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「"Brookes AJ"[Author]」の検索結果

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Genetic association analysis: lessons from the study of Alzheimers disease.

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction.

Sequence variants of IDE are associated with the extent of beta-amyloid deposition in the Alzheimer's disease brain.

Human neuropeptide Y signal peptide gain-of-function polymorphism is associated with increased body mass index: possible mode of function.

Linkage disequilibrium patterns vary substantially among populations.

Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene.

Lower rate of genomic variation identified in the trans-membrane domain of monoamine sub-class of Human G-Protein Coupled Receptors: the Human GPCR-DB Database.

Genotyping by dynamic heating of monolayered beads on a microheated surface.

Genetic analysis of the RNASEL gene in hereditary, familial, and sporadic prostate cancer.

Haplotype block structures show significant variation among populations.

Quantitative trait loci near the insulin-degrading enzyme (IDE) gene contribute to variation in plasma insulin levels.

Complex SNP-related sequence variation in segmental genome duplications.

DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applications.

Integrative annotation of 21,037 human genes validated by full-length cDNA clones.

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

Genetic variation in CTNNA3 encoding alpha-3 catenin and Alzheimer's disease.

Variants of CYP46A1 may interact with age and APOE to influence CSF Abeta42 levels in Alzheimer's disease.

Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism.

Common variants of ACE contribute to variable age-at-onset of Alzheimer's disease.

A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.

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