Zobrazeno 1 - 10
of 41
pro vyhledávání: '"T L, Murphy"'
Autor:
Kim R. Bridle, Gregory J. Anderson, Darrell H. G. Crawford, Claudia Popa, Linda M. Fletcher, T. L. Murphy
Publikováno v:
Hepatology. 46:822A-901A
Introduction: Co-toxicity is an important factor in determining the pathogenesis of progressive liver disease. The mRNA expression of the hepatic iron sensor peptide hepcidin, is decreased in human subjects and in animal models of HFE-related hemochr
Publikováno v:
Hepatology. 40:676A-735A
Introduction: Oxidative stress plays a pivotal role in the pathogenesis of alcoholic liver disease (ALD). Iron homeostasis has been reported to be altered in ALD and available free iron may catalyse reactions generating reactive oxygen species (ROS).
Autor:
Gregory J. Anderson, Andrew T. McKie, David M. Frazer, T. L. Murphy, Chris D. Vulpe, Sarah J. Wilkins, E. M. Becker
Publikováno v:
Gut. 52:340-346
Background: A large oral dose of iron will reduce the absorption of a subsequent smaller dose of iron in a phenomenon known as mucosal block. Molecular analysis of this process may provide insights into the regulation of intestinal iron absorption. A
Autor:
Herman H. Shugart, A. S. Isaev, T. L. Murphy, Anthony C. Janetos, B. E. Orlick, Dmitry Ershov, Eric S. Kasischke, Sergey Bartalev, Nancy H. F. French, G. N. Korovin
Publikováno v:
Climatic Change. 55:235-249
Russian boreal forests are subject to frequent wildfires. The resulting combustion of large amounts of biomass not only transforms forest vegetation, but it also creates significant carbon emissions that total, according to some authors, from 35–94
Autor:
T. L. Murphy, Natasha Libina, Gregory J. Anderson, Jane Gitschier, Yien-Ming Kuo, L. Cowley, Candice C. Askwith, Chris D. Vulpe
Publikováno v:
Nature Genetics. 21:195-199
Iron is essential for many cellular functions; consequently, disturbances of iron homeostasis, leading to either iron deficiency or iron overload, can have significant clinical consequences. Despite the clinical prevalence of these disorders, the mec
Autor:
Gordon D. McLaren, T. L. Murphy, June W. Halliday, Gregory J. Anderson, L. Cowley, Betty A. Evans
Publikováno v:
Genomics. 48:34-39
The sex-linked anemic (sla) mouse carries an anemia that results from an inherited defect of intestinal iron absorption and provides an ideal model with which to investigate this poorly understood yet clinically important process. We have precisely m
Autor:
Darrell H. G. Crawford, Gregory J. Anderson, V. Nathan Subramaniam, N. Santrampurwala, Lesley Jaskowski, Denis I. Crane, Andrew D. Clouston, T. L. Murphy, Terrence C. H. Tan, Linda M. Fletcher
Publikováno v:
Alcoholism: Clinical and Experimental Research.
Combined iron overload and alcohol may promote synergistic chronic liver injury and toxicity. The role of specific dietary fats in influencing the development of co-toxic alcoholic liver disease needs further evaluation and is investigated in this st
Autor:
Kenneth Sosnowski, Patricia L. Featherston, June W. Halliday, Linda M. Fletcher, Stephen H. Caldwell, Mark Kulaga, T. L. Murphy, Xuiming Li, Phillip K. Kiyasu, Rolland C. Dickson
Publikováno v:
Journal of Gastroenterology and Hepatology. 10:174-178
To assess the relationship between carbohydrate-deficient transferrin (CDT) and alcoholic liver disease, we measured the ratio of carbohydrate-deficient transferrin to total transferrin (rCDT) in 32 male alcoholics with liver disease (Child-Pugh clas
Autor:
T. L. Murphy, Sarah J. Wilkins, Gregory J. Anderson, Andrew T. McKie, K N Millard, E. M. Becker, David M. Frazer, Chris D. Vulpe
Publikováno v:
Biochemical Society Transactions. 30:724-726
Hepcidin is an anti-microbial peptide predicted to be involved in the regulation of intestinal iron absorption. We have examined the relationship between the expression of hepcidin in the liver and the expression of the iron-transport molecules dival
Publikováno v:
Molecular and Cellular Biology. 13:4793-4805
Activity of the murine interleukin-4 (IL-4) promoter was localized to several cis-acting elements present within the first 300 bp from the transcriptional initiation site. Five repeated elements, P0 to P4, that share the common consensus ATTTTCCNNT w