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Research 571–600 of 1000+
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Pathophysiological mechanisms implicated in postpartum depression
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- FGF5 is a crucial regulator of hair length in humans
- The Pathobiology of Skin Aging
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- The Many Faces of Calcineurin Inhibitor Toxicity—What the FK?
- Nanomaterials-Based Wound Dressing for Advanced Management of Infected Wound
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The biology and genetics of curly hair
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Epidermal pigmentation in the human lineage is an adaptation to ultraviolet radiation
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits