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Research 31–60 of 95
- Molecular Genetics of Alopecias
- Keratin disorders: from gene to therapy
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- <i>Hoxc13</i> mutant mice lack external hair
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Current Genetics in Hair Diseases
- Woolly Antics between the Sheaths
- Molecular Genetics of Human Hair Diseases
- Trichoscopy in genetic hair shaft abnormalities
- Advances in Hair Diseases
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Sequences and differential expression of three novel human type-II hair keratins
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Hair Anomalies in a 6-Year-Old Girl
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Monilethrix – Case report of a rare disease
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Alopezien und Hypotrichosen im Kindesalter
- Monilethrix
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele