Latest papers

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.

Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.

Array CGH ends diagnostic odyssey for infant with features of Williams and Alagille syndrome

Ductal Malformation and Pancreatitis in Mice Caused by Conditional Jag1 Deletion

Alagille Syndrome Associated with Myelinated Retinal Nerve Fibers

Hepatobiliary scan in Alagille syndrome; arteriohepatic dysplasia.

Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype.

Clinical and pathological characteristics of Alagille syndrome in Chinese children.

Gene symbol: JAG1. Disease: Alagille syndrome.

Gene symbol: JAG1. Disease: Alagille syndrome.

Functional role of Notch signaling in the developing and postnatal heart

Gene symbol: JAG1. Disease: Alagille syndrome.

Williams syndrome in a preterm infant with phenotype of Alagille syndrome.

SIR 2008 annual meeting film panel case: Alagille syndrome.

Histiocytic osteolysis secondary to hyperbilirubinaemia: a case report.

Successful arterial thrombolysis and percutaneous transluminal angioplasty for early hepatic artery thrombosis after split liver transplantation in a four-month-old baby.

Fluctuation of lipoprotein metabolism linked with bile acid-activated liver nuclear receptors in Alagille syndrome.

[Aortic aneurysm in Alagille syndrome]

Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders.