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Martin Brand

Showing results (81-90 of 109) with videos related to

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Orphanet Journal of Rare Diseases|May 5, 2016
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variantMalte Lenders, Frank Weidemann, Christine Kurschat, et al.
Journal of Lipid Research|February 18, 2005
Alcohol intake modulates the genetic association between HDL cholesterol and the PPARgamma2 Pro12Ala polymorphismStefan-Martin Brand-Herrmann, Tatiana Kuznetsova, Andreas Wiechert, et al.
Journal of Hypertension|December 5, 2006
-391 C to G substitution in the regulator of G-protein signalling-2 promoter increases susceptibility to the metabolic syndrome in white European men: consistency between molecular and epidemiological studiesKathleen Freson, Katarzyna Stolarz, Raymond Aerts, et al.
Hypertension (Dallas, Tex. : 1979)|April 17, 2008
Blood pressure and renal sodium handling in relation to genetic variation in the DRD1 promoter and GRK4Jan A Staessen, Tatiana Kuznetsova, Haifeng Zhang, et al.
American Journal of Physiology. Renal Physiology|January 9, 2009
Hypertension in mice lacking the CXCR3 chemokine receptorHsiang-Hao Hsu, Kerstin Duning, Hans Henning Meyer, et al.
American Journal of Hypertension|January 3, 2007
The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathyRalph Telgmann, Bassam A Harb, Cemil Ozcelik, et al.
Journal of the American Society of Nephrology : JASN|July 18, 2015
Patients with Fabry Disease after Enzyme Replacement Therapy Dose Reduction and Switch-2-Year Follow-UpMalte Lenders, Sima Canaan-Kühl, Johannes Krämer, et al.
Atherosclerosis|October 1, 2013
Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation in vitroBoris Schmitz, Peter Vischer, Eva Brand, et al.
Plos One|January 4, 2013
Transport mechanisms and their pathology-induced regulation govern tyrosine kinase inhibitor delivery in rheumatoid arthritisChristian Schmidt-Lauber, Saliha Harrach, Thomas Pap, et al.
Pharmacogenetics and Genomics|July 12, 2007
Neutrophil elastase gene variation and coronary heart diseaseJacqueline Schönfelder, Ralph Telgmann, Viviane Nicaud, et al.
Pageof 11

Showing results (81-90 of 109) with videos related to

Sort By:
Pageof 11
Orphanet Journal of Rare Diseases|May 5, 2016
Alpha-Galactosidase A p.A143T, a non-Fabry disease-causing variantMalte Lenders, Frank Weidemann, Christine Kurschat, et al.
Journal of Lipid Research|February 18, 2005
Alcohol intake modulates the genetic association between HDL cholesterol and the PPARgamma2 Pro12Ala polymorphismStefan-Martin Brand-Herrmann, Tatiana Kuznetsova, Andreas Wiechert, et al.
Journal of Hypertension|December 5, 2006
-391 C to G substitution in the regulator of G-protein signalling-2 promoter increases susceptibility to the metabolic syndrome in white European men: consistency between molecular and epidemiological studiesKathleen Freson, Katarzyna Stolarz, Raymond Aerts, et al.
Hypertension (Dallas, Tex. : 1979)|April 17, 2008
Blood pressure and renal sodium handling in relation to genetic variation in the DRD1 promoter and GRK4Jan A Staessen, Tatiana Kuznetsova, Haifeng Zhang, et al.
American Journal of Physiology. Renal Physiology|January 9, 2009
Hypertension in mice lacking the CXCR3 chemokine receptorHsiang-Hao Hsu, Kerstin Duning, Hans Henning Meyer, et al.
American Journal of Hypertension|January 3, 2007
The G-231A polymorphism in the endothelin-A receptor gene is associated with lower aortic pressure in patients with dilated cardiomyopathyRalph Telgmann, Bassam A Harb, Cemil Ozcelik, et al.
Journal of the American Society of Nephrology : JASN|July 18, 2015
Patients with Fabry Disease after Enzyme Replacement Therapy Dose Reduction and Switch-2-Year Follow-UpMalte Lenders, Sima Canaan-Kühl, Johannes Krämer, et al.
Atherosclerosis|October 1, 2013
Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation in vitroBoris Schmitz, Peter Vischer, Eva Brand, et al.
Plos One|January 4, 2013
Transport mechanisms and their pathology-induced regulation govern tyrosine kinase inhibitor delivery in rheumatoid arthritisChristian Schmidt-Lauber, Saliha Harrach, Thomas Pap, et al.
Pharmacogenetics and Genomics|July 12, 2007
Neutrophil elastase gene variation and coronary heart diseaseJacqueline Schönfelder, Ralph Telgmann, Viviane Nicaud, et al.
Pageof 11