Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erica L Boetefuer"'
Autor:
Robert J Lake, Erica L Boetefuer, Pei-Fang Tsai, Jieun Jeong, Inchan Choi, Kyoung-Jae Won, Hua-Ying Fan
Publikováno v:
PLoS Genetics, Vol 10, Iss 4, p e1004284 (2014)
Cockayne syndrome is an inherited premature aging disease associated with numerous developmental and neurological defects, and mutations in the gene encoding the CSB protein account for the majority of Cockayne syndrome cases. Accumulating evidence s
Externí odkaz:
https://doaj.org/article/8028cbe89872461cbdfdf92577e401f7
Publikováno v:
Journal of Biological Chemistry. 293:17863-17874
Cockayne syndrome protein B (CSB) is an ATP-dependent chromatin remodeler that relieves oxidative stress by regulating DNA repair and transcription. CSB is proposed to participate in base-excision repair (BER), the primary pathway for repairing oxida
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e104a40625d3aef1d91b3a3270274d7
https://doi.org/10.1074/jbc.ra118.004548
https://doi.org/10.1074/jbc.ra118.004548
Publikováno v:
Nucleic Acids Research
Cockayne syndrome protein B (CSB) is a member of the SNF2/SWI2 ATPase family and is essential for transcription-coupled nucleotide excision DNA repair (TC-NER). CSB also plays critical roles in transcription regulation. CSB can hydrolyze ATP in a DNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af1ddb87abec98e020b1367de4aadde2
https://doi.org/10.1093/nar/gky660
https://doi.org/10.1093/nar/gky660
The CSB chromatin remodeler and CTCF architectural protein cooperate in response to oxidative stress
Publikováno v:
Nucleic Acids Research
Cockayne syndrome is a premature aging disease associated with numerous developmental and neurological abnormalities, and elevated levels of reactive oxygen species have been found in cells derived from Cockayne syndrome patients. The majority of Coc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2eae9fe2199e2c8e5a63037645ca396d
https://doi.org/10.1093/nar/gkv1219
https://doi.org/10.1093/nar/gkv1219
Autor:
Pei-Fang Tsai, Kyoung-Jae Won, Jieun Jeong, Erica L. Boetefuer, Inchan Choi, Hua-Ying Fan, Robert J. Lake
Publikováno v:
PLoS Genetics, Vol 10, Iss 4, p e1004284 (2014)
PLoS Genetics
PLoS Genetics
Cockayne syndrome is an inherited premature aging disease associated with numerous developmental and neurological defects, and mutations in the gene encoding the CSB protein account for the majority of Cockayne syndrome cases. Accumulating evidence s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a840f7ece522f460c40fd0bc5db6250b
http://europepmc.org/articles/PMC3990521?pdf=render
http://europepmc.org/articles/PMC3990521?pdf=render