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Research 601–630 of 1000+
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Hair follicles’ transit-amplifying cells govern concurrent dermal adipocyte production through Sonic Hedgehog
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Role of FGFR2-signaling in the pathogenesis of acne
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- Skin tissue engineering
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Global Trends in Research of Androgen Receptor Associated With Breast Cancer From 2011 to 2020: A Scientometric Analysis
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Acne Syndromes and Mosaicism
- Current Genetics in Hair Diseases