Mutations inLPAR6/P2RY5andLIPHare associated with woolly hair and/or hypotrichosis
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2012.04472.x/fullpdf
Reference15 articles.
1. Hereditary woolly hair and keratosis pilaris;Chien;J Am Acad Dermatol,2006
2. Woolly hair. Clinical and general aspects;Hutchinson;Trans St Johns Hosp Dermatol Soc,1974
3. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease);McKoy;Lancet,2000
4. Recessive mutation in desmoplakin disrupts desmoplakinintermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma;Norgett;Hum Mol Genet,2000
5. Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair;Shimomura;Nat Genet,2008
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1. Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies;Journal of the European Academy of Dermatology and Venereology;2021-06-04
2. Autosomal recessive woolly hair and hypotrichosis in two Caucasian dizygotic twins. Description of a novel biallelic mutation in the LPAR6 gene;International Journal of Dermatology;2020-10-05
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4. Regulation of tumor cell – Microenvironment interaction by the autotaxin-lysophosphatidic acid receptor axis;Advances in Biological Regulation;2019-01
5. MOLECULAR BASIS OF HAIR LOSS-A MINI REVIEW;INDO AM J PHARM SCI;2018
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