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Zeitschriftenartikel zum Thema "Lipoproteins Analysis"

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Huang, Haibin, Mingqun Lin, Xueqi Wang, Takane Kikuchi, Heather Mottaz, Angela Norbeck, and Yasuko Rikihisa. "Proteomic Analysis of and Immune Responses to Ehrlichia chaffeensis Lipoproteins." Infection and Immunity 76, no. 8 (May 19, 2008): 3405–14. http://dx.doi.org/10.1128/iai.00056-08.

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ABSTRACT Ehrlichia chaffeensis is an obligately intracellular gram-negative bacterium and is the etiologic agent of human monocytic ehrlichiosis (HME). Although E. chaffeensis induces the generation of several cytokines and chemokines by leukocytes, E. chaffeensis lacks lipopolysaccharide and peptidoglycan. Bioinfomatic analysis of the E. chaffeensis genome, however, predicted genes encoding 15 lipoproteins and 3 posttranslational lipoprotein-processing enzymes. The present study showed that by use of multidimensional liquid chromatography followed by tandem mass spectrometry, all predicted li
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Polyakov, L. M., D. V. Sumenkova, R. A. Knyazev, and L. E. Panin. "The analysis of interaction between lipoproteins and steroid hormones." Biomeditsinskaya Khimiya 57, no. 3 (2011): 308–13. http://dx.doi.org/10.18097/pbmc20115703308.

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Using the methods of ultracentrifugation, gel-filtration and fluorescence quenching, we demonstrated, that plasma lipoproteins bind steroid hormones and can therefore play a role of their active transport form in an organism. High density lipoproteins have revealed the highest affinity to steroids for. It has been found, that protein component of lipoproteins takes part in the formation of lipoprotein-steroid complex. The apolipoprotein A-I, the main protein component of high density lipoproteins, is responsible for binding of steroid hormones. The calculated constants formation of the complex
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März, W., R. Siekmeier, H. Scharnagl, U. B. Seiffert, and W. Gross. "Fast lipoprotein chromatography: new method of analysis for plasma lipoproteins." Clinical Chemistry 39, no. 11 (November 1, 1993): 2276–81. http://dx.doi.org/10.1093/clinchem/39.11.2276.

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Abstract Fast lipoprotein chromatography (FLPC) is a novel method for quantifying lipoproteins. Plasma proteins are separated by fast-flow gel filtration. Lipoproteins are detected by post-column derivatization with an enzymatic cholesterol reagent. FLPC resolves very-low-, low-, and high-density lipoproteins (VLDL, LDL, and HDL, respectively) and completely separates apolipoprotein Al- and apolipoprotein B-containing lipoproteins. CVs for VLDL-cholesterol, LDL-cholesterol, and HDL-cholesterol are 5.8%, 2.0%, and 1.9%, respectively. We compared FLPC with a combined ultracentrifugation and prec
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Remans, Kim, Ken Vercammen, Josselin Bodilis, and Pierre Cornelis. "Genome-wide analysis and literature-based survey of lipoproteins in Pseudomonas aeruginosa." Microbiology 156, no. 9 (September 1, 2010): 2597–607. http://dx.doi.org/10.1099/mic.0.040659-0.

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Pseudomonas aeruginosa is a Gram-negative opportunistic pathogen able to cause acute or chronic infections. Like all other Pseudomonas species, P. aeruginosa has a large genome, >6 Mb, encoding more than 5000 proteins. Many proteins are localized in membranes, among them lipoproteins, which can be found tethered to the inner or the outer membrane. Lipoproteins are translocated from the cytoplasm and their N-terminal signal peptide is cleaved by the signal peptidase II, which recognizes a specific sequence called the lipobox just before the first cysteine of the mature lipoprotein. A majorit
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Storf, Stefanie, Friedhelm Pfeiffer, Kieran Dilks, Zhong Qiang Chen, Saheed Imam, and Mechthild Pohlschröder. "Mutational and Bioinformatic Analysis of Haloarchaeal Lipobox-Containing Proteins." Archaea 2010 (2010): 1–11. http://dx.doi.org/10.1155/2010/410975.

