(Q46121033)

English

The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T among G6PD deficient individuals from Western Iran

scientific article published on 15 February 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T among G6PD deficient individuals from Western Iran (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Factor V Leiden

1 reference

based on heuristic

inferred from title

Prothrombin G20210A

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

author name string

Hadi Mozafari

1

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Azadeh Heidarpour

3

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Mahsa Fallahi

4

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Adraiana Muniz

5

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

publication date

15 February 2009

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Molecular Biology Reports

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

36

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

8

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

2361-2364

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

Methylenetetrahydrofolate reductase polymorphism (C677T), hyperhomocysteinemia, and risk of ischemic cardiovascular disease and venous thromboembolism: prospective and case-control studies from the Copenhagen City Heart Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Portal vein thrombosis: what is the role of genetics?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of G6PD deficiency in Cyprus

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fulminant Rocky Mountain spotted fever. Its pathologic characteristics associated with glucose-6-phosphate dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in coagulation factor genes and their impact on arterial and venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

International Committee for Standardization in Haematology: Recommended Screening Test for Glucose-6-Phosphate Dehydrogenase (G-6-PD) Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sickle-cell trait, thalassemia, G-6-PD deficiency and puerperal pulmonary embolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish Jews

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of common methylenetetrahydrofolate reductase gene mutation on coronary artery disease in familial hypercholesterolemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase polymorphism associated with susceptibility to coronary heart disease in Chinese type 2 diabetic patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of factor V Leiden and G6PD 1311 silent mutations in Dalmatian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine and atherothrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of the G6PD nt 1311 C/T polymorphism in English and Iranian populations: relevance to studies of X chromosome inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19219640

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S11033-009-9458-X

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

release_fijkbj6mzzc3xn4ixvsldz2pv4

1 reference

https://api.fatcat.wiki/v0/release/fijkbj6mzzc3xn4ixvsldz2pv4

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 December 2017

http://europepmc.org/abstract/MED/19219640

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