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H Funke

Showing results (101-110 of 203) with videos related to

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Human Molecular Genetics|January 1, 1995
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT geneH Wiebusch, P Cullen, J S Owen, et al.
Molecular Biology & Medicine|June 1, 1986
Polymorphisms in the apolipoprotein AI-CIII gene complexR T Coleman, P A Gonzalez, H Funke, et al.
Journal of Lipid Research|August 1, 1994
Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45-->Asn), in a Turkish patientS Lüttmann, A von Eckardstein, W Wei, et al.
Arteriosclerosis (Dallas, Tex.)|March 1, 1988
Metabolism of canine beta-very low density lipoproteins in normal and cholesterol-fed dogsM Fainaru, H Funke, J K Boyles, et al.
Journal of Cardiovascular Pharmacology|May 22, 1998
Endothelial expression of endothelin-converting enzyme-1 beta mRNA is regulated by the transcription factor Ets-1H D Orzechowski, A Günther, S Menzel, et al.
The Journal of Clinical Investigation|July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Human Mutation|January 1, 1996
Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT geneJ S Owen, H Wiebusch, P Cullen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|February 1, 1993
Glutamine/histidine polymorphism in apo A-IV affects plasma concentrations of lipoprotein(a) and fibrin split products in coronary heart disease patientsA von Eckardstein, J Heinrich, H Funke, et al.
Deutsche Medizinische Wochenschrift (1946)|September 11, 1999
[Clinical aspects and molecular genetics of the long QT-syndrome]W Haverkamp, G Mönnig, H Wedekind, et al.
Angewandte Chemie (International Ed. in English)|March 14, 2015
High ethene/ethane selectivity in 2,2'-bipyridine-based silver(i) complexes by removal of coordinated solventMatthew G Cowan, William M McDanel, Hans H Funke, et al.
Pageof 21

Showing results (101-110 of 203) with videos related to

Sort By:
Pageof 21
Human Molecular Genetics|January 1, 1995
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT geneH Wiebusch, P Cullen, J S Owen, et al.
Molecular Biology & Medicine|June 1, 1986
Polymorphisms in the apolipoprotein AI-CIII gene complexR T Coleman, P A Gonzalez, H Funke, et al.
Journal of Lipid Research|August 1, 1994
Electrophoretic screening for genetic variation in apolipoprotein C-III: identification of a novel apoC-III variant, apoC-III(Asp45-->Asn), in a Turkish patientS Lüttmann, A von Eckardstein, W Wei, et al.
Arteriosclerosis (Dallas, Tex.)|March 1, 1988
Metabolism of canine beta-very low density lipoproteins in normal and cholesterol-fed dogsM Fainaru, H Funke, J K Boyles, et al.
Journal of Cardiovascular Pharmacology|May 22, 1998
Endothelial expression of endothelin-converting enzyme-1 beta mRNA is regulated by the transcription factor Ets-1H D Orzechowski, A Günther, S Menzel, et al.
The Journal of Clinical Investigation|July 15, 1996
An intronic mutation in a lariat branchpoint sequence is a direct cause of an inherited human disorder (fish-eye disease)J A Kuivenhoven, H Weibusch, P H Pritchard, et al.
Human Mutation|January 1, 1996
Complete deficiency of plasma lecithin-cholesterol acyltransferase (LCAT) activity due to a novel homozygous mutation (Gly-30-Ser) in the LCAT geneJ S Owen, H Wiebusch, P Cullen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology|February 1, 1993
Glutamine/histidine polymorphism in apo A-IV affects plasma concentrations of lipoprotein(a) and fibrin split products in coronary heart disease patientsA von Eckardstein, J Heinrich, H Funke, et al.
Deutsche Medizinische Wochenschrift (1946)|September 11, 1999
[Clinical aspects and molecular genetics of the long QT-syndrome]W Haverkamp, G Mönnig, H Wedekind, et al.
Angewandte Chemie (International Ed. in English)|March 14, 2015
High ethene/ethane selectivity in 2,2'-bipyridine-based silver(i) complexes by removal of coordinated solventMatthew G Cowan, William M McDanel, Hans H Funke, et al.
Pageof 21