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PubMed
22678782
[Genome-wide association study with memory measures as a quantitative trait locus for schizophrenia]. OBJECTIVE: To assess the association between gene polymorphisms and memory function through a geno
1.12 KB
2025-10-02
6
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PubMed
23276211
Genetic effects on old-age cognitive functioning: a population-based study. Associations between genotypes and cognitive outcomes may provide clues as to which mechanisms cause individual differences
1.73 KB
2025-10-02
8
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PubMed
21461582
Lack of association between methylenetetrahydrofolate reductase genetic polymorphisms and postmenopausal breast cancer risk. Published data on the association between methylenetetrahydrofolate reducta
1.32 KB
2025-10-02
7
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PubMed
24491138
Association of CDKN2A polymorphisms with the severity of cervical neoplasia in a Brazilian population. Variants of p16(INK4a) and p14(ARF), encoded by the CDKN2A locus, may respond differently to the
865 Bytes
2025-10-02
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PubMed
17327385
Genetic variations in PPARD and PPARGC1A determine mitochondrial function and change in aerobic physical fitness and insulin sensitivity during lifestyle intervention. CONTEXT: Mitochondrial function
1.97 KB
2025-10-02
6
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PubMed
21497535
Association of interleukin-4 receptor gene polymorphisms with rheumatoid arthritis in Egyptian female patients. OBJECTIVES: The imbalance between proinflammatory and anti-inflammatory cytokines is a f
1.25 KB
2025-10-02
10
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PubMed
25560469
COMT Val158Met and 5-HT1A-R -1019 C/G polymorphisms: effects on the negative symptom response to clozapine. AIM: Clozapine is still considered the gold standard for treatment-resistant schizophrenia p
1.7 KB
2025-10-02
7
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PubMed
23186209
Mitochondriogenesis genes and extreme longevity. Genes of the proliferator-activated receptor delta (PPARD)-peroxisome proliferator-activated receptor γ coactivator 1α (PPARGC1A, also termed PGC1-α)-n
1003 Bytes
2025-10-02
6
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PubMed
23456610
SOX10 rs139883 polymorphism is associated with the age of onset in schizophrenia. Schizophrenia is a common psychiatric disorder with high heritability. The age of onset is an important phenotype of s
1.26 KB
2025-10-02
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PubMed
22801813
The GC, CYP2R1 and DHCR7 genes are associated with vitamin D levels in northeastern Han Chinese children. Vitamin D deficiency is associated with risk in several diseases. Vitamin D status has high he
1.4 KB
2025-10-02
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