Literature DB >> 19174834

Hair lost in translation.

Lorin Weiner, Janice L Brissette.   

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Year:  2009        PMID： 19174834     DOI： 10.1038/ng0209-141

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


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  15 in total

1.  Regulated translation termination at the upstream open reading frame in s-adenosylmethionine decarboxylase mRNA.

Authors:  Alexa Raney; G Lynn Law; Gregory J Mize; David R Morris
Journal:  J Biol Chem       Date:  2001-12-12       Impact factor: 5.157

2.  The skin of hairless mice. I. The formation of cysts and the distribution of lipids.

Authors:  W MONTAGNA; H B CHASE; H P MELARAGNO
Journal:  J Invest Dermatol       Date:  1952-07       Impact factor: 8.551

3.  Four dominant autosomal mutations affecting skin and hair development in the mouse.

Authors:  K F Stelzner
Journal:  J Hered       Date:  1983 May-Jun       Impact factor: 2.645

4.  Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia.

Authors:  S Cichon; M Anker; I R Vogt; H Rohleder; M Pützstück; A Hillmer; S A Farooq; K S Al-Dhafri; M Ahmad; S Haque; M Rietschel; P Propping; R Kruse; M M Nöthen
Journal:  Hum Mol Genet       Date:  1998-10       Impact factor: 6.150

5.  Polyamine regulation of ribosome pausing at the upstream open reading frame of S-adenosylmethionine decarboxylase.

Authors:  G L Law; A Raney; C Heusner; D R Morris
Journal:  J Biol Chem       Date:  2001-08-06       Impact factor: 5.157

6.  Alopecia universalis associated with a mutation in the human hairless gene.

Authors:  W Ahmad; M Faiyaz ul Haque; V Brancolini; H C Tsou; S ul Haque; H Lam; V M Aita; J Owen; M deBlaquiere; J Frank; P B Cserhalmi-Friedman; A Leask; J A McGrath; M Peacocke; M Ahmad; J Ott; A M Christiano
Journal:  Science       Date:  1998-01-30       Impact factor: 47.728

7.  The near-naked hairless (Hr(N)) mutation disrupts hair formation but is not due to a mutation in the Hairless coding region.

Authors:  Yutao Liu; Suchita Das; Robert E Olszewski; Donald A Carpenter; Cymbeline T Culiat; John P Sundberg; Patricia Soteropoulos; Xiaochen Liu; Mitchel J Doktycz; Edward J Michaud; Brynn H Voy
Journal:  J Invest Dermatol       Date:  2007-03-01       Impact factor: 8.551

8.  Molecular basis for the rhino (hrrh-8J) phenotype: a nonsense mutation in the mouse hairless gene.

Authors:  W Ahmad; A A Panteleyev; J P Sundberg; A M Christiano
Journal:  Genomics       Date:  1998-11-01       Impact factor: 5.736

9.  Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis.

Authors:  Yaran Wen; Yang Liu; Yiming Xu; Yiwei Zhao; Rui Hua; Kaibo Wang; Miao Sun; Yuanhong Li; Sen Yang; Xue-Jun Zhang; Roland Kruse; Sven Cichon; Regina C Betz; Markus M Nöthen; Maurice A M van Steensel; Michel van Geel; Peter M Steijlen; Daniel Hohl; Marcel Huber; Giles S Dunnill; Cameron Kennedy; Andrew Messenger; Colin S Munro; Alessandro Terrinoni; Alain Hovnanian; Christine Bodemer; Yves de Prost; Amy S Paller; Alan D Irvine; Rod Sinclair; Jack Green; Dandan Shang; Qing Liu; Yang Luo; Li Jiang; Hong-Duo Chen; Wilson H-Y Lo; W H Irwin McLean; Chun-Di He; Xue Zhang
Journal:  Nat Genet       Date:  2009-01-04       Impact factor: 38.330

10.  Modulation of murine hair follicle function by alterations in ornithine decarboxylase activity.

Authors:  A P Soler; G Gilliard; L C Megosh; T G O'Brien
Journal:  J Invest Dermatol       Date:  1996-05       Impact factor: 8.551
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