Loss of TAF8 causes TFIID dysfunction and p53-mediated apoptotic neuronal cell death
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Title
Loss of TAF8 causes TFIID dysfunction and p53-mediated apoptotic neuronal cell death
Authors
Keywords
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Journal
CELL DEATH AND DIFFERENTIATION
Volume 29, Issue 5, Pages 1013-1027
Publisher
Springer Science and Business Media LLC
Online
2022-03-31
DOI
10.1038/s41418-022-00982-5
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- The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote
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- Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
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- Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
- (2009) Da Wei Huang et al. Nature Protocols
- Neural Differentiation of Embryonic Stem Cells In Vitro: A Road Map to Neurogenesis in the Embryo
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- (2008) Da Wei Huang et al. NUCLEIC ACIDS RESEARCH
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