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Research 631–660 of 1000+
- The nude gene and the skin
- Genetic Basis of Alopecia Areata
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Immuno-Endocrinology of COVID-19: The Key Role of Sex Hormones
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- The significance of the apelinergic system in doxorubicin-induced cardiotoxicity
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- A functional role of S100A4/non-muscle myosin IIA axis for pro-tumorigenic vascular functions in glioblastoma
- CD44 signaling in skin wound healing and regeneration
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Monilethrix in three generations
- Developmental and functional roles of androgen and interactive signals for external genitalia and erectile tissues
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia