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G Wolfram

Showing results (191-200 of 252) with videos related to

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Klinische Wochenschrift|November 15, 1991
Identification of a 76-year-old patient with compound heterozygous familial hypercholesterolemia by haplotype analysis of the LDL receptor geneH J Fischer, H Schuster, C Keller, et al.
Human Genetics|April 1, 1993
Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemiaH Schuster, H J Fischer, C Keller, et al.
European Journal of Clinical Pharmacology|January 1, 1986
Effect of acarbose on carbohydrate tolerance during administration of a fibre-free formula diet on healthy subjectsI E Walter-Sack, A Ittner-Holland, G Wolfram, et al.
Hearing Research|August 1, 1997
Transcripts encoding three types of guanylyl-cyclase-coupled trans-membrane receptors in inner ear tissues of guinea pigsG Krause, A M Meyer zum Gottesberge, G Wolfram, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1988
Evidence for a nonspecific factor interfering in the radioimmunoassay of somatoliberin-like immunoreactivity in human seminal plasmaM Losa, G Wolfram, J Schopohl, et al.
European Journal of Clinical Investigation|August 1, 1987
Inhibition of muscular amino acid release by lipid infusion in manM Wicklmayr, K Rett, B Schwiegelshohn, et al.
Biological Psychiatry|May 1, 1990
Disturbances in the hypothalamo-pituitary-adrenal and other neuroendocrine axes in bulimiaM M Fichter, K M Pirke, J Pöllinger, et al.
Clinical Genetics|August 1, 1995
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemiaH Schuster, C Manke, J Fischer, et al.
Clinical Nutrition (Edinburgh, Scotland)|November 1, 1986
Inhibition of muscular glucose uptake by lipid infusion in manK Rett, M Wicklmayr, G Dietze, et al.
Journal of Medical Genetics|December 1, 1991
Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German familiesH Schuster, G Rauh, C Gerl, et al.
Pageof 26

Showing results (191-200 of 252) with videos related to

Sort By:
Pageof 26
Klinische Wochenschrift|November 15, 1991
Identification of a 76-year-old patient with compound heterozygous familial hypercholesterolemia by haplotype analysis of the LDL receptor geneH J Fischer, H Schuster, C Keller, et al.
Human Genetics|April 1, 1993
Identification of the 408 valine to methionine mutation in the low density lipoprotein receptor in a German family with familial hypercholesterolemiaH Schuster, H J Fischer, C Keller, et al.
European Journal of Clinical Pharmacology|January 1, 1986
Effect of acarbose on carbohydrate tolerance during administration of a fibre-free formula diet on healthy subjectsI E Walter-Sack, A Ittner-Holland, G Wolfram, et al.
Hearing Research|August 1, 1997
Transcripts encoding three types of guanylyl-cyclase-coupled trans-membrane receptors in inner ear tissues of guinea pigsG Krause, A M Meyer zum Gottesberge, G Wolfram, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1988
Evidence for a nonspecific factor interfering in the radioimmunoassay of somatoliberin-like immunoreactivity in human seminal plasmaM Losa, G Wolfram, J Schopohl, et al.
European Journal of Clinical Investigation|August 1, 1987
Inhibition of muscular amino acid release by lipid infusion in manM Wicklmayr, K Rett, B Schwiegelshohn, et al.
Biological Psychiatry|May 1, 1990
Disturbances in the hypothalamo-pituitary-adrenal and other neuroendocrine axes in bulimiaM M Fichter, K M Pirke, J Pöllinger, et al.
Clinical Genetics|August 1, 1995
Identification of the valine 408 to methionine mutation in the LDL receptor in a Greek patient with homozygous familial hypercholesterolemiaH Schuster, C Manke, J Fischer, et al.
Clinical Nutrition (Edinburgh, Scotland)|November 1, 1986
Inhibition of muscular glucose uptake by lipid infusion in manK Rett, M Wicklmayr, G Dietze, et al.
Journal of Medical Genetics|December 1, 1991
Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German familiesH Schuster, G Rauh, C Gerl, et al.
Pageof 26