Permanent correction of an inherited ectodermal dysplasia with recombinant EDA. (Q40561373)

21 September 2017

Permanent correction of an inherited ectodermal dysplasia with recombinant EDA. (English)

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21 September 2017

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2

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21 September 2017

Olivier Gaide

1

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PubMed ID

12692542

21 September 2017

language of work or name

English

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publication date

7 April 2003

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21 September 2017

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21 September 2017

9

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21 September 2017

5

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21 September 2017

614-618

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https://scigraph.springernature.com/pub.10.1038/nm861

21 September 2017

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cites work

Ectodermal dysplasias: a clinical classification and a causal review

1 reference

7 January 2021

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia

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7 January 2021

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

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7 January 2021

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

1 reference

7 January 2021

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

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7 January 2021

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

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7 January 2021

Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice

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7 January 2021

Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organization.

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7 January 2021

Two adjacent trimeric Fas ligands are required for Fas signaling and formation of a death-inducing signaling complex

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7 January 2021

TROY, a newly identified member of the tumor necrosis factor receptor superfamily, exhibits a homology with Edar and is expressed in embryonic skin and hair follicles

1 reference

7 January 2021

Postnatal lower jaw dentition in different phenotypes of tabby mice

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7 January 2021

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

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7 January 2021

TRAF6-deficient mice display hypohidrotic ectodermal dysplasia

1 reference

7 January 2021

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

1 reference

7 January 2021

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

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7 January 2021

The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone

1 reference

7 January 2021

Materno-fetal immunoglobulin transfer and passive immunity during the first trimester of human pregnancy

1 reference

7 January 2021

Production of recombinant TRAIL and TRAIL receptor: Fc chimeric proteins

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7 January 2021

Identifiers

DOI

10.1038/NM861

1 reference

21 September 2017

1 reference

PubMed ID

12692542