Zobrazeno 1 - 10
of 180
pro vyhledávání: '"F.M. van Bockxmeer"'
Publikováno v:
Journal of Lipid Research, Vol 41, Iss 3, Pp 481-488 (2000)
Abstract: We examined the effect of genetic polymorphisms of proteins regulating intrahepatic processing of apolipoprotein B-100 (apoB) and the supply of neutral lipids to the liver on the hepatic secretion of very low density lipoprotein (VLDL) apoB
Externí odkaz:
https://doaj.org/article/2d16b85b019b4fa0bf10f49879c8657b
Publikováno v:
Journal of Lipid Research, Vol 39, Iss 9, Pp 1752-1758 (1998)
We aimed to examine the effect of genetic polymorphisms of apolipoprotein B-100 (apoB) signal peptide and apolipoprotein E (apoE) on the hepatic secretion of very low density lipoprotein (VLDL) apoB in 29 men with visceral obesity. We studied apoB se
Externí odkaz:
https://doaj.org/article/6d00fcd9ba2f464b99ea63832bc7aa36
Autor:
Jing Pang, F.M. van Bockxmeer, Dick C. Chan, David R. Sullivan, John R. Burnett, P. H. R. Barrett, Gerald F. Watts, Trevor A. Mori
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 26:1140-1145
Increased arterial stiffness is closely linked with raised blood pressure that contributes substantially to enhanced risk of coronary heart disease in high risk individuals with familial hypercholesterolaemia (FH). Omega-3 fatty acid (ω3-FA) supplem
Autor:
Christopher Chen, Wasim Uddin, Jose C. Navarro, John Gommans, F.M. van Bockxmeer, R. Schmidt, Qilong Yi, Udaya K. Ranawaka, John W. Eikelboom, Kennedy R. Lees, Osvaldo P. Almeida, Andrew H. Ford, Stefano Ricci, Graeme J. Hankey, Denis Xavier
Publikováno v:
Stroke. 44:2232-2239
Background and Purpose— High plasma total homocysteine (tHcy) has been associated with cognitive impairment but lowering tHcy with B-vitamins has produced equivocal results. We aimed to determine whether B-vitamin supplementation would reduce tHcy
Autor:
F.M. van Bockxmeer, Robert Bender, Glenn Edwards, Damon A. Bell, Jenny McMahon, Gerald F. Watts, Amanda J. Hooper, John R. Burnett
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 49:534-537
Background Familial hypercholesterolaemia (FH) is an inherited disorder characterized by increased serum low-density lipoprotein (LDL)-cholesterol concentrations and premature atherosclerotic cardiovascular disease. The majority of people with FH are
Autor:
F.M. van Bockxmeer, Osvaldo P. Almeida, Andrew H. Ford, Graeme J. Hankey, Paul Norman, L. Flicker
Publikováno v:
Molecular Psychiatry
High total plasma homocysteine (tHcy) has been associated with cognitive impairment in later life, but it is unclear if this association is causal or is due to confounding. The C677T polymorphism of the 5,10 methylenetetrahydrofolate reductase gene (
Autor:
Richard J.N. Allcock, Barry Iacopetta, F.M. van Bockxmeer, Nicole M. Warrington, Jonathan Golledge, L. Smallwood, Paul Norman, Lyle J. Palmer
Publikováno v:
British Journal of Surgery. 95:1239-1244
Background Increased matrix metalloproteinase (MMP) 9 activity has been implicated in the formation of abdominal aortic aneurysm (AAA). The aim was to explore the association between potentially functional variants of the MMP-9 gene and AAA. Methods
Publikováno v:
HIV Medicine. 9:677-680
Objectives Host genetic factors implicated in AIDS dementia complex (ADC) were studied. Methods DNA from ADC patients (n=56), unselected HIV-seropositive patients (n=112, 171, 185 and 204) and HIV-seronegative controls (n=204, 60, 60, 96 and 624) wer
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 24:2188-2191
Objective— We examined the influence of genetic variation of the ATP-binding cassette (ABC) transporter G8 on apolipoprotein B (apoB) kinetics in overweight/obese men. Methods and Results— Very low–density lipoprotein (VLDL) and low-density lip
Autor:
Richard J.N. Allcock, L. Smallwood, F.M. van Bockxmeer, Jonathan Golledge, Paul Norman, Barry Iacopetta, Nicole M. Warrington, Lyle J. Palmer
Publikováno v:
Europe PubMed Central
Objective: To investigate associations between two polymorphisms of the matrix metalloproteinase-2 gene (MMP2) and the incidence and progression of abdominal aortic aneurysm (AAA). Methods: Cases and controls were recruited from a trial of screening