Five common gene variants identify elevated genetic risk for coronary heart disease. - Wikidata - wikimedia - TriplyDB

Five common gene variants identify elevated genetic risk for coronary heart disease.

Five common gene variants identify elevated genetic risk for coronary heart disease.

http://www.wikidata.org/entity/Q34724256

about

Investigation of KIF6 Trp719Arg in a case-control study of myocardial infarction: a Costa Rican population Submicroscopic deletions of 11q24-25 in individuals without Jacobsen syndrome: re-examination of the critical region by high-resolution array-CGH Sequencing and analysis of a South Asian-Indian personal genome Gene variants associated with ischemic stroke: the cardiovascular health study Single nucleotide polymorphisms associated with coronary heart disease predict incident ischemic stroke in the atherosclerosis risk in communities study Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study Child development and molecular genetics: 14 years later No association of VAMP8 gene polymorphisms with glioma in a Chinese Han population No evidence for cardiac dysfunction in Kif6 mutant mice Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).Myosin individualized: single nucleotide polymorphisms in energy transduction.Polymorphisms associated with both noncardioembolic stroke and coronary heart disease: vienna stroke registry.KIF6 p.Trp719Arg Testing to Assess Risk of Coronary Artery Disease and/or Statin Response.The contribution of a 9p21.3 variant, a KIF6 variant, and C-reactive protein to predicting risk of myocardial infarction in a prospective study.Survival bias and drug interaction can attenuate cross-sectional case-control comparisons of genes with health outcomes. An example of the kinesin-like protein 6 (KIF6) Trp719Arg polymorphism and coronary heart disease.A common KIF6 polymorphism increases vulnerability to low-density lipoprotein cholesterol: two meta-analyses and a meta-regression analysis Genome-wide association study of swine farrowing traits. Part II: Bayesian analysis of marker data.Genetic variants in the KIF6 region and coronary event reduction from statin therapy.Applying genome-wide gene-based expression quantitative trait locus mapping to study population ancestry and pharmacogenetics The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease.Statin pharmacogenomics: opportunities to improve patient outcomes and healthcare costs with genetic testing Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.Myosin heavy chain 15 is associated with bovine pulmonary arterial pressure.Novel KIF6 polymorphism increases susceptibility to type 2 diabetes mellitus and coronary heart disease in Han Chinese men GOSR2 Lys67Arg is associated with hypertension in whites.Development of a learning-oriented computer assisted instruction designed to improve skills in the clinical assessment of the nutritional status: a pilot evaluation VAMP-8 gene variant is associated with increased risk of early myocardial infarction.Genotyping and meta-analysis of KIF6 Trp719Arg polymorphism in South Indian Coronary Artery Disease patients: A case-control study.Genetic predictors for cardiovascular disease in hispanics.Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease Investigation of Pathogenic Genes in Chinese sporadic Hypertrophic Cardiomyopathy Patients by Whole Exome Sequencing A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies.Emerging risk factors for cardiovascular diseases: Indian context Genetic determinants of response to statins.Insights into the PX (phox-homology) domain and SNX (sorting nexin) protein families: structures, functions and roles in disease.Pharmacogenetics of statins: achievements, whole-genome analyses and future perspectives.The Trp719Arg polymorphism of the KIF6 gene and coronary heart disease risk: systematic review and meta-analysis.Polymorphism of the palladin gene and cardiovascular outcome in patients with atherosclerosis.Investigation of KIF6 Trp719Arg gene polymorphism in a case-control study of coronary artery disease and non-fatal myocardial infarction in the Eastern Province of Saudi Arabia.

P2860

Q21091102-4D081E3F-6A06-44D4-86C0-0A08BE3958DC Q21202043-5CFE8843-86BF-47AC-BFAE-2E4FFF3243DD Q21266697-24A56520-0D6A-46AD-9A88-E4383F772789 Q24599770-F17A5C1D-7878-48C7-B73A-7E0B16C452B1 Q24650973-4DA48F57-B6B7-4359-A1C3-88E77B30164B Q24657646-F1D624F9-E0B8-4684-8A7D-710E3E223E75 Q26853446-3D1614BE-0F30-4C45-8DE8-071903C6A0CB Q28383460-76736EA2-7337-4B30-87CA-F89260F37CC2 Q28485242-B307003D-6903-410D-85C7-3B1A165D7AC0 Q30499949-AAA16978-7260-48C5-958D-3B09EFDCEE8D Q33387469-D15A763C-79FB-455A-9CDB-DD724057F0E3 Q33540368-F57E4F11-DE10-46E9-90AD-C66A57C4890F Q33637520-EE9D0C3B-DF38-4777-8516-DB736BAE2D86 Q33727868-C2E1001C-7C27-4C72-9FB2-3E70A66F1006 Q33846673-DCBA840D-C04B-4313-9BD8-75076583A400 Q33854825-CBE0474F-24C8-4C74-9223-A7CF9B37823C Q34117006-3FE49BB5-9259-4E2C-BA51-8C5EB324DA42 Q34268862-C0B0BB6B-153E-47AE-AE96-04FB7BF6E52B Q34467745-AA226A96-851F-4E57-B3FB-7989253E2A7C Q34539515-3D1E45B8-94FD-466A-A576-6062EF68E6AA Q34579841-8911F3B3-E2A9-4338-B9D5-0B003298213D Q34608646-1EE265B8-9E95-414E-9534-E0550D0A5B50 Q34611998-3AD70261-8E29-4F92-8B64-D2A10C97A0BD Q34782501-E0DF0304-11D1-45FA-B9CF-AA2E6389B96B Q34979907-F2E27F69-4EEE-4F04-B51D-62FB4ECF212D Q35136694-3B5FBBED-A848-479B-8DC2-C7D78C136E01 Q35610711-5BD0B3B6-FB51-4562-B7D9-E66EA7724F6C Q35674159-8D6F1C76-5F76-42D5-AB78-7CB0B0E3D352 Q35884049-2FD30137-8EE9-4CF2-8F28-A84897EF3A8A Q35889009-71D65409-08A8-4342-A381-76DB42EB033F Q36049194-4FAD7E1C-F459-4C01-B447-8B8795AE5710 Q36287303-ED51B912-1CD8-4A8E-99DE-CC1655127B35 Q36677207-6E856E99-E069-4D5D-893A-154B1565F744 Q37201644-A28F4AE1-0480-461E-AAAE-4DCB48E06946 Q37578563-AD5D832A-0121-4A93-A41F-6AF630A60F44 Q37968311-D1DEE39A-D466-4CAE-A1E8-6B1910121C17 Q38010751-D2504750-8F40-4207-BC56-14984695E8ED Q39092864-D03CF149-EB2E-438F-934D-CDB0E25869EE Q39820137-89DCD0C7-C89C-41F1-8569-BBE67A94CB9C Q39903121-599E1877-A152-4E55-A698-71CF9F5F808B

P2860

Five common gene variants identify elevated genetic risk for coronary heart disease.

http://www.wikidata.org/entity/Q34724256

description

2007 nî lūn-bûn

@nan

2007 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

@ja

2007年論文

@yue

2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

@zh-tw

2007年论文

@wuu

name

Five common gene variants identify elevated genetic risk for coronary heart disease.

@ast

Five common gene variants identify elevated genetic risk for coronary heart disease.

@en

Five common gene variants identify elevated genetic risk for coronary heart disease.

@nl

type

label

Five common gene variants identify elevated genetic risk for coronary heart disease.

@ast

Five common gene variants identify elevated genetic risk for coronary heart disease.

@en

Five common gene variants identify elevated genetic risk for coronary heart disease.

@nl

prefLabel

Five common gene variants identify elevated genetic risk for coronary heart disease.

@ast

Five common gene variants identify elevated genetic risk for coronary heart disease.

@en

Five common gene variants identify elevated genetic risk for coronary heart disease.

