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Markus Pfister

Showing results (31-40 of 57) with videos related to

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Human Mutation|May 18, 2004
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern HungaryTímea Tóth, Susan Kupka, Birgit Haack, et al.
Ear, Nose, & Throat Journal|May 6, 2005
Surgical-handling properties of the titanium prosthesis in ossiculoplastyMarcus M Maassen, Hubert Löwenheim, Markus Pfister, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisationFarhad Mirghomizadeh, Bettina Bardtke, Marcella Devoto, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 6, 2008
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusisMaria Lubka, Marcus Müller, Mirela Baus-Loncar, et al.
Human Mutation|February 22, 2002
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patientsSusan Kupka, Tímea Tóth, Maciej Wróbel, et al.
Molecular and Cellular Endocrinology|September 10, 2013
Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cellsJuliane Dettling, Christoph Franz, Ulrike Zimmermann, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Human Genetics|October 23, 2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populationsIsabelle Schrauwen, Megan Ealy, Erik Fransen, et al.
Human Molecular Genetics|May 7, 2009
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cellPaulina Heidrych, Ulrike Zimmermann, Stephanie Kuhn, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Human Mutation|May 18, 2004
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern HungaryTímea Tóth, Susan Kupka, Birgit Haack, et al.
Ear, Nose, & Throat Journal|May 6, 2005
Surgical-handling properties of the titanium prosthesis in ossiculoplastyMarcus M Maassen, Hubert Löwenheim, Markus Pfister, et al.
European Journal of Human Genetics : EJHG|April 9, 2002
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisationFarhad Mirghomizadeh, Bettina Bardtke, Marcella Devoto, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|May 6, 2008
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusisMaria Lubka, Marcus Müller, Mirela Baus-Loncar, et al.
Human Mutation|February 22, 2002
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patientsSusan Kupka, Tímea Tóth, Maciej Wróbel, et al.
Molecular and Cellular Endocrinology|September 10, 2013
Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cellsJuliane Dettling, Christoph Franz, Ulrike Zimmermann, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 21, 2004
A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutationsMarkus Pfister, Holger Thiele, Guy Van Camp, et al.
Human Genetics|October 23, 2009
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populationsIsabelle Schrauwen, Megan Ealy, Erik Fransen, et al.
Human Molecular Genetics|May 7, 2009
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cellPaulina Heidrych, Ulrike Zimmermann, Stephanie Kuhn, et al.
Pageof 6