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Research 271–300 of 368
- Screening of Tyrosinase, Xanthine Oxidase, and α-Glucosidase Inhibitors from Polygoni Cuspidati Rhizoma et Radix by Ultrafiltration and HPLC Analysis
- The Roles of Non-coding RNA in the Development and Regeneration of Hair Follicles: Current Status and Further Perspectives
- Docking and Molecular Dynamics Identify Leads against 5 Alpha Reductase 2 for Benign Prostate Hyperplasia Treatment
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Cuprorivaite/hardystonite/alginate composite hydrogel with thermionic effect for the treatment of peri-implant lesion
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Impact of mTORC1 inhibition on keratinocyte proliferation during skin tumor promotion in wild‐type and BK5.Akt<sup>WT</sup> mice
- Ontogeny of Skin Stem Cells and Molecular Underpinnings
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Histological and Gene Expression Analysis of the Effects of Menopause Status and Hormone Therapy on the Vaginal Introitus and Labia Majora
- Assessment of the Chemical Profile and Potential Medical Effects of a Flavonoid-Rich Extract of Eclipta prostrata L. Collected in the Central Highlands of Vietnam
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- The Role of Hormones in Hidradenitis Suppurativa: A Systematic Review
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Mechanistic and therapeutic insight into the effects of cinnamon in polycystic ovary syndrome: a systematic review
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- HSP90 Inhibition and Cellular Stress Elicits Phenotypic Plasticity in Hematopoietic Differentiation
- Advancing Design Strategy of PROTACs for Cancer Therapy
- Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells
- Transcriptional Control of Epidermal Stem Cells
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita