(Q28344711)

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The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans

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scholarly article

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The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans (English)

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7

object named as

Uri Seligsohn

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author name string

Nurit Rosenberg

1

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Mitsuru Murata

2

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Yasuo Ikeda

3

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Ohene Opare-Sem

4

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Ariella Zivelin

5

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Eli Geffen

6

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language of work or name

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publication date

March 2002

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American Journal of Human Genetics

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70

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3

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758-62

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Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

20 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

20 March 2017

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

7 April 2017

Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

29 September 2017

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

2 June 2018

Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

27 November 2018

Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=384952

27 November 2018

Pathogenicity of thermolabile methylenetetrahydrofolate reductase for vascular dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

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Thrombophilia as a multigenic disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic risk factor for unexplained recurrent early pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic selection and folate intake during pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cobalamin and folate deficiency: acquired and hereditary disorders in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent--the Nîmes Obstetricians and Haematologists Study5 (NOHA5)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between platelet glycoprotein Ibalpha genotype and ischemic cerebrovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11781870

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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