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Research 61–90 of 129
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dermatoscopy of hair shaft disorders
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- t-Flavanone Improves the Male Pattern of Hair Loss by Enhancing Hair-Anchoring Strength: A Randomized, Double-Blind, Placebo-Controlled Study
- Value of dermoscopy for the diagnosis of monilethrix
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Integrated Meta-Analysis of Scalp Transcriptomics and Serum Proteomics Defines Alopecia Areata Subtypes and Core Disease Pathways
- Effect of Oral Minoxidil on Monilethrix
- A Comparative Clinical study of Nasya Karma and Shirodhara with Yashtimadhwadi tail for the management of Khalitya with special reference to "Telogen effluvium"
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- The molecular basis of human keratin disorders
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Genetic Hair Disorders: A Review
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- The Genetics of Human Skin Disease
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Protein extraction from human anagen head hairs 1-millimeter or less in total length
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function