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Research 61–90 of 95
- Monilethrix – Case report of a rare disease
- The Catalog of Human Hair Keratins
- Minoxidil and its use in hair disorders: a review
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Hox in hair growth and development
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- The molecular basis of human keratin disorders
- Trichoscopy in genetic hair shaft abnormalities
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Alopezien und Hypotrichosen im Kindesalter
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks