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Research 91–120 of 1000+
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- 0877 Activated wound phenotype and microbial dysbiosis are driven by AhR suppression in hidradenitis suppurativa tunnels
- Faculty Opinions recommendation of Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.
- 489 Seborrhea-like dermatitis phenotype in the Mpzl3 knockout mice
- 333 Poor perifollicular vascularization is associated with nutrient insufficiency and a quiescent metabolic phenotype in intermediate hair follicles from patients with female pattern hair loss
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Metabolic risk in PCOS: phenotype and adiposity impact
- Cardiovascular disease risk in women with hyperandrogenism, oligomenorrhea/menstrual irregularity or polycystic ovaries (components of polycystic ovary syndrome): a systematic review and meta-analysis
- Minoxidil Regulates Aging-Like Phenotypes in Rat Cortical Astrocytes <i>In Vitro</i>
- Genomic Portraiture: The Science and Ethics of DNA Phenotyping in Identity Prediction
- FORENSIC DNA PHENOTYPING FOR CRIMINAL IDENTIFICATION
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Iron deficient toxic milk leads to the mask phenotype in hephaestin knockout mice (907.4)
- Changes in the PCOS phenotype with age
- 0439 Temporal–phenotype signatures of alopecia associated with GLP-1–based therapies: A PRISMA-ScR scoping review
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Digit-length ratios (2D:4D) as a phenotypic indicator of in utero androgen exposure is not prognostic for androgenic alopecia: a descriptive-analytic study of 1200 Iranian men
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Effects of α-Synuclein on the Lipid Phenotype of SZ95 Human Sebocytes: A Preliminary Study in the Context of Parkinson’s Disease
- 261 Tissue and circulating microRNA co-expression analysis reveals potential involvement of miRNAs in the pathobiology of frontal fibrosing alopecia
- Disease modifying osteoarthritis drug discovery using a temporal phenotypic reporter in 3D aggregates of primary human chondrocytes
- The Effect of High Spice Consumption on the Phenotypic and Histological Structure of the Mouse Liver
- The Effect of High Spice Consumption on the Phenotypic and Histological Structure of the Mouse Liver
- Disease Modifying Osteoarthritis Drug Discovery Using A Temporal Phenotypic Reporter In 3D Aggregates of Primary Human Chondrocytes
- Long-Term Bezafibrate Treatment Improves Skin and Spleen Phenotypes of the mtDNA Mutator Mouse