508 results on '"Arinami, T."'
Search Results
2. DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia
3. Meta-analysis of 32 genome-wide linkage studies of schizophrenia
4. Genome-wide association study identifies a potent locus associated with human opioid sensitivity
5. Involvement of cannabinoid CB2 receptor in alcohol preference in mice and alcoholism in humans
6. RGS4 is not a susceptibility gene for schizophrenia in Japanese: Association study in a large case-control population
7. Human cannabinoid receptor 1: 5′ exons, candidate regulatory regions, polymorphisms, haplotypes and association with polysubstance abuse
8. Insertion/deletion coding polymorphisms in hHAVcr-1 are not associated with atopic asthma in the Japanese population
9. Association between serotonin 4 receptor gene polymorphisms and bipolar disorder in Japanese case-control samples and the NIMH Genetics Initiative Bipolar Pedigrees
10. An association between a missense polymorphism in the close homologue of L1 (CHL1, CALL) gene and schizophrenia
11. A genome-wide linkage analysis of orchard grass-sensitive childhood seasonal allergic rhinitis in Japanese families
12. Association analysis of the pituitary adenyl cyclase activating peptide gene (PACAP) on chromosome 18p11 with schizophrenia and bipolar disorders
13. Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia
14. Mutation and association analysis of the 5′ region of the dopamine D3 receptor gene in schizophrenia patients: identification of the Ala38Thr polymorphism and suggested association between DRD3 haplotypes and schizophrenia
15. Identification of a polymorphism in the promoter region of DRD4associated with the human novelty seeking personality trait
16. Identification of a novel polymorphism of the human dopamine transporter (DAT1) gene and the significant association with alcoholism
17. The 5′ region of the tryptophan hydroxylase gene: mutation search and association study with alcoholism
18. Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history
19. Associations between decay-accelerating factor polymorphisms and allergic respiratory diseases
20. Species differences in cannabinoid receptor 2 (CNR2 gene): identification of novel human and rodent CB2 isoforms, differential tissue expression and regulation by cannabinoid receptor ligands
21. Expression profiling of genes related to asthma exacerbations
22. Support for association of the PPP3CC gene with schizophrenia
23. Failure to confirm association between AKT1 haplotype and schizophrenia in a Japanese case–control population
24. ADAM33 polymorphisms are associated with asthma susceptibility in a Japanese population
25. Association between polymorphisms in the SPINK5 gene and atopic dermatitis in the Japanese
26. Haplotype analysis of a 100 kb region spanning TNF–LTA identifies a polymorphism in the LTA promoter region that is associated with atopic asthma susceptibility in Japan
27. An association study of asthma and total serum immunoglobin E levels for Toll-like receptor polymorphisms in a Japanese population
28. Identification of missense mutation in the IL12B gene: lack of association between IL12B polymorphisms and asthma and allergic rhinitis in the Japanese population
29. No evidence for association between the — 112G/A polymorphism of UGRP1 and childhood atopic asthma
30. A Val227Ala polymorphism in the peroxisome proliferator activated receptor α (PPARα) gene is associated with variations in serum lipid levels
31. New polymorphisms of haematopoietic prostaglandin D synthase and human prostanoid DP receptor genes
32. Mutation screening of interferon regulatory factor 1 gene (IRF-1) as a candidate gene for atopy/asthma
33. Lack of association of atopy/asthma and the interleukin-4 receptor α gene in Japanese
34. Association of asthma and the interleukin-4 promoter gene in Japanese
35. Subclinical cerebral lesion accumulation on serial magnetic resonance imaging (MRI) in patients with hypertension: risk factors
36. No evidence for association between CNTF null mutant allele and schizophrenia
37. Screening for 22q11 deletions in a schizophrenia population
38. Association of ZNF74 gene genotypes with age-at-onset of schizophrenia
39. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan
40. Frequency of the fragile X syndrome in Japanese mentally retarded males
41. A fragile X female with Down syndrome
42. Genome-wide association study identifies a potent locus associated with human opioid sensitivity
43. DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia
44. A nonsynonymous polymorphism in cannabinoid CB2 receptor gene is associated with eating disorders in humans and food intake is modified in mice by its ligands
45. Species differences in cannabinoid receptor 2 (CNR2gene): identification of novel human and rodent CB2 isoforms, differential tissue expression and regulation by cannabinoid receptor ligands
46. Subclinical cerebral lesion accumulation on serial magnetic resonance imaging (MRI) in patients with hypertension: risk factors
47. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations
48. PICK1 is not a susceptibility gene for schizophrenia in a Japanese population: Association study in a large case–control population
49. Chromosomal assignments of the human endothelin family genes: the endothelin-1 gene (EDN1) to 6p23-p24, the endothelin-2 gene (EDN2) to 1p34, and the endothelin-3 gene (EDN3) to 20q13.2-q13.3
50. Involvement of cannabinoid CB2 receptor in alcohol preference in mice and alcoholism in humans
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