Zobrazeno 1 - 6
of 6
pro vyhledávání: '"LinXi Cheng"'
Publikováno v:
Cell Reports, Vol 42, Iss 8, Pp 112867- (2023)
Summary: The POGZ gene has been found frequently mutated in neurodevelopmental disorders (NDDs) such as autism spectrum disorder (ASD) and intellectual disability (ID). We have recently shown that POGZ maintains mouse embryonic stem cells (ESCs). How
Externí odkaz:
https://doaj.org/article/b0cc31bcade14a0fa7b73d31c5c1cf58
Publikováno v:
Molecular Autism, Vol 13, Iss 1, Pp 1-18 (2022)
Abstract Background The POGZ gene has been found frequently mutated in neurodevelopmental disorders (NDDs), particularly autism spectrum disorder (ASD) and intellectual disability (ID). However, little is known about its roles in embryonic stem cells
Externí odkaz:
https://doaj.org/article/e918f593efae475993d3a12c618de020
Autor:
LinXi Cheng, MingHui Xie, WeiHua Qiao, Yu Song, YanYong Zhang, YingChao Geng, WeiLin Xu, Lin Wang, Zheng Wang, Kai Huang, NianGuo Dong, YuHua Sun
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-15 (2021)
Cheng et al. provide a detailed characterization of the differentiation of human pluripotent stem cells to valve endothelial cells and their function. Their results show that the valve endothelial-like cells express key markers for valve endothelial
Externí odkaz:
https://doaj.org/article/00f4479e6cab46848b34a82b21781d66
Autor:
MingHui Xie, Weilin Xu, Zheng Wang, Yuhua Sun, Nianguo Dong, Lin Wang, WeiHua Qiao, YanYong Zhang, Yu Song, Kai Huang, Yingchao Geng, Linxi Cheng
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-15 (2021)
Communications Biology
Communications Biology
The cardiac valvular endothelial cells (VECs) are an ideal cell source that could be used for making the valve organoids. However, few studies have been focused on the derivation of this important cell type. Here we describe a two-step chemically def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f1b7ce26e29a6dca02d7d3d5321dcbe
https://doaj.org/article/00f4479e6cab46848b34a82b21781d66
https://doaj.org/article/00f4479e6cab46848b34a82b21781d66
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcb1d062b47383541aff3a1359ea0856
https://doi.org/10.2139/ssrn.4288933
https://doi.org/10.2139/ssrn.4288933
POGZ, which encodes a multi-domain transcription factor, has been found frequently mutated in neurodevelopmental disorders, particularly autism spectrum disorder (ASD) and intellectual disability (ID). However, little is known about its functions in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c587c2a76beeadc8a394c42d4836da3
https://doi.org/10.1101/2021.02.07.430173
https://doi.org/10.1101/2021.02.07.430173
