𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A meta-analysis of association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and hypertension

✍ Scribed by Qian, Xueqing; Lu, Zhigang; Tan, Miao; Liu, Hongliang; Lu, Daru

Book ID
110027214
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
144 KB
Volume
15
Category
Article
ISSN
1018-4813

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Association between methylenetetrahydrof
Association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and age of onset in schizophrenia
✍ Maria Vares; Peter Saetre; Hong Deng; Guiqing Cai; Xiehe Liu; Thomas Hansen; Hen πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 163 KB πŸ‘ 2 views

## Abstract Different lines of evidence indicate that methylenetetrahydrofolate reductase (__MTHFR__) functional gene polymorphisms, causative in aberrant folate–homocysteine metabolism, are associated with increased vulnerability to several heritable developmental disorders. Opposing views are exp

Association of the C677T polymorphism in
Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss
✍ Yasue Uchida; Saiko Sugiura; Fujiko Ando; Hiroshi Shimokata; Tsutomu Nakashima πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 88 KB

## Abstract ## Objectives/Hypothesis: To investigate the recently reported association of the C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with sudden sensorineural hearing loss (SSNHL), we analyzed data from a community‐based Japanese population. ## Study Design: N

Association of the C677T and A1298C poly
Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene in patients with essential tremor in Turkey
✍ Ali Sazci; Emel Ergul; Kemal Bayulkem πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 69 KB

## Abstract Essential tremor (ET) is a most common human movement disorder of unknown etiology. Previous reports have shown that the C677T polymorphism of methylenetetrahydrofolate reductase gene has been associated with neurodegenerative disorders. To investigate the role of methylenetetrahydrofol