-derived treatment (red line) in patients with macular degeneration over the course of 360 days. (Schwartz et al., The Lancet, October 15, 2014)

While the controversy has calmed down, stem-cell research is taking off and scientists are making advances with both embryonic and non-embryonic cells.

Much of the initial research on stem-cell therapies has focused on eye treatments. (That's because stem-cell therapies can be unpredictable and have sometimes lead to tumors in previous experiments. A tumor in an eye would be relatively easier to deal with and remove than tumors hidden deeper inside the body.)

In October 2014, researchers from the company Advanced Cell Technology (now called Ocata Therapeutics)showed that they had created new retina cells from embryonic stem cells for 18 patients who were going blind. Afterward, 10 of them had improved eyesight. Another group of researchers in Japan is trying to do the same thing with non-embryonic cells (those aforementioned IPSCs).

10 PEOPLE WHO WERE GOING BLIND HAD Improved eyesight AFTER EMBRYONIC STEM-CELL THERAPY

Other embryonic stem-cell research has focused on developing cells that can help treat spinal-cord injuries. A company called Geron startedsafety tests in such patients in 2010.

Although a few groups are continuing to work on embryonic stem cells, many are now focusing on non-embryonic stem cells like IPSCs because they're less contentious. "Everyone jumped very, very quickly on the IPS[C] bandwagon because it was eligible for federal funding, and then also any of the controversy [regarding embryos] was dropped," says Susan Solomon, CEO of the nonprofit New York Stem Cell Foundation.

But Solomon also thinks researchers have moved away from embryonic stem cells too quickly. "We felt that it was way too early to do that," she adds. Her organization still studies embryonic stem cells, among others in part because they may be able to do things that non-embryonic stem cells can't. It's just too early to tell.

It's important to note that despite all the overhype over the years, stem-cell science has been moving at the same slow pace as most scientific fields. There are still no FDA-approved treatments that use either embryonic stem cells or IPSCs. And that means that controversy over whether embryonic stem cells are needed for science and medicine is still unresolved.

(Shutterstock)

That said, the fight over stem cells hasn't gone away forever. And there's likely to be more conflict in the future.

Even after the Obama administration relaxed the rules on funding stem-cell research, there are still plenty of hurdles. For example, federal funding is currently prohibited for research on embryonic stem-cell lines made through a technique calledSCNT or cloning, which requires creating embryos in the lab.

This technique could one day prove useful because it can turn a person's own cells into a customized embryonic stem-cell line and would therefore stop people's immune systems from rejecting stem-cell treatments.

In 2013 and 2014, two groups published the firstdemonstrations of this technique with human cells. But all such research in the US must be done with private funds.

On top of all of this, some states directly ban some or all stem-cell research within their borders no matter who's paying for it:

Note: Minnesota has a vague law on the books that's currently interpreted to mean that embryonic stem-cell research is ok. Missouri's law is a bit self-conflicting. For more details, check out The Hinxton Group's site, which includes quotations from the relevant regulations themselves.

"We went from more of a legislative vacuum to our current patchwork quilt, with legislation enacted in all of the jurisdictions where interest groups had enough clout to get the job done," Alan Regenberg, Director of Outreach and Research Support at the Johns Hopkins Berman Institute of Bioethics, told me in an email.

Several things could bring the stem-cell fight back. For example, a clinical trial could come out with some really impressive results on some sort of stem-cell treatment renewing the debate over whether regulations should be loosened. Conversely, a social conservative could run for president and bring up the ethical issues on the campaign trail. And no matter who lands in the White House in 2016, its reasonable to expect some major changes in federal policy and fast. Both George W. Bush and Barack Obama implemented their rules within the first year in office.

In 2013, Obama's stem-cell policy survived Supreme Court case Sherley v. Sebelius.

A piece on the first embryonic stem-cellmedical trials in people, by Sarah Boseley at the Guardian

Update: Clarified the current interpretation of Minnesota's stem cell laws and changed the map to match.

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Stem cells were one of the biggest controversies of 2001. Where are they now? - Vox

Protein that kick-starts gene expression in developing embryos. – Science Daily

Protein that kick-starts gene expression in developing embryos.
Science Daily
Next, they looked at mouse embryonic stem cells, which contain the mouse version of the DUX4 gene (called simply DUX). When in culture, a small fraction of these cells exhibit a any given time the gene expression pattern of 2-cell stage embryos, before ...

and more »

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Protein that kick-starts gene expression in developing embryos. - Science Daily

Lab-grown ‘mini-brains’ mimic brain development – Spectrum

Download PDF Multicolored mind: Fluorescent markers pinpoint cells inside a 'mini-brain' grown from human stem cells.

