Literature DB >> 11410842

Variant 1859G-->A (Arg620Gln) of the "hairless" gene: absence of association with papular atrichia or androgenic alopecia.

A M Hillmer, R Kruse, R C Betz, J Schumacher, U Heyn, P Propping, M M Nöthen, S Cichon.   

Abstract

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Year:  2001        PMID： 11410842      PMCID： PMC1226040          DOI： 10.1086/321273

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  2 in total

1.  Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.

Authors:  R Kruse; S Cichon; M Anker; A M Hillmer; P Barros-Núñez; J M Cantú; E Leal; G Weinlich; M Schmuth; P Fritsch; T Ruzicka; P Propping; M M Nöthen
Journal:  J Invest Dermatol       Date:  1999-12       Impact factor: 8.551

2.  A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.

Authors:  W Ahmad; A D Irvine; H Lam; C Buckley; E A Bingham; A A Panteleyev; M Ahmad; J A McGrath; A M Christiano
Journal:  Am J Hum Genet       Date:  1998-10       Impact factor: 11.025
  2 in total
  2 in total

1.  Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

Authors:  Axel M Hillmer; Sandra Hanneken; Sibylle Ritzmann; Tim Becker; Jan Freudenberg; Felix F Brockschmidt; Antonia Flaquer; Yun Freudenberg-Hua; Rami Abou Jamra; Christine Metzen; Uwe Heyn; Nadine Schweiger; Regina C Betz; Bettina Blaumeiser; Jochen Hampe; Stefan Schreiber; Thomas G Schulze; Hans Christian Hennies; Johannes Schumacher; Peter Propping; Thomas Ruzicka; Sven Cichon; Thomas F Wienker; Roland Kruse; Markus M Nothen
Journal:  Am J Hum Genet       Date:  2005-05-18       Impact factor: 11.025

Review 2.  [Androgenetic alopecia. Current aspects of a common phenotype].

Authors:  S Hanneken; S Ritzmann; M M Nöthen; R Kruse
Journal:  Hautarzt       Date:  2003-08       Impact factor: 0.751
  2 in total

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