Gene defect in ectodermal dysplasia implicates a death domain adapter in development - sprookjes - yvandenbroek - TriplyDB

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

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

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Role of TRAF3 and -6 in the activation of the NF-kappa B and JNK pathways by X-linked ectodermal dysplasia receptor TRAF6-deficient mice display hypohidrotic ectodermal dysplasia.EDA signaling and skin appendage development Scratching the surface of skin development The tumor suppressor CYLD interacts with TRIP and regulates negatively nuclear factor kappaB activation by tumor necrosis factor Molecular basis of hypohidrotic ectodermal dysplasia: an update Historical perspectives on tumor necrosis factor and its superfamily: 25 years later, a golden journey NF-kappaB-related genetic diseases Essential role for NFI-C/CTF transcription-replication factor in tooth root development Tinkering signaling pathways by gain and loss of protein isoforms: the case of the EDA pathway regulator EDARADD Development and evolution of the amniote integument: current landscape and future horizon Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma.Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.A genome-wide association study identifies multiple loci for variation in human ear morphology Deficient natural killer cell cytotoxicity in patients with IKK-gamma/NEMO mutations.Distinct impacts of Eda and Edar loss of function on the mouse dentition.Microarray analysis of Shigella flexneri-infected epithelial cells identifies host factors important for apoptosis inhibition Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families.Positive selection in East Asians for an EDAR allele that enhances NF-kappaB activation.Non-syndromic tooth agenesis in two Chinese families associated with novel missense mutations in the TNF domain of EDA (ectodysplasin A)Dkk4 and Eda regulate distinctive developmental mechanisms for subtypes of mouse hair.Dental abnormalities associated with X-linked hypohidrotic ectodermal dysplasia in dogs.Inflammatory mediator TAK1 regulates hair follicle morphogenesis and anagen induction shown by using keratinocyte-specific TAK1-deficient mice EDAR-induced hypohidrotic ectodermal dysplasia: a clinical study on signs and symptoms in individuals with a heterozygous c.1072C > T mutation.A mutation of Ikbkg causes immune deficiency without impairing degradation of IkappaB alpha.A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene Death receptor signaling giving life to ectodermal organs.A common founder mutation in the EDA-A1 gene in X-linked hypodontia.Epidermal patterning and induction of different hair types during mouse embryonic development.Generation of the primary hair follicle pattern.Ectodysplasin regulates the lymphotoxin-beta pathway for hair differentiation A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness.Pharmacological stimulation of Edar signaling in the adult enhances sebaceous gland size and function To the Root of the Curl: A Signature of a Recent Selective Sweep Identifies a Mutation That Defines the Cornish Rex Cat Breed X-linked anhidrotic ectodermal dysplasia disruption yields a mouse model for ocular surface disease and resultant blindness Genetic architecture of skeletal evolution in European lake and stream stickleback.Genetically altered mouse models: the good, the bad, and the ugly.Towards a new classification of ectodermal dysplasias.Molecular and therapeutic characterization of anti-ectodysplasin A receptor (EDAR) agonist monoclonal antibodies

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P2860

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

http://www.wikidata.org/entity/Q24292109

description

2001 nî lūn-bûn

@nan

2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2001年の論文

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2001年学术文章

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2001年学术文章

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2001年学术文章

@zh-hans

2001年学术文章

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2001年学术文章

@zh-sg

2001年學術文章

@yue

name

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

@ast

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

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

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

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type

label

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

@ast

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

@en

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

@en-gb

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

@nl

prefLabel

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

@ast

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

@en

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

@en-gb

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

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

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P2093

A S Tucker

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

B M Ferguson

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D J Headon

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J Zonana

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M J Justice

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P A Overbeek

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P T Sharpe

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S A Emmal

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P2860

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

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

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

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

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

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

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

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

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

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

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