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Research 61–90 of 1000+
- 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
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Genetically separable determinants of hair keratin gene expression
- The genetics of alopecia areata
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- 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
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Natural variation in trichome density and biochemistry in Antirrhinum
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Lichen Planopilaris
- Lab Quality Management and Methodology
- Mice humanised for the EGF receptor display hypomorphic phenotypes in skin, bone and heart
- 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
- Insertional mutation of the hairless locus on mouse Chromosome 14
- 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
- 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
- Adiponectin serum levels and ADIPOQ (rs2241766) polymorphism in alopecia areata Egyptian patients
- Association between angiotensin‐converting enzyme gene insertion deletion polymorphism and androgenetic alopecia susceptibility among Egyptian patients: A preliminary case‐controlled study
- Association of Human Beta – Defensin 1 Gene Polymorphisms with Alopecia Areata Patients