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Research 31–60 of 153
- Genetic Susceptibility to Alopecia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Evolving approaches to profiling the microbiome in skin disease
- Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Ichthyosis
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Construction of transcriptome atlas of white yak hair follicle during anagen and catagen using single-cell RNA sequencing
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Wnt signaling: the good and the bad
- Inherited Disorders of the Hair
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Human umbilical cord mesenchymal stem cell treatment alleviates symptoms in an atopic dermatitis-like mouse model
- Genetics
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genetic Hair Disorders: A Review
- Skin, Genetic Defects, and Aging