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Research 61–90 of 1000+
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Investigating bioactive phytochemicals in bulb and shoot of <i>Allium longisepalum</i> Bertol. from Iran
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Autoimmunity: Alopecia Areata
- Mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart
- Male-pattern baldness susceptibility locus at 20p11
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Evaluation of DNA Variants Associated with Androgenetic Alopecia and Their Potential to Predict Male Pattern Baldness
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Genetic Fate Mapping Using Site-Specific Recombinases
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Genetically separable determinants of hair keratin gene expression
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Insertional mutation of the hairless locus on mouse Chromosome 14
- The genetics of alopecia areata
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or 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
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- Association of follicle-stimulating hormone receptor gene ser680 asn (rs6166) polymorphism with polycystic ovarian syndrome
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage