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Research 151–180 of 1000+
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Observation of phenotypic variation among Indian women with polycystic ovary syndrome (PCOS) from Delhi and Srinagar
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- Influence of Immune Cells and Circulating Inflammatory Cytokines on Pathological Scars: A Mendelian Randomization Study
- КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2)
- Clinical features and presentation of polycystic ovary syndrome
- POLİKİSTİK OVER SENDROMU FENOTİPLERİ VE METABOLİK DİSFONKSİYON İLİŞKİSİ
- Analysis of the human diseasome using phenotype similarity between common, genetic and infectious diseases
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Reconsidering the Polycystic Ovary Syndrome (PCOS)
- Metabolic syndrome and metabolic risk profile according to polycystic ovary syndrome phenotype
- A Transcriptome Sequencing Study on Genome-Wide Gene Expression Differences of Lung Cancer Cells Modulated by Fucoidan
- MmuPV1 infection and tumor development of T cell-deficient mice is prevented by passively transferred hyperimmune sera from normal congenic mice immunized with MmuPV1 virus-like particles (VLPs)
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Phenotype-Specific Lifestyle Prediction for PCOS Using Machine Learning Multi-Class Classification and SHAP Explainability
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Trichoscopy of Dark Scalp
- Epidermal pigmentation in the human lineage is an adaptation to ultraviolet radiation
- Auxin Input Pathway Disruptions Are Mitigated by Changes in Auxin Biosynthetic Gene Expression in Arabidopsis
- The evolutionary impact of androgen levels on prostate cancer in a multi-scale mathematical model
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome
- Finding Long-COVID: temporal topic modeling of electronic health records from the N3C and RECOVER programs
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Development and evaluation of novel rodent model of PCOS mimicking clinical phenotype in human disease
- 加齢に伴うミトコンドリア枯渇は皮膚老化と肥満を加速する
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2