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CRISPR

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24.05.2019
11:36 Nature.ComAuthor Correction: A CRISPR/Cas system mediates bacterial innate immune evasion and virulence

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09:26 Technology.orgCRISPR Fingers Drug-Resistant Microbes in a ‘FLASH’

A research team led by scientists at UC San Francisco and the Chan Zuckerberg Biohub has developed a

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23.05.2019
16:03 Phys.orgCRISPR/Cas9 improves with better gene knockout method in aneuploid cell lines

CRISPR/Cas9 technology enables convenient and effective genome editing in diploid cell lines based on the isolation and expansion of edited single-cell clones. However, this approach is ineffective for aneuploid cell lines, and a group has now reported an improved method for genome editing based on multiple rounds of modification. The article is published in Tissue Engineering.

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02:06 Yahoo.com BusinessBrainstorm Health: CRISPR V. Superbugs, Gottlieb to NEA, UniQure Gene Therapy

Brainstorm Health: CRISPR V. Superbugs, Gottlieb to NEA, UniQure Gene Therapy

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22.05.2019
17:47 Nature.ComCRISPR-baby rules, fake-news law and kilogram retires

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16:53 Nature.ComCRISPR zeroes in on antibiotic-resistance genes

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01:30 TechInvestorNews.comWe need to resolve ethics of CRISPR technology as China awaits third genetically modified baby (CNBC: Top News)

CNBC: Top NewsWe need to resolve ethics of CRISPR technology as China awaits third genetically modified baby - The scientific community is now struggling to grapple with the ethics of human germline editing as another woman pregnant with a gene-edited baby is soon due to give birth. ...

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00:43 CNBC.comWe need to resolve ethics of CRISPR technology as China awaits third genetically modified baby

The scientific community is now struggling to grapple with the ethics of human germline editing as another woman pregnant with a gene-edited baby is soon due to give birth.

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00:41 CNBC health careWe need to resolve ethics of CRISPR technology as China awaits third genetically modified baby

The scientific community is now struggling to grapple with the ethics of human germline editing as another woman pregnant with a gene-edited baby is soon due to give birth.

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20.05.2019
13:10 Technology.orgResearchers identify molecules that rein in CRISPR systems

Scientists have identified the first chemical compounds able to inhibit and regulate CRISPR systems, which could ultimately make

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10:34 Nature.ComChina set to tighten gene-editing laws following CRISPR-baby furore

Nature is the international weekly journal of science: a magazine style journal that publishes full-length research papers in all disciplines of science, as well as News and Views, reviews, news, features, commentaries, web focuses and more, covering all branches of science and how science impacts upon all aspects of society and life.

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16.05.2019
15:57 ScienceDaily.comCRISPR catches out critical cancer changes: New drug target for multiple cancers

In the first large-scale analysis of cancer gene fusions, researchers used CRISPR to uncover which gene fusions are critical for the growth of cancer cells. The team also identified a new gene fusion that presents a novel drug target for multiple cancers, including brain and ovarian cancers. The results give more certainty for the use of specific gene fusions to diagnose and guide the treatment of patients.

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14:34 News-Medical.NetCRISPR uncovers which gene fusions are critical for growth of cancer cells

In the first large-scale analysis of cancer gene fusions, which result from the merging of two previously separate genes, researchers at the Wellcome Sanger Institute, EMBL-EBI, Open Targets, GSK and their collaborators have used CRISPR to uncover which gene fusions are critical for the growth of cancer cells.

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15.05.2019
17:05 SingularityHub.ComThe Hunt for a CRISPR Antidote Just Heated Up

When scientists behind the Manhattan Project heard of the destruction of Hiroshima and Nagasaki, their earlier exuberance gradually turned into morose and regret. What began as a physics revolution had mutated into a weapon of mass destruction—with no feasible “off switch” to cripple its power. For biology, CRISPR has that same nuclear-scale destructive power. And […]

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08.05.2019
15:39 Yahoo.com BusinessWhy CRISPR Therapeutics Gained 13.4% in April

CRISPR and partner Vertex bagged an important regulatory designation for CTX001 last month.