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A conserved lipid-modified cysteine found in a protein motif commonly referred to as a lipobox mediates the membrane anchoring of a subset of proteins transported across the bacterial cytoplasmic membrane via the Sec pathway. Sequenced haloarchaeal genomes encode many putative lipoproteins and recent studies have confirmed the importance of the conserved lipobox cysteine for signal peptide processing of three lipobox-containing proteins in the model archaeonHaloferax volcanii. We have extended thesein vivoanalyses to additionalHfx. volcaniisubstrates, supporting our previousin silicoprediction
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Mahmoodi, Bakhtawar, Ron Gansevoort, Friso Muntinghe, Robin Dullaart, Hanneke Kluin-Nelemans, Nic Veeger, Inge van Schouwenburg, and Karina Meijer. "Lipid levels do not influence the risk of venous thromboembolism." Thrombosis and Haemostasis 108, no. 11 (2012): 923–29. http://dx.doi.org/10.1160/th12-06-0426.

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SummaryStudies on the association between lipid profile and venous thromboembolism (VTE) are inconsistent. This could be caused by classical lipoproteins being inferior to apolipoproteins as markers for VTE risk. Therefore, we examined whether apolipoproteins are more strongly related to VTE than lipoproteins. For this analysis we used the PREVEND prospective community based observational cohort study. Levels of apolipoprotein A1 (ApoA1), apolipoprotein B (ApoB), total cholesterol (TC), high-density lipoprotein (HDL), non-HDL, low-density lipoprotein (LDL), triglycerides (TG), lipoprotein(a),
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Trentalance, A., G. Bruscalupi, L. Conti Devirgiliis, S. Leoni, M. T. Mangiantini, L. Rossini, S. Spagnuolo, and S. K. Erickson. "Changes in lipoprotein binding and uptake by hepatocytes during rat liver regeneration." Bioscience Reports 9, no. 2 (April 1, 1989): 231–41. http://dx.doi.org/10.1007/bf01116000.

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The binding and uptake of cholesterol enriched lipoproteins by isolated hepatocytes was decreased at 16 hours after partial hepatectomy, with a tendency to return to control values as the regeneration proceeds. The number of lipoprotein binding sites of total cellular membranes remained similar to control at 16 and 24 hours. The plasma lipoprotein pattern, determined by electrophoretic analysis, showed a lower per cent of very low density lipoproteins (VLDL) and a higher per cent of low density lipoproteins (LDL) at 16 and 24 hours post-partial hepatectomy. At these times, plasma lecithin: cho
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Edelberg, J. M., M. Weissler, and S. V. Pizzo. "Kinetic analysis of the effects of glycosaminoglycans and lipoproteins on urokinase-mediated plasminogen activation." Biochemical Journal 276, no. 3 (June 15, 1991): 785–91. http://dx.doi.org/10.1042/bj2760785.

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The glycosaminoglycans (GAGs) heparin, heparan sulphate and chondroitin 6-sulphate stimulate the rate of urokinase activation of human plasminogen. Kinetic analysis of plasminogen activation demonstrates that heparin, heparan sulphate and chondroitin 6-sulphate increased the catalytic rate (Kcat) by 5.3-, 3.5- and 2.5-fold respectively. These stimulatory GAGs had no effect on the affinity of urokinase for plasminogen, since the Km of the reaction is unaltered by the GAGs. The GAGs may enhance the rate of plasminogen activation through an interaction with the catalytic domain of the urokinase,
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Asmal, A. Cader. "Kinetic Analysis of Lipoproteins." JAMA: The Journal of the American Medical Association 253, no. 7 (February 15, 1985): 978. http://dx.doi.org/10.1001/jama.1985.03350310060015.

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Asmal, A. C. "Kinetic analysis of lipoproteins." JAMA: The Journal of the American Medical Association 253, no. 7 (February 15, 1985): 978–79. http://dx.doi.org/10.1001/jama.253.7.978.

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Dissertationen zum Thema "Lipoproteins Analysis"

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Barrett, P. Hugh R. "The kinetic analysis and computer modelling of lipoprotein metabolism in man." Title page, table of contents and abstract only, 1989. http://web4.library.adelaide.edu.au/theses/09PH/09phb274.pdf.

