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PubMed 15022315 Haplotype analysis in simplex families and novel analytic approaches in a case-control cohort reveal no evidence of association of the CTLA-4 gene with rheumatoid arthritis. OBJECTIVE: Cytotoxic T lym 1.79 KB 2025-10-02 6 0
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PubMed 15024396 Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder. Mouse mutants of the homeobox transcription factor Engrailed2 (En2) and autistic individuals display si 1.52 KB 2025-10-02 6 0
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PubMed 15567072 A case-control study of the relationship between the metabotropic glutamate receptor 3 gene and schizophrenia in the Chinese population. Recent studies of the association between the metabotropic glut 1.22 KB 2025-10-02 6 0
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PubMed 15569484 Single nucleotide polymorphisms of deoxyribonuclease I and their expression in Chinese systemic lupus erythematosus patients. BACKGROUND: Previous studies have suggested that interrupted clearance of 2.46 KB 2025-10-02 5 0
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PubMed 15570643 Epistatic interactions between HLA-DRB1 and interleukin 4, but not interferon-gamma, increase susceptibility to giant cell arteritis. OBJECTIVE: To assess the roles of the interleukin 4 (IL-4) and int 1.62 KB 2025-10-02 6 0
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PubMed 15034781 Variants of CYP46A1 may interact with age and APOE to influence CSF Abeta42 levels in Alzheimer's disease. Recent studies have suggested that variants of CYP46A1, encoding cholesterol 24-hydroxylase ( 1.62 KB 2025-10-02 5 0
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PubMed 15047632 A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for l 1.72 KB 2025-10-02 6 0
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PubMed 15047633 Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes. The Finland-United States Investigation Of NIDDM Genetics (FUSION) study aims to identify 1.49 KB 2025-10-02 5 0
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PubMed 15056512 Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. OBJECTIVE: Autism/autistic disorder (MIM number 209850) is a complex, largely genetic psychiatric di 2.09 KB 2025-10-02 6 0
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PubMed 15077008 Nicotine dependence in a prospective population-based study of adolescents: the protective role of a functional tyrosine hydroxylase polymorphism. Dopamine is a key neurotransmitter of the mesolimbic 1.49 KB 2025-10-02 4 0
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