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07.05.2019
19:51 Phys.orgTeaching CRISPR and antibiotic resistance to high school students

How can high school students learn about a technology as complex and abstract as CRISPR? It's simple: just add water.

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19:45 ScienceDaily.comTeaching CRISPR and antibiotic resistance to high school students

A team has developed BioBits, a suite of hands-on educational kits that enable students to perform a range of biological experiments by adding water and simple reagents to freeze-dried cell-free reactions.

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13:13 TechnologyReview.comGoogle backs a bid to use CRISPR to prevent heart disease

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03.05.2019
15:39 News-Medical.NetDiscovery of small-molecule inhibitors could enable precise control over CRISPR-Cas9 genome editing

The discovery of the first small-molecule inhibitors of the Streptococcus pyogenes Cas9 (SpCas9) protein could enable more precise control over CRISPR-Cas9-based genome editing, researchers report May 2 in the journal Cell.

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08:33 GizmagAnti-CRISPR molecules discovered that can block the gene editing technology


As we dive into the brave new world of gene editing, CRISPR technologies are undoubtedly becoming increasingly precise, but alongside enhanced precision is also the necessity for developing ways to inhibit or block the process – an anti-CRISPR molecule, if you will. New work from the Broad Institute and Brigham and Women's Hospital has presented a study that homes in on small molecules that may have the ability to safely block the CRISPR gene editing process.
.. Continue Reading Anti-CRISPR molecules discovered that can block the gene editing technology Category: Medical Tags: Brigham and Women’s Hospital Broad Institute CRISPR Genetic engineering Genetics

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02:03 ScienceDaily.comDrugs that block CRISPR-Cas9 genome editing identified

The discovery of the first small-molecule inhibitors of the Streptococcus pyogenes Cas9 (SpCas9) protein could enable more precise control over CRISPR-Cas9-based genome editing, researchers report.

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02.05.2019
18:41 TechnologyReview.comThe search for the kryptonite that can stop CRISPR

Powerful gene-editing tools have the potential to heal—or to harm. Now there’s a race to develop the antidote to the next bioweapon.

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18:25 Nature.ComCompound stops CRISPR enzyme running amok

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18:24 NewScientist.ComTwo molecules could give us finer control over CRISPR gene editing

Molecules that act like off switches for CRISPR may one day be used as a drug to make gene editing therapies safer and less likely to cause unwanted mutations

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18:06 Phys.orgResearchers identify drugs that block CRISPR-Cas9 genome editing

The discovery of the first small-molecule inhibitors of the Streptococcus pyogenes Cas9 (SpCas9) protein could enable more precise control over CRISPR-Cas9-based genome editing, researchers report May 2nd in the journal Cell.

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17:02 SingularityHub.ComCRISPR Used in Human Trials for the First Time in the US

CRISPR just hit another landmark. Last week, the University of Pennsylvania (UPenn) confirmed that they have treated two cancer patients using the gene editing darling married with another biomedical wizard, CAR-T. For now, it’s too early to tell if the treatment proved beneficial in either patient, but the team hopes to release a first batch […]

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06:45 SingularityHub.ComA Deceptively Simple Tweak to CRISPR Makes It 50 Times More Accurate

CRISPR may be the premiere gene editing progeny poised to upend natural genomes and erase inherited diseases. But since its inception, one thing has always stood in the way: accuracy. Back in 2017, a contentious report using CRISPR found massive off-target edits in mice, in which the tool went rogue to snip away at innocent […]

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01.05.2019
15:34 ScienceDaily.comDeadly box jellyfish antidote discovered using CRISPR genome editing

Researchers studying how pain works have discovered an antidote to the deadly sting delivered by the most venomous creature on Earth -- the Australian box jellyfish. A single sting to a human causes necrosis of the skin, excruciating pain and, if the dose of venom is large enough, cardiac arrest and death within minutes. The new antidote, discovered using CRISPR genome editing techniques, blocks the symptoms within 15 minutes after contact.

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30.04.2019
19:28 Geek.comAntidote to Deadly Box Jellyfish Venom Discovered With CRISPR Genome Editing

It’s one of the deadliest creatures on Earth: The infamous box jellyfish developed its powerful venom to be so overpoweringly painful, human victims have been known to go into shock or die of […]
The post Antidote to Deadly Box Jellyfish Venom Discovered With CRISPR Genome Editing appeared first on Geek.com.

