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Research 10 of 495

1. The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71 Mammalian genome · 2010 · 75 citations
2. A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2005 · 33 citations
3. Buschke-Ollendorff syndrome British Journal of Dermatology · 2016 · 1 citations
4. The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes Journal of Biological Chemistry · 2008 · 35 citations
5. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
6. <i>WNT10A</i> , dermatology and dentistry British Journal of Dermatology · 2021 · 30 citations
7. Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism? Human & Experimental Toxicology · 1996 · 48 citations
8. Familial and Sporadic Porphyria Cutanea Tarda Medicine · 2010 · 38 citations
9. Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis Amino Acids · 2024 · 3 citations
10. Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis Bioinformation · 2012 · 3 citations

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