نتایج جستجو برای: apolipoprotein cii deficiency

تعداد نتایج: 160006  

Journal: :Carcinogenesis 2000
S E Andrew X S Xu A Baross-Francis L Narayanan K Milhausen R M Liskay F R Jirik P M Glazer

DNA mismatch repair (MMR) deficiency leads to an increased mutation frequency and a predisposition to neoplasia. 'Knockout' mice deficient in the MMR proteins Msh2 and Pms2 crossed with mutation detection reporter (supF, lacI and cII) transgenic mice have been used to facilitate a comparison of the changes in mutation frequency and spectra. We find that the mutation frequency was consistently h...

Journal: :Journal of lipid research 2007
Leslie K Pulawa Dalan R Jensen Alison Coates Robert H Eckel

LPL and its specific physiological activator, apolipoprotein C-II (apoC-II), regulate the hydrolysis of triglycerides (TGs) from circulating TG-rich lipoproteins. Previously, we developed a skeletal muscle-specific LPL transgenic mouse that had lower plasma TG levels. ApoC-II transgenic mice develop hypertriglyceridemia attributed to delayed clearance. To investigate whether overexpression of L...

Journal: :British medical journal 1986
A L Meredith S M Huson P W Lunt M Sarfarazi H G Harley J D Brook D J Shaw P S Harper

The close genetic linkage between the loci for apolipoprotein CII (ApoC2) and myotonic dystrophy makes ApoC2 the closest fully validated marker for prediction of myotonic dystrophy. Application to genetic counselling and presymptomatic and prenatal prediction is reported in seven families with myotonic dystrophy, including one case in which the disorder was excluded prenatally. Only one of the ...

Journal: :The Journal of Japan Atherosclerosis Society 1979

Journal: :Journal of Korean Medical Science 1998
J. Q. Kim J. Song Y. B. Park S. H. Hong

Coronary heart disease (CHD) has been considered as a multifactorial disorder with the involvement of both environmental and genetic factors. The advent of tools to investigate individual variability of DNA has allowed us to perform the association studies of candidate genes. However, an association between genetic trait and phenotypic variations is not easy to demonstrate and several reported ...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2007
Michael Torzewski Viola Ochsenhirt Andrei L Kleschyov Matthias Oelze Andreas Daiber Huige Li Heidi Rossmann Sotirios Tsimikas Kurt Reifenberg Fei Cheng Hans-Anton Lehr Stefan Blankenberg Ulrich Förstermann Thomas Münzel Karl J Lackner

BACKGROUND We have recently demonstrated that activity of red blood cell glutathione peroxidase-1 is inversely associated with the risk of cardiovascular events in patients with coronary artery disease. The present study analyzed the effect of glutathione peroxidase-1 deficiency on atherogenesis in the apolipoprotein E-deficient mouse. METHODS AND RESULTS Female apolipoprotein E-deficient mic...

2012

Twenty-four male weanling rats were randomly divided into two treatment groups, namely a copper-adequate (8 mg Cu/kg diet) or a copper-deficient (0.85 mg Cu/kg diet) group. Feed and distilled, deionized water were provided ad libitum. After 7 weeks, plasma lipid, protein and apolipoprotein concentrations of high density lipoproteins (HDL) and subfractions of HDL were determined. Significant ele...

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