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Research 631–660 of 993
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Use of Leukocyte Platelet (L-PRF) Rich Fibrin in Diabetic Foot Ulcer with Osteomyelitis (Three Clinical Cases Report)
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- Ichthyosis with confetti: clinics, molecular genetics and management
- Cidea Control of Lipid Storage and Secretion in Mouse and Human Sebaceous Glands
- Betacellulin Regulates Hair Follicle Development and Hair Cycle Induction and Enhances Angiogenesis in Wounded Skin
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Monitoring of clinical signs in goats with transmissible spongiform encephalopathies
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Miz1 is required for hair follicle structure and hair morphogenesis
- The cellular basis of mechanosensory Merkel-cell innervation during development
- Dutasteride reduces alcohol’s sedative effects in men in a human laboratory setting and reduces drinking in the natural environment
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- The crest phenotype in domestic chicken is caused by a 195 bp duplication in the intron of <i>HOXC10</i>
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Current evidence for the involvement of sex steroid receptors and sex hormones in benign prostatic hyperplasia
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- The impact of VDR expression and regulation in vivo