L
Lei Chen
Researcher at Stanford University
Publications - 16
Citations - 4126
Lei Chen is an academic researcher from Stanford University. The author has contributed to research in topics: NFATC Transcription Factors & Gene. The author has an hindex of 14, co-authored 14 publications receiving 3922 citations. Previous affiliations of Lei Chen include Howard Hughes Medical Institute.
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Journal ArticleDOI
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
Joseph R. Arron,Monte M. Winslow,Alberto Polleri,Ching Pin Chang,Hai Wu,Xin Gao,Joel R. Neilson,Lei Chen,Jeremy J Heit,Seung K. Kim,Nobuyuki Yamasaki,Tsuyoshi Miyakawa,Uta Francke,Isabella A. Graef,Gerald R. Crabtree +14 more
TL;DR: It is suggested that the 1.5-fold increase in dosage of DSCR1 and DYRK1A cooperatively destabilizes a regulatory circuit, leading to reduced NFATc activity and many of the features of Down's syndrome, and the destabilization of regulatory circuits can underlie human disease.
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NF-AT components define a family of transcription factors targeted in T-cell activation
Jeffrey P. Northrop,Steffan N. Ho,Lei Chen,Daryl J. Thomas,Luika A. Timmerman,Garry P. Nolan,Arie Admon,Gerald R. Crabtree +7 more
TL;DR: This work purify two proteins encoded by separate genes that represent the pre-existing and cytosolic components of NF-AT, indicating that distinct signalling pathways converge onNF-ATc to regulate its function.
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MicroRNA-mediated switching of chromatin-remodelling complexes in neural development
TL;DR: It is found that BAF53a repression is mediated by sequences in the 3′ untranslated region corresponding to the recognition sites for miR-9* and miR -124, which are selectively expressed in post-mitotic neurons.
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An embryonic stem cell chromatin remodeling complex, esBAF, is essential for embryonic stem cell self-renewal and pluripotency.
Lena Ho,Jehnna L. Ronan,Jiang Wu,Brett T. Staahl,Lei Chen,Ann Kuo,Julie A. Lessard,Julie A. Lessard,Alexey I. Nesvizhskii,Jeff Ranish,Gerald R. Crabtree +10 more
TL;DR: It is shown that BAF complexes are required for the self-renewal and pluripotency of mouse ES cells but not for the proliferation of fibroblasts or other cells, suggesting that esBAF complexes are specialized to interact with ES cell-specific regulators, providing a potential explanation for the requirement of BAF complex in pluripOTency.
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Signals Transduced by Ca2+/Calcineurin and NFATc3/c4 Pattern the Developing Vasculature
TL;DR: It is shown that calcineurin function is transiently required between E7.5 and E8.5, which initiates the later cross-talk between vessels and surrounding tissues that pattern the vasculature.