Association of matrix metalloproteinase-2 gene promoter polymorphism with myocardial infarction susceptibility in a Mexican population
โ Scribed by Ivan Delgado-Enciso; Nelida A. Gonzalez-Hernandez; Luz M. Baltazar-Rodriguez; Rebeca O. Millan-Guerrero; Oscar Newton-Sanchez; Alfonso Bayardo-Noriega; Alfonso Aleman-Mireles; Irma G. Enriquez-Maldonado; Ma J. Anaya-Carrillo; Augusto Rojas-Martinez; Rocio Ortiz-Lopez
- Publisher
- Indian Academy of Sciences
- Year
- 2009
- Tongue
- English
- Weight
- 89 KB
- Volume
- 88
- Category
- Article
- ISSN
- 0022-1333
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
## Abstract A key feature in the malignant behavior of glioblastoma is the tendency to invade host brain tissue surrounding the primary tumor site. Several members of the matrix metalloproteinase family are thought to contribute to this invasive capacity. A single nucleotide polymorphism has been d
The Werner syndrome (WS) is a rare autosomal recessive progeroid syndrome characterized by the premature onset of multiple age-related disorders, including atherosclerosis, cancer, non-insulin-dependent diabetes mellitus (NIDDM), ocular cataracts and osteoporosis [Epstein et al., 1966]. The major ca