Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables

: Numerous transgenic, targeted mutagenesis (so‐called knockouts), conditional (so‐called “gene switch”) and spontaneous mutant mice develop abnormal hair phenotypes. The number of mice that exhibit such abnormalities is increasing exponentially as genetic engineering methods become routine. Since d...

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Bibliographic Details
Published in:Experimental dermatology Vol. 10; no. 6; pp. 369 - 390
Main Authors: Nakamura, M., Sundberg, J. P., Paus, R.
Format: Journal Article
Language:English
Published: Copenhagen Munksgaard International Publishers 01-12-2001
Blackwell
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Summary:: Numerous transgenic, targeted mutagenesis (so‐called knockouts), conditional (so‐called “gene switch”) and spontaneous mutant mice develop abnormal hair phenotypes. The number of mice that exhibit such abnormalities is increasing exponentially as genetic engineering methods become routine. Since defined abnormalities in hair follicle morphogenesis, cycling and/or structure in such mutant mice provide important clues to the as yet poorly understood functional roles of many gene products, it is useful to summarize and classify these mutant mice according to their hair phenotype. This review provides a corresponding, annotated table of mutant mice with hair abnormalities, classifying the latter into 6 categories, 1) abnormally low number of hair follicles, 2) disorders of hair morphogenesis, 3) of hair follicle cycling, 4) of hair follicle structure 5) of sebaceous gland structure, and 6) hair growth disorders as a consequence of immunological abnormalities. This annotated table should serve as a useful source of reference for anyone who is interested in the molecular controls of hair growth, for investigators who are looking for mouse models to explore or compare the functional activities of their gene of interest, and for comparing the hair phenotype of newly generated mouse mutants with existing ones.
Bibliography:istex:5D8F20B8A77291D10C1B03B32CA1FA5070CAD595
ArticleID:EXD100601
ark:/67375/WNG-6CXDG6RT-R
ISSN:0906-6705
1600-0625
DOI:10.1034/j.1600-0625.2001.100601.x