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Research 121–150 of 1000+
- Prediction of male-pattern baldness from genotypes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Regulatory T cells in dominant immunologic tolerance
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Androgen Receptor Mutations and Polymorphisms in African American Prostate Cancer
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genetic analysis of interleukin 18 gene polymorphisms in alopecia areata
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- Azathioprine‐induced alopecia and leukopenia associated with NUDT15 polymorphisms
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Inhibition of T-cell activity in alopecia areata: recent developments and new directions
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Predominant expression of interleukin (IL)‐17 in chronic alopecia areata compared to IFN‐γ in pathogenic Th17 cells, tissue‐resident memory T cells and natural killer cells
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Regulatory T cells in skin regeneration and wound healing
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- The effect of GGC and CAG repeat polymorphisms on the androgen receptor gene in response to finasteride therapy in men with androgenetic alopecia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Genetic Polymorphisms of the 3'-Untranslated Regions (3'-UTR) of the HSP 70 Gene in Moa Buffalo (Bubalus bubalis)
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women