Gene defect in ectodermal dysplasia implicates a death domain adapter in development (Q24292109)

ORCID Public Data File 2021

GOA release 2020-03-11

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author name string

D J Headon

1

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S A Emmal

2

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B M Ferguson

3

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A S Tucker

4

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M J Justice

5

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P T Sharpe

6

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J Zonana

7

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P A Overbeek

Death receptors: signaling and modulation

8

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language of work or name

English

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publication date

December 2001

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414

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issue

6866

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page(s)

913-6

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cites work

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The TNF and TNF receptor superfamilies: integrating mammalian biology

21 January 2018

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Involvement of a novel Tnf receptor homologue in hair follicle induction.

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

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

The modular nature of apoptotic signaling proteins

21 January 2018

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The TNF receptor 1-associated protein TRADD signals cell death and NF-kappa B activation

21 January 2018

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FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis

21 January 2018

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Death receptor 5, a new member of the TNFR family, and DR4 induce FADD-dependent apoptosis and activate the NF-kappaB pathway

21 January 2018

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Signal transduction by DR3, a death domain-containing receptor related to TNFR-1 and CD95

21 January 2018

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Identification and functional characterization of DR6, a novel death domain-containing TNF receptor

21 January 2018

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

21 January 2018

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The Mouse Genome Database (MGD): integration nexus for the laboratory mouse

21 January 2018

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MyD88 is an adaptor protein in the hToll/IL-1 receptor family signaling pathways

21 January 2018

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Tumor necrosis factor receptor-associated factor (TRAF) family: adapter proteins that mediate cytokine signaling

21 January 2018

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Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder

21 January 2018

1 reference

The involvement of multiple tumor necrosis factor receptor (TNFR)-associated factors in the signaling mechanisms of receptor activator of NF-kappaB, a member of the TNFR superfamily

21 January 2018

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Hedgehog and Bmp genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo

21 January 2018

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

21 January 2018

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

21 January 2018

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Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications

21 January 2018

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Hypohidrotic ectodermal dysplasia

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

The genetics and development of 'crinkled', a new mutant in the house mouse

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Comparative Mapping in thebeige–satinRegion of Mouse Chromosome 13

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/414913A

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Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1532813

1042703745

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Fatcat ID

release_otlbcqr5zvep3exdsyeicgxqhi

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1532813

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference