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Research 781–810 of 1000+
- Knockout of the ING5 epigenetic regulator confirms roles in stem cell maintenance and tumor suppression in vivo
- Dermal Papilla Cells: From Basic Research to Translational Applications
- Pharmacotherapy for Keloids and Hypertrophic Scars
- Pathogenesis of Alopecia Areata and Vitiligo: Commonalities and Differences
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer
- PLCD1 and Pilar Cysts
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart
- Siberian cats help in solving part of the mystery surrounding golden cats
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Natural variation in trichome density and biochemistry in Antirrhinum
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- Effect of PTPN22, FAS/FASL, IL2RA and CTLA4 genetic polymorphisms on the risk of developing alopecia areata: A systematic review of the literature and meta-analysis
- Genotyping of the rs1800440 Polymorphism in CYP1B1 Gene and the rs9258883 Polymorphism in HLA-B Gene in a Spanish Cohort of 223 Patients with Frontal Fibrosing Alopecia
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- The genetics of alopecia areata
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study