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Research 181–210 of 1000+
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Hair & Cutaneous Development
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Nutritional Disorders of the Hair and Their Management
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Diseases of Hair
- Diseases of Hair
- The biology and genetics of curly hair
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- Cronkhite-Canada Syndrome: A Case Report
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Diversity of Trichocyte Keratins and Keratin Associated Proteins