Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Hsuan-Chung Ho"'
Autor:
Hsuan-Chung Ho, Sean M Burgess
Publikováno v:
PLoS Genetics, Vol 7, Iss 11, p e1002351 (2011)
Proper segregation of chromosomes during meiosis requires the formation and repair of double-strand breaks (DSBs) to form crossovers. Repair is biased toward using the homolog as a substrate rather than the sister chromatid. Pch2 is a conserved membe
Externí odkaz:
https://doaj.org/article/0c570413a01d4b2ebf5a1e8b0206396d
Autor:
Hesso Farhan, Jeffrey L. Brodsky, Muhammad Zahoor, Patrick G. Needham, Susan Ferro-Novick, Smriti Parashar, Muriel Mari, Ming Zhu, Hsuan-Chung Ho, Fulvio Reggiori, Shuliang Chen, Yixian Cui
Publikováno v:
Science, 365(6448), 53-60. AMER ASSOC ADVANCEMENT SCIENCE
ER-phagy keeps cells healthy In eukaryotic cells, about one-third of all proteins are targeted to the endoplasmic reticulum (ER), which serves as a hub for secretory protein traffic and quality control. Cui et al. studied a protein known as Lst1 in y
Publikováno v:
The Journal of Cell Biology
Lee et al. show that methionine triggers Ppz phosphatase-dependent dephosphorylation of the E3 ubiquitin ligase adaptor Art1. Art1 dephosphorylation promotes its interaction with the methionine transporter Mup1, as well as subsequent endocytosis and
Publikováno v:
Molecular Biology of the Cell
The ART-Rsp5 network is regulated by the ubiquitin system. Ubp2 and Ubp15 prevent hyperubiquitination and proteasomal degradation of ARTs. Ubp2 and Ubp15 ensure efficient endocytosis by stabilizing ARTs.
Endocytic down-regulation of cell-surface
Endocytic down-regulation of cell-surface
Publikováno v:
Current Biology. 20:1707-1716
Summary Background Homologous recombination promotes proper segregation of chromosomes during meiosis. Programmed double-strand breaks (DSBs) initiate recombination and are repaired preferentially using the homolog rather than the sister chromatid te
Publikováno v:
The EMBO Journal. 29:1748-1761
Death-associated protein kinase (DAPK) was identified as a mediator of interferon (IFN)-induced cell death. How IFN controls DAPK activation remains largely unknown. Here, we identify the BTB-Kelch protein KLHL20 as a negative regulator of DAPK. KLHL
Autor:
Sora Lee1, Hsuan-Chung Ho2, Tumolo, Jessica M.1, Pi-Chiang Hsu2, MacGurn, Jason A.1 jason.a.macgurn@vanderbilt.edu
Publikováno v:
Journal of Cell Biology. Mar2019, Vol. 218 Issue 3, p977-992. 16p.
Homologous recombination promotes proper segregation of chromosomes during meiosis. Programmed double-strand breaks (DSBs) initiate recombination and are repaired preferentially using the homolog rather than the sister chromatid template. In yeast, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a438a3552a60d9313955e0017735dfc
https://europepmc.org/articles/PMC2989795/
https://europepmc.org/articles/PMC2989795/
Autor:
Chun-Hau Chen, Yu-Ru Lee, Wei-Chien Yuan, Che-Hung Shen, Hsiu Ming Shih, Hsuan-Chung Ho, Ruey-Hwa Chen
Publikováno v:
Cancer Research. 70:LB-18
Death-associated protein kinase (DAPK) is a pro-apoptotic, calmodulin-regulated serine/threonine kinase and was originally identified based on its involvement in interferon- -induced cell death. Whether and how interferon-γ-signaling regulates the a