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Markus Pfister

Showing results (11-20 of 57) with videos related to

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Lab on a Chip|January 27, 2005
A new two-chip concept for continuous measurements on PMMA-microchipsOliver Vogt, Markus Pfister, Ulrich Marggraf, et al.
The Laryngoscope|March 17, 2006
In vitro model for intraoperative adjustments in an implantable hearing aid (MET)Jesus Rodriguez Jorge, Markus Pfister, Hans P Zenner, et al.
Oncology Reports|February 13, 2003
Epigenetic control of E-cadherin (CDH1) by CpG methylation in metastasising laryngeal cancerPia Azarschab, Agnieszka Stembalska, Mirela Baus Loncar, et al.
Human Mutation|May 10, 2005
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patientsClaudia Schulte, Urban Geisthoff, Andreas Lux, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Ergic2, a brain specific interacting partner of OtoferlinMagdalena Żak, Andreas Bress, Niels Brandt, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Genetic heterogeneity of deafness phenotypes linked to DFNA4Tao Yang, Markus Pfister, Nikolaus Blin, et al.
International Journal of Molecular Medicine|August 3, 2007
Coincidence of mutations in different connexin genes in Hungarian patientsTímea Tóth, Susan Kupka, Birgit Haack, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|February 13, 2003
A patient database application for Hereditary Deafness Epidemiology and Clinical Research (H.E.A.R.): an effort for standardization in multiple languagesMarkus Pfister, Serdar Akyildiz, Ovunc Gunhan, et al.
Journal of Vascular Surgery|August 31, 2016
Computer-aided endovascular aortic repair using fully automated two- and three-dimensional fusion imagingGiuseppe Panuccio, Giovanni Federico Torsello, Markus Pfister, et al.
Human Molecular Genetics|September 6, 2008
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness formPaulina Heidrych, Ulrike Zimmermann, Andreas Bress, et al.
Pageof 6

Showing results (11-20 of 57) with videos related to

Sort By:
Pageof 6
Lab on a Chip|January 27, 2005
A new two-chip concept for continuous measurements on PMMA-microchipsOliver Vogt, Markus Pfister, Ulrich Marggraf, et al.
The Laryngoscope|March 17, 2006
In vitro model for intraoperative adjustments in an implantable hearing aid (MET)Jesus Rodriguez Jorge, Markus Pfister, Hans P Zenner, et al.
Oncology Reports|February 13, 2003
Epigenetic control of E-cadherin (CDH1) by CpG methylation in metastasising laryngeal cancerPia Azarschab, Agnieszka Stembalska, Mirela Baus Loncar, et al.
Human Mutation|May 10, 2005
High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patientsClaudia Schulte, Urban Geisthoff, Andreas Lux, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 23, 2012
Ergic2, a brain specific interacting partner of OtoferlinMagdalena Żak, Andreas Bress, Niels Brandt, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Genetic heterogeneity of deafness phenotypes linked to DFNA4Tao Yang, Markus Pfister, Nikolaus Blin, et al.
International Journal of Molecular Medicine|August 3, 2007
Coincidence of mutations in different connexin genes in Hungarian patientsTímea Tóth, Susan Kupka, Birgit Haack, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|February 13, 2003
A patient database application for Hereditary Deafness Epidemiology and Clinical Research (H.E.A.R.): an effort for standardization in multiple languagesMarkus Pfister, Serdar Akyildiz, Ovunc Gunhan, et al.
Journal of Vascular Surgery|August 31, 2016
Computer-aided endovascular aortic repair using fully automated two- and three-dimensional fusion imagingGiuseppe Panuccio, Giovanni Federico Torsello, Markus Pfister, et al.
Human Molecular Genetics|September 6, 2008
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness formPaulina Heidrych, Ulrike Zimmermann, Andreas Bress, et al.
Pageof 6