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G Utermann

Showing results (101-110 of 208) with videos related to

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The Journal of Clinical Investigation|January 1, 1989
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesisH G Kraft, H J Menzel, F Hoppichler, et al.
Orvosi Hetilap|September 23, 1990
[Plasma concentration of lipoprotein(a) and distribution of its subtypes in the healthy population of Hungary]A Császár, L Romics, C Lackner, et al.
The Journal of Biological Chemistry|June 5, 1998
Physical interaction of ApoE with amyloid precursor protein independent of the amyloid Abeta region in vitroS Hass, F Fresser, S Köchl, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Atherosclerosis|August 23, 1996
The relative electrophoretic mobility of apo(a) isoforms depends on the gel system: proposal of a nomenclature for apo(a) phenotypesH G Kraft, A Lingenhel, G Bader, et al.
Human Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasmaG Utermann, H G Kraft, H J Menzel, et al.
Atherosclerosis|August 1, 1984
The conformation of apolipoprotein E isoforms in phospholipid complexes and their interaction with human Hep G2 cellsD L Cassel, M C Phillips, P Rostron, et al.
Nature Genetics|April 7, 1999
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISHM Erdel, M Hubalek, A Lingenhel, et al.
International Journal of Oncology|November 18, 2000
Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemiaH C Duba, W Hilbe, A Mehringer, et al.
American Journal of Medical Genetics|April 15, 2000
Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7)J Löffler, B Utermann, H C Duba, et al.
Pageof 21

Showing results (101-110 of 208) with videos related to

Sort By:
Pageof 21
The Journal of Clinical Investigation|January 1, 1989
Changes of genetic apolipoprotein phenotypes caused by liver transplantation. Implications for apolipoprotein synthesisH G Kraft, H J Menzel, F Hoppichler, et al.
Orvosi Hetilap|September 23, 1990
[Plasma concentration of lipoprotein(a) and distribution of its subtypes in the healthy population of Hungary]A Császár, L Romics, C Lackner, et al.
The Journal of Biological Chemistry|June 5, 1998
Physical interaction of ApoE with amyloid precursor protein independent of the amyloid Abeta region in vitroS Hass, F Fresser, S Köchl, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Atherosclerosis|August 23, 1996
The relative electrophoretic mobility of apo(a) isoforms depends on the gel system: proposal of a nomenclature for apo(a) phenotypesH G Kraft, A Lingenhel, G Bader, et al.
Human Genetics|January 1, 1988
Genetics of the quantitative Lp(a) lipoprotein trait. I. Relation of LP(a) glycoprotein phenotypes to Lp(a) lipoprotein concentrations in plasmaG Utermann, H G Kraft, H J Menzel, et al.
Atherosclerosis|August 1, 1984
The conformation of apolipoprotein E isoforms in phospholipid complexes and their interaction with human Hep G2 cellsD L Cassel, M C Phillips, P Rostron, et al.
Nature Genetics|April 7, 1999
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISHM Erdel, M Hubalek, A Lingenhel, et al.
International Journal of Oncology|November 18, 2000
Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemiaH C Duba, W Hilbe, A Mehringer, et al.
American Journal of Medical Genetics|April 15, 2000
Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7)J Löffler, B Utermann, H C Duba, et al.
Pageof 21