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18:04 Phys.orgDeadly box jellyfish antidote discovered using CRISPR genome editing

Researchers at the University of Sydney have discovered an antidote to the deadly sting delivered by the most venomous creature on earth—the Australian box jellyfish.

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27.04.2019
20:45 Yahoo.com BusinessBetter Buy: Editas Medicine vs. CRISPR Therapeutics

Which stock wins in a match-up between these two CRISPR gene-editing pioneers?

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26.04.2019
06:06 Yahoo ScienceA New Frontier for CRISPR Stocks: Gene Therapy Cures 10 Babies

Imagine being able to cure diseases the same way you fix a typo.That's a bit of an oversimplification because the process is more involved than a "delete" button on a keyboard. But it helps make clear the breakthrough possibilities of gene editing.Last week was big for the industry. Scientists from St. Jude Children's Research Hospital and UCSF Benioff Children's Hospital announced the cures of 10 newborn babies with the rare "bubble boy" disease.InvestorPlace - Stock Market News, Stock Advice & Trading TipsScientists took out stem cells from the babies and used a modified HIV virus to deliver the "corrected" copy of the gene back into the patient. It cured the babies with no apparent side effects. This is huge. A previous trial was discontinued in 2003 after some children developed leukemia."Bubble boy" disease is

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01:15 InvestorPlace.comA New Frontier for CRISPR Stocks: Gene Therapy Cures 10 Babies

InvestorPlace - Stock Market News, Stock Advice & Trading Tips
Scientists took out stem cells from the babies and used a modified HIV virus to deliver the “corrected” copy of the gene back into the patient. It cured the babies with no apparent side effects. This is huge.
The post A New Frontier for CRISPR Stocks: Gene Therapy Cures 10 Babies appeared first on InvestorPlace.
More From InvestorPlace 2 Toxic Pot Stocks You Should Avoid 7 Dividend Stocks That Could Double Over the Next Five Years 6 S&P 500 Stocks Ready to Break Out 5 Mining ETFs to Dig Into

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25.04.2019
13:08 Technology.orgEngineering ‘hairpins’ increases CRISPR accuracy

Biomedical engineers at Duke University have developed a method for improving the accuracy of the CRISPR genome editing

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10:05 Technology.orgUC receives fourth CRISPR patent; three more on the way

The U.S. Patent Office today issued a fourth patent for the revolutionary CRISPR-Cas9 gene-editing technology to the University

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24.04.2019
16:53 Yahoo.com BusinessSome CRISPR Therapeutics (NASDAQ:CRSP) Shareholders Are Down 19%

While not a mind-blowing move, it is good to see that the CRISPR Therapeutics AG (NASDAQ:CRSP) share price has gained 20% in the last three months. But in truth the last year hasn't been good for the share price. The cold...

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23.04.2019
22:56 TechnologyReview.comStanford has cleared its professors over the CRISPR baby scandal

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22:56 TechnologyReview.comThe scientist who created CRISPR babies is on Time’s most-influential list—but not in a good way

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14:23 Nature.ComCRISPR gene-editing creates wave of exotic model organisms

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20.04.2019
00:14 ScienceMag.orgTop stories: Vaccine durability, the universe’s first molecule, and CRISPR’s powerful cousin

This week’s top Science news

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19.04.2019
21:19 ScienceDaily.comNew method to detect off-target effects of CRISPR

Since the CRISPR genome editing technology was invented in 2012, it has shown great promise to treat a number of intractable diseases. However, scientists have struggled to identify potential off-target effects in therapeutically relevant cell types, which remains the main barrier to moving therapies to the clinic. Now, a group of scientists have developed a reliable method to do just that.

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18:17 Phys.orgNew method to detect off-target effects of CRISPR

Since the CRISPR genome editing technology was invented in 2012, it has shown great promise to treat a number of intractable diseases. However, scientists have struggled to identify potential off-target effects in therapeutically relevant cell types, which remains the main barrier to moving therapies to the clinic. Now, a group of scientists at the Gladstone Institutes and the Innovative Genomics Institute (IGI), with collaborators at AstraZeneca, have developed a reliable method to do just that.