@nl

P1433

Q34724256-C6EB02EB-0C16-4AB9-949B-CCBAF0B0EE4A

P1476

Q34724256-0597513E-7758-4D02-A854-411270E43D83

P2093

Q34724256-2136860A-4C08-4349-B5FA-1AB6607040ED

Q34724256-4AFA2FDC-14A2-4179-96A6-FB79ECB03549

Q34724256-510AC20A-497D-448A-B1A9-E58C97D070C9

Q34724256-5780DD53-8B1E-472D-8940-1DADE55A53C2

Q34724256-89FB7FD8-53ED-419F-8267-8E8E5E21648B

Q34724256-B02D0413-1EF4-4909-8834-E4F3C15FB70C

Q34724256-B3FAAE14-9891-45D1-96D6-3F8A6A30DED0

Q34724256-B51E5C42-2DB4-48DE-9C54-71E5D6C0E1DB

Q34724256-F8E2F253-9311-4EE4-8AE2-29670A38837A

P2860

Q34724256-1BD4FAA6-4825-4D47-A588-79D86BFF82BF

Q34724256-23CC3096-96A0-495F-8A1B-F8A9675BA0C0

Q34724256-278A3981-973F-4FB7-9FE6-20E04D83156C

Q34724256-2AEE444D-5077-476A-BA8F-990273D46F4F

Q34724256-3A6E6B25-CF94-4E6B-9385-ECA99B9878BA

Q34724256-3A95DBE7-D8B8-4104-BD76-84B9A9BAC5A9

Q34724256-517CB972-6706-403B-9D8B-5E105EF8B080

Q34724256-5879CE58-EC7B-4ABA-94BF-207FA59E0AD9

Q34724256-67D29270-D758-449F-9FFC-94201DCDDADC

Q34724256-6C4303D2-EA54-4A9D-887C-770447EB3DB2

P2888

Q34724256-CCE01B7B-078D-426F-B06E-87575548F986

P304

Q34724256-95F227E5-DA5B-40A3-A0F6-991E5EDB3DC3

P31

Q34724256-929A15D0-AADF-48CF-ACE8-ECF5E17B0EC6

P356

Q34724256-BD7963C8-C0DF-4D7D-BBAD-497AD8907DB5

P407

Q34724256-11FC76C8-5594-410D-A08C-0426272443DF

P433

Q34724256-7C6A320A-0C0C-45BF-A2B6-40CAC7DC1DFD

P478

Q34724256-F9853A15-9966-4BAB-A4A8-25064EE73DD7

P50

Q34724256-4F1EC0F3-F76A-43FC-9FC9-FB80388BA95D

Q34724256-BBBAAAC3-3631-4B8C-B3D0-8C39F50F847A

Q34724256-C8EFFAFC-263B-47F4-9928-F232214DD3AE

Q34724256-CB4C7AFF-18DF-4AED-87A0-486169142A44

P577

Q34724256-A55032BF-36C7-4CD4-A67F-084AE8364FE5

P5875

Q34724256-F42FB605-872B-4C01-8A4D-75C8BC9361EF

P6179

Q34724256-8E61E1F3-6E2D-4751-ADC0-B7AABD539896

P698

Q34724256-11523207-D0EF-4EB6-B19B-E06799B44DB0

P356

GIM.0B013E318156FB62

P1433

Genetics in Medicine

P1476

Five common gene variants identify elevated genetic risk for coronary heart disease.

@en

P2093

Charles M Rowland

http://www.w3.org/2001/XMLSchema#string

Dov Shiffman

http://www.w3.org/2001/XMLSchema#string

James J Devlin

http://www.w3.org/2001/XMLSchema#string

James T Willerson

http://www.w3.org/2001/XMLSchema#string

John P Kane

http://www.w3.org/2001/XMLSchema#string

Lance A Bare

http://www.w3.org/2001/XMLSchema#string

Mary J Malloy

http://www.w3.org/2001/XMLSchema#string

May M Luke

http://www.w3.org/2001/XMLSchema#string

Olga A Iakoubova

http://www.w3.org/2001/XMLSchema#string

P2860

Characterization of human palladin, a microfilament-associated protein

Vesicle-associated membrane protein 3 (VAMP-3) and VAMP-8 are present in human platelets and are required for granule secretion

All kinesin superfamily protein, KIF, genes in mouse and human

Sorting out the cellular functions of sorting nexins

Alternative projections of mortality and disability by cause 1990-2020: Global Burden of Disease Study

Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction

The Atherosclerosis Risk in Communities (ARIC) Study: design and objectives. The ARIC investigators

A common variant on chromosome 9p21 affects the risk of myocardial infarction

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

Implications of recent clinical trials for the National Cholesterol Education Program Adult Treatment Panel III guidelines

P2888

gim.0b013e318156fb62

P304

682-689

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1097/GIM.0B013E318156FB62

http://www.w3.org/2001/XMLSchema#string

P407

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

9

http://www.w3.org/2001/XMLSchema#string

P50

Eric Boerwinkle

James S. Pankow

Alanna Morrison

Stephen G. Ellis

P577

2007-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5774085

http://www.w3.org/2001/XMLSchema#string

P6179

1006189386

http://www.w3.org/2001/XMLSchema#string

P698

18073581

http://www.w3.org/2001/XMLSchema#string