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Research 721–750 of 1000+
- Tofacitinib in alopecia areata and HIV: A curious intersection of immunomodulation, hair regrowth, and hypertrichosis
- Enanthem in Patients With COVID-19 and Skin Rash
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- HAIR AND SYSTEMATIC DISEASE
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Bovine besnoitiosis in Germany
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Pubic Hair Transplantation
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Growth Hormone and the Human Hair Follicle
- Disorders of hair in infants and children other than alopecia
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- A new type of pachyonychia congenita.
- Genital Rejuvenation: The Next Frontier in Medical and Cosmetic Dermatology
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- The biodisposition and hypertrichotic effects of bimatoprost in mouse skin
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Manganese Ethylene Bis(Maneb)-Induced Degeneration of Hair Follicle Epithelia in the Dosal Skin of WBN/ILA-Ht Rats.
- Sebaceous adenitis in a cat.
- Cardiomiopatia dilatada em cão com hipotireoidismo e megaesôfago
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- [Wooly hair syndrome. Clinical and microscopic study].
- Canine pododermatitis: A retrospective study of 300 cases
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix