Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mairi J. Hunter"'
Autor:
Mairi J Hunter, Kate J Treharne, Alexandra K Winter, Diane M Cassidy, Stephen Land, Anil Mehta
Publikováno v:
PLoS ONE, Vol 5, Iss 7, p e11598 (2010)
Mutation of the cystic fibrosis transmembrane-conductance regulator (CFTR) causes cystic fibrosis (CF) but not all CF aspects can easily be explained by deficient ion transport. CF-inflammation provides one example but its pathogenesis remains contro
Externí odkaz:
https://doaj.org/article/e1fc60751cda44efaf32e91362d618b6
Autor:
Yun Wah Lam, Eric Jan, Sonia Paytubi, Luis Izquierdo, Mairi J. Hunter, Harinder S. Hundal, Christopher G. Proud, Xuemin Wang
Publikováno v:
Journal of Biological Chemistry. 284:24061-24073
ABC50 is an ATP-binding cassette (ABC) protein, which, unlike most ABC proteins, does not possess membrane-spanning domains. ABC50 interacts with eukaryotic initiation factor 2 (eIF2), which plays a key role in translation initiation and its control.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7054301ec2d63b8b8ffe0236af4c8457
https://doi.org/10.1074/jbc.m109.031625
https://doi.org/10.1074/jbc.m109.031625
Autor:
Rudolf Nenutil, Ted R. Hupp, Mairi J. Hunter, Joanne Darragh, Peter E. Ross, John F. Dillon, Neil M. Kernohan, Elizabeth Pohler, Lenny Nelson, Borek Vojtesek
Publikováno v:
FEBS Journal. 273:1930-1947
Stress protein responses have evolved in part as a mechanism to protect cells from the toxic effects of environmental damaging agents. Oesophageal squamous epithelial cells have evolved an atypical stress response that results in the synthesis of a 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::018e53edae345597bb0d61e3d63c297b
https://doi.org/10.1111/j.1742-4658.2006.05206.x
https://doi.org/10.1111/j.1742-4658.2006.05206.x
Autor:
Stephen C. Land, Diane Cassidy, Anil Mehta, Kate J. Treharne, Mairi J. Hunter, Alexandra K. Winter
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 7, p e11598 (2010)
PLoS ONE, Vol 5, Iss 7, p e11598 (2010)
BACKGROUND Mutation of the cystic fibrosis transmembrane-conductance regulator (CFTR) causes cystic fibrosis (CF) but not all CF aspects can easily be explained by deficient ion transport. CF-inflammation provides one example but its pathogenesis rem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95e325430d5e5c0103e841fa41246342
https://doi.org/10.1371/journal.pone.0011598
https://doi.org/10.1371/journal.pone.0011598