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12:54 Technology.orgResearchers Use Gene Editing with CRISPR to Treat Lethal Lung Diseases Before Birth

Using CRISPR gene editing, a team from Penn Medicine and Children’s Hospital of Philadelphia (CHOP) have thwarted a lethal lung disease, in an

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09:10 News-Medical.NetBreakthrough CRISPR gene-editing tool engineer multiple edits to DNA fragments from human cell

Scientists at Christiana Care Health System's Gene Editing Institute and NovellusDx, an Israeli biotechnology company, have deployed a breakthrough CRISPR gene-editing tool to successfully engineer multiple edits simultaneously to fragments of DNA extracted from a human cell, according to a new study published today in The CRISPR Journal.

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00:52 SingularityHub.ComNew CRISPR Method Can Edit Over 13,000 Spots in a Single Cell

Dr. George Church, the legendary godfather of synthetic biology, just made another push towards massively editing life’s base code. Since the inception of gene editing, long before the CRISPR revolution, scientists have struggled with simultaneously altering multiple spots on a genome. This difficult feat, dubbed multiplex editing, challenges both scientists and their genomic toolkit: the […]

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00:17 ScienceDaily.comResearchers use gene editing with CRISPR to treat lethal lung diseases before birth

Using CRISPR gene editing, researchers have thwarted a lethal lung disease in an animal model in which a harmful mutation causes death within hours after birth. This proof-of-concept study showed that in utero editing could be a promising new approach for treating lung diseases before birth.

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18.04.2019
17:40 TechnologyReview.comThe scientist who created CRISPR babies is on TIME’s most influential list—but not in a good way

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17.04.2019
23:47 ScienceMag.orgPowerful CRISPR cousin accidentally mutates RNA while editing DNA target

Off-target editing could complicate developing safe “base-edited” therapies

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21:04 FierceBiotech.comCRISPR edits out a deadly lung disease in mice before birth

Some inherited diseases, including those that affect the lung, can lead to death at the time of or shortly after birth. Scientists from the Children’s Hospital of Philadelphia and UPenn have used CRISPR gene editing to silence a congenital lung disorder in mouse fetuses.

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20:25 Nature.ComTranscriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors

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20:05 Phys.orgCRISPR base editors can induce wide-ranging off-target RNA edits

A Massachusetts General Hospital (MGH) research team reports that several of the recently developed CRISPR base editors, which create targeted changes in a single DNA base, can induce widespread off-target effects in RNA, extending beyond the targeted DNA. Their report receiving advance online publication in Nature also describes engineering variant base editors that significantly reduced the incidence of RNA edits while also increasing the precision of on-target DNA editing.

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20:05 TechnologyReview.comStanford has cleared its professors over the CRISPR baby scandal

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19:49 Nature.ComUS university clears three scientists in CRISPR-babies probe

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18:24 ScientificAmerican.ComStanford Clears Three Faculty Members of "CRISPR Babies" Involvement

A review concluded that the scientists did not take part in a Chinese researcher’s experiment to edit the genomes of twin human embryos -- Read more on ScientificAmerican.com

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16:18 TechnologyReview.comCRISPR has been used to treat US cancer patients for the first time

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10:28 GizmagCRISPR used to build dual-core computers inside human cells


The CRISPR gene-editing system is usually known for helping scientists treat genetic diseases, but the technology has a whole range of possible uses in synthetic biology too. Now researchers at ETH Zurich have used CRISPR to build functional biocomputers inside human cells.
.. Continue Reading CRISPR used to build dual-core computers inside human cells Category: Science Tags: Cells Computer CRISPR Enzyme molecular biology

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16.04.2019
17:00 Technology.orgCRISPR-Cas3 innovation holds promise for disease cures, advancing science

A Cornell researcher, who is a leader in developing a new type of gene editing CRISPR system, and

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16:35 FierceBiotech.comEx-Blueprint R&D exec takes up CMO post at Meeker's CRISPR biotech

As CRISPRomics biotech KSQ Therapeutics gears up for its first clinical trial next year, it’s hired biopharma vet Beni Wolf, M.D., Ph. D as its chief medical officer.

