Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear. - Wikidata - wikimedia - TriplyDB

Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear.

Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear.

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Essential Role of Nr2f Nuclear Receptors in Patterning the Vertebrate Upper Jaw.

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P2860

Requirement for Jagged1-Notch2 signaling in patterning the bones of the mouse and human middle ear.

http://www.wikidata.org/entity/Q30355432

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2017 nî lūn-bûn

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2017 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2017 թվականի մայիսին հրատարակված գիտական հոդված

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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name

Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Requirement for Jagged1-Notch2 ...... he mouse and human middle ear.

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Scientific Reports

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Requirement for Jagged1-Notch2 ...... the mouse and human middle ear

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Bea Smith

http://www.w3.org/2001/XMLSchema#string

Hai-Yun Yen

http://www.w3.org/2001/XMLSchema#string

J Gage Crump

http://www.w3.org/2001/XMLSchema#string

John Go

http://www.w3.org/2001/XMLSchema#string

Juan Llamas

http://www.w3.org/2001/XMLSchema#string

Neil Segil

http://www.w3.org/2001/XMLSchema#string

Pedro A Sanchez-Lara

http://www.w3.org/2001/XMLSchema#string

Robert E Maxson

http://www.w3.org/2001/XMLSchema#string

P2860

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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

The Notch ligand JAG1 is required for sensory progenitor development in the mammalian inner ear

New perspectives on pharyngeal dorsoventral patterning in development and evolution of the vertebrate jaw

Competition between Jagged-Notch and Endothelin1 Signaling Selectively Restricts Cartilage Formation in the Zebrafish Upper Face

New insights into craniofacial malformations

A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency

Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients

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