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 - Wikidata - wikimedia - TriplyDB

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

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

http://www.wikidata.org/entity/Q36717195

about

Population genomics of parallel adaptation in threespine stickleback using sequenced RAD tags Gene defect in ectodermal dysplasia implicates a death domain adapter in development 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.Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia EDA signaling and skin appendage development Molecular basis of hypohidrotic ectodermal dysplasia: an update Mesenchymal-epithelial interactions during hair follicle morphogenesis and cycling The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A Mutation analysis of the ED1 gene in two Chinese Han families with X-linked hypohidrotic ectodermal dysplasia Identification of a highly polymorphic microsatellite within the bovine ectodysplasin A (ED1) gene on BTA Xq22-24 Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease Morphoregulation of teeth: modulating the number, size, shape and differentiation by tuning Bmp activity A novel point mutation within the EDA gene causes an exon dropping in mature RNA in Holstein Friesian cattle breed affected by X-linked anhidrotic ectodermal dysplasia.The role of tumor necrosis factor receptor superfamily members in mammalian brain development, function and homeostasis Subtle Morphological Changes in the Mandible of Tabby Mice Revealed by Micro-CT Imaging and Elliptical Fourier Quantification.EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families.Salivary gland branching morphogenesis: a quantitative systems analysis of the Eda/Edar/NFkappaB paradigm.Enhanced Edar signalling has pleiotropic effects on craniofacial and cutaneous glands.The genetic basis of normal and abnormal craniofacial development.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 A mutation of Ikbkg causes immune deficiency without impairing degradation of IkappaB alpha.Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome.A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene Ectodermal dysplasias: a new clinical-genetic classification Genetic basis of tooth development and dental defects.Ectodermal dysplasias: not only 'skin' deep.Death receptor signaling giving life to ectodermal organs.Collagens and collagen-related diseases.The genetics of human skin disease.Epidermal patterning and induction of different hair types during mouse embryonic development.Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables.Ectodysplasin regulates the lymphotoxin-beta pathway for hair differentiation Pharmacological stimulation of Edar signaling in the adult enhances sebaceous gland size and function Partial deletion of the bovine ED1 gene causes anhidrotic ectodermal dysplasia in cattle.X-linked anhidrotic ectodermal dysplasia disruption yields a mouse model for ocular surface disease and resultant blindness The Tabby cat locus maps to feline chromosome B1.

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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

http://www.wikidata.org/entity/Q36717195

description

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Proceedings of the National Academy of Sciences of the United States of America

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An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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

Fine mapping of the EDA gene: a translocation breakpoint is associated with a CpG island that is transcribed

LEF-1, a gene encoding a lymphoid-specific protein with an HMG domain, regulates T-cell receptor alpha enhancer function [corrected]

Functional interaction of beta-catenin with the transcription factor LEF-1

Nuclear localization of beta-catenin by interaction with transcription factor LEF-1

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice

Beta-catenin mediates the interaction of the cadherin-catenin complex with epidermal growth factor receptor.

Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.

Ectodermal dysplasias: a clinical classification and a causal review.

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13069-13074

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