Gene Therapy With Lipoprotein Lipase Variant S447X
Author:
Affiliation:
1. Blackburn Cardiovascular Genetics Laboratory, Robarts Research Institute, London, Ontario, Canada
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Link
https://www.ahajournals.org/doi/pdf/10.1161/01.ATV.0000203502.01793.8d
Reference44 articles.
1. Complete Rescue of Lipoprotein Lipase–Deficient Mice by Somatic Gene Transfer of the Naturally Occurring LPL S447X Beneficial Mutation
2. Rip J Nierman MC Sierts JA Petersen W Den Oever KV Raalte DV Ross CJ Hayden MR Bakker AC Dijkhuizen P Hermens WT Twisk J Stroes E Kastelein JJ Kuivenhoven JA Meulenberg JM. Gene therapy for lipoprotein lipase deficiency: working toward clinical application. Hum Gene Ther . 2005. [Epub ahead of print].
3. Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
4. Gain-of-Function Mutations and Therapeutic Implications
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1. Lipoprotein Lipase Deficiency: Clinical, Biochemical and Molecular Characteristics in Three Patients with Novel Mutations in the LPL Gene;Folia Biologica;2014
2. Genetic polymorphism of S447X lipoprotein lipase (LPL) and the susceptibility to hypertension;Journal of Critical Care;2009-09
3. NovelLPLmutations associated with lipoprotein lipase deficiency: two case reports and a literature review;Canadian Journal of Physiology and Pharmacology;2009-03
4. Genetic Differences between the Determinants of Lipid Profile Phenotypes in African and European Americans: The Jackson Heart Study;PLoS Genetics;2009-01-16
5. Association of lipase lipoprotein polymorphisms with myocardial infarction and lipid levels;Clinical Chemical Laboratory Medicine;2007-01-01
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