Gender and single nucleotide polymorphisms in MTHFR, BHMT, SPTLC1, CRBP2, CETP, and SCARB1 are significant predictors of plasma homocysteine normalized by RBC folate in healthy adults. (Q36160345)

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English	Gender and single nucleotide polymorphisms in MTHFR, BHMT, SPTLC1, CRBP2, CETP, and SCARB1 are significant predictors of plasma homocysteine normalized by RBC folate in healthy adults.	scientific article

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9 February 2020

Gender and single nucleotide polymorphisms in MTHFR, BHMT, SPTLC1, CRBP2, CETP, and SCARB1 are significant predictors of plasma homocysteine normalized by RBC folate in healthy adults (English)

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9 February 2020

single-nucleotide polymorphism

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9 February 2020

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Andrew J Clifford

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9 February 2020

Kehui Chen

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9 February 2020

Laura McWade

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9 February 2020

Seung-Hyun Kim

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9 February 2020

Dirk M Holstege

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9 February 2020

Janel E Owens

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9 February 2020

Bitao Liu

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9 February 2020

Hans-Georg Müller

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9 February 2020

Juan F Medrano

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9 February 2020

James G Fadel

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9 February 2020

Alanna J Moshfegh

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9 February 2020

David J Baer

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9 February 2020

Janet A Novotny

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9 February 2020

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25 July 2012

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9 February 2020

Journal of Nutrition

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9 February 2020

142

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9 February 2020

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9 February 2020

1764-1771

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9 February 2020

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2 October 2017

MTHFR polymorphisms, folate intake and carcinogen DNA adducts in the lung

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2 October 2017

Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1.

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2 October 2017

Common variants of homocysteine metabolism pathway genes and risk of type 2 diabetes and related traits in Indians.

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Signaling by vitamin A and retinol-binding protein regulates gene expression to inhibit insulin responses

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2 October 2017

Impact of gene variants on sex-specific regulation of human Scavenger receptor class B type 1 (SR-BI) expression in liver and association with lipid levels in a population-based study

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Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations

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2 October 2017

The molecular basis of retinoid absorption: a genetic dissection

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2 October 2017

Quantitation of total folate in whole blood using LC-MS/MS.

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2 October 2017

Gene-gene and gene-environment interactions in mild hyperhomocysteinemia.

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Inflammation and emerging risk factors in diabetes mellitus and atherosclerosis

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2 October 2017

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2 October 2017

Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

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2 October 2017

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

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2 October 2017

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

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2 October 2017

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

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2 July 2018

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23 September 2018

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23 September 2018

Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I.

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Newborn serum retinoic acid level is associated with variants of genes in the retinol metabolism pathway

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23 September 2018

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23 September 2018

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1 reference

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1 reference

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23 September 2018

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1 reference

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5 December 2018

Racial/Ethnic Variation in the Association of Lipid-Related Genetic Variants With Blood Lipids in the US Adult Population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22833659

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Quantitative Assessment of Plasma Homocysteine as a Risk Factor for Vascular Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/22833659

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homocysteine levels in morbidly obese patients: its association with waist circumference and insulin resistance

1 reference

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12 December 2020

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inferred from PubMed ID database lookup

Methionine metabolism in mammals. Distribution of homocysteine between competing pathways

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variant of the scavenger receptor BI in humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/22833659

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene polymorphisms and low dietary intake of micronutrients in coronary artery disease

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://pubmed.ncbi.nlm.nih.gov/22833659

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.3945/JN.112.160333

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9 February 2020

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Europe PubMed Central

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9 February 2020

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9 February 2020

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