Detection of a point mutation in cholesteryl ester transfer protein gene by polymerase chain reaction-mediated site-directed mutagenesis
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry,Biophysics
Reference14 articles.
1. Deficiency of serum cholesteryl-ester transfer activity in patients with familial hyperalphalipoproteinaemia
2. Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
3. Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene Mutation
4. Total deficiency of plasma cholesteryl ester transfer protein in subjects homozygous and heterozygous for the intron 14 splicing defect
5. Approach to identification of a point mutation in apo B100 gene by means of a PCR-mediated site-directed mutagenesis
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1. Study of Cholesteryl Ester Transfer Protein (CETP) I405v Genotype and Its Association with Lipid Fractions in Myocardial Infarction Patients: A Case Control Study;JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH;2014
2. Characterization of a naturally occurring new version of the cholesterol ester transfer protein (CETP) from small intestine;Molecular and Cellular Biochemistry;2003
3. Elevated HDL Cholesterol Is a Risk Factor for Ischemic Heart Disease in White Women When Caused by a Common Mutation in the Cholesteryl Ester Transfer Protein Gene;Circulation;2000-04-25
4. Skipping of Exon 14 and Possible Instability of Both the mRNA and the Resultant Truncated Protein Underlie a Common Cholesteryl Ester Transfer Protein Deficiency in Japan;Arteriosclerosis, Thrombosis, and Vascular Biology;1997-07
5. Genetic Cholesteryl Ester Transfer Protein Deficiency Is Extremely Frequent in the Omagari Area of Japan;Arteriosclerosis, Thrombosis, and Vascular Biology;1997-06
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