M. Renner et al. / The EMBO Journal

A new method for examining lab-grown mini-brains reveals structures like those in the human brain1.

Mini-brains, also known as cerebral organoids, can provide clues to brain development. To build them, scientists coax clusters of stem cells into becoming neurons and other brain cells. They can even start with skin cells from a person with autism to see how the persons genes influence the mini-brains structure. But researchers debate how closely mini-brains resemble human brains.

In the new study, published 10 March in The EMBO Journal, researchers probed the cellular and regional structure of 104 mini-brains grown from human embryonic stem cells. They first froze the mini-brains and cut them into ultra-thin sections, which they mounted onto glass slides. They then labeled the sections with different combinations of colored fluorescent tags that are specific to certain cell types, and imaged the sections using an automated scanner.

The tags revealed a mixture of cells, including mature neurons and star-shaped support cells called astrocytes. The mini-brains are irregular blobs with small inner chambers, but the researchers found that they contain complex tissues.

A region within each mini-brain resembles the human forebrain, which governs complex cognitive tasks such as integrating sensory information. This region often develops as a folded, ribbon-like structure near the outside of the organoid. It contains layers of cells like those seen in the human cortex.

The researchers used a chemical cocktail to render some of the mini-brains transparent. This revealed bridges of tissue that connect different parts of the forebrain-like region.

The researchers also examined mini-brains at various time points from 33 to 160 days old, when their cells are fully mature. The cells matured into neurons and other brain cells at a speed and in a sequence similar to those in the developing human brain.

Some mini-brains formed patches of cells that secrete chemical cues that spur the development of certain cell types or delineate regions. These patches are similar to so-called organizing centers in the developing human brain.

The method revealed significant variability in the size and location of the forebrain. This may arise from when and where the organizing centers form, or whether they form, the researchers say.

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Lab-grown 'mini-brains' mimic brain development - Spectrum

‘Growing brains in a dish’ will help in fight against disorders – Irish Independent

Neural circuits from the most advanced part of the human brain have been recreated in tiny 3D balls of cells that could help scientists investigate psychiatric disorders.

The "brains in a dish", known as spheroids, were grown from stem cells and followed the same developmental process that takes place in the womb.

Two linked spheroids were made, each measuring about one-sixteenth of an inch across.

They modelled different areas of the forebrain including the cerebral cortex, the most highly evolved "thinking" part of the brain.

The research is the first to allow key events unfolding in the brain at late stages of foetal development to be viewed in real time.

As part of the proof-of-concept study, the scientists generated abnormal brain circuits typical of Timothy syndrome, a rare inherited condition leading to heart problems, autism and epilepsy. They were able to pinpoint the defective development path and correct it using two drugs.

Lead scientist Dr Sergiu Pasca, from Stanford University in the US, said: "We've never been able to recapitulate these human brain developmental events in a dish before.

"The process happens in the second half of pregnancy, so viewing it live is challenging. Our method lets us see the entire movie, not just snapshots.

"Our method of assembling and carefully characterising neuronal circuits in a dish is opening up new windows through which we can view the normal development of the foetal human brain.

"More importantly, it will help us see how this goes awry in individual patients."

The research, reported in the journal 'Nature', is expected to open a new window on a wide range of brain conditions including mental disorders such as schizophrenia.

To create the "brains" the scientists first reprogrammed ordinary skin cells, transforming them into induced pluripotent stem cells (IPS cells) with the properties of embryonic stem cells. Floating in a nutrient-rich broth, the stem cells were coaxed into becoming precursor neurons and finally mature brain circuits.

