Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,General Medicine,Biotechnology
Reference19 articles.
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2. C-cadherin ectodomain structure and implications for cell adhesion mechanisms;Boggon;Science,2002
3. Structure and function of desmosomal proteins and their role in development and disease;Huber;Cell Mol Life Sci,2003
4. Clustered cadherin genes: A sequence-ready contig for the desmosomal cadherin locus on human chromosome 18;Hunt;Genomics,1999
5. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene;Jahoda;Genomics,2004
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1. Desmoglein-4 Deficiency Exacerbates Psoriasiform Dermatitis in Rats While Psoriasis Patients Displayed a Decreased Gene Expression of DSG4;Frontiers in Immunology;2021-04-29
2. Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice;Veterinary Dermatology;2021-01-19
3. An Autosomal Recessive Mutation of DSG4 Causes Monilethrix through the ER Stress Response;Journal of Investigative Dermatology;2015-05
4. Inherited desmosomal disorders;Cell and Tissue Research;2014-12-09
5. Genetic skin diseases related to desmosomes and corneodesmosomes;Journal of Dermatological Science;2014-05
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