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Research 271–300 of 1000+
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.
- Reversal of male-pattern baldness, hypertrichosis, and accelerated hair and nail growth in patients receiving benoxaprofen.
- Tofacitinib in alopecia areata and HIV: A curious intersection of immunomodulation, hair regrowth, and hypertrichosis
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Enanthem in Patients With COVID-19 and Skin Rash
- Biology and Genetics of Hair
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Enhancing the Growth of Natural Eyelashes: The Mechanism of Bimatoprost-Induced Eyelash Growth
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- HAIR AND SYSTEMATIC DISEASE
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- 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
- Genetic Hair Disorders: A Review
- 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
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Growth Hormone and the Human Hair Follicle
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Disorders of hair in infants and children other than alopecia
- Dermatopathology and molecular genetics