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Research 121–150 of 1000+
- News in brief
- Low-dose oral minoxidil in a case of short anagen syndrome
- HAIR AND SYSTEMATIC DISEASE
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- A new type of pachyonychia congenita.
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Síndrome do nevo de Becker
- Low prevalence of twisted hair in anorexia nervosa
- Acquired and inheritedhair disorders
- Hair Disorders
- Hair and scalp disorders
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.