Alagille syndrome—a notch up for the Notch receptor

This publication has 12 references indexed in Scilit:

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• Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1
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• TAN-1, the human homolog of the Drosophila Notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms
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