Association between CFL1gene polymorphisms and spina bifida risk in a California population
Open Access
- 12 March 2007
- journal article
- research article
- Published by Springer Nature in BMC Medical Genetics
- Vol. 8 (1) , 12
- https://doi.org/10.1186/1471-2350-8-12
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Neural tube defects and folate: case far from closedNature Reviews Neuroscience, 2006
- FASTSNP: an always up-to-date and extendable service for SNP function analysis and prioritizationNucleic Acids Research, 2006
- The actin depolymerizing factor n-cofilin is essential for neural tube morphogenesis and neural crest cell migrationDevelopmental Biology, 2004
- The Structure of Haplotype Blocks in the Human GenomeScience, 2002
- Prevention of Neural-Tube Defects with Folic Acid in ChinaNew England Journal of Medicine, 1999
- Maternal Vitamin Use, Genetic Variation of Infant Methylenetetrahydrofolate Reducatase, and Risk for spina BifidaAmerican Journal of Epidemiology, 1998
- Mapping of human non‐muscle type cofilin (CFL1) to chromosome 11q13 and muscle‐type cofilin (CFL2) to chromosome 14Annals of Human Genetics, 1996
- Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin SupplementationNew England Journal of Medicine, 1992
- Prevention of neural tube defects: Results of the Medical Research Council Vitamin StudyPublished by Elsevier ,1991
- Cofilin, a protein in porcine brain that binds to actin filaments and inhibits their interactions with myosin and tropomyosinBiochemistry, 1984