Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

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Distinct impacts of Eda and Edar loss of function on the mouse dentition.Patterning of palatal rugae through sequential addition reveals an anterior/posterior boundary in palatal development.Lrp4/Wise regulates palatal rugae development through Turing-type reaction-diffusion mechanisms

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P2860

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

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http://www.wikidata.org/entity/Q52583543

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2007 nî lūn-bûn

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2007年の論文

@ja

2007年学术文章

@wuu

2007年学术文章

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2007年学术文章

@zh-cn

2007年学术文章

@zh-hans

2007年学术文章

@zh-my

2007年学术文章

@zh-sg

2007年學術文章

@yue

2007年學術文章

@zh-hant

name

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

@en

Disruption of the palatal rugae pattern in Tabby

@nl

type

Item

label

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

@en

Disruption of the palatal rugae pattern in Tabby

@nl

prefLabel

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

@en

Disruption of the palatal rugae pattern in Tabby

@nl

P1476

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

@en

P2093

Renata Peterkova

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

Sophie Pantalacci

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

P2860

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

Palatal ruga anomaly induced by all-trans-retinoic acid in the Crj:SD rat: possible warning sign of teratogenicity.

TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis.

Generation of the primary hair follicle pattern.

Ectodysplasin signaling in development.

Establishing identity using cheiloscopy and palatoscopy.

Molecular control of secondary palate development.

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain.

Anhidrosis and absence of sweat glands in mice hemizygous for the Tabby gene: supportive evidence for the hypothesis of homology between Tabby and human anhidrotic (hypohidrotic) ectodermal dysplasia (Christ-Siemens-Touraine syndrome).

P304

441-448

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P31

scholarly article

P356

10.1111/J.1600-0722.2007.00482.X

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P433

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

P478

115

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P577

2007-12-01T00:00:00Z

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P5875

5819386

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P698

18028050

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Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

about

P2860

P2860

Disruption of the palatal rugae pattern in Tabby (eda) mutant mice.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698