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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 24
1954 76
1955 108
1956 122
1957 143
1958 131
1959 121
1960 115
1961 129
1962 68
1963 1
1964 8
1965 13
1966 89
1967 142
1968 161
1969 197
1970 193
1971 271
1972 352
1973 319
1974 350
1975 344
1976 348
1977 381
1978 418
1979 488
1980 563
1981 595
1982 672
1983 614
1984 619
1985 620
1986 647
1987 589
1988 696
1989 650
1990 698
1991 697
1992 783
1993 702
1994 750
1995 843
1996 746
1997 756
1998 813
1999 771
2000 791
2001 726
2002 756
2003 675
2004 767
2005 820
2006 859
2007 850
2008 867
2009 926
2010 877
2011 915
2012 971
2013 1103
2014 1101
2015 1114
2016 992
2017 1001
2018 969
2019 389
2020 10
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34,481 results
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Page 1
Plasma lipoproteins: apolipoprotein structure and function.
Mahley RW, et al. J Lipid Res 1984 - Review. PMID 6099394 Free article.
Plasma lipoprotein metabolism is regulated and controlled by the specific apolipoprotein (apo-) constituents of the various lipoprotein classes. ...Specific apolipoproteins function in the regulation of lipoprotein metabolism through their involvement in the transport and redistribution of lipids among various cells and tissues, through their role as cofactors for enzymes of lipid metabolism, or through their maintenance of the structure of the lipoprotein particles. ...
Plasma lipoprotein metabolism is regulated and controlled by the specific apolipoprotein (apo-) constituents of the various lipopr
Feasibility of a plasma bioassay to assess oxidative protection of low-density lipoproteins by high-density lipoproteins.
Swertfeger DK, et al. J Clin Lipidol 2018. PMID 30244943 Free PMC article.
BACKGROUND: Traditionally, the impact of lipoproteins on vascular disease has been evaluated in light of their quantity, that is, cholesterol content, in plasma. ...As a result, attention has focused on developing plasma-based assays for other putative HDL protective functions including protecting low-density lipoproteins (LDLs) from oxidative damage. ...
BACKGROUND: Traditionally, the impact of lipoproteins on vascular disease has been evaluated in light of their quantity, that is, cho …
Hemoglobin level and lipoprotein particle size.
Hämäläinen P, et al. Lipids Health Dis 2018. PMID 29321013 Free PMC article.
The concentrations and sizes of lipoprotein subclass particles were analyzed by high-throughput nuclear magnetic resonance (NMR) spectroscopy. ...There was a strong relationship between smaller high density lipoprotein (HDL) particle size and higher hemoglobin concentration in both men and women as well as with smaller low density lipoprotein (LDL) particle size and higher hemoglobin concentration in men and women (p < 0.001; p = 0.009, p = 0.008). ...
The concentrations and sizes of lipoprotein subclass particles were analyzed by high-throughput nuclear magnetic resonance (NMR) spec …
Phospholipids in lipoproteins: compositional differences across VLDL, LDL, and HDL in pregnant women.
Rauschert S, et al. Lipids Health Dis 2019. PMID 30670033 Free PMC article.
Wilcoxon-Mann-Whitney U test and principal component analysis (PCA) were used to investigate if metabolite profiles differed between the lean/obese group and between lipoprotein species. ...Obese and lean pregnant women showed no significant differences in their lipoprotein associated metabolite profile....
Wilcoxon-Mann-Whitney U test and principal component analysis (PCA) were used to investigate if metabolite profiles differed between the lea …
Lipoprotein apheresis to treat elevated lipoprotein (a).
Waldmann E and Parhofer KG. J Lipid Res 2016 - Review. PMID 26889050 Free PMC article.
