Precipitation of LDL with Sulphopolyanions: A Comparison of Two Methods for LDL Cholesterol Determination
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Bibliographic citation
-
In: Clinical Chemistry and Laboratory Medicine, Band 22, Ausgabe 11, Seite 781-786, 2009
- Event
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Veröffentlichung
- (where)
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Berlin
- (who)
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Humboldt-Universität zu Berlin
- (when)
-
1984
- Creator
-
Assmann, G.
Jabs, H.-U.
Nolte, W.
Schriewer, H.
- DOI
-
10.1515/cclm.1984.22.11.781
- URN
-
urn:nbn:de:kobv:11-100123488
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:49 PM CET
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Assmann, G.
- Jabs, H.-U.
- Nolte, W.
- Schriewer, H.
- Humboldt-Universität zu Berlin
Time of origin
- 1984
Other Objects (12)
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VLDL Apolipoprotein B Determination in Blood Serum Following Precipitation of LDL with Polyvinylsulphate
Lowering LDL cholesterol reduces cardiovascular risk independently of presence of inflammation
Apolipoprotein B Determination in the Dissolved Precipitate Obtained after Precipitation of LDL with Polyvinylsulphate. An Alternative Method for the Determination of LDL Apolipoprotein B without Using Ultracentrifugation
Performance of a Direct, Immunoseparation Based LDL-Cholesterol Method Compared to Friedewald Calculation and a Polyvinyl Sulphate Precipitation Method
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Die LDL-Rezeptoraktivität
Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children
Influence of E-LDL and Ox-LDL on the metabolism of ApoE, cholesterol, sphingolipids and glycosphingolipids as well as on the raft-composition in human macrophages
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Determination of LDL Cholesterol and LDL Apolipoprotein B Following Precipitation of VLDL in Blood Serum with Phosphotungstic Acid/MgCl2
Studien zur Bindungscharakteristik von Cholesterol bzw. LDL an verschiedene Chargen LDL-adsorbierender Perlzellulose
VLDL Apolipoprotein B Determination in Blood Serum Following Precipitation of LDL with Polyvinylsulphate
Lowering LDL cholesterol reduces cardiovascular risk independently of presence of inflammation
Apolipoprotein B Determination in the Dissolved Precipitate Obtained after Precipitation of LDL with Polyvinylsulphate. An Alternative Method for the Determination of LDL Apolipoprotein B without Using Ultracentrifugation
Performance of a Direct, Immunoseparation Based LDL-Cholesterol Method Compared to Friedewald Calculation and a Polyvinyl Sulphate Precipitation Method
Philips LDL 1002
Die LDL-Rezeptoraktivität
Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children
Influence of E-LDL and Ox-LDL on the metabolism of ApoE, cholesterol, sphingolipids and glycosphingolipids as well as on the raft-composition in human macrophages
LDL-Rezeptordiagnostik bei Hyperlipidämie
Grundig LDL 1000/70
Determination of LDL Cholesterol and LDL Apolipoprotein B Following Precipitation of VLDL in Blood Serum with Phosphotungstic Acid/MgCl2
Studien zur Bindungscharakteristik von Cholesterol bzw. LDL an verschiedene Chargen LDL-adsorbierender Perlzellulose
VLDL Apolipoprotein B Determination in Blood Serum Following Precipitation of LDL with Polyvinylsulphate
Lowering LDL cholesterol reduces cardiovascular risk independently of presence of inflammation
Apolipoprotein B Determination in the Dissolved Precipitate Obtained after Precipitation of LDL with Polyvinylsulphate. An Alternative Method for the Determination of LDL Apolipoprotein B without Using Ultracentrifugation
Performance of a Direct, Immunoseparation Based LDL-Cholesterol Method Compared to Friedewald Calculation and a Polyvinyl Sulphate Precipitation Method
Philips LDL 1002
Die LDL-Rezeptoraktivität
Genetic Contribution of Variants near SORT1 and APOE on LDL Cholesterol Independent of Obesity in Children
Influence of E-LDL and Ox-LDL on the metabolism of ApoE, cholesterol, sphingolipids and glycosphingolipids as well as on the raft-composition in human macrophages
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