Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.

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Association between polymorphisms in genes encoding methylenetetrahydrofolate reductase and the risk of Ménière's disease.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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Association between polymorphi ...... the risk of Ménière's disease.

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Association between polymorphi ...... the risk of Ménière's disease.

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Item

label

Association between polymorphi ...... the risk of Ménière's disease.

@en

Association between polymorphi ...... the risk of Ménière's disease.

@nl

prefLabel

Association between polymorphi ...... the risk of Ménière's disease.

@en

Association between polymorphi ...... the risk of Ménière's disease.

@nl

P1476

Association between polymorphi ...... the risk of Ménière's disease.

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P2093

Fujiko Ando

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Hironao Otake

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Hiroshi Shimokata

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Ken Kato

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Masaaki Teranishi

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Michihiko Sone

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Naoki Nishio

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Saiko Sugiura

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Tadao Yoshida

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Tsutomu Nakashima

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P2860

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

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

Polymorphisms in KCNE1 or KCNE3 are not associated with Ménière disease in the Caucasian population

Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3

Hearing impairment risk and interaction of folate metabolism related gene polymorphisms in an aging study.

Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study

MTHFR 677 C>T Polymorphism reveals functional importance for 5-methyltetrahydrofolate, not homocysteine, in regulation of vascular redox state and endothelial function in human atherosclerosis.

5,10-Methylenetetrahydrofolate reductase polymorphisms and leukemia risk: a HuGE minireview.

The methylenetetrahydrofolate reductase C677T mutation induces cell-specific changes in genomic DNA methylation and uracil misincorporation: a possible molecular basis for the site-specific cancer risk modification

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5-10

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scholarly article

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10.3109/01677063.2013.770510

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1-2

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P478

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2013-03-13T00:00:00Z

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23484733

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