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Leigh, Spencer A. "Functional analysis of the mycoplasma fermentans P29 adhesin." free to MU campus, to others for purchase, 2000. http://wwwlib.umi.com/cr/mo/fullcit?p9999300.

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Chandra, Richa. "The analysis of triglyceride-rich lipoproteins in human serum for clinical studies." [College Station, Tex. : Texas A&M University, 2006. http://hdl.handle.net/1969.1/ETD-TAMU-1745.

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Kung, Sin-yan. "Analysis of vitellogenin gene (MeVg2) from the sand shrimp (Metapenaeusensis): gene organization andexpression study." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B30497292.

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Huang, Haibin. "Analysis of lipoproteins, outer membrane proteins, and genetic diversities of Ehrlichia and Anaplasma species." Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1155154668.

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Ayyobi, Amir Fardad. "Analysis of lecithin : cholesterol acyltransferase (LCAT) protein structure and its influence on binding to plasma lipoproteins." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0014/NQ56499.pdf.

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YAMADA, SHIN'YA, KATSUMI YAMANAKA, SHIN'YA ISHIHARA, HISATAKA SAKAKIBARA, TAKA-AKI KONDO, MASASHI FURUTA, and MASARU MIYAO. "The Relationship of High-Density Lipoprotein Cholesterol to Obesity, Drinking and Smoking Habits." Nagoya University School of Medicine, 1993. http://hdl.handle.net/2237/17534.

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Conway, James Patrick. "Systems biology analysis of macrophage foam cells finding a novel function for Peroxiredoxin I /." Connect to text online, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=case1156961185.

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Thesis (Ph. D.)--Case Western Reserve University, 2006.<br>[School of Medicine] Department of Physiology and Biophysics. Includes bibliographical references. Available online via OhioLINK's ETD Center.
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Amigó, Grau Núria. "Lipoprotein analysis by 2d diffusion-ordered 1h-nmr spectroscopy." Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/665148.

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The need for predictors of cardiovascular disease is increasing due to the pandemic levels that metabolic disorders are achieving. One of the main areas where new biomarkers can be looked for is in the lipids and lipoproteins field. NMR spectroscopy appears to be a suitable analytical tool to develop novel methodologies, which will aid in the assessment and management of cardiovascular events and cardio-metabolic disease, due to its sensitivity to the lipoprotein content and size, robustness and the possibility of automation. Part of the research presented in this thesis is focused on the dev
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Douvris, Adrianna. "Functional Analysis of the TRIB1 Locus in Coronary Artery Disease." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20115.

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The TRIB1 locus (8q24.13) is a novel locus associated with plasma TGs and CAD risk. Trib1 is a regulator of MAPK activity, and has been shown to regulate hepatic lipogenesis and VLDL production in mice. However, the functional relationship between common SNPs at the TRIB1 locus and plasma lipid traits is unknown; TRIB1 has not been identified as an eQTL. This cluster of SNPs falls within an intergenic region 25kb to 50kb downstream of the TRIB1 coding region. By phylogenetic footprinting analysis and DNA genotyping, we identified an evolutionarily conserved region (CNS1) within the risk locus
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Bücher zum Thema "Lipoproteins Analysis"

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National Cholesterol Education Program (U.S.). Working Group on Lipoprotein Measurement. Recommendations on lipoprotein measurement: From the Working Group on Lipoprotein Measurement. [Bethesda, MD]: National Institutes of Health, National Heart, Lung and Blood Institute, 1995.

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Workshop on Lipoprotein Heterogeneity (1986 Rockville, Md.). Proceedings of the Workshop on Lipoprotein Heterogeneity, Rockville, Maryland, September 29, 30, and October 1, 1986. Edited by Lippel Kenneth. [Bethesda, Md.]: U.S. Dept. of Health and Human Services, National Institutes of Health, 1987.

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Walker, Janice. Analysis of the long term effect of physical activity level on high-density and low-density lipoproteins. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1992.

