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Division Of Genetic Diagnosis Institute Of Medical Science The University Of Tokyo | 論文
- ADAM33 polymorphisms are associated with aspirin-intolerant asthma in the Japanese population
- The Small Heat Shock Protein αB-Crystallin Inhibits Differentiation-Induced Caspase 3 Activation and Myogenic Differentiation(Molecular and Cell Biology)
- Gender-specific haplotype association of collagen α2 (XI) gene in ossification of the posterior longitudinal ligament of the spine
- Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?
- Association of positional and functional candidate genes FGF1, FBN2, and LOX on 5q31 with intracranial aneurysm
- COL6A1, the Candidate Gene for Ossification of the Posterior Longitudinal Ligament, Is Associated With Diffuse Idiopathic Skeletal Hyperostosis in Japanese
- Akaike's information criterion for a measure of linkage disequilibrium
- 4 Polymorphisms in the prostaglandin E2 receptor subtype 2 gene confer susceptibility to aspirin-intolerant asthma(II. Asthma Genetics)
- Genomewide linkage analysis of familial prostate cancer in the Japanese population
- Current Topics in Pharmacological Research on Bone Metabolism : Promyelotic Leukemia Zinc Finger (PLZF) and Tumor Necrosis Factor-α-Stimulated Gene 6 (TSG-6) Identified by Gene Expression Analysis Play Roles in the Pathogenesis of Ossification of the Post
- Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in children
- A frameshift variant of CYP2C8 was identified in a patient who suffered from rhabdomyolysis after administration of cerivastatin
- Characterization of six base pair deletion in the putative HNF 1-binding site of human PXR promoter
- The genetics of intracranial aneurysms
- Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis
- Mitochondrial DNA polymorphisms in Yunnan nationalities in China
- Genome-wide association analysis of copy number variations in subarachnoid aneurysmal hemorrhage
- Next-generation sequencing : impact of exome sequencing in characterizing Mendelian disorders
- Meta-analysis of genetic association studies : methodologies, between-study heterogeneity and winner's curse