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10:47 GizmagCRISPR breakthrough uses "hairpin lock" for more precise genetic engineering


The CRISPR gene-editing system is incredibly accurate, but when there are billions of base pairs of DNA to scroll through, it's not unusual for it to be a little bit off target sometimes. Now, biomedical engineers at Duke University have created an RNA "lock" that can apparently make the system far more precise, and it works with all kinds of CRISPR variations.
.. Continue Reading CRISPR breakthrough uses "hairpin lock" for more precise genetic engineering Category: Biology Tags: CRISPR DNA Duke University Genetic engineering Genetics RNA

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10:11 Technology.orgNew DNA “shredder” technique goes beyond CRISPR’s scissors

In the last six years, a tool called CRISPR-Cas9 has transformed genetic research, allowing scientists to snip and

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09:32 News-Medical.NetCRISPR-scanning could lead to more effective treatments for cancer

11,000 people are predicted to die from acute myeloid leukemia in 2019, according to the American Cancer Society. The cancer starts in the bone marrow. There, mutated genes fail to prevent blood cells from replicating again and again and again, growing tumors.

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15.04.2019
22:53 ScienceDaily.comEngineering 'hairpins' increases CRISPR accuracy

Biomedical engineers have developed a method for improving the accuracy of the CRISPR genome editing technology by an average of 50-fold. The approach adds a short tail to the guide RNA that folds back and binds onto itself, creating a 'lock' that can only be undone by the targeted DNA sequence.

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18:11 FierceBiotech.comA better CRISPR? RNA 'hairpins' could improve gene editing

Engineers at Duke University have devised a solution to the dangerous off-target gene editing that CRISPR can cause. It's a short tail that's added to guide RNA and that locks when it reaches the DNA sequence being targeted.

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18:11 Phys.orgEngineering 'hairpins' increases CRISPR accuracy

Biomedical engineers at Duke University have developed a method for improving the accuracy of the CRISPR genome editing technology by an average of 50-fold. They believe it can be easily translated to any of the editing technology's continually expanding formats.

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10:32 StemCellsPortal.comlWhat’s the Stem Cells Buzz this Week? - hCPC Releases EVs, Bone Marrow Nestin-expressing Cells, CRISPR Screen in Cardiac Fibroblasts, and Melanoma Initiating Cell Plasticity!

The Stem Cells Portal brings you a roundup of some of the new and exciting stories in the ever-changing world of stem cells, regenerative medicine, and beyond!
Allogeneic-Driven-Benefit of hCPC-Released Extracellular Vesicles

Recent research from the lab of Reem Al‐Daccak (Hôpital Saint Louis, Paris, France) established that paracrine acting factors released from allogeneic human cardiac stem/progenitor cells (hCPC) positively impacted cardiac repair/regeneration post-myocardial infarction (MI). Now the team returns with a STEM CELLS Translational Medicine article that now reports proof‐of‐concept for the active contribution of extracellular vesicles. Hocine et al.

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12.04.2019
18:29 ScienceDaily.comCRISPR-Cas3 innovation holds promise for disease cures, advancing science

Scientists have used a new type of gene editing CRISPR system for the first time in human cells - a major advance in the field.

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11.04.2019
16:13 News-Medical.NetHundreds of new anti-cancer drug targets identified using CRISPR

A team of scientists from the Wellcome Sanger Institute have identified the genes that are essential for the survival of thirty types of cancer cells.

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10.04.2019
20:24 Nature.ComPrioritization of cancer therapeutic targets using CRISPR–Cas9 screens

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20:12 FierceBiotech.comUsing CRISPR to identify a new cancer drug target

With the help of CRISPR, two separate teams of scientists led by the Wellcome Trust Sanger Institute and the Broad Institute have identified a gene essential for survival of microsatellite instability tumors, pinpointing a promising drug target.

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16:20 ScienceDaily.comCRISPR-based 'allelic drive' allows genetic editing with selective precision and broad implications

Scientists developed a new version of a gene drive that allows the spread of specific, favorable genetic variants, also known as 'alleles,' throughout a population. The new 'allelic drive' is equipped with a guide RNA that directs CRISPR to cut undesired variants of a gene and replace it with a preferred version. Using a word processing analogy, CRISPR-based gene drives allow scientists to edit sentences of genetic information, while the new allelic drive offers letter-by-letter editing.

