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Mashup Score: 1Hans-Peter Kiem, M.D., Ph.D. - 2 year(s) ago
Dr. Kiem is a physician-scientist studying hematopoietic stem cell (HSC) biology, transplantation,…
Source: asgct.orgCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 3Introducing Our 2022 Annual Meeting Award Winners - 2 year(s) ago
The American Society of Gene @ Cell Therapy is proud to announce the winners of the Outstanding Achievement Award, the Outstanding New Investigator Award, the Sonia Skarlatos Public Service Award, and the Jerry Mendell Award for Translational Science.
Source: asgct.orgCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 8DOK7 Gene Therapy Enhances Neuromuscular Junction Innervation and Motor Function in Aged Mice - 2 year(s) ago
Clinical Genetics; Molecular Mechanism of Gene Regulation; Musculoskeletal Medicine
Source: iScienceCategories: General Medicine News, Latest HeadlinesTweet
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Mashup Score: 5Preclinical Efficacy and Safety of a Human Embryonic Stem Cell-Derived Midbrain Dopamine Progenitor Product, MSK-DA01 - 2 year(s) ago
Tabar et al. report the development of an hESC-derived dopamine neuron product for clinical applications.
Source: Cell Stem CellCategories: General Medicine News, Latest HeadlinesTweet
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Mashup Score: 1Agenda Details | ASGCT 25th Annual Meeting - 2 year(s) ago
Detailed Program …
Source: annualmeeting.asgct.orgCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 1Cell Press: Molecular Therapy - 2 year(s) ago
Suppression of RNA editing by miR-17 inhibits the stemness of melanoma stem cellsMiR-17 inhibits RNA editing to achieve post-transcriptional regulation of DOCK2, leading to the suppression of the stemness of melanoma stem cells. Our findings indicate that miRNA-regulated RNA editing plays important roles in tumor progression and that miR-17, a tumor suppressor, may be a potential therapeutic…
Source: www.cell.comCategories: General Medicine News, Latest HeadlinesTweet
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Mashup Score: 7Acute gene inactivation in the adult mouse liver using the CRISPR-Cas9 technology: STAR Protocols - 2 year(s) ago
Summary Genetic manipulation in mice allows the discovery of gene function and biological mechanisms in vivo. The widely used Cre/LoxP system usually takes months to years especially when starting with the production of floxed alleles of a new gene of interest (GOI). Here, we describe a protocol using the CRISPR-Cas9 system to acutely inactivate the GOI in adult mice. This…
Source: star-protocols.cell.comCategories: General Medicine News, Latest HeadlinesTweet
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Mashup Score: 0Agenda Details | ASGCT 25th Annual Meeting - 2 year(s) ago
Wednesday, May 18 2022 08:50 AM – 09:15 AM ET. Breaking Down Gene Therapy and CRISPR Topics for Non-scientific Audiences Jennifer E. Adair, PhD. Fred Hutch, Seattle, WA …
Source: annualmeeting.asgct.orgCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 0Agenda Details | ASGCT 25th Annual Meeting - 2 year(s) ago
Wednesday, May 18 2022 08:00 AM – 09:45 AM ET. Challenges and Status in Development of Gene Therapies in LMICs (Organized by the Global Outreach Committee) This symposium will highlight the barriers to the development of gene therapies in…
Source: annualmeeting.asgct.orgCategories: Hem/Onc News and Journals, Latest HeadlinesTweet
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Mashup Score: 2Best of Molecular Therapy 2021 - 2 year(s) ago
Best of Molecular Therapy 2021
Source: info.cell.comCategories: General Medicine News, Latest HeadlinesTweet
Closing out #ASGCT22 with a warm congratulations to Dr. Hans-Peter Kiem @HPKiem of Fred Hutch as he steps into his role as president of @ASGCTherapy. https://t.co/hJkaayeIyK https://t.co/u879oUscU5