Ectodermal Dysplasia

Known as: Congenital ectodermal dysplasia, Dysplasias, Ectodermal, Ectodermal Dysplasia [Disease/Finding] 
A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of… (More)
National Institutes of Health

Papers overview

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Highly Cited
2007
Highly Cited
2007
Odonto-onycho-dermal dysplasia is a rare autosomal recessive syndrome in which the presenting phenotype is dry hair, severe… (More)
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Highly Cited
2003
Highly Cited
2003
X-linked anhidrotic ectodermal dysplasia with immunodeficiency (XL-EDA-ID) is caused by hypomorphic mutations in the gene… (More)
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Highly Cited
2003
Highly Cited
2003
X-linked hypohidrotic ectodermal dysplasia (XLHED; OMIM 305100) is a genetic disorder characterized by absence or deficient… (More)
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Highly Cited
2002
Highly Cited
2002
Keratitis-ichthyosis-deafness syndrome (KID) is a rare ectodermal dysplasia characterized by vascularizing keratitis, profound… (More)
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Highly Cited
2001
Highly Cited
2001
The molecular basis of X-linked recessive anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) has remained elusive… (More)
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Highly Cited
2001
Highly Cited
2001
Members of the tumour-necrosis factor receptor (TNFR) family that contain an intracellular death domain initiate signalling by… (More)
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Highly Cited
2001
Highly Cited
2001
The gene that encodes nuclear factor κ (NF-κB) essential modulator (or NEMO, also known as IKKγ) is required for activation of… (More)
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Highly Cited
1999
Highly Cited
1999
X-linked hypohidrotic ectodermal dysplasia results in abnormal morphogenesis of teeth, hair and eccrine sweat glands. The gene… (More)
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Highly Cited
1997
Highly Cited
1997
Members of the armadillo protein gene family, which includes plakoglobin and β-catenin, have important functions in cytoskeleton… (More)
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Highly Cited
1996
Highly Cited
1996
Ectodermal dysplasias comprise over 150 syndromes of unknown pathogenesis. X–linked anhidrotic ectodermal dysplasia (EDA) is… (More)
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