3 天
GlobalData on MSNUSC receives grant for gene therapy targeting glioblastomaUSC has received a $6m grant from the California Institute for Regenerative Medicine (CIRM) to advance a new gene therapy for ...
Medera, Inc., (“Medera”), a clinical-stage biotechnology company, announced today that the management team will participate ...
6 小时
AZoLifeSciences on MSNNew CRISPR Tool Reveals Key Lymphoma GenesThis study presents an optimized CRISPR-Cas12a system for large-scale genetic screening, revealing critical genes involved in lymphoma development and therapy.
5 小时
Zacks.com on MSNCRISPR Therapeutics Stock Before Q4 Earnings: To Buy or Not to Buy?CRISPR Therapeutics CRSP is expected to report fourth-quarter and full-year 2024 earnings later this month. The Zacks ...
Forkhead box protein L2 (FOXL2) is a protein involved in ovary development and maintenance, among other functions. Mutations in its gene are involved in ovarian failure and granulosa cell tumors, ...
Stargardt disease type 1 (STGD1) is an inherited retinal recessive disease caused by biallelic variants in the ABCA4 gene. One of the recurrent variants is located at the exon-intron junction of exon ...
3 天
News Medical on MSNUSC receives $6 million grant for pioneering glioblastoma gene therapyThe California Institute for Regenerative Medicine has awarded a $6 million grant to USC investigators pioneering a new first ...
By creating gene editors not found in nature, or optimizing existing editors, AI can improve the accuracy, effectiveness, and accessibility of gene editing.
Gene silencing is a negative feedback mechanism that regulates gene expression to define cell fate and also regulates metabolism and gene expression throughout the life of an organism. In plants, gene ...
Gene-editing strategies involving engineered nucleases [i.e., zinc-finger nucleases ... and transcription activator-like effector nucleases (TALENs), the versatility of CRISPR targeting has rapidly ...
Potent in vivo gene editing in skeletal muscle of non-human primates by a novel, ultracompact CRISPR system delivered via a single AAV vector.
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