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Research 61–90 of 1000+
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Study on genetic polymorphisms of androgen receptor gene and 5α-reductase genes of Han men with androgenetic alopecia in the Eastern China
- BJD Editor's Choice
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- Intermittent nitrate transdermal therapy
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Male-pattern baldness susceptibility locus at 20p11
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- Lichen Planopilaris
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Lab Quality Management and Methodology
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Alopecia Areata
- Alopecia Areata
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )