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Research 151–180 of 1000+
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Activation of TRPV4 Induces Exocytosis and Ferroptosis in Human Melanoma Cells
- The Genetics of Human Skin Disease
- Double-stranded RNA induces inflammation via the NF-κB pathway and inflammasome activation in the outer root sheath cells of hair follicles
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Somatic Mutations in Normal Tissues: New Perspectives on Early Carcinogenesis
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Cyproterone Acetate: A Genotoxic Carcinogen?
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Activation of extrasynaptic δ-GABAA receptors globally or within the posterior-VTA has estrous-dependent effects on consumption of alcohol and estrous-independent effects on locomotion
- Reduced SMAD2/3 activation independently predicts increased depth of human cutaneous squamous cell carcinoma
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- What causes hidradenitis suppurativa ?—15 years after
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Prevalent founder mutation c.736T>A of <i>LIPH</i> in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
- Clonal analysis of stem cells in differentiation and disease
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Molecular Genetics of Alopecias
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit