(Q34032296)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Neural tube defects and a disturbed folate dependent homocysteine metabolism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

N M van der Put

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

publication date

1 September 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Obstetrics Gynecology and Reproductive Biology

10 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

57-61

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

Heterogeneity of neural tube defects in Europe: the significance of site of defect and presence of other major anomalies in relation to geographic differences in prevalence

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The embryonic development of mammalian neural tube defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The role of nutrition in neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Altered folate and vitamin B12 metabolism in families with spina bifida offspring

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Absorption of pteroylpolyglutamates in mothers of infants with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Folic acid absorption in women with a history of pregnancy with neural tube defect.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Neural-tube defects and derangement of homocysteine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Risk of neural tube defect-affected pregnancy is associated with a block in maternal one-carbon metabolism at the level of N-5-methyltetrahydrofolate:homocysteine methyltransferase.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Folate levels and neural tube defects. Implications for prevention

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Vitamin B12 and anencephaly

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The methylfolate axis in neural tube defects: in vitro characterisation and clinical investigation.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Impaired regeneration of monoglutamyl tetrahydrofolate leads to cellular folate depletion in mothers affected by a spina bifida pregnancy.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Amniotic fluid B12 and folate levels associated with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Neural-tube defects are associated with low concentrations of cobalamin (vitamin B12) in amniotic fluid

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Genetic control of cobalamin binding in normal and mutant cells: Assignment of the gene for 5-methyltetrahydrofolate:L-homocysteine S -methyltransferase to human chromosome 1

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Cloning, mapping and RNA analysis of the human methionine synthase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Methionine synthase and neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The effects of folic acid supplementation on plasma total homocysteine are modulated by multivitamin use and methylenetetrahydrofolate reductase genotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The structure and properties of methylenetetrahydrofolate reductase from Escherichia coli suggest how folate ameliorates human hyperhomocysteinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Spina bifida, 677T-->C mutation, and role of folate

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Methylenetetrahydrofolate reductase and neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Relevance to spina bifida of mutated methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

MTHFR 677C-->T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0301-2115%2800%2900426-7

7 January 2021

10.1016/S0301-2115(00)00426-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10986435%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference