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PMC 6338815 Association between TMPRSS2:ERG fusion gene and the prostate cancer: systematic review and meta-analysis Abstract Introduction To identify the association between the TMPRSS2:ERG fusion gene, their v 24.9 KB 2025-10-02 5 0
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PMC 7048686 The association of miR34b/c and TP53 gene polymorphisms with Wilms tumor risk in Chinese children Abstract Abstract Wilms tumor is the most common pediatric malignancy in the kidney. The miR34b/c is 15.7 KB 2025-10-02 5 0
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PMC 10994991 Association of Blood MicroRNA Expression and Polymorphisms with Cognitive and Biomarker Changes in Older Adults Abstract Background Identifying individuals before the onset of overt symptoms is key i 44.3 KB 2025-10-02 3 0
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PMC 7606308 Understanding Behçet’s Disease in the Context of Innate Immunity Activation Abstract Behçet´s disease (BD) is a heterogeneous condition consisting of idiopathic systemic vasculitis affecting large an 37.1 KB 2025-10-02 4 0
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PMC 9381810 Sexual dimorphism in the relationship between Forkhead-Box P2 and BMI with cognitive deficits in schizophrenia Abstract FOXP2, cognitive deficits, and schizophrenia are associated with neurodegenerat 30 KB 2025-10-02 3 0
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PMC 4910552 Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil Abstract Abstract In Brazil, 40.1 KB 2025-10-02 5 0
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PMC 6525128 The Role of Stressful Parenting and Mineralocorticoid Receptor Haplotypes on Social Development During Adolescence and Young Adulthood Abstract The development of social behavior could be affected by 59.4 KB 2025-10-02 5 0
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PMC 1559631 The IMAGE project: methodological issues for the molecular genetic analysis of ADHD Abstract The genetic mechanisms involved in attention deficit hyperactivity disorder (ADHD) are being studied with 50.8 KB 2025-10-02 6 0
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PMC 6702638 Autoantibodies Directed Toward a Novel IA-2 Variant Protein Enhance Prediction of Type 1 Diabetes Abstract We identified autoantibodies (AAb) reacting with a variant IA-2 molecule (IA-2var) that has 30.3 KB 2025-10-02 5 0
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PMC 5352434 Identification and characterization of novel PAX8 mutations in Congenital Hypothyroidism(CH) in a Chinese population Abstract Objective Based on mutations in PAX8 is associated with thyroid dysgenesi 28.8 KB 2025-10-02 5 0
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