Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts. (Q33490988)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19657388%20AND%20SRC:MED&resulttype=core&format=json

4 February 2020

title

Lack of association between genetic polymorphisms in enzymes associated with folate metabolism and unexplained reduced sperm counts (English)

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4 February 2020

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3

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Luis B Barreiro

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Ken McElreavey

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12

Anu Bashamboo

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Jean-Pierre Siffroi

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Sandra Chantot-Bastaraud

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object named as

Sandra Chantot-Bastaraud

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author name string

Celia Ravel

1

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Isabelle Aknin-Seifer

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Jerome Pfeffer

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Isabelle Berthaut

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E Emmanuelle Mathieu

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Jacqueline Mandelbaum

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language of work or name

English

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publication date

6 August 2009

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volume

4

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issue

8

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page(s)

e6540

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Creative Commons Attribution 4.0 International

4 February 2020

copyright license

start time

6 August 2009

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

21 June 2018

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The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

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Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

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The human Y chromosome and male infertility

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A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

21 June 2018

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A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 June 2018

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Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

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Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks

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Folinic acid in the treatment of human male infertility

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Komrower Lecture. Molecular basis of phenotype expression in homocystinuria

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

21 June 2018

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High frequency (71%) of cystathionine β-synthase mutation G307S in Irish homocystinuria patients

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5,10-methylenetetrahydrofolate reductase (MTHFR) 677C-->T and 1298A-->C mutations are associated with DNA hypomethylation

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MTRR and MTHFR polymorphism: link to Down syndrome?

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Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.

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Molecular basis of phenotype expression in homocystinuria

21 January 2018

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Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility

21 January 2018

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MTHFR C677T polymorphism associates with unexplained infertile male factors

21 January 2018

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Mutation C677T in the methylenetetrahydrofolate reductase gene is associated with male infertility in an Indian population

21 January 2018

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Associations of MTHFR DNMT3b 4977 bp deletion in mtDNA and GSTM1 deletion, and aberrant CpG island hypermethylation of GSTM1 in non-obstructive infertility in Indian men.

21 January 2018

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C677T methylenetetrahydrofolate reductase polymorphism interferes with the effects of folic acid and zinc sulfate on sperm concentration

21 January 2018

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The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy

21 January 2018

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Infertility in 5,10-methylenetetrahydrofolate reductase (MTHFR)-deficient male mice is partially alleviated by lifetime dietary betaine supplementation

21 January 2018

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Identification of a Y chromosome haplogroup associated with reduced sperm counts

21 January 2018

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Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring

21 January 2018

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12 December 2020

Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR)

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12 December 2020

Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility

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12 December 2020

Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia

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12 December 2020

10.1371/JOURNAL.PONE.0006540

Identifiers

DOI

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4 February 2020

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4 February 2020

PubMed publication ID

19657388

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