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Research 211–240 of 762
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Association between <i>EGF</i> and <i>EGFR</i> Gene Polymorphisms and Susceptibility to Alopecia Areata in the Korean Population
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Integration of Point-of-Care Technology in the Decoding Process of Single Nucleotide Polymorphism for Healthcare Application †
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Genetic Dissection of Leg and Back Feather Follicle Density in Yellow-feathered Broiler: Integrative GWAS and Transcriptome Analysis Reveal the Regulatory Role of SERPINF1
- Exploring imputation performance of phenotype-associated SNPs for forensic prediction models
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats
- Landmark native breed of the Orenburg goats: progress in its breeding and genetics and future prospects
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Association between epidermal growth factor and epidermal growth factor receptor gene polymorphisms and susceptibility to alopecia areata in Korean population
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Defining the identity of mouse embryonic dermal fibroblasts
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Prevalence of vitamin D deficiency in Slovak women with polycystic ovary syndrome and its relation to metabolic and reproductive abnormalities
- The Genetics of Seborrheic Dermatitis: A Candidate Gene Approach and Pilot Genome-Wide Association Study
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- The Effect of Alfacalcidiol and Metformin on Phenotype Manifestations in Women with Polycystic Ovary Syndrome – a Preliminary Study
- Relationship Between Steroid Hormones and Metabolic Profile in Women With Polycystic Ovary Syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Association of Rs231775 Genetic Variant of Cytotoxic T-lymphocyte Associated Protein 4 with Alopecia Areata Disease in Males: A Case–Control Study
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Associations between genetically predicted sex and growth hormones and facial aging in the UK Biobank: a two−sample Mendelian randomization study