Literature DB >> 11599924

The nude mouse skin phenotype: the role of Foxn1 in hair follicle development and cycling.

L Mecklenburg1, M Nakamura, J P Sundberg, R Paus.   

Abstract

The original nude mouse mutation has proven to be an incredibly valuable biomedical tool since its discovery in 1966. Initially its value was as a tool to study the immune system. The immunodeficiency in this mutant mouse made nude mice valuable as hosts for xenografts, primarily for cancer research. More recently, the most obvious clinical feature of this mutant mouse, lack of hair, has been capitalized on to define the role of Foxn1 in normal and pathological skin and hair follicle physiology. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11599924     DOI: 10.1006/exmp.2001.2386

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  24 in total

1.  Control of hair follicle cell fate by underlying mesenchyme through a CSL-Wnt5a-FoxN1 regulatory axis.

Authors:  Bing Hu; Karine Lefort; Wenying Qiu; Bach-Cuc Nguyen; Renuga Devi Rajaram; Einar Castillo; Fenglei He; Yiping Chen; Peter Angel; Cathrin Brisken; G Paolo Dotto
Journal:  Genes Dev       Date:  2010-07-15       Impact factor: 11.361

2.  The nude mutant gene Foxn1 is a HOXC13 regulatory target during hair follicle and nail differentiation.

Authors:  Christopher S Potter; Nathanael D Pruett; Michael J Kern; Mary Ann Baybo; Alan R Godwin; Kathleen A Potter; Ron L Peterson; John P Sundberg; Alexander Awgulewitsch
Journal:  J Invest Dermatol       Date:  2010-12-30       Impact factor: 8.551

3.  A Single Amino Acid in the Hinge Loop Region of the FOXP Forkhead Domain is Significant for Dimerisation.

Authors:  Kershia Perumal; Heini W Dirr; Sylvia Fanucchi
Journal:  Protein J       Date:  2015-04       Impact factor: 2.371

Review 4.  Research-Relevant Conditions and Pathology of Laboratory Mice, Rats, Gerbils, Guinea Pigs, Hamsters, Naked Mole Rats, and Rabbits.

Authors:  Timothy K Cooper; David K Meyerholz; Amanda P Beck; Martha A Delaney; Alessandra Piersigilli; Teresa L Southard; Cory F Brayton
Journal:  ILAR J       Date:  2021-12-31       Impact factor: 1.521

Review 5.  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

6.  Impaired synthesis of erythropoietin, glutamine synthetase and metallothionein in the skin of NOD/SCID/gamma(c)(null) and Foxn1 nu/nu mice with misbalanced production of MHC class II complex.

Authors:  L Danielyan; S Verleysdonk; M Buadze; C H Gleiter; G H Buniatian
Journal:  Neurochem Res       Date:  2009-10-14       Impact factor: 3.996

7.  Agammaglobulinemia and Staphylococcus aureus botryomycosis in a cohort of related sentinel Swiss Webster mice.

Authors:  Erin C Bridgeford; James G Fox; Prashant R Nambiar; Arlin B Rogers
Journal:  J Clin Microbiol       Date:  2008-03-05       Impact factor: 5.948

Review 8.  Keloids: Animal models and pathologic equivalents to study tissue fibrosis.

Authors:  Jaana Marttala; Jonathan P Andrews; Joel Rosenbloom; Jouni Uitto
Journal:  Matrix Biol       Date:  2016-01-29       Impact factor: 11.583

9.  Alopecia in a viable phospholipase C delta 1 and phospholipase C delta 3 double mutant.

Authors:  Fabian Runkel; Maik Hintze; Sebastian Griesing; Marion Michels; Birgit Blanck; Kiyoko Fukami; Jean-Louis Guénet; Thomas Franz
Journal:  PLoS One       Date:  2012-06-19       Impact factor: 3.240

10.  Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes.

Authors:  Zhongya Song; Xi Chen; Qian Zhao; Vesna Stanic; Zhimiao Lin; Shuxia Yang; Ting Chen; Jiang Chen; Yong Yang
Journal:  J Invest Dermatol       Date:  2021-03-03       Impact factor: 7.590

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