An elevated plasma concentration of lipoprotein (a) [Lp(a)] is an independent risk factor for cardiovascular disease. Life style modification and currently available drugs either fail to effectively lower plasma Lp(a) levels or do not result in clinical benefit. ...While most apheresis systems (heparin-induced extracorporeal LDL precipitation, direct adsorption of lipoproteins, lipoprotein apheresis with dextran-sulfate, lipid filtration, immunoadsorption) decrease LDL and Lp(a), Lipopac is specific and only decreases Lp(a). ...
An elevated plasma concentration of lipoprotein (a) [Lp(a)] is an independent risk factor for cardiovascular disease. Life style modi …
Current therapies for lowering lipoprotein (a).
van Capelleveen JC, et al. J Lipid Res 2016 - Review. PMID 26637277 Free PMC article.
Lipoprotein (a) [Lp(a)] is a human plasma lipoprotein with unique structural and functional characteristics. Lp(a) is an assembly of two components: a central core with apoB and an additional glycoprotein, called apo(a). ...
Lipoprotein (a) [Lp(a)] is a human plasma lipoprotein with unique structural and functional characteristics. Lp(a) is an assem
Oxidized lipoproteins.
Bruckdorfer KR. Baillieres Clin Endocrinol Metab 1995 - Review. PMID 8593122
The understanding of the role of lipoprotein oxidation is still incomplete. Much is still to be learned about the mechanism of action of oxidized lipoproteins on different types of cell, as well as the origin of the oxidation process, and how it links to the situation in vivo. ...
The understanding of the role of lipoprotein oxidation is still incomplete. Much is still to be learned about the mechanism of action …
Asymmetrical flow field-flow fractionation for improved characterization of human plasma lipoproteins.
Bria CRM, et al. Anal Bioanal Chem 2019. PMID 30470915 Free PMC article.
Additionally, lipoprotein size distributions are determined using analytical scale AF4 coupled with multiangle light scattering (MALS) and dynamic light scattering (DLS) detectors. These developments position SP-AF4 as a sample preparation method of choice for lipoprotein biomarker characterization and identification. ...
Additionally, lipoprotein size distributions are determined using analytical scale AF4 coupled with multiangle light scattering (MALS …
Development of an integrated model for analysis of the kinetics of apolipoprotein B in plasma very low density lipoproteins, intermediate density lipoproteins, and low density lipoproteins.
Beltz WF, et al. J Clin Invest 1985. PMID 4031063 Free PMC article.
To quantify more precisely the metabolism of apolipoprotein B (apo B) in human beings, an integrated model was developed for the analysis of the isotope kinetics of apo B in very low density lipoproteins (VLDL), intermediate density lipoproteins (IDL), and low density lipoproteins (LDL). ...The model appears to be consistent with specific activity curves from the current triple-isotope studies and with present concepts of lipoprotein physiology; it also can be used to quantify pathways of lipoprotein apo B transport in normal and abnormal states....
To quantify more precisely the metabolism of apolipoprotein B (apo B) in human beings, an integrated model was developed for the analysis of …
[THE LIPOLYSIS IN PHYLOGENETICALLY EARLY LIPOPROTEINS OF LOW DENSITY AND MORE LATER LIPOPROTEINS OF VERY LOW DENSITY: FUNCTION AND DIAGNOSTIC VALUE OF APOE AND APOC-III].
Rozhkova TA, et al. Klin Lab Diagn 2015 - Review. PMID 27032246 Russian.
According to phylogenetic theory of general pathology, the function of low density lipoproteins (LDL) and hydrolysis of triglycerides (TG) in them under the effect of hepatic glycerol hydrolase apoC-III (HGH) developed at much earlier stages of phylogenesis than functioning of insulin-dependent phylogenetically late very low density lipoproteins (VLDL). For millions ofyears, lipolysis and HGH+apoC-III have activated transfer of polyenic fatty acids (FA) in the form of cholesteryl polyesters (CLE) from high density lipoproteins (HDL) to linoleic and linolenic LDL under the effect of cholesteryl ester transfer protein. ...
According to phylogenetic theory of general pathology, the function of low density lipoproteins (LDL) and hydrolysis of triglycerides …
34,481 results
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