Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Cyrus A. Martin"'
Autor:
Shelley R. Allen, Brian P. Flemming, Cyrus C. Martin, James K. Oeser, Richard M. O'Brien, Yingda Wang, John C. Hutton, Jay A. Walters
Publikováno v:
Diabetes. 57:133-141
OBJECTIVE—Islet-specific glucose-6-phosphatase catalytic subunit–related protein (IGRP) is selectively expressed in islet β-cells and is a major autoantigen in both mouse and human type 1 diabetes. This study describes the use of a combination o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818462f92dc7db6ed4e786d7a6c0bf36
https://doi.org/10.2337/db07-0092
https://doi.org/10.2337/db07-0092
Autor:
John C. Hutton, Suparna A. Sarkar, Owen P. McGuinness, James K. Oeser, Richard M. O'Brien, Yingda Wang, Cyrus C. Martin
Publikováno v:
Diabetologia. 50:774-778
Islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP, now known as glucose-6-phosphatase, catalytic, 2 [G6PC2]) has recently been identified as a major autoantigen in mouse and human type 1 diabetes. Strategies designed to sup
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4671d206a6041fea62f18d0ad6dd0857
https://doi.org/10.1007/s00125-006-0564-1
https://doi.org/10.1007/s00125-006-0564-1
Publikováno v:
Journal of Biological Chemistry. 279:34277-34289
Islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP) is selectively expressed in islet beta cells and is a major autoantigen in a mouse model of type I diabetes. The analysis of IGRP-chloramphenicol acetyltransferase (CAT) fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::475a009f357a8710c5934c59f137cd69
https://doi.org/10.1074/jbc.m404830200
https://doi.org/10.1074/jbc.m404830200
Autor:
Carrie A. Everett, Lauri A. Hornbuckle, Stephanie S. Gustavson, James K. Oeser, Cyrus C. Martin, Alan D. Cherrington, Doss W. Neal, Christina A. Svitek, Richard M. O'Brien
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 286:E795-E808
We recently compared the regulation of glucose-6-phosphatase (G-6-Pase) catalytic subunit and glucose 6-phosphate (G-6- P) transporter gene expression by insulin in conscious dogs in vivo (Hornbuckle LA, Edgerton DS, Ayala JE, Svitek CA, Neal DW, Car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acc84f75b56e5260222a77f4ee1f3ea3
https://doi.org/10.1152/ajpendo.00455.2003
https://doi.org/10.1152/ajpendo.00455.2003
Autor:
Christina A. Svitek, Cyrus C. Martin, John C. Hutton, James K. Oeser, Richard M. O'Brien, SI Hunter
Publikováno v:
Journal of Molecular Endocrinology. 29:205-222
Glucose-6-phosphatase (G6Pase) catalyzes the final step in the gluconeogenic and glycogenolytic pathways, the hydrolysis of glucose-6-phosphate (G6P) to glucose and phosphate. This paper describes the identification and characterization of a human cD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bee0c4a0d4d9d7398473f5a9844762ae
https://doi.org/10.1677/jme.0.0290205
https://doi.org/10.1677/jme.0.0290205
Autor:
John C. Hutton, Joshua K. Goldman, Larry J. Bischof, Lauri A. Hornbuckle, Beth T. Stadelmaier, James K. Oeser, Cyrus C. Martin, Christina A. Svitek, Richard M. O'Brien
Publikováno v:
Diabetes. 50:502-514
Glucose-6-phosphatase (G6Pase) is a multicomponent system located in the endoplasmic reticulum comprising a catalytic subunit and transporters for glucose-6-phosphate, inorganic phosphate, and glucose. We have recently cloned a novel gene that encode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cec15b11ad28c60fd153b6430733e45
https://doi.org/10.2337/diabetes.50.3.502
https://doi.org/10.2337/diabetes.50.3.502
Publikováno v:
Journal of molecular endocrinology. 41(5)
Islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP/G6PC2) is a major autoantigen in both mouse and human type 1 diabetes. IGRP is selectively expressed in islet β cells and polymorphisms in the IGRP gene have recently been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0325112116a44798d606ae44d3c73b76
https://pubmed.ncbi.nlm.nih.gov/18753309
https://pubmed.ncbi.nlm.nih.gov/18753309
Autor:
John C. Hutton, Cyrus C. Martin, Richard M. O'Brien, James K. Oeser, Claudia Frigeri, Christina A. Svitek, Maureen Gannon
Publikováno v:
Diabetes. 53(7)
We have previously reported the discovery of an islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP) that is predominantly expressed in islet beta-cells. IGRP has recently been identified as a major autoantigen in a mouse mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9798439f5df82b91cd871eee6c76203
https://pubmed.ncbi.nlm.nih.gov/15220199
https://pubmed.ncbi.nlm.nih.gov/15220199
Autor:
Richard M. O'Brien, Cyrus C. Martin, Jared N. Boustead, Christina A. Svitek, John C. Hutton, James K. Oeser, SI Hunter
Publikováno v:
Journal of molecular endocrinology. 32(1)
Glucose-6-phosphatase (G6Pase) catalyzes the final step in the gluconeogenic and glycogenolytic pathways, the hydrolysis of glucose-6-phosphate (G6P) to glucose and phosphate. This paper describes the identification and characterization of a cDNA and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93757060e42f76d2050ee19372898d6e
https://pubmed.ncbi.nlm.nih.gov/14765991
https://pubmed.ncbi.nlm.nih.gov/14765991
Autor:
Richard M. O'Brien, Eva Henderson, Cyrus C. Martin, Christina A. Svitek, Roland Stein, James K. Oeser
Publikováno v:
The Biochemical journal. 371(Pt 3)
Islet-specific glucose-6-phosphatase (G6Pase) catalytic-subunit-related protein (IGRP) is a homologue of the catalytic subunit of G6Pase, the enzyme that catalyses the final step of the gluconeogenic pathway. The analysis of IGRP-chloramphenicol acet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5b510a355751aba815044368d8bbe4e
https://pubmed.ncbi.nlm.nih.gov/12540293
https://pubmed.ncbi.nlm.nih.gov/12540293