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Research 31–60 of 1000+
- The E211 G>A Androgen Receptor Polymorphism Is Associated with a Decreased Risk of Metastatic Prostate Cancer and Androgenetic Alopecia
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- Adiponectin serum levels and ADIPOQ (rs2241766) polymorphism in alopecia areata Egyptian patients
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Association of follicle-stimulating hormone receptor gene ser680 asn (rs6166) polymorphism with polycystic ovarian syndrome
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Drugs affecting blood coagulation, fibrinolysis, and hemostasis
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Gene-wide association study between the aromatase gene (<i>CYP19A1</i>) and female pattern hair loss
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- The association between HDAC9 gene polymorphisms and stroke risk in the Chinese population: A meta-analysis
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- Effects of <i>KISS1</i> structural polymorphism on the risk of polycystic ovary syndrome and reproductive hormones in Iraqi women who take metformin
- Transgenic mouse models support HCR as an effector gene in the PSORS1 locus
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Association of Human Beta – Defensin 1 Gene Polymorphisms with Alopecia Areata Patients
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- 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
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- Lab Quality Management and Methodology