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B Hölzl

Showing results (1-10 of 14) with videos related to

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Journal of Internal Medicine|December 23, 2003
Lack of association of the Gly972Arg mutation of the insulin receptor substrate-1 gene with coronary artery disease in the Austrian populationB Strohmer, R Reiter, B Hölzl, et al.
Lancet (London, England)|August 12, 1989
Genetics of coronary heart diseaseB Paulweber, W Friedl, B Hölzl, et al.
Clinical Nephrology|November 14, 1997
Acute renal failure after ingestion of Cortinarius speciocissimusB Hölzl, H Regele, M Kirchmair, et al.
Acta Medica Austriaca|January 1, 1987
[Cytochemical study of macrophages in sarcoidosis patients in skin window exudates]N Sepp, B Hölzl, F Schmalzl, et al.
Journal of Internal Medicine|March 6, 1998
Hypertriglyceridemia and insulin resistanceB Hölzl, B Paulweber, F Sandhofer, et al.
Rheuma Plus|August 25, 2020
[The Gastein Healing Gallery and a Potential Risk of Viral Infections in the Treatment Area]M Offenbächer, B Hölzl, M Gaisberger, et al.
Journal of Lipid Research|December 1, 1994
Lipoprotein lipase deficiency due to a 3' splice site mutation in intron 6 of the lipoprotein lipase geneB Hölzl, R Huber, B Paulweber, et al.
Molecular and Cellular Biology|September 1, 1997
Functional domains of the human orphan receptor ARP-1/COUP-TFII involved in active repression and transrepressionG Achatz, B Hölzl, R Speckmayer, et al.
Diabetologia|March 27, 2002
Insulin sensitivity is impaired in heterozygous carriers of lipoprotein lipase deficiencyB Hölzl, B Iglseder, A Sandhofer, et al.
Journal of Lipid Research|April 29, 2000
Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23B Hölzl, H G Kraft, H Wiebusch, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Internal Medicine|December 23, 2003
Lack of association of the Gly972Arg mutation of the insulin receptor substrate-1 gene with coronary artery disease in the Austrian populationB Strohmer, R Reiter, B Hölzl, et al.
Lancet (London, England)|August 12, 1989
Genetics of coronary heart diseaseB Paulweber, W Friedl, B Hölzl, et al.
Clinical Nephrology|November 14, 1997
Acute renal failure after ingestion of Cortinarius speciocissimusB Hölzl, H Regele, M Kirchmair, et al.
Acta Medica Austriaca|January 1, 1987
[Cytochemical study of macrophages in sarcoidosis patients in skin window exudates]N Sepp, B Hölzl, F Schmalzl, et al.
Journal of Internal Medicine|March 6, 1998
Hypertriglyceridemia and insulin resistanceB Hölzl, B Paulweber, F Sandhofer, et al.
Rheuma Plus|August 25, 2020
[The Gastein Healing Gallery and a Potential Risk of Viral Infections in the Treatment Area]M Offenbächer, B Hölzl, M Gaisberger, et al.
Journal of Lipid Research|December 1, 1994
Lipoprotein lipase deficiency due to a 3' splice site mutation in intron 6 of the lipoprotein lipase geneB Hölzl, R Huber, B Paulweber, et al.
Molecular and Cellular Biology|September 1, 1997
Functional domains of the human orphan receptor ARP-1/COUP-TFII involved in active repression and transrepressionG Achatz, B Hölzl, R Speckmayer, et al.
Diabetologia|March 27, 2002
Insulin sensitivity is impaired in heterozygous carriers of lipoprotein lipase deficiencyB Hölzl, B Iglseder, A Sandhofer, et al.
Journal of Lipid Research|April 29, 2000
Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23B Hölzl, H G Kraft, H Wiebusch, et al.
Pageof 2