Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ziye Rong"'
Publikováno v:
Cell Death Discovery, Vol 10, Iss 1, Pp 1-11 (2024)
Abstract Carboxy-terminal domain small phosphatase like 2 (CTDSPL2), one of the haloacid dehalogenase phosphatases, is associated with several diseases including cancer. However, the role of CTDSPL2 and its regulatory mechanism in lung cancer remain
Externí odkaz:
https://doaj.org/article/2f84d53f91b14c41a5a2087d6a8a61e0
Publikováno v:
Cell Death and Disease, Vol 14, Iss 1, Pp 1-11 (2023)
Abstract The alteration of cellular energy metabolism is a hallmark of colorectal cancer (CRC). Accumulating evidence has suggested oxidative phosphorylation (OXPHOS) is upregulated to meet the demand for energy in tumor initiation and development. H
Externí odkaz:
https://doaj.org/article/a3d62021a0c243e8928c5976c6a94a2a
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Mitochondria are double membrane organelles in eukaryotic cells that provide energy by generating adenosine triphosphate (ATP) through oxidative phosphorylation. They are crucial to many aspects of cellular metabolism. Mitochondria contain their own
Externí odkaz:
https://doaj.org/article/814884c8c7f647a880331d4455dba31c
The alteration of cellular energy metabolism is a hallmark of colorectal cancer (CRC). Accumulating evidence has suggested oxidative phosphorylation (OXPHOS) is upregulated to meet the demand for energy in tumor initiation and development. However, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e532e0e1308dd5940d1a39fb3bf8ca4
https://doi.org/10.21203/rs.3.rs-2080235/v1
https://doi.org/10.21203/rs.3.rs-2080235/v1
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Mitochondria are double membrane organelles in eukaryotic cells that provide energy by generating adenosine triphosphate (ATP) through oxidative phosphorylation. They are crucial to many aspects of cellular metabolism. Mitochondria contain their own
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92abe1b651670f7ec8ca99c9fe42f786
https://pubmed.ncbi.nlm.nih.gov/34055802
https://pubmed.ncbi.nlm.nih.gov/34055802
Autor:
David R. Corey, Chao Xing, Jiaxin Hu, Vivek Sharma, Jonathan K. Watts, Zhengyang Zhou, Venkateswara Mootha, Xin Gong, Ziye Rong
Publikováno v:
Human Molecular Genetics
Fuchs’ endothelial corneal dystrophy (FECD) is the most common repeat expansion disorder. FECD impacts 4% of U.S. population and is the leading indication for corneal transplantation. Most cases are caused by an expanded intronic CUG tract in the T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e056799c0197b7b11e99c40a510968f
https://doi.org/10.1093/hmg/ddy018
https://doi.org/10.1093/hmg/ddy018
Publikováno v:
Journal of Biological Chemistry. 291:19079-19091
During the cell cycle, sister-chromatid cohesion tethers sister chromatids together from S phase to the metaphase-anaphase transition and ensures accurate segregation of chromatids into daughter cells. N-terminal acetylation is one of the most preval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22aa459c0b559a54966b27dda07934dc
https://doi.org/10.1074/jbc.m116.737585
https://doi.org/10.1074/jbc.m116.737585
Publikováno v:
Translational Vision Science & Technology
Purpose Fuchs’ endothelial corneal dystrophy (FECD) is the leading indication for corneal transplantation. Seventy percent of cases are caused by an intronic CTG triplet repeat expansion in the TCF4 gene that results in accumulation of pathogenic e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b2624c4a794ac18b8aa512f911cad03
https://doi.org/10.1167/tvst.9.9.47
https://doi.org/10.1167/tvst.9.9.47
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose Fuchs' endothelial corneal dystrophy (FECD) is a major cause of vision loss and the most common nucleotide repeat disorder, affecting 4% of United States population greater than 40 years of age. Seventy percent of FECD cases are due to an int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e462c83c425083b37bb3f10cbdfb57
https://doi.org/10.1167/iovs.19-27641
https://doi.org/10.1167/iovs.19-27641
Autor:
Jiaxin Hu, Ziye Rong, Xin Gong, Zhengyang Zhou, Sharma, Vivek K., Chao Xing, Watts, Jonathan K., Corey, David R., Mootha, V. Vinod
Publikováno v:
Human Molecular Genetics; Mar2018, Vol. 27 Issue 6, p1015-1026, 12p, 1 Diagram, 2 Charts, 4 Graphs