Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients - Wikidata - awgldk - TriplyDB

Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients

Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients

http://www.wikidata.org/entity/Q36569149

about

Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.Role of ApoB-516C/T promoter gene polymorphism in the risk of Hepatitis C virus infection in Egyptian patients and in gender susceptibility.

P2860

Q36249248-D1CC9117-D858-48CB-AD63-A4737609D180 Q39131373-03F0221C-688B-4D5C-B94B-74ED3609606C

P2860

Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients

http://www.wikidata.org/entity/Q36569149

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@ast

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@en

type

label

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@ast

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@en

prefLabel

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@ast

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@en

P1433

Q36569149-62AD9A4D-4142-434D-BDB5-678DF37C7088

P1476

Q36569149-C14A798C-D9C2-4397-8DBE-EE6280070515

P2093

Q36569149-2A336A76-0191-4E36-BC08-32C5534EA99A

Q36569149-2B76E437-4362-4F49-8D06-EBDA0B60EEBC

Q36569149-5BB4EAC2-0314-4A13-BBFE-367E9F062279

Q36569149-DA99E82E-8AFC-4123-96BB-CEBA33558665

Q36569149-EA12B082-0FDF-4A86-86D9-880228FF0B5E

Q36569149-FD577C74-7711-4D8A-9D71-880EC0841F55

Q36569149-FD9CFECC-B458-48AE-BC0F-C6B8CF91A217

P2860

Q36569149-034E9CF1-2972-4215-B8B4-7D92298CF144

Q36569149-05F761DF-26D6-4CD2-8DA5-1F8DB3796633

Q36569149-14C57F4D-9FED-4DBA-A463-E87A8944F438

Q36569149-18070F86-E855-4853-BD89-8E376C5D24AC

Q36569149-1F80EDA5-87A8-4DCC-8294-1AF8FCC25DB2

Q36569149-29FBF98B-4D6A-4205-92DE-8CE38AE2AF6C

Q36569149-2B2062B5-7871-4F3F-927E-2D5824971DDF

Q36569149-36C2A84A-9BE7-4E39-B0BA-3BFE54609733

Q36569149-3F70FED6-0F61-45F2-9633-80740716E4F7

Q36569149-4532D8E5-8177-4E84-BA7C-2E07A16FD489

P304

Q36569149-1DCA78B3-DB89-4D06-9442-F8CD35F33362

P31

Q36569149-C43F09CD-883F-454F-A7EE-FB5E2C412A62

P356

Q36569149-4210FA19-C1B4-4715-9497-A3F679607525

P433

Q36569149-9C7B31DA-994A-4A02-8398-91BCC70C9C9F

P478

Q36569149-33395D66-6824-43CD-9A6C-9CE16A3C6F7A

P577

Q36569149-89FF5D70-87C1-4B71-B5AD-DF445CE272DB

P5875

Q36569149-35EB04CC-79C3-452D-9B5E-1F944EE02B20

P698

Q36569149-3622424C-2313-44A6-82F5-6D681DCC8B0C

P921

Q36569149-701DA350-9BEE-4B73-AAA8-FC8E216927D0

P932

Q36569149-F5B96998-865E-4CA7-9587-24CDD8270D82

P356

CARDIOVASCMED.29134

P1433

Research in cardiovascular medicine

P1476

Polymorphisms in NOS3, MTHFR, ...... ic Lesions in Iranian Patients

@en

P2093

Mahbobeh Kazemi

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

Massomeh Mirjalili

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

Mehdi Hadadzadeh

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

Mehri Khatami

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

Mohammad Mehdi Heidari

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

Pegah Malekzadeh

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

Sahar Mahamed

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

P2860

Genomics of Cardiovascular Disease

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Familial hypercholesterolemia in St-Petersburg: the known and novel mutations found in the low density lipoprotein receptor gene in Russia

A common variant of endothelial nitric oxide synthase (Glu298Asp) is associated with collateral development in patients with chronic coronary occlusions.

Molecular biology of 5,10-methylenetetrahydrofolate reductase

Endothelial nitric oxide synthase (eNOS) 4b/a gene polymorphisms and coronary artery disease: evidence from a meta-analysis.

Nutrition, physical activity, and cardiovascular disease: an update.

Evidence for association of a common variant of the endothelial nitric oxide synthase gene (Glu298-->Asp polymorphism) to the presence, extent, and severity of coronary artery disease.

Polymorphisms in endothelial nitric oxide synthase and carotid artery atherosclerosis.

Endothelial nitric oxide synthase gene polymorphisms and cardiovascular disease: a HuGE review.

P304

e29134

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

P31

scholarly article

P356

10.5812/CARDIOVASCMED.29134

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

P433

1

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

P478

5

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

P577

2015-12-23T00:00:00Z

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

P5875

284705592

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

P698

26878010

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

P921

atherosclerosis

P932

4749848

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