NewLink Genetics (NLNK) and Editas Medicine (EDIT) Critical ReviewThe Lincolnian OnlineIt is developing a genome editing platform based on clustered, regularly interspaced short palindromic repeats (CRISPR) technology. CRISPR uses a protein-ribonucleic… Continue reading
GlobeNewswire (press release) |
Predictive Technology Group, Inc.’s (PRED) Subsidiary Provides a Sponsorship at 4th Annual Perinatal Stem Cell …
GlobeNewswire (press release) Dr. Doug Schmid, Chief Science and Lab Officer, at Predictive Biotech, Inc. presented his topic during the March 1-2, 2018 4th Annual Perinatal Stem Cell Society Congress, Salt Lake City, UT, titled: “Wharton’s Jelly: A Perinatal Cytokine Reservoir … |
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International Stem Cell Corporation Completes Dosing Of Second Cohort In Parkinson’s Disease Clinical Trial
GlobeNewswire (press release) CARLSBAD, Calif., March 05, 2018 (GLOBE NEWSWIRE) — International Stem Cell Corporation (OTCQB:ISCO), a California-based clinical stage biotechnology company developing stem cell-based therapies and biomedical products, announced today that the eighth … |
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International Stem Cell Corporation Completes Dosing Of Second Cohort In Parkinson’s Disease Clinical Trial
Nasdaq CARLSBAD, Calif., March 05, 2018 (GLOBE NEWSWIRE) — International Stem Cell Corporation (OTCQB:ISCO), a California-based clinical stage biotechnology company developing stem cell-based therapies and biomedical products, announced today that the eighth … |
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International Stem Cell Corporation Completes Dosing Of Second Cohort In Parkinson’s Disease Clinical Trial
Nasdaq CARLSBAD, Calif., March 05, 2018 (GLOBE NEWSWIRE) — International Stem Cell Corporation (OTCQB:ISCO), a California-based clinical stage biotechnology company developing stem cell-based therapies and biomedical products, announced today that the eighth … |
Genetic Literacy Project |
Targeted evolution: Why are we so afraid of CRISPR gene editing?
Genetic Literacy Project The potential applications of CRISPR are enormous. It’s the closest we’ve ever come to a cure for cancer. We’ve already been able to cure HIV infection in animal models, and even in human cell cultures, by removing the viral genes that insert … |