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Research 991–1000 of 1000+
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Assessment of copper and zinc status in hair and urine of young women descendants of NIDDM parents
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Localization of S100A2, S100A4, S100A6, S100A7, and S100P in the human hair follicle.
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands