Ectodysplasin A, Isoform 1

Known as: Ectodysplasin A1 
An ectodysplasin isoform with specificity for the EDAR RECEPTOR.
National Institutes of Health

Papers overview

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2019
2019
Hypohidrotic ectodermal dysplasia (HED) is a rare genetic condition resulting from defective development of ectodermal… (More)
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2018
2018
OBJECTIVE In X-linked hypohidrotic ectodermal dysplasia (XLHED), dysfunction of ectodysplasin A1 (EDA1) due to EDA mutations… (More)
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2018
2018
Hypohidrotic ectodermal dysplasias (HED) are hereditary differentiation disorders of multiple ectodermal structures including the… (More)
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2014
2014
Background Disorders that irremediably affect fetuses make early stage therapies desirable. X-linked hypohidrotic ectodermal… (More)
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Review
2014
Review
2014
The TNF family ligand ectodysplasin A (EDA) regulates the induction, morphogenesis and/or maintenance of skin-derived structures… (More)
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2014
2014
Abstract Mice with skin and hair follicle (HF) defects are common models of human skin disorders. A mutant strain with the we/we… (More)
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2012
2012
BACKGROUND Hypohidrotic/anhidrotic ectodermal dysplasia (HED) is a rare Mendelian disorder affecting ectodermal tissues. The… (More)
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2005
2005
BACKGROUND Hypohidrotic ectodermal dysplasia (HED) is a human heritable disorder characterized by sparse hair, a lack of sweat… (More)
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2005
2005
We characterized a movement disorder of Chinese Crested dogs clinically and pathologically indistinguishable from canine multiple… (More)
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