Search
for
Sort by
Research 31–60 of 1000+
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- An evaluation of the RapidHIT™ ID system for hair roots stained with Diamond™ Nucleic Acid Dye
- 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
- Unexpectedly high carrier rates and genotype/phenotype correlation; LIPH mutations in Japanese autosomal recessive woolly hair/hypotrichosis
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Genetic association of complement component 2 polymorphism with systemic lupus erythematosus
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- 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
- 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
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Association of Human Beta – Defensin 1 Gene Polymorphisms with Alopecia Areata Patients
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- Androgenetic alopecia and polymorphism of the androgen receptor gene (SNP rs6152) in patients with benign prostate hyperplasia or prostate cancer
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women