(Q43202822)

16 November 2017

title

Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India (English)

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single-nucleotide polymorphism

16 November 2017

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Shaik Mohammad Naushad

object named as

Shaik Mohammad Naushad

series ordinal

1

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author name string

Akella Radha Rama Devi

series ordinal

2

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16 November 2017

publication date

1 January 2010

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Journal of Perinatal Medicine

16 November 2017

number of pages

7

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based on heuristic

inferred from page(s)

published in

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16 November 2017

volume

38

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16 November 2017

issue

1

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16 November 2017

page(s)

63-69

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MTHFR 677C-->T and 1298A-->C polymorphisms: evaluation of maternal genotypic risk and association with level of neural tube defect

16 November 2017

cites work

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https://api.crossref.org/works/10.1515%2FJPM.2009.119

Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

High incidence of neural-tube defects in South India

21 January 2018

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https://api.crossref.org/works/10.1515%2FJPM.2009.119

Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Evaluation of the levels of folate, vitamin B12, homocysteine and fluoride in the parents and the affected neonates with neural tube defect and their matched controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Genetic susceptibility to neural tube defect pregnancy varies with offspring phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Mechanisms of homocysteine-induced oxidative stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Effects of common polymorphisms on the properties of recombinant human methylenetetrahydrofolate reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPM.2009.119

21 January 2018

Identifiers

DOI

10.1515/JPM.2009.119

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16 November 2017

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