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image: Researchers Make Knockout Stem Cell Lines in One Step

Researchers Make Knockout Stem Cell Lines in One Step

By | December 1, 2017

Combining gene editing and stem-cell induction improves efficiency of functional genetic analyses.

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image: Infographic: Combo Method of Stem Cell Generation

Infographic: Combo Method of Stem Cell Generation

By | December 1, 2017

Simultaneous exposure to reprogramming and gene-editing plasmids efficiently produces edited pluripotent colonies.

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Professionals in the genetics field generally support editing the genomes of somatic cells, mirroring public opinion, but diverge from nonexperts when it comes to germline editing.

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image: Gene Drive Limitations

Gene Drive Limitations

By | October 9, 2017

In lab populations of genetically engineered mosquitoes, mutations arose that blocked the gene drive’s spread and restored female fertility.

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image: First CAR T-Cell Therapy Approved in U.S.

First CAR T-Cell Therapy Approved in U.S.

By | August 30, 2017

The genetically modified blood cells will be used for patients with a type of acute lymphoblastic leukemia, when other treatments fail.

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image: Skin Graft-based Gene Therapy Treats Diabetes in Mice

Skin Graft-based Gene Therapy Treats Diabetes in Mice

By | August 4, 2017

A small patch of engineered cells makes an enzyme that stimulates insulin release.

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image: Final Nail Hammered into NgAgo Coffin

Final Nail Hammered into NgAgo Coffin

By | August 3, 2017

The paper describing the gene-editing method is retracted.

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image: Scientists Edit Viable Human Embryos in U.S.

Scientists Edit Viable Human Embryos in U.S.

By | July 27, 2017

The embryos, whose genes were altered by CRISPR, were not intended for implantation. 

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image: CRISPR Restores Muscle Function in Mice

CRISPR Restores Muscle Function in Mice

By | July 17, 2017

Scientists use the gene-editing tool to treat animals with a rare form of congenital muscular dystrophy.

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image: CRISPR Corrects Duchenne-Causing Mutations

CRISPR Corrects Duchenne-Causing Mutations

By | April 12, 2017

Using CRISPR-Cpf1 gene editing, researchers have fixed mutations that cause a form of muscular dystrophy in cultured human cardiomyocytes and a mouse model.

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