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Research 871–900 of 1000+
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Congenital alopecia areata
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Ethnomedicinal plants used by traditional healers in the management of HIV/AIDS opportunistic diseases in Rundu, Kavango East Region, Namibia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Necrosis of the donor site after hair restoration with follicular unit extraction (FUE): A case report
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- <i>De novo</i> mutations in monilethrix
- Bioinformatics analysis of evolutionary characteristics and biochemical structure of FGF5 Gene in sheep
- The Proteins of Normal and Aberrant Hair Keratins
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Adenovirus-Mediated Wnt5a Expression Inhibits the Telogen-To-Anagen Transition of Hair Follicles in Mice
- Sequence and expression of human hair keratin genes
- Evolution of Trichocyte Keratins
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Clinical presentation and etiologic factors of hirsutism in premenopausal Iranian women.
- Sjogren-Larsson syndrome
- A novel calmodulin‐interacting Domain of Unknown Function 506 protein represses root hair elongation in <i>Arabidopsis</i>
- Female pattern hair loss: A retrospective study in a tertiary referral center
- Alopecia Areata
- The role of oxidative stress in early-onset androgenetic alopecia
- Biotinidase deficiency – clinching the diagnosis rapidly can make all the difference!
- Lupus erythematosus-like lesions in a carrier of X-linked chronic granulomatous disease: A case report and personal considerations
- Uncombable-hair Syndrome
- NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: A new disease association
- Diphencyprone Induced Vitiligo: A Case Report
- Finasteride-Induced Pseudoporphyria
- Koebnerization secondary to microblading