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Kurt, Widhalm, and Naito Herbert K, eds. Detection and treatment of lipid and lipoprotein disorders of childhood: Proceedings of the Third International Atherosclerosis Conference, held in Vienna, Austria, April 4-9, 1983. New York: Liss, 1985.

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Tagg, Lesley J. Molecular analysis of a lipoprotein, TpN24-28, from Treponema pallidum subspecies. Birmingham: University of Birmingham, 1993.

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Weyer, Karl Aloys. Isolierung und Sequenzierung der Proteinuntereinheiten des photosynthetischen Reaktionszentrums von Rhodopseudomonas viridis: Entdeckung und Strukturaufklärung des Lipoprotein-Membranankers der Cytochrom-Untereinheit. Gauting bei München: Intemann, 1987.

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A, Converse Carolyn, and Skinner E. Roy, eds. Lipoprotein analysis. Oxford [England]: IRL Press at Oxford University Press, 1992.

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1934-, Perkins Edward George, ed. Analyses of fats, oils, and lipoproteins. Champaign, Ill: American Oil Chemists' Society, 1991.

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Lipoprotein Analysis: Practical Approach. I. R. L. P., 1992.

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Nader, Rifai, Warnick G. Russell, and Dominiczak Marek H, eds. Handbook of lipoprotein testing. Washington, DC: AACC Press, 1997.

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Buchteile zum Thema "Lipoproteins Analysis"

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de Lalla, Oliver F., and John W. Gofman. "Ultracentrifugal Analysis of Serum Lipoproteins." In Methods of Biochemical Analysis, 459–78. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/9780470110171.ch16.

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Fruchart, Jean-Charles, Monique Koffigan, Catherine Fievet, Claude Cachera, Ngoc Vu Dac, Jean-Claude Gesquière, and Pascal Puchois. "Molecular Analysis of Lipoproteins: Clinical Applications." In Advances in Experimental Medicine and Biology, 225–31. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-1268-0_33.

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Yang, Chao-Yuh, Natalia V. Valentinova, Manlan Yang, Zi-Wei Gu, John R. Guyton, and Antonio M. Gotto. "Immunological Approach to Study the Structure of Oxidized Low Density Lipoproteins." In Methods in Protein Structure Analysis, 327–34. Boston, MA: Springer US, 1995. http://dx.doi.org/10.1007/978-1-4899-1031-8_28.

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Burillo, Elena, Jesus Vazquez, and Inmaculada Jorge. "Quantitative Proteomics Analysis of High-Density Lipoproteins by Stable 18O-Isotope Labeling." In Methods in Molecular Biology, 139–56. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-405-0_11.

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Thomas, C. E. "Nitrone spin traps as reagents for the study of oxidative modification of low density lipoproteins: Implications for atherosclerosis." In Analysis of Free Radicals in Biological Systems, 127–43. Basel: Birkhäuser Basel, 1995. http://dx.doi.org/10.1007/978-3-0348-9074-8_10.

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Lehmann, Rainer. "Lipoprotein Analysis." In Clinical and Forensic Applications of Capillary Electrophoresis, 113–44. Totowa, NJ: Humana Press, 2001. http://dx.doi.org/10.1007/978-1-59259-120-6_7.

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King, Sarah M., and Ronald M. Krauss. "Ion Mobility Lipoprotein Analysis." In Contemporary Cardiology, 537–44. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-56514-5_28.

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Angelberger, P. "Lipoprotein Labeling and Analysis Techniques." In Radiolabeled Blood Elements, 221–30. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2462-5_32.

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Sasaki, Jun. "Molecular Analysis of Apolipoprotein A-I and E Mutants in Japan." In Lipoprotein Metabolism and Atherogenesis, 44–47. Tokyo: Springer Japan, 2000. http://dx.doi.org/10.1007/978-4-431-68424-4_7.

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Miyake, Yasuko, Taku Yamamura, Keiko Oi, and Hideshi Hori. "Molecular Analysis on the LDL Receptors in Two Patients with Homozygous Familial Hypercholesterolemia." In Lipoprotein Metabolism and Atherogenesis, 59–61. Tokyo: Springer Japan, 2000. http://dx.doi.org/10.1007/978-4-431-68424-4_12.

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Konferenzberichte zum Thema "Lipoproteins Analysis"

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Robbins, David L., John P. Nolan, James H. Jett, Richard A. Keller, and Larry A. Sklar. "Analysis of individual lipoproteins and liposomes." In BiOS '97, Part of Photonics West, edited by Gerald E. Cohn and Steven A. Soper. SPIE, 1997. http://dx.doi.org/10.1117/12.274353.

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Damirchi, Behzad, Amir Rouhollahi, Salman Sohrabi, and Seyyed Mahdi Nemati Mehr. "Modeling and Stability Analysis of Truncated High Density Lipoprotein (HDL) System Using Martini Coarse Grain Technique." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-64808.

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Lipoproteins are biochemical compounds containing both proteins and lipids. These particles carry chemicals like cholesterol and triglycerides that are not soluble in aqueous solutions. This paper presents modeling of lipoprotein system using coarse grain molecular dynamics technique and stability analysis of this system in a water solution like blood. A high density lipoprotein (HDL) that consists of two annular monomers is modeled. Also there are lipid bilayers located in center of the rings, so the whole HDL and lipid bilayers are called lipoprotein system. First, all atom model is provided
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Aursnes, I., P. Smith, and H. Arnesen. "EPIDEMIOLOGICAL ASPECTS OF ANTITHROMBIN-III, SELENIUM AND LIPOPROTEIN COMPONENTS IN CORONARY DISEASE." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643030.

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The known risk factors for coronary disease can only “explain” a proportion of the incidence of the disease. Looking for supplementary risk factors we thus selected for detailed study both a group of patients with normal levels of risk factors (normo-tensives, non-smokers with normal serum cholesterol) and a group with high conventional risk factors, comparing both groups with an age and sex matched control group. Subgroups were formed by individuals aged below (young) and above (old) 60 years.Total- and HDL-cholesterol, apo-lipoproteins A-I and B and triglycerides showed co-variation with eac
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Prabhu, Anmiv S., Alejandro Moraga, Michael Cecchini, Rafael Mulero, Stephen Olsen, Young I. Cho, and Min Jun Kim. "Synthetic Nanoscale Architectures for Lipoprotein Separation." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-66535.

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Current low density lipoprotein (LDL) apheresis procedures are expensive and time consuming. We report here a novel technique to detect and separate nanoparticles using solid state nanopores. Our technique relies on the resistive pulse phenomenon used in coulter counters. We used a 150nm diameter nanopore to detect nanoparticles that closely resembled HDL and LDL in terms of their size and surface charge. Statistical analysis of the translocation data revealed that our setup preferentially allowed the particles resembling HDL to pass thorough while restricting the translocation of the particle
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Adelita, Sela Putri, Eti Poncorini Pamungkasari, and Bhisma Murti. "Meta Analysis: The Effect of High-Intensity Interval Training on Low Density Lipoprotein Level in Patients with Type 2 Diabetes Melitus." In The 7th International Conference on Public Health 2020. Masters Program in Public Health, Universitas Sebelas Maret, 2020. http://dx.doi.org/10.26911/the7thicph.05.42.

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ABSTRACT Background: High intensity interval training (HIIT) is a protocol of short work intervals of vigorous to high intensity interspersed with active or passive (cessation of movement) recovery periods. HIIT has been employed since the mid-20th century to improve athletic exercise performance. Regular exercise reduces elevated low-density lipoprotein (LDL), atherosclerosis formation, and risk factors of cardiovascular disease (CVD). This study aimed to examine the effect of high-intensity interval training on low density lipoprotein level in patients with type 2 diabetes mellitus (DM). Sub
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Zinman, B., C. Mathieu, S. Kaspers, HJ Woerle, and D. Fitchett. "Empagliflozin reduces mortality in analyses adjusted for control of blood pressure, low density lipoprotein cholesterol and HbA1c over time." In Diabetes Kongress 2018 – 53. Jahrestagung der DDG. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1641901.

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Roan, Esra, Alex Bada, and Randy Buddington. "Mechanical Characterization of Preterm Neonate Pig Liver as a Function of High-Density Lipoprotein (HDL)." In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-39363.

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Elastography, a non-invasive imaging modality, utilizes mechanical properties of tissue as markers for disease diagnosis or staging. In the case of liver, there have been a number of studies focusing on the relationship between elastic mechanical properties and underlying disease, i.e. fibrosis and cirrhosis. In summary, these studies indicate the feasibility of elastographic tools in detecting liver diseases such as fibrosis and steatosis. There have not been any studies looking at the mechanical properties of the preterm neonate liver to date, which is important, because preterm neonates are
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Hassall, D. C., R. F. G. Booth, A. C. Honey, and J. F. Martin. "EXTRAVASCULAR INJURY CAUSES FOAM CELL FORMATION, ACCUMULATION OF CHOLESTEROL (C) and CHOLESTEROL ESTER (CE) IN THE CAROTID ARTERY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643414.

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In atherosclerotic arterial tissue, cholesterol is delivered to smooth muscle cells by low-density lipoprotein (LDL) and to macrophages via modified LDL. The reasons for accumulation of excess lipid are unknown although increased uptake of C and CE occurs in regions of arterial de-endothelialisation. We now report that the positioning of a silastic collar containing saline around the outside of arteries induces accumulation of C and CE within those tissues. 9 rabbits were separated into 3 groups, each group was fed a normal laboratory chow, 2 groups were supplemented with lg/day cholesterol; t
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Scheefers, H., A. Kobus, and R. Geyer. "CARBOHYDRATE COMPOSITION AND LECTIN BINDING AFFINITIES OF HUMAN PLACENTAL TISSUE FACTOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643737.

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Tissue factor (TF) is a widely distibuted membrane glycoprotein and the most potent trigger of bloodcoagulation. It serves as an essential cofactor for the activation of Factor IX and X by Factor Vll/VIIa.TF is a lipoprotein composed of a phospholipid portion and a glycosylated apoprotein (apo-TF). The procoagulant activity of bovine brain TF is inhibited bythe lectin Con A indicating that the carbohydrates of TF might play a functional role in its interactionwith Factor Vll/VIIa.In the present study apo-TF was purified from human placenta by repeated SDS-PAGE to a purity of 95%. The carbohydr
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Weigensberg, B. I., M. Alavi, S. Moore, J. O. Lough, H. Riml, and M. H. Lee. "PROTEOGLYCAN IN AORTIC WHITE MURAL THROMBUS AND IN RESULTING THROMBOATHEROSCLEROTIC LESIONS IN RABBITS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643408.

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Thromboatherosclerotic lesions in normolipidemic rabbits may contain variable amounts of lipid but the cause of this variable lipid content is not understood. Proteoglycan (PG) has been implicated in the trapping of lipoproteins in atherosclerosis. The object of this investigation was to study the quantity and quality of PG and glycosaminoglycan (GAG ) in early white mural thrombus induced with an indwelling catheter in the aorta of the rabbit as it evolves into thrombo atherosclerosis and to determine if the Alcian Blue stainable PG correlates with lipid accumulation. Lesions were compared wi
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Berichte der Organisationen zum Thema "Lipoproteins Analysis"

1

Cheng, Wenke, Julia Boettner, Tina Fischer-Schaepman, Sarah Werner, Angela Kricke, Holger Thiele, and Petra Buettner. High-density lipoprotein Cholesterol Efflux Capacity and the Risk of Cardiovascular Diseases: A Systematic Review and Meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, July 2021. http://dx.doi.org/10.37766/inplasy2021.7.0006.

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2

Wang, Zeng-mian. Association between serum lipoprotein levels and cognitive impairment in acute cerebral infarction: a protocol for systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review Protocols, April 2020. http://dx.doi.org/10.37766/inplasy2020.4.0018.

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3

Wang, Zeng-mian. Association between serum lipoprotein levels and neurological function in patients with acute ischemic stroke: a protocol of systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, April 2020. http://dx.doi.org/10.37766/inplasy2020.4.0043.

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