(Q28189557)

2

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Ying-Xue Song

3

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Sen Yang

4

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Xiao-Yan Xiong

5

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An-Ping Zhang

6

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Ping-Ping He

7

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Min Gao

8

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Yue-Bin Li

9

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Da Lin

10

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Wei Huang

Archives of Dermatological Research

11

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language of work or name

English

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publication date

April 2003

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published in

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volume

295

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issue

1

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page(s)

38-42

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cites work

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodermal dysplasias: a clinical classification and a causal review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodermal dysplasias: a new clinical-genetic classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Ectodermal dysplasias: not only 'skin' deep

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7

The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00403-003-0394-7