Arginine

ectodysplasin A ; Homo sapiens







7 Article(s)
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1 20486090 Missense mutation of the EDA gene in a Jordanian family with X-linked hypohidrotic ectodermal dysplasia: phenotypic appearance and speech problems. 2010 May 18 2
2 19127222 Two novel mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia. 2009 Apr 1
3 16583127 A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia. 2006 1
4 12568929 Inhibition of cryogelation by the novel synthetic peptide (Gly-Arg-Lys-Lys-Thr): recognition site of extra domain A containing fibronectin for heparin in cryogelation. 2003 Jan 15 4
5 11416205 Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia. 2001 Jun 19 6
6 10733677 Overexpression of the oncofetal Fn variant containing the EDA splice-in segment in the dermal-epidermal junction of psoriatic uninvolved skin. 2000 Apr 1
7 10951256 A novel arginine-->Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia. 2000 Aug 1