(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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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

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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

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

1 reference

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

12 December 2020

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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

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V677 mutation of methylenetetrahydrofolate reductases and cardiovascular disease in Canadian Inuit

1 reference

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

12 December 2020

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Thrombophilia as a multigenic disorder

1 reference

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

12 December 2020

based on heuristic

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Genetic risk factor for unexplained recurrent early pregnancy loss

1 reference

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

12 December 2020

based on heuristic

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Genetic selection and folate intake during pregnancy

1 reference

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

12 December 2020

based on heuristic

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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

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Cobalamin and folate deficiency: acquired and hereditary disorders in children

1 reference

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

12 December 2020

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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

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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

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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

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