Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Robert C. De Lisle"'
Autor:
Robert C. De Lisle, Andrew Ballabio, Thomas R. Kolodecik, Hong-Min Ni, Pal Pacher, Shaogui Wang, Xiaowen Ma, Wen-Xing Ding, Xiaojuan Chao
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology, Vol 10, Iss 1, Pp 59-81 (2020)
Background & Aims Alcohol abuse is the major cause of experimental and human pancreatitis but the molecular mechanisms remain largely unknown. We investigated the role of transcription factor EB (TFEB), a master regulator of lysosomal biogenesis, in
Autor:
Jim Geiser, Robert C De Lisle, David Finkelstein, Paul A Adlard, Ashley I Bush, Glen K Andrews
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e72543 (2013)
BackgroundZinc deficiency due to poor nutrition or genetic mutations in zinc transporters is a global health problem and approaches to providing effective dietary zinc supplementation while avoiding potential toxic side effects are needed.Methods/pri
Externí odkaz:
https://doaj.org/article/83a06b4ef9494a5aab94221ac8aff609
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e82149 (2013)
ZIP5 localizes to the baso-lateral membranes of intestinal enterocytes and pancreatic acinar cells and is internalized and degraded coordinately in these cell-types during periods of dietary zinc deficiency. These cell-types are thought to control zi
Externí odkaz:
https://doaj.org/article/7c89b091af7d4f3e934652a5bc218e4b
Publikováno v:
PLoS Genetics, Vol 8, Iss 6, p e1002766 (2012)
Mutations in the human Zip4 gene cause acrodermatitis enteropathica, a rare, pseudo-dominant, lethal genetic disorder. We created a tamoxifen-inducible, enterocyte-specific knockout of this gene in mice which mimics this human disorder. We found that
Externí odkaz:
https://doaj.org/article/6114b6f5a14b40c5a81eabaeb4b40098
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4283 (2009)
BACKGROUND: Cystic fibrosis (CF) has many effects on the gastrointestinal tract and a common problem in this disease is poor nutrition. In the CF mouse there is an innate immune response with a large influx of mast cells into the muscularis externa o
Externí odkaz:
https://doaj.org/article/37b1af70df8547ef8ab72db5ce73c0e1
Autor:
Pal Pacher, Hua Wang, Anna S. Gukovskaya, Sean C. Kumer, Robert C. De Lisle, Shaogui Wang, Olga A. Mareninova, Brian Bridges, Hong-Min Ni, Andrea Ballabio, Xiaojuan Chao, Wen-Xing Ding, Timothy M. Schmitt
Publikováno v:
Autophagy. 15(11)
Impaired macroautophagy/autophagy has been implicated in experimental and human pancreatitis. However, the transcriptional control governing the autophagy-lysosomal process in pancreatitis is largely unknown. We investigated the role and mechanisms o
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 55:689-694
Intestinal dysmotility is one of the effects of cystic fibrosis (CF), but when and how this develops is not well understood. The goal of the present study was to use the Cftr knockout mouse to determine when in development circular smooth muscle of t
Publikováno v:
American Journal of Physiology-Gastrointestinal and Liver Physiology. 294:G717-G727
The Dmbt1 gene encodes alternatively spliced glycoproteins that are either membrane-associated or secreted epithelial products. Functions proposed for Dmbt1 include it being a tumor suppressor, having roles in innate immune defense and inflammation,
Publikováno v:
Molecular and Cellular Biochemistry. 302:157-167
The C-terminal PDZ-binding motifs are required for polarized apical/basolateral localization of many membrane proteins. Ezrin-radixin-moesin (ERM) proteins regulate the organization and function of specific cortical structures in polarized epithelial
Autor:
Robert C. De Lisle
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 62(4)
OBJECTIVES Cystic fibrosis (CF) has major effects on the intestinal tract with potential consequences on nutrition, but these are not fully understood. I investigated the possibility of altered enterocyte maturation in CF, as suggested by decreased e