(Q34127400)

31 July 2017

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title

Death receptor signaling giving life to ectodermal organs (English)

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31 July 2017

1

Irma Thesleff

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31 July 2017

Marja L Mikkola

2

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31 July 2017

publication date

7 May 2002

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Science's STKE : signal transduction knowledge environment

31 July 2017

published in

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31 July 2017

volume

2002

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31 July 2017

issue

131

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31 July 2017

page(s)

pe22

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

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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/10.1126%2FSTKE.2002.131.PE22

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/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Involvement of a novel Tnf receptor homologue in hair follicle induction

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

TAJ, a novel member of the tumor necrosis factor receptor family, activates the c-Jun N-terminal kinase pathway and mediates caspase-independent cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

The TNF and TNF receptor superfamilies: integrating mammalian biology

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

The IKK complex: an integrator of all signals that activate NF-kappaB?

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Signaling and subcellular localization of the TNF receptor Edar

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma)

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Reiterative signaling and patterning during mammalian tooth morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Splitting hairs: dissecting roles of signaling systems in epidermal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Local inhibitory action of BMPs and their relationships with activators in feather formation: implications for periodic patterning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSTKE.2002.131.PE22

10.1126/STKE.2002.131.PE22

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference