Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Collin Shaw"'
Autor:
Collin Shaw, Gary Sweeney, Ravi Retnakaran, Anthony J. Hanley, Rungsunn Tungtrongchitr, Ying Liu
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 92:4313-4318
Decreased total adiponectin has been associated with metabolic disorders, including obesity, diabetes, fatty liver, and the metabolic syndrome. Although circulating adiponectin is composed of trimers, hexamers, and high molecular weight (HMW) multime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e486c62975e54eec51fb6c9f71b3f015
https://doi.org/10.1210/jc.2007-0890
https://doi.org/10.1210/jc.2007-0890
Autor:
Collin Shaw, Malu Govindan, Bruce A. Stanton, Dominique Loffing-Cueni, Caitlin R. Stanton, Jan Loffing, Amilyn M. Taplin
Publikováno v:
American Journal of Physiology-Cell Physiology. 281:C1889-C1897
The ΔF508 mutation reduces the amount of cystic fibrosis transmembrane conductance regulator (CFTR) expressed in the plasma membrane of epithelial cells. However, a reduced temperature, butyrate compounds, and “chemical chaperones” allow ΔF508-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ed0e934f53473c06c352db486caf49c
https://doi.org/10.1152/ajpcell.2001.281.6.c1889
https://doi.org/10.1152/ajpcell.2001.281.6.c1889
Increased functional cell surface expression of CFTR and ΔF508-CFTR by the anthracycline doxorubicin
Publikováno v:
American Journal of Physiology-Cell Physiology. 280:C1031-C1037
Cystic fibrosis (CF) is a disease that is caused by mutations within the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The most common mutation, DeltaF508, accounts for 70% of all CF alleles and results in a protein that is defecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfca781d9fc8ad3e69c259734e4b559e
https://doi.org/10.1152/ajpcell.2001.280.5.c1031
https://doi.org/10.1152/ajpcell.2001.280.5.c1031
Publikováno v:
Cellular Physiology and Biochemistry. 11:93-98
Cystic fibrosis is caused by mutations in the CFTR gene. The most common of these mutations, DeltaF508, results in a protein that is not trafficked to the apical plasma membrane but instead is retained and degraded in the endoplasmic reticulum (ER) b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c91b1f7f8d6218eb488f296d4b04ead
https://doi.org/10.1159/000047796
https://doi.org/10.1159/000047796
Autor:
Bryan D. Moyer, Marc Duhaime, Collin Shaw, Jerod Denton, Donna Reynolds, Katherine H. Karlson, Jason Pfeiffer, Shusheng Wang, John E. Mickle, Michal Milewski, Garry R. Cutting, William B. Guggino, Min Li, Bruce A. Stanton
Publikováno v:
Journal of Biological Chemistry. 275:27069-27074
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f99f5d80fed4bba20fbda28e831d8b4
https://doi.org/10.1016/s0021-9258(19)61481-x
https://doi.org/10.1016/s0021-9258(19)61481-x
Autor:
Anthony J. Hanley, Ji Woo Park, Gary Sweeney, Michael M. Swarbrick, Nam Seok Lee, Eun Sun Song, Ravi Retnakaran, Ying Liu, Wi Kim, Byung Soo Youn, Collin Shaw, Rungsunn Tungtrongchitr, Vivian Vu, Peter J. Havel
Publikováno v:
Clinical endocrinology. 69(6)
Author(s): Retnakaran, Ravi; Youn, Byung-Soo; Liu, Ying; Hanley, Anthony JG; Lee, Nam Seok; Park, Ji Woo; Song, Eun Sun; Vu, Vivian; Kim, Wi; Tungtrongchitr, Rungsunn; Havel, Peter J; Swarbrick, Michael M; Shaw, Collin; Sweeney, Gary | Abstract: Obje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da34035f597507e81a627196af246078
https://pubmed.ncbi.nlm.nih.gov/18410550
https://pubmed.ncbi.nlm.nih.gov/18410550
Autor:
Bryan D. Moyer, Garry R. Cutting, Collin Shaw, Michal Milewski, John E. Mickle, Marc Duhaime, Jason R. Pfeiffer, Katherine H. Karlson, Jerod S. Denton, Bruce A. Stanton, Min Li, Donna Reynolds, Shusheng Wang, William B. Guggino
Publikováno v:
Journal of Biological Chemistry.
Polarization of cystic fibrosis transmembrane conductance regulator (CFTR), a cAMP-activated chloride channel to the apical plasma membrane in epithelial cells is critical for vectorial chloride transport. Previously, we reported that the C terminus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1182aa9301d417a5333bdceb02311192
https://doi.org/10.1074/jbc.m004951200
https://doi.org/10.1074/jbc.m004951200
Autor:
Collin Shaw
An abstract of the thesis of Collin M. Shaw for the Master of Science in Biology presented November 9,1998. Title: Increased glutathione metabolic defense capabilities In cultured Alzheimer's diseased lymphoblast cell lines. The hypothesis to be test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6440c15956e46019f72bc093d7044a75
https://doi.org/10.15760/etd.1702
https://doi.org/10.15760/etd.1702
