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Research 301–330 of 1000+
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Hair & Cutaneous Development
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Gsdma3 is required for hair follicle differentiation in mice
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- The Rotterdam Study: objectives and design update
- The JAK/STAT signaling pathway: from bench to clinic
- Biotin and biotinidase deficiency
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- FGF5 is a crucial regulator of hair length in humans
- HOXC13 Is Involved in the Regulation of Human Hair Keratin Gene Expression
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- The biology and genetics of curly hair
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Oxidative DNA Damage Accelerates Skin Inflammation in Pristane-Induced Lupus Model