Literature DB >> 12754508

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin.

Etgar Levy-Nissenbaum1, Regina C Betz, Moshe Frydman, Michel Simon, Hadas Lahat, Tengiz Bakhan, Boleslaw Goldman, Anette Bygum, Monika Pierick, Axel M Hillmer, Nathalie Jonca, Jaime Toribio, Roland Kruse, Georg Dewald, Sven Cichon, Christian Kubisch, Marina Guerrin, Guy Serre, Markus M Nöthen, Elon Pras.   

Abstract

We have identified nonsense mutations in the gene CDSN (encoding corneodesmosin) in three families suffering from hypotrichosis simplex of the scalp (HSS; OMIM 146520). CDSN, a glycoprotein expressed in the epidermis and inner root sheath (IRS) of hair follicles, is a keratinocyte adhesion molecule. Truncated CDSN aggregates were detected in the superficial dermis and at the periphery of hair follicles. Our findings suggest that CDSN is important in normal scalp hair physiology.

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Year:  2003        PMID: 12754508     DOI: 10.1038/ng1163

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  31 in total

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Journal:  Am J Hum Genet       Date:  2018-10-25       Impact factor: 11.025

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Journal:  J Histochem Cytochem       Date:  2018-09-10       Impact factor: 2.479

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6.  Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.

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Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

7.  Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.

Authors:  Sandra M Pasternack; Melanie Refke; Elham Paknia; Hans Christian Hennies; Thomas Franz; Niklas Schäfer; Alan Fryer; Maurice van Steensel; Elizabeth Sweeney; Miquel Just; Clemens Grimm; Roland Kruse; Carlos Ferrándiz; Markus M Nöthen; Utz Fischer; Regina C Betz
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

8.  Hair abnormalities in genetic disorders of junctions.

Authors:  Paul D Yesudian
Journal:  Int J Trichology       Date:  2009-01

Review 9.  To grow or not to grow: hair morphogenesis and human genetic hair disorders.

Authors:  Olivier Duverger; Maria I Morasso
Journal:  Semin Cell Dev Biol       Date:  2013-12-17       Impact factor: 7.727

10.  Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2.

Authors:  A Wali; G Ali; P John; K Lee; M S Chishti; S M Leal; W Ahmad
Journal:  Ann Hum Genet       Date:  2007-04-19       Impact factor: 1.670

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