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Items: 6

1.
Retinal blood vessel‐origin yes‐associated protein (YAP) governs astrocytic maturation via leukaemia inhibitory factor (LIF)
Li‐Qian‐Yu Ai, Rong‐Di Yuan, Xi Chen, Yun‐Jia Liu, Wen‐Yi Liu, Jing‐Yi Zhu, Zhou Zhang, Jun Yan, Chun‐Lin Chen, Sen Lin, Jian Ye
Cell Prolif. 2020 Feb; 53(2): e12757. Published online 2020 Jan 8. doi: 10.1111/cpr.12757
PMCID:
PMC7046482
AbstractArticlePDF–2.3M
2.
YAP promotes the proliferation of neuroblastoma cells through decreasing the nuclear location of p27Kip1 mediated by Akt
Xiya Shen, Xingxing Xu, Changnan Xie, Huitao Liu, Danlu Yang, Jingjing Zhang, Qian Wu, Wenjin Feng, Ling Wang, Leilei Du, Lina Xuan, Chaobo Meng, Haitao Zhang, Wei Wang, Ying Wang, Tian Xie, Zhihui Huang
Cell Prolif. 2020 Feb; 53(2): e12734. Published online 2019 Dec 20. doi: 10.1111/cpr.12734
PMCID:
PMC7046475
AbstractArticlePDF–1.9M
3.
LncRNA-ATB promotes autophagy by activating Yes-associated protein and inducing autophagy-related protein 5 expression in hepatocellular carcinoma
Chuan-Zhuo Wang, Guang-Xin Yan, De-Shuo Dong, He Xin, Zhao-Yu Liu
World J Gastroenterol. 2019 Sep 21; 25(35): 5310–5322. Published online 2019 Sep 21. doi: 10.3748/wjg.v25.i35.5310
PMCID:
PMC6761242
AbstractArticlePDF–13M
4.
Identification, basic characterization and evolutionary analysis of differentially spliced mRNA isoforms of human YAP1 gene
Christian J Gaffney, Tsutomu Oka, Virginia Mazack, Dror Hilman, Uri Gat, Tomoki Muramatsu, Johji Inazawa, Alicia Golden, David J Carey, Amjad Farooq, Gerard Tromp, Marius Sudol
Gene. Author manuscript; available in PMC 2013 Nov 10.
Published in final edited form as: Gene. 2012 Nov 10; 509(2): 215–222. Published online 2012 Aug 24. doi: 10.1016/j.gene.2012.08.025
PMCID:
PMC3455135
AbstractArticlePDF–1.6M
5.
The WW domain of Yes-associated protein binds a proline-rich ligand that differs from the consensus established for Src homology 3-binding modules.
H I Chen, M Sudol
Proc Natl Acad Sci U S A. 1995 Aug 15; 92(17): 7819–7823. doi: 10.1073/pnas.92.17.7819
PMCID:
PMC41237
SummaryPage BrowsePDF–1.5M
6.
Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects
Kathleen A. Williamson, Joe Rainger, James A.B. Floyd, Morad Ansari, Alison Meynert, Kishan V. Aldridge, Jacqueline K. Rainger, Carl A. Anderson, Anthony T. Moore, Matthew E. Hurles, Angus Clarke, Veronica van Heyningen, Alain Verloes, Martin S. Taylor, Andrew O.M. Wilkie, UK10K Consortium, David R. FitzPatrick
Am J Hum Genet. 2014 Feb 6; 94(2): 295–302. doi: 10.1016/j.ajhg.2014.01.001
PMCID:
PMC3928658
AbstractArticlePDF–1.4M

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