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'Growing brains in a dish' will help in fight against disorders - Irish Independent

California’s deadly ‘social legislation’ parallels its economic and political death spiral – Desert Dispatch

By Richard Reeb

The Golden States well-known descent from its years of prosperity and political clout, which stands in sharp contrast to the nations recently renewed growth and turn to the right, has another side. That is its Democrat leaders determination to facilitate the death of unwanted unborn babies, the elderly and terminally ill. Indeed, this session of the California State Legislature provides more evidence of this ominous trend.We Californians already legalize and finance abortion on demand and last year sanctioned so-called assisted suicide. Now attention is turning to new means and new victims of this misguided movement.In the State Senate, four bills have been introduced to this end, while one constitutional amendment has been proposed to stem the billions in funding for embryonic stem cell research.First, the bill (SB 743) of Sen. Richard Pan, D-Sacramento, would guarantee that Planned Parenthood and other abortion providers could still receive federal Medicaid funds via Medi-Cal family planning services. This is a perfect example of California Democrats defiance of the national conservative trend. Fortunately, it will probably go nowhere as President Donald Trump has recently rescinded his immediate predecessors executive order to force states to finance abortions.Exemplifying abortion advocates virtual sanctification of fetal homicide is SB 309, originally introduced by Sen. Pan, which would actually establish a specialty license plate celebrating reproductive freedom. Revenue generated would go to the California Reproductive Freedom Fund, whatever that is.One wonders: did the Third Reich authorize plates for Volkwagens to celebrate the killing of members of inferior races?Sen. Pans SB 481 would allow nursing homes to declare patients unfit to make their own decisions, and then implement medical procedures which may include assisted suicide. The state already permits persons believed to be facing deathin six monthsto end their lives, justified on the grounds of their own consent. This new development demonstrates just how hollow that premise was.While unlikely to make it out of committee, Senate Constitutional Amendment 7 would repeal the (embryonic) Stem Cell Research and Cures Act approved by the states voters in 2004. That misguided measure was sold on the failed promise that embryonic cells offered the greatest potential. But experience with adult stem cells and from placentas has been far more fruitful.Though not directly aimed at death, SB 18, also the work of Sen. Pan, originally sought to challenge parental authority in the name of childrens rights. Of course, parents natural concern for their childrens very lives cannot be surpassed. Yet this bill would have directly threatened parents ability to provide in-home education for their children or to send them to private schools.But Senate committee action has changed the focus of the bill to establish an 18-member Children and Youth joint committee (half from the Senate and half from the Assembly) to direct the legislature to maximize spending on that class of persons. It would undo current code on this subject by the year 2025. The original alarming objectives doubtless will be implemented in bits and pieces through the new committees efforts. Do only children who have been permitted to be born deserve this intense concern?Meanwhile, California's new Attorney General Xavier Becerra has slapped 15 felony charges 14 counts of illegally recording conversations without consent and one count of conspiracy against David Daleiden, the project lead at the Center for Medical Progress (CMP), and his associate Sandra Merritt.In the past 20 months, the Center for Medical Progress has released a series of undercover videos that feature high end Planned Parenthood officials and employees of tissue procurement companies associated with the nation's largest abortion provider. They admitted in recorded conversations various illegalities about how the companies skirted state and federal law to engage in the selling of highly-desired aborted baby tissue, organs and limbs."At the end of the day, the only thing that is different from the work that I did and the work that CMP did and the work that undercover journalists and investigative journalists are doing every single day here in California ... is who I went after," Daleiden said during a telephone interview with the Washington Times."The only difference is that I happened to go after and expose the political ally and financial backers of the establishment power structure in California and in the country. That is the only reason why I am being prosecuted with these bogus charges under California Penal Code 632 and why the local reporters with NBC Los Angeles and other places are not. That really says it all."One can only hope that Californias political leadership would be as zealous in saving lives as they are in ending them. But alas they are not. Such is the situation in our coming sanctuary state.

Richard Reeb taught political science, philosophy and journalism at Barstow College from 1970 to 2003. He is the author of "Taking Journalism Seriously: 'Objectivity' as a Partisan Cause" (University Press of America, 1999). He can be contacted at rhreeb@verizon.net

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California's deadly 'social legislation' parallels its economic and political death spiral - Desert Dispatch

Custer considered for stem cell study | The Miami Student – Miami Student

WSU student fractured spine at Oxford party

Ryan Custer, a Wright State University student who was severely injured at an Oxford party, is being considered for a stem cell study at Rush University Hospital in Chicago. The 19-year-old, a first-year forward for the Raiders varsity basketball team, will be evaluated for five days before doctors determine if he qualifies for the study.

Custer suffered a severe spinal injury after jumping into a makeshift pool at a party on S. Main Street on Saturday, April 8. Custer collided with another persons knee when he slid into the pool, causing the injury. Custer was immediately transported to the University of Cincinnati Medical Center where he underwent surgery on his spine that night.

