(Q43004431)

English

Genotypes 677TT and 677CT+1298AC of methylenetetrahydrofolate reductase are associated with the severity of ulcerative colitis in central China

scientific article published in May 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

Genotypes 677TT and 677CT+1298AC of methylenetetrahydrofolate reductase are associated with the severity of ulcerative colitis in central China (English)

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

author name string

M Chen

1

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

B Xia

2

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

R M Rodriguez-Gueant

3

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

M Bigard

4

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

J-L Gueant

5

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

language of work or name

0 references

publication date

1 May 2005

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

54

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

5

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

733-734

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

26 May 2018

Review article: inherited thrombophilia in inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

26 May 2018

Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

26 May 2018

Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with inflammatory bowel disease, and its clinical implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

26 May 2018

High prevalence of hyperhomocysteinemia related to folate deficiency and the 677C-->T mutation of the gene encoding methylenetetrahydrofolate reductase in coastal West Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

16 August 2018

Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

16 August 2018

Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

16 August 2018

Increased prevalence of methylenetetrahydrofolate reductase C677T variant in patients with IBD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1774509

16 August 2018

Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informed consent

1 reference

https://pubmed.ncbi.nlm.nih.gov/15831933

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/GUT.2004.062539

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 November 2017

ResearchGate publication ID

0 references

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