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09:51 Phys.orgCRISPR-based 'allelic drive' allows genetic editing with selective precision and broad implications

New CRISPR-based gene drives and broader active genetics technologies are revolutionizing the way scientists engineer the transfer of specific traits from one generation to another.

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07:25 News-Medical.NetScientists develop new CRISPR-based 'allelic drive'

New CRISPR-based gene drives and broader active genetics technologies are revolutionizing the way scientists engineer the transfer of specific traits from one generation to another.

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09.04.2019
11:57 GizmagA DNA "shredder" is the latest CRISPR gene-editing tool


The CRISPR gene-editing system is one of the most important medical breakthroughs of recent years, but that doesn't mean it's perfect. The most common enzyme in use is Cas9, which acts like a pair of molecular scissors and enables precise cut-and-paste DNA edits. But now, researchers have developed a new genetic tool that, they say, acts more like a motorized DNA "shredder."
.. Continue Reading A DNA "shredder" is the latest CRISPR gene-editing tool Category: Medical Tags: CRISPR DNA Enzyme Genetic engineering Genetics Genome University of Michigan

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02:38 ScienceDaily.comNew DNA 'shredder' technique goes beyond CRISPR's scissors

An international team has unveiled a new CRISPR-based tool that acts more like a shredder than the usual scissor-like action of CRISPR-Cas9. The new approach, based on Type I CRISPR-Cas3, is able to wipe out long stretches of DNA in human cells with programmable targeting, and has been shown to work in human cells for the first time.

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08.04.2019
23:32 Phys.orgNew DNA 'shredder' technique goes beyond CRISPR's scissors

In the last six years, a tool called CRISPR-Cas9 has transformed genetic research, allowing scientists to snip and edit DNA strands at precise locations like a pair of tiny scissors.

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15:38 Phys.orgResearchers find a way to use CRISPR Cas-9 on reptiles

A team of researchers at the University of Georgia has found a way to use the CRISPR-Cas9 gene editing tool on reptiles. In their paper uploaded to the bioRxiv preprint server, the group describes the technique they developed and how well it worked on test lizards.

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04.04.2019
15:39 Phys.orgA light-based carrier system for CRISPR-Cas9 gene editing

A team of researchers from Nanjing and Xiamen Universities in China has developed an alternative to using viruses to transport CRISPR-Cas9 gene editing tools into a desired cell—and it involves two types of light. In their paper published in the journal Science Advances, the group describes their new type of carrier and how well it worked with test mice.

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30.03.2019
12:23 NewScientist.ComGiant viruses have weaponised CRISPR against their bacterial hosts

Hundreds of giant viruses that infect bacteria have been discovered. Some seem to deploy CRISPR – the system used for gene editing – to fight their hosts

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28.03.2019
15:38 Yahoo.com BusinessBetter Buy: CRISPR Therapeutics vs. Sangamo Therapeutics

Which of these gene editing stocks will come out on top?

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27.03.2019
12:16 Technology.orgNew CRISPR-powered device detects genetic mutations in minutes

A team of engineers at the UC Berkeley and the Keck Graduate Institute (KGI) of The Claremont Colleges

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26.03.2019
20:43 Nature.ComThe CRISPR fix that could combat inherited blood disorders

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19:09 ScienceDaily.comCRISPR-chip enables digital detection of DNA without amplification

Researchers have found multiple applications for the CRISPR gene editing technology since it came into use by the scientific community.

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12:21 TechnologyReview.comGenome engineers made more than 13,000 CRISPR edits in a single cell

A team at George Church’s Harvard lab wants to redesign species with large-scale DNA changes.

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25.03.2019
19:08 Phys.orgNew CRISPR-powered device detects genetic mutations in minutes

A team of engineers at the University of California, Berkeley and the Keck Graduate Institute (KGI) of The Claremont Colleges combined CRISPR with electronic transistors made from graphene to create a new hand-held device that can detect specific genetic mutations in a matter of minutes.

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21.03.2019
17:33 ScienceDaily.comCRISPR/Cas libraries open new avenues in cancer research

CRISPR/Cas enables the targeted deactivation of genes by cutting DNA at pre-determined sites. This is accomplished by providing the Cas enzyme with a genetic zip code. Using an entire library of zip codes, it is then possible to simultaneously probe multiple sites within the genome, for example to determine which genes are essential for cancer cell survival. This could revolutionize drug discovery.

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15:53 Phys.orgCRISPR/Cas libraries open new avenues in cancer research

CRISPR/Cas enables the targeted deactivation of genes by cutting DNA at pre-determined sites. This is accomplished by providing the Cas enzyme with a genetic zip code. Using an entire library of zip codes, it is then possible to simultaneously probe multiple sites within the genome, for example to determine which genes are essential for cancer cell survival. This could revolutionize drug discovery.

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20.03.2019
21:13 News-Medical.NetCRISPR/Cas libraries could revolutionize drug discovery

CRISPR/Cas enables the targeted deactivation of genes by cutting DNA at pre-determined sites. This is accomplished by providing the Cas enzyme with a genetic zip code.

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02:08 Nature.ComWorld Health Organization panel weighs in on CRISPR-babies debate

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00:20 ScienceMag.orgWHO panel proposes new global registry for all CRISPR human experiments

The World Health Organization should also step up governance of human genome-editing research, group says

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19.03.2019
18:10 Phys.orgCRISPR gene editing: Why we need Slow Science

In a newly published article in Nature, a group of prominent scientists and ethicists have called for a moratorium on clinical research using CRISPR/Cas9 gene editing.

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16.03.2019
00:28 ScienceMag.orgCuring HIV just got more complicated. Can CRISPR help?

Scientists probe cellular hideouts for HIV and show that CRISPR can still cut the AIDS virus from DNA in monkeys

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15.03.2019
13:46 Technology.orgUC awarded third CRISPR patent, expanding its gene-editing portfolio

The University of California announced today that the U.S. Patent and Trademark Office (USPTO) issued U.S. Patent Number

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14.03.2019
19:09 FierceBiotech.comNew enzyme boosts 'CRISPR toolbox' for disease detection

Mammoth Biosciences is harnessing CRISPR to create diagnostic tools that can detect any biomarker containing DNA or RNA, with the ultimate goal of making tests that are as accessible and easy to use as a pregnancy test. It has just added the Cas14 enzyme to its arsenal.

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13.03.2019
21:08 TechnologyReview.comCRISPR experts are calling for a global moratorium on heritable gene editing

Some of the biggest names in gene editing want to stop anyone from playing around with cells that pass on changes to the next generation.

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15:33 NewScientist.ComHandheld device could detect CRISPR bioweapons before they spread

Bits of DNA known as gene drives that force themselves through a population could be use maliciously, but thankfully there is a way to detect them before they spread

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12.03.2019
12:53 Technology.orgNew CRISPR technique for studying gene function developed

When researchers want to understand a gene’s function, they silence or disable that gene in a model organism,

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11.03.2019
17:27 FierceBiotech.comSnipr raises $50M to use CRISPR to modulate the microbiome

Snipr Biome has raised $50 million to take CRISPR-based microbiome drugs into clinical trials. The Danish biotech is using CRISPR/Cas to selectively target and kill bacteria with specific DNA sequences. 

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07.03.2019
20:57 News-Medical.NetResearchers develop new method to boost efficiency of CRISPR gene editing in DMD

Scientists have developed a method to boost the efficiency of CRISPR gene editing in Duchenne muscular dystrophy (DMD), according to a study that could have implications for optimizing gene therapies for other diseases.

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02:44 ScienceDaily.comScientists find method to boost CRISPR efficiency

Scientists have developed a method to boost the efficiency of CRISPR gene editing in Duchenne muscular dystrophy (DMD), according to a study that could have implications for optimizing gene therapies for other diseases.

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00:35 Phys.orgScientists find method to boost CRISPR efficiency

Scientists have developed a method to boost the efficiency of CRISPR gene editing in Duchenne muscular dystrophy (DMD), according to a study that could have implications for optimizing gene therapies for other diseases.

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