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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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NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21

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

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.

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.