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Ulrich Brinkmann

Showing results (51-60 of 97) with videos related to

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British Journal of Clinical Pharmacology|May 8, 2002
MDR1 gene polymorphisms and disposition of the P-glycoprotein substrate fexofenadineSiegfried Drescher, Elke Schaeffeler, Monika Hitzl, et al.
European Journal of Clinical Pharmacology|April 17, 2003
Digoxin pharmacokinetics and MDR1 genetic polymorphismsCéline Verstuyft, Mathias Schwab, Elke Schaeffeler, et al.
Pharmacogenetics|November 20, 2002
Identification of genetic variations of the human organic cation transporter hOCT1 and their functional consequencesReinhold Kerb, Ulrich Brinkmann, Natalia Chatskaia, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Identification of proangiogenic genes and pathways by high-throughput functional genomics: TBK1 and the IRF3 pathwayChristian Korherr, Hendrik Gille, Rolf Schäfer, et al.
Antibodies (Basel, Switzerland)|September 24, 2019
Back-to-Germline (B2G) Procedure for Antibody DevolutionAnja Schrade, Alexander Bujotzek, Christian Spick, et al.
Molecular & Cellular Proteomics : MCP|June 8, 2004
High-throughput functional genomics identifies genes that ameliorate toxicity due to oxidative stress in neuronal HT-22 cells: GFPT2 protects cells against peroxideJürgen Zitzler, Dieter Link, Rolf Schäfer, et al.
International Journal of Molecular Sciences|November 24, 2015
TriFabs--Trivalent IgG-Shaped Bispecific Antibody Derivatives: Design, Generation, Characterization and Application for Targeted Payload DeliveryKlaus Mayer, Anna-Lena Baumann, Michael Grote, et al.
Biomed Research International|July 4, 2014
Zirconium-89 labeled antibodies: a new tool for molecular imaging in cancer patientsFloor C J van de Watering, Mark Rijpkema, Lars Perk, et al.
European Journal of Human Genetics : EJHG|June 25, 2020
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathyHarmen Hawer, Bryce A Mendelsohn, Klaus Mayer, et al.
Pharmacogenetics and Genomics|February 1, 2007
Risk of coronary artery disease as influenced by variants of the human endothelin and endothelin-converting enzyme genesKatrin Bühler, Mike Ufer, Alexis Müller-Marbach, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
British Journal of Clinical Pharmacology|May 8, 2002
MDR1 gene polymorphisms and disposition of the P-glycoprotein substrate fexofenadineSiegfried Drescher, Elke Schaeffeler, Monika Hitzl, et al.
European Journal of Clinical Pharmacology|April 17, 2003
Digoxin pharmacokinetics and MDR1 genetic polymorphismsCéline Verstuyft, Mathias Schwab, Elke Schaeffeler, et al.
Pharmacogenetics|November 20, 2002
Identification of genetic variations of the human organic cation transporter hOCT1 and their functional consequencesReinhold Kerb, Ulrich Brinkmann, Natalia Chatskaia, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Identification of proangiogenic genes and pathways by high-throughput functional genomics: TBK1 and the IRF3 pathwayChristian Korherr, Hendrik Gille, Rolf Schäfer, et al.
Antibodies (Basel, Switzerland)|September 24, 2019
Back-to-Germline (B2G) Procedure for Antibody DevolutionAnja Schrade, Alexander Bujotzek, Christian Spick, et al.
Molecular & Cellular Proteomics : MCP|June 8, 2004
High-throughput functional genomics identifies genes that ameliorate toxicity due to oxidative stress in neuronal HT-22 cells: GFPT2 protects cells against peroxideJürgen Zitzler, Dieter Link, Rolf Schäfer, et al.
International Journal of Molecular Sciences|November 24, 2015
TriFabs--Trivalent IgG-Shaped Bispecific Antibody Derivatives: Design, Generation, Characterization and Application for Targeted Payload DeliveryKlaus Mayer, Anna-Lena Baumann, Michael Grote, et al.
Biomed Research International|July 4, 2014
Zirconium-89 labeled antibodies: a new tool for molecular imaging in cancer patientsFloor C J van de Watering, Mark Rijpkema, Lars Perk, et al.
European Journal of Human Genetics : EJHG|June 25, 2020
Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathyHarmen Hawer, Bryce A Mendelsohn, Klaus Mayer, et al.
Pharmacogenetics and Genomics|February 1, 2007
Risk of coronary artery disease as influenced by variants of the human endothelin and endothelin-converting enzyme genesKatrin Bühler, Mike Ufer, Alexis Müller-Marbach, et al.
Pageof 10