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Markus Pfister

Showing results (41-50 of 57) with videos related to

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The Laryngoscope|October 29, 2004
Safe and reliable sound threshold measures with direct vibration of the ossicular chainMarcus M Maassen, Jesus Rodriguez Jorge, Stephan Herberhold, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|January 12, 2011
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing lossMostafa R Mohamed, Ioana Alesutan, Michael Föller, et al.
Hearing Research|March 22, 2006
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholdsAndreas Frey, Angelika Lampert, Siegfried Waldegger, et al.
Neurobiology of Disease|July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cellsLut Van Laer, Markus Pfister, Sofie Thys, et al.
Neurobiology of Disease|August 1, 2006
Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndromeKaren Vrijens, Sofie Thys, Marcel T De Jeu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2004
Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing lossLukas Rüttiger, Matthias Sausbier, Ulrike Zimmermann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2009
Deafness in TRbeta mutants is caused by malformation of the tectorial membraneHarald Winter, Lukas Rüttiger, Marcus Müller, et al.
Clinical Genetics|April 13, 2020
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing lossBirgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, et al.
American Journal of Human Genetics|March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)Francesca Donaudy, Rik Snoeckx, Markus Pfister, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
The Laryngoscope|October 29, 2004
Safe and reliable sound threshold measures with direct vibration of the ossicular chainMarcus M Maassen, Jesus Rodriguez Jorge, Stephan Herberhold, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|January 12, 2011
Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing lossMostafa R Mohamed, Ioana Alesutan, Michael Föller, et al.
Hearing Research|March 22, 2006
Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholdsAndreas Frey, Angelika Lampert, Siegfried Waldegger, et al.
Neurobiology of Disease|July 19, 2005
Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cellsLut Van Laer, Markus Pfister, Sofie Thys, et al.
Neurobiology of Disease|August 1, 2006
Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndromeKaren Vrijens, Sofie Thys, Marcel T De Jeu, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2004
Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing lossLukas Rüttiger, Matthias Sausbier, Ulrike Zimmermann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 27, 2009
Deafness in TRbeta mutants is caused by malformation of the tectorial membraneHarald Winter, Lukas Rüttiger, Marcus Müller, et al.
Clinical Genetics|April 13, 2020
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing lossBirgit S Budde, Maha Abdelgaber Aly, Mostafa R Mohamed, et al.
American Journal of Human Genetics|March 12, 2004
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4)Francesca Donaudy, Rik Snoeckx, Markus Pfister, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
Pageof 6