Sequence diversity in 36 candidate genes for cardiovascular disorders.
about
Prediction of deleterious nonsynonymous single-nucleotide polymorphism for human diseasesHuman non-synonymous SNPs: server and surveySelecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibriumGenome-wide association studies for common diseases and complex traitsHighly multiplexed genotyping of coronary artery disease-associated SNPs using MALDI-TOF mass spectrometry.Use of molecular variation in the NCBI dbSNP database.New polymorphisms in the interleukin-10 gene--relationships to myocardial infarction.Relative effects of mutability and selection on single nucleotide polymorphisms in transcribed regions of the human genomeSingle nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populationsEtiology and pathophysiology of stroke as a complex trait.Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populationsMining for SNPs: putting the common variants--common disease hypothesis to the test.Genetic variation in coronary heart disease and myocardial infarction: methodological overview and clinical evidence.A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequenceSequence diversity in genes of lipid metabolismPharmacogenomics of multigenic diseases: sex-specific differences in disease and treatment outcome.Novel technology and the development of pharmacogenetics within the pharmaceutical industry.Inducible nitric oxide synthase promoter polymorphism affords protection against cognitive dysfunction after carotid endarterectomyExtensive and breed-specific linkage disequilibrium in Canis familiaris.Apolipoprotein molecular variation in Moroccan Berbers: pentanucleotide (TTTTA)n repeat in the LPA gene and APOE-C1-C2 gene cluster.Robust and accurate single nucleotide polymorphism genotyping by dynamic allele-specific hybridization (DASH): design criteria and assay validation.A cSNP map and database for human chromosome 21.Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity.Genetic variation in mRNA coding sequences of highly conserved genes.cDNA microarray analysis of vascular gene expression after nitric oxide donor infusions in rats: implications for nitrate tolerance mechanisms.Matters of the heart transcriptome: a brief history of cardiovascular genomics.SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease.Genetic variation in COL17A1 and the development of bullous pemphigoid.Detection of regulatory variation in mouse genes.A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm.Angiotensin II type 2 receptor gene polymorphism and cardiovascular phenotypes: the GLAECO and GLAOLD studies.Genetic Variation at the Chromosome 16 Chemokine Gene Cluster: Development of a Strategy for Association Studies in Complex Disease
P2860
Q28708958-FC87C94A-0391-4475-BAE1-48E151E3D739Q29547603-B88E6CB3-9229-4E10-AC7F-754A12EE94F3Q29615642-1652F351-7959-4535-8F55-0286544A5F82Q29615822-88569309-C249-4D08-8987-373E540B6F63Q30711968-B0E72FC7-0F72-43FF-8D62-C90C68868DFDQ30829552-D2C4D323-ACA7-4548-81AF-69BF591AA0ECQ31898120-07747897-DBA4-4985-B08F-1E01493648AFQ33344253-EAA84F3D-99E3-41D8-B1E9-B7DAAC76AFADQ33679056-544FC219-A688-414D-AFA4-BE14AC760F11Q33909698-78EC52A6-0D15-451E-9E0D-FA748DC818C5Q34065857-CAD3E81B-A2D0-44F1-830E-A96F515444EBQ34146133-A1DA131F-7B75-4C61-A4D5-32FE3E75B59DQ34189877-132055C1-7E83-4365-8149-B4FFD4372AEEQ34189907-DBED6F84-D88B-4F41-B878-198221ED0CB6Q35031627-C53E8D3B-9840-41DB-8F29-F04698114A13Q35032382-EE260BB3-2731-4543-B91A-D329976D512AQ35805941-ADEED92D-D35B-4194-BE9A-C457EC8B5B36Q36186950-0527FAD6-7C31-404B-B685-0915B0F711B4Q37172702-7BA05246-4EF7-4FB9-982B-6D52466561B6Q37694592-440C3D7F-4094-4D0A-AE9B-ADB46034C28FQ39047716-0DECE0BF-E1F3-4D28-BDDB-F7BC3C314051Q40414773-63969D38-F14D-4A5E-AABF-97B4F0A9FB21Q40414860-AF621F3A-762D-4040-8A58-883CE003C3C3Q40416831-9D54E35D-B2BF-4F61-8FCD-E6AC12F59E8FQ40791331-342804BE-F0F2-4467-ADE8-D0343B6DB3CCQ40815231-EFD0FB04-1715-4B40-B050-792A371BCE8CQ41892733-759714B8-30E3-490B-B30A-CAA230E722ADQ42761037-C6C6D9A1-D040-4C6C-B62C-46329E8C5A0FQ44670795-D958E773-32E9-451B-AE12-FAF3E970B5BDQ48031026-384FF522-36A7-4C9D-9100-A0CB33493D45Q48456623-6145D184-8036-4EB5-9846-DE76E6A1E78FQ52001789-4EAD6259-CA01-4E84-A5C8-511B641C1FECQ52954250-F28E83E8-4989-4255-BF92-3CC915F36138Q57436406-3FB5D2AC-A739-4246-B4ED-F027DBE0BA87
P2860
Sequence diversity in 36 candidate genes for cardiovascular disorders.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Sequence diversity in 36 candidate genes for cardiovascular disorders.
@en
type
label
Sequence diversity in 36 candidate genes for cardiovascular disorders.
@en
prefLabel
Sequence diversity in 36 candidate genes for cardiovascular disorders.
@en
P2093
P2860
P356
P1476
Sequence diversity in 36 candidate genes for cardiovascular disorders.
@en
P2093
Arveiler D
Herrmann SM
P2860
P304
P356
10.1086/302448
P407
P577
1999-07-01T00:00:00Z