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Research 91–120 of 186
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Trichoscopy in genetic hair shaft abnormalities
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- Characteristics of Androgenetic Alopecia in Asian
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Recently Identified Forms of Epidermolysis Bullosa
- Genetic hair and nail disorders
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- The Genetics of Human Skin Disease
- Parsing patterns: Emerging roles of tissue self-organization in health and disease
- New developments in the molecular treatment of ichthyosis: review of the literature
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- Chronic overlapping pain conditions and nociplastic pain
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Tabby pattern genetics – a whole new breed of cat