The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene. (Q47814016)

5 February 2018

title

The human and mouse methylenetetrahydrofolate reductase (MTHFR) genes: genomic organization, mRNA structure and linkage to the CLCN6 gene. (English)

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5 February 2018

author name string

Gaughan DJ

1

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5 February 2018

Barbaux S

2

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5 February 2018

Kluijtmans LA

3

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5 February 2018

Whitehead AS

4

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5 February 2018

language of work or name

English

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publication date

1 October 2000

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5 February 2018

published in

Gene

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5 February 2018

volume

257

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5 February 2018

issue

2

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5 February 2018

page(s)

279-289

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5 February 2018

Characterization of the human aldehyde reductase gene and promoter

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ClC-6 and ClC-7 are two novel broadly expressed members of the CLC chloride channel family

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Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification

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Alternative poly(A) site selection in complex transcription units: means to an end?

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MTHFR association with arteriosclerotic vascular disease?

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

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The methylenetetrahydrofolate reductase (Mthfr) gene maps to distal mouse chromosome 4.

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Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

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7 January 2021

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

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7 January 2021

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

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The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

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Expanding the TRANSFAC database towards an expert system of regulatory molecular mechanisms

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Identification of a functional role for the 3' region of the human oestrogen receptor gene

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Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.

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Complete genomic structure of the CLCN6 and CLCN7 putative chloride channel genes(1).

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

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Sequence analysis and compositional properties of untranslated regions of human mRNAs.

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The cytoskeleton and mRNA localization

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mRNA translation: influence of the 5' and 3' untranslated regions

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Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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

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The role of the 5' untranslated region of an mRNA in translation regulation during development

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Loss of heterozygosity at the 5,10-methylenetetrahydrofolate reductase locus in human ovarian carcinomas

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

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A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

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Identifiers

DOI

1 reference

5 February 2018

PubMed ID

11080594

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5 February 2018