Concepedia

Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome

Karen Vrijens, Sofie Thys, Marcel T. De Jeu, Andrei Postnov, Markus Pfister, Luk Cox, An Zwijsen, Viviane Van Hoof, Marcus Mueller, Nora M. De Clerck

Neurobiology of Disease · 2006 · 23 citations · 35 references

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35

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

Linheng Li, Ian D. Krantz, Yu Deng et al. · Nature Genetics · 1997 · 1.3K citations

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Mutations in the human Jagged1 gene are responsible for Alagille syndrome

Takaya Oda, Abdel Elkahloun, Brian L. Pike et al. · Nature Genetics · 1997 · 1.2K citations

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Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

Derek C. Rogers, Elizabeth Fisher, Steve D. M. Brown et al. · Mammalian Genome · 1997 · 803 citations

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Embryonic Lethality and Vascular Defects in Mice Lacking the Notch Ligand Jagged1

Yun Xue, Xiang Gao, C.E. Lindsell et al. · Human Molecular Genetics · 1999 · 762 citations · Full text

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Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): Review of 80 cases

D Alagille, Andrea Estrada, Michelle Hadchouel et al. · The Journal of Pediatrics · 1987 · 669 citations

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