A novel transgenic mouse model of CBS-deficient homocystinuria does not incur hepatic steatosis or fibrosis and exhibits a hypercoagulative phenotype that is ameliorated by betaine treatment
Open Access
- 30 November 2010
- journal article
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 101 (2-3), 153-162
- https://doi.org/10.1016/j.ymgme.2010.06.010
Abstract
No abstract availableKeywords
Funding Information
- Jerome Lejeune Foundation
- NICHD (P30 HD04024-39, HD17449)
- Special Products U.K.
- William R. Hummel Homocystinuria Research Fund
- Denver Children's Hospital (6703)
- NIH (HL65217)
- Wellcome Trust International Senior Fellowship in Biomedical Science in Central Europe (070255/Z/03/Z)
- Research Project from the Ministry of Education, Youth and Sports of the Czech Republic (MSM0021620806)
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