Jagged1 Ablation Results in Cerebellar Granule Cell Migration Defects and Depletion of Bergmann Glia
Jagged1 Ablation Results in Cerebellar Granule Cell Migration Defects and Depletion of Bergmann Glia
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Basel, Switzerland: S. Karger AG
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English
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Basel, Switzerland: S. Karger AG
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Jagged1 is a ligand for members of the Notch family of receptors. Mutations in the human JAG1 gene are the major cause of Alagille syndrome, an autosomal dominant disorder affecting the liver, heart, eye, skeleton, kidneys, and craniofacial structures. Although expressed throughout mammalian embryonic development and in the adult, the function of J...
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Jagged1 Ablation Results in Cerebellar Granule Cell Migration Defects and Depletion of Bergmann Glia
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TN_cdi_proquest_journals_221141552
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_221141552
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ISBN
9783805580861,380558086X
ISSN
0378-5866
E-ISSN
1421-9859
DOI
10.1159/000090754