𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women

✍ Scribed by Kobashi, Gen ;Yamada, Hideto ;Asano, Toshimichi ;Nagano, Shunsuke ;Hata, Akira ;Kishi, Reiko ;Fujimoto, Seiichiro ;Kondo, Kiyotaro


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
83 KB
Volume
93
Category
Article
ISSN
0148-7299

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A common haplotype for the 677T thermola
✍ M. Linnebank; A. Homberger; U. Nowak-GΓΆttl; H. G. Koch πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 18 KB

The common polymorphic transition 677C>T in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene causes a thermolabile enzyme variant. This variant is associated with moderate hyperhomocysteinemia, a risk factor for vascular disease and thrombophilia. Up to now, it remained unclear if the therm

Association of the C677T and A1298C poly
✍ 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

No association between a common single n
✍ Sarah Curran; Patrick Bolton; Kinga Rozsnyai; Andreas Chiocchetti; Sabine M. Kla πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 142 KB πŸ‘ 1 views

## Abstract The Autism Genome Project (AGP) Consortium recently reported genome‐wide significant association between autism and an intronic single nucleotide polymorphism marker, rs4141463, within the MACROD2 gene. In the present study we attempted to replicate this finding using an independent cas