Feeling in Custers legs has not returned, and he has only recently regained some movement in his fingers.

Custer was transported from the UC Medical Center to Rush Hospital on Sunday, April 22. According to a post from the Ryan Custer Recovery Care Page, a Facebook page updated almost daily by Custers family, he spent the first day in Chicago getting acclimated in his new room in Rushs ICU and meeting the doctor who will lead the study, Dr. Richard Fessler.

Dr. Fessler, a renowned spinal surgeon, has focused his research on developing and refining new ways to perform minimally invasive spinal surgeries. In 2010, Fessler performed surgery on former Indianapolis Colts quarterback Peyton Manning, which Custer was happy to learn, the post said.

The five-day period of testing began Monday, and, if selected for the study, treatment for Custer will begin on Friday. The study, called the SCiStar study, will evaluate how the injection of AST-OPC1, particular neural cells produced from human embryonic stem cells, at a single time 14 to 30 days after an injury can benefit the patients recovery.

According to the SCiStar webpage, the studys researchers are seeking adults between the ages of 18 and 69 who recently experienced a spinal cord injury in the neck which resulted in a loss of feeling below the site of the injury in addition to some paralysis in the arms and legs.

HBO has contacted Dr. Fessler about following a patient through this research process.

Ryan thinks it would be cool to do it, so we said yes,an April 22 Facebook post reads. Another step in the plan God has mapped out for Ryan.

A fundraising page created for Custer, The Ryan Custer 33 Recovery Fund, is close to raising its entire $100,000 goal. At the time of publication, the fund was just about $4,000 shy of the 100k mark.

Over 6,500 people have liked the page and are following along with Custers recovery through the familys Facebook updates.

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Custer considered for stem cell study | The Miami Student - Miami Student

We need a new NIH director: Column – USA TODAY

David A. Prentice 6:04 a.m. ET April 25, 2017

Francis Collins speaks to the USA TODAY Editorial Board in 2014.(Photo: Jack Gruber, USA TODAY)

Over his first 100 days in office, President Trump has set a new direction for the country in a variety of areas, from Defense policy to health care and federal hiring.One by one, he has been making good on his campaign promises.He is burnishing his pro-life credentials as well as proving his drive to innovate and put America back in a position of global leadership.Next on the presidents list should be a new director for the National Institutes of Health (NIH).

The incumbent, Dr. Francis Collins, is a leftover from the Obama administration.That is startling enough for such a vital role, but Collins is most definitely not pro-life nor in the same leadership class as Trump.Collins left the NIH in 2008 to work for the Obama campaign team, where he helped set the Obama research priorities, including creating the NIH registry of human embryonic stem cell lines. The registry is a listing of cells created by destroying human embryos that are eligible for federal taxpayer dollars, and the power to approve for this deathly listing rests with the NIH director.

Collins also supports human cloning to create embryos for experiments.Some call such a technique clone and kill since the cloned human embryo is not allowed to survive and develop, but is disaggregated to use her cells in laboratory tests.

He takes the completely unscientific view that a cloned embryo is not really an embryo, because, he says, this is not the natural way that embryos come into existence.This makes any cloned human beings fair game to be used, including destroyed, for experiments.By Collins logic, Dolly the cloned sheep was not really a sheep.

Democrats aren't the party of science: Jonah Goldberg

Why I march for life: Column

Unethical research under the Collins-led NIH doesnt stop there.In 2016, NIH began consideration of allowing creation with taxpayer dollars of human-animal chimeras,including creation of animals that could contain human sperm, human eggsor a human brain. This macabre, unethical science certainly does not represent innovation in healthcare.

Even though we are now in the Trump era, Collins continues to approve more cell lines from destroyed human embryos for use intaxpayer-funded research; the most recent approvals were last month.Embryonic stem cell science relies on destroying embryos to harvest their cells.Collins not only approves of this technique but continues to award federal dollars to the destroyers of young embryos.He has called it important, life-saving research, despite the fact that embryonic stem cells have not saved a single human life nor had any proven success in patients.Its all about destruction and lives lost.

POLICING THE USA:Alook atrace, justice, media

We're scaring off future Einsteins: USD president

Personnel, the adage goes, is policy.Leftovers represent stale policy.Trump needs someone in this critical leadership role for American research who aligns with his strong pro-life ethic and his desire to unleash American ingenuity.There arewell-qualified candidates to rev up Americas biomedical engine and to make it a fountainhead of new therapies against some of the worst diseases facing our world.

In this enterprise, we havent a moment to lose.We just need a new NIH Director.

David A. Prentice is vice president & director of research at Charlotte Lozier Institute, research and education institute of the Susan B. Anthony List, an organization dedicated to electing candidates and pursuing policies that will reduce and ultimately end abortion..

You can readdiverse opinions from ourBoard of Contributorsand other writers ontheOpinion front page,on Twitter@USATOpinionand in our dailyOpinion newsletter.To respond to a column, submit a comment toletters@usatoday.com.

Read or Share this story: http://usat.ly/2pZSabK

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We need a new NIH director: Column - USA TODAY

Are human space babies conceivable? – Space Daily

As astronauts continue to break records for time spent in space and manned Mars exploration is under discussion, scientists in China have begun a groundbreaking study to determine if humans can reproduce in space.

Scientists will for the first time conduct an experiment to induce the differentiation of human embryonic stem cells into germ cells on China's first cargo spacecraft, Tianzhou-1.

The experiment aims to study the effects of the space environment on human reproduction, beginning with the study of microgravity on human stem cells and germ cells, says Kehkooi Kee, lead researcher on the project.

Kee, a Malaysia Chinese professor at China's prestigious Tsinghua University, says the unprecedented experiment will study the basic development and maturation of germ cells in the micro-gravity environment, and the developmental potential of human embryonic stem cells.

The research is expected to provide a theoretical basis and technical support to solve the possible problems of human reproduction caused by the space environment, Kee said.

"It's an important experiment because it is the first step towards directly understanding human reproduction during space exploration," he says.

What kind of difficulties could people face by having children in space?

Experts say that in the known space environment, micro-gravity, radiation and magnetic fields could have a great impact on human reproduction. Among these factors, micro-gravity could be the largest challenge.

At the cellular level, micro-gravity might affect cell division or polarity. The cells of living organisms contain many organic molecules. These molecules and cells are evolved to function under the earth gravitational force. But scientists are still not clear how micro-gravity could affect the physical force governing the molecular interactions and developments of the cells, says Kee.

The United States, Russia and Europe have conducted many space experiments to examine if micro-gravity is harmful to astronauts, especially the effects on the muscle and bones. However, microgravity effect on human reproductive capacity has been rarely studied.

Previous research in this area mainly focused on monitoring the reproductive hormone levels of astronauts. Due to the ethical and physical constraints, it has been very difficult to directly obtain and study their germ cells.

"If we aim to directly study human reproductive biology in space, we need to build an in-vitro platform to study the germ cells. So we chose to use human embryonic stem cells to differentiate into germ cells," says Kee.

In 2009, he and his colleagues used human embryonic stem cells to create human primordial germ cells and sperm-like cells for the first time. They published their research in the academic journal Nature.

Currently, the team has successfully obtained egg-like cells from human embryonic stem cells and will be publishing this novel finding soon.

Human embryonic stem cells can be induced into primordial germ cells and further differentiate into sperm-like or egg-like cells. But differentiating embryonic stem cells into sperm-like or egg-like cells is very difficult because they require more developmental steps and more cellular factors, says Kee.

Although other scientists have conducted similar experiments, none has made human germ cells differentiate into such a mature state as Kee's team has.

"We have compared the in-vitro cultured cells with in-vivo cells, and found they have many similar characteristics. But we can only call the in-vitro ones sperm-like cells or egg-like cells, because we still can't prove they are exactly the same until we conduct functional experiments," Kee says.

So far, all such experiments have been conducted on the ground, so scientists do not know whether micro-gravity will affect the differentiation of human embryonic stem cells and the formation of germ cells.

"In the experiments on the ground, it usually takes six days to culture and obtain primordial germ cells, and about two weeks to form sperm-like or egg-like cells," says Kee.

"The experiment on Tianzhou-1 will last 30 days. To what extent the human embryonic stem cell can differentiate in space is still unknown. Will the process be delayed? If so, by how much?" asks Kee, adding they expect to see at least the first stage of the primordial germ cells appear.

Scientists on the ground will remotely control the research equipment to change the cell-culture medium to induce the human embryonic stem cells to differentiate into germ cells. Images of the cells under the microscope will be transmitted to earth.

Source: Xinhua News Agency

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