Literature DB >> 11916127

Mutant laboratory mice with abnormalities in pigmentation: annotated tables.

Motonobu Nakamura1, Desmond J Tobin, Beverly Richards-Smith, John P Sundberg, Ralf Paus.   

Abstract

Mammalian pigment cell research has recently entered a phase of significantly increased activity due largely to the exploitation of the many mutant mouse stocks that are coming on stream. Numerous transgenic, targeted mutagenesis (so-called 'knockouts'), conditional (so-called 'gene switch') and spontaneous mutant mice develop abnormal coat color phenotypes. The number of mice that exhibit such abnormalities is increasing exponentially as genetic engineering methods become routine. Since defined abnormalities in such mutant mice provide important clues to the as yet often poorly understood functional roles of many gene products, this overview includes a corresponding, annotated table of mutant mice with pigmentation alterations. These range from early developmental defects via a large array of coat color abnormalities to a melanoma metastasis model. This overview should provide helpful pointers to investigators who are looking for mouse models to explore or to compare functional activities of genes of interest and for comparing coat color phenotypes of spontaneous or genetically engineered mouse mutants with novel ones. Secondly, this review includes a table of mouse models of specific human diseases with genetically defined pigmentation abnormalities. In summary, this annotated table should serve as a useful reference for anyone interested in the molecular controls of pigmentation.

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Year:  2002        PMID: 11916127     DOI: 10.1016/s0923-1811(01)00158-x

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  7 in total

Review 1.  Hair follicle pigmentation.

Authors:  Andrzej Slominski; Jacobo Wortsman; Przemyslaw M Plonka; Karin U Schallreuter; Ralf Paus; Desmond J Tobin
Journal:  J Invest Dermatol       Date:  2005-01       Impact factor: 8.551

2.  Somatolactin selectively regulates proliferation and morphogenesis of neural-crest derived pigment cells in medaka.

Authors:  Shoji Fukamachi; Masazumi Sugimoto; Hiroshi Mitani; Akihiro Shima
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-12       Impact factor: 11.205

Review 3.  Genetically modified laboratory mice with sebaceous glands abnormalities.

Authors:  Carmen Ehrmann; Marlon R Schneider
Journal:  Cell Mol Life Sci       Date:  2016-07-25       Impact factor: 9.261

4.  A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

Authors:  Qing-he Xing; Ming-tai Wang; Xiang-dong Chen; Guo-yin Feng; Hong-yun Ji; Jian-dong Yang; Jian-jun Gao; Wei Qin; Xue-qing Qian; Sheng-nan Wu; Lin He
Journal:  Am J Hum Genet       Date:  2003-06-12       Impact factor: 11.025

5.  Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse.

Authors:  Vicky Tsipouri; John A Curtin; Pat M Nolan; Lucie Vizor; Claire A Parsons; Colin M Clapham; Ian D Latham; Lesley J Rooke; Jo E Martin; Jo Peters; A Jackie Hunter; Derek Rogers; Sohaila Rastan; Steve D M Brown; Elizabeth M C Fisher; Nigel K Spurr; Ian C Gray
Journal:  Comp Funct Genomics       Date:  2004

6.  Zebrafish endzone regulates neural crest-derived chromatophore differentiation and morphology.

Authors:  Brigitte L Arduini; Glen R Gallagher; Paul D Henion
Journal:  PLoS One       Date:  2008-07-30       Impact factor: 3.240

Review 7.  Proliferative and non-proliferative lesions of the rat and mouse integument.

Authors:  Lars Mecklenburg; Donna Kusewitt; Carine Kolly; Silke Treumann; E Terence Adams; Kelly Diegel; Jyoji Yamate; Wolfgang Kaufmann; Susanne Müller; Dimitry Danilenko; Alys Bradley
Journal:  J Toxicol Pathol       Date:  2013       Impact factor: 1.628

  7 in total

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