Review on JAG1 (jagged 1 (Alagille syndrome)), with data on DNA, on the protein encoded, and where the gene is implicated
Notch proteins are a family of closely related transmembrane receptors proven to be instrumental in ...
Abstract Alagille syndrome (ALGS) is an autosomal domi-nant disorder characterized by developmental ...
Alagille syndrome is an autosomal dominant multisystem disorder with variable phenotypic penetrance,...
SummaryAlagille syndrome (AGS) is a dominantly inherited disorder characterized by liver disease in ...
Alagille syndrome (AGS) is an autosomal dominant disease characterized by five major abnormalities i...
Review on JAG2 (human jagged2), with data on DNA, on the protein encoded, and where the gene is impl...
Alagille syndrome (AGS) is an autosomal dominant disorder with developmental abnormalities affecting...
Alagille syndrome (AGS) is an autosomal dominant disorder characterized by abnormal development of t...
Alagille syndrome (AGS) is an autosomal-dominant disorder characterized by intrahepatic cholestasis ...
Alagille syndrome (AGS) is an autosomal dominant disorder with developmental abnormalities affecting...
International audienceHeterozygous mutations in JAGGED1 (JAG1), encoding a ligand for Notch receptor...
Mutations of Jagged 1 (JAG1), a ligand in the Notch signaling pathway, cause Alagille syndrome (AGS)...
Mutations in the Notch signaling cell surface ligand Jagged1 (JAG1) predominantly cause Alagille syn...
We have summarized data on 233 Alagille syndrome patients reported with mutations in Jagged1 (JAG1)....
Mutations in the Notch signaling cell surface ligand Jagged1 (JAG1) predominantly cause Alagille syn...
Notch proteins are a family of closely related transmembrane receptors proven to be instrumental in ...
Abstract Alagille syndrome (ALGS) is an autosomal domi-nant disorder characterized by developmental ...
Alagille syndrome is an autosomal dominant multisystem disorder with variable phenotypic penetrance,...
SummaryAlagille syndrome (AGS) is a dominantly inherited disorder characterized by liver disease in ...
Alagille syndrome (AGS) is an autosomal dominant disease characterized by five major abnormalities i...
Review on JAG2 (human jagged2), with data on DNA, on the protein encoded, and where the gene is impl...
Alagille syndrome (AGS) is an autosomal dominant disorder with developmental abnormalities affecting...
Alagille syndrome (AGS) is an autosomal dominant disorder characterized by abnormal development of t...
Alagille syndrome (AGS) is an autosomal-dominant disorder characterized by intrahepatic cholestasis ...
Alagille syndrome (AGS) is an autosomal dominant disorder with developmental abnormalities affecting...
International audienceHeterozygous mutations in JAGGED1 (JAG1), encoding a ligand for Notch receptor...
Mutations of Jagged 1 (JAG1), a ligand in the Notch signaling pathway, cause Alagille syndrome (AGS)...
Mutations in the Notch signaling cell surface ligand Jagged1 (JAG1) predominantly cause Alagille syn...
We have summarized data on 233 Alagille syndrome patients reported with mutations in Jagged1 (JAG1)....
Mutations in the Notch signaling cell surface ligand Jagged1 (JAG1) predominantly cause Alagille syn...
Notch proteins are a family of closely related transmembrane receptors proven to be instrumental in ...
Abstract Alagille syndrome (ALGS) is an autosomal domi-nant disorder characterized by developmental ...
Alagille syndrome is an autosomal dominant multisystem disorder with variable phenotypic penetrance,...