| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 6096400 | Gastroenterology | 2010 | 9 Pages | 
Abstract
												These results imply a role for PHD1 as a positive regulator of intestinal epithelial cell apoptosis in the inflamed colon. Genetic loss of PHD1 is protective against colitis through decreased epithelial cell apoptosis and consequent enhancement of intestinal epithelial barrier function. Thus, targeted PHD1 inhibition may represent a new therapeutic approach in IBD.
											Keywords
												PBSDMOGPHDHIFTEERIL-1βFITCDSSshort interfering RNAsiRNAColitisinterleukin-1 βterminal deoxynucleotidyl transferase–mediated deoxyuridine triphosphate nick-end labelingTUNELApoptosisdextran sulphate sodiumHypoxia Inducible Factorfluorescein isothiocyanatePhosphate-buffered salinetransepithelial electrical resistancehydroxylaseHypoxiaProlyl hydroxylase
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											Authors
												Murtaza M. Tambuwala, Eoin P. Cummins, Colin R. Lenihan, Judit Kiss, Markus Stauch, Carsten C. Scholz, Peter Fraisl, Felix Lasitschka, Martin Mollenhauer, Sean P. Saunders, Patrick H. Maxwell, Peter Carmeliet, Padraic G. Fallon, Martin Schneider, 
											