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2009 JAN 5 ... liver diseases with potential renal involvement including inborn errors of metabolism, Alagille syndrome, and hepatic fibrosis (P=0.003) were associated with CRI. Renal function is a major ...
2009 APR 13 ... of these harboured a single gene, BMP2. In two individuals with additional features of Alagille syndrome, deletion of both JAG1 and BMP2 were identified. Deletion of this region has not been ...
2009 JUN 22 ... According to recent research from the United States, "Alagille syndrome is an autosomal dominant disorder caused by mutations in Notch signaling pathway genes, ...
2009 JAN 22 ... According to a study from the United States, "Alagille syndrome (AGS) is a heterogeneous developmental disorder associated with bile duct paucity and ...
2009 OCT 19 ... dilate into the biliary tree," scientists in Basel, Switzerland report. "Alagille syndrome patients, who suffer from bile duct paucity, carry Jagged1 and Notch2 mutations, ...
2008 SEP 8 ... all four organs from the same donor. He needed a transplant because he was born with Alagille syndrome, a rare, hereditary disorder characterized by a reduced number of bile ducts in the ...
2007 DEC 10 ... A new study, 'Biological function of mutant forms of JAGGED1 proteins in Alagille syndrome: inhibitory effect on Notch signaling,' is now available. "Heterozygous mutations in ...
2007 NOV 12 ... autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) and Alagille syndrome," wrote C. Roca and colleagues, Cancer Research UK London Research Institute.
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2008 MAY 26 ... in vascular smooth muscle development and the cardiovascular defects associated with Alagille syndrome."
Varadkar and colleagues published their study in Developmental ...
2008 JAN 21 ... (NEA) has been recommended as a marker of cholestasis in adults but not in children with Alagille syndrome (AGS)."
"We investigated ontogenic and disease-related differences in ...
2008 JAN 21 ... adult hepatology practice. Among four congenital cholestatic syndromes (biliary atresia, Alagille syndrome, Caroli disease and congenital hepatic fibrosis, and progressive familial intrahepatic ...
2007 OCT 1 ... for antibodies to maternal and other HLA. Two cases of neonatal hepatitis, 2 cases of Alagille syndrome, and I case of Byler syndrome acted as controls. All male BA livers were found to ...
2008 DEC 24 ... The syndrome is clearly distinct from other previously described syndromes such as Alagille syndrome, congenital hepatic fibrosis, Caroli disease, and Kabuki make-up syndrome, To date, only ...
2008 DEC 22 ... concluded: "It is intriguing to speculate, that HS could he genetically related to Alagille syndrome (AS), since both conditions share an unusual number of phenotypic abnormalities."
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2008 MAR 3 ... (Williams 22q11-deletion, 1p-deletion, Miller-Dieker, Smith-Magenis, Prader-Willi, Alagille, Saethre-Chotzen and Sotos syndrome). Feasibility: prior to the consent procedure, for ...
