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Markus Pfister

Showing results (21-30 of 57) with videos related to

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Molecular Medicine (Cambridge, Mass.)|December 13, 2002
A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10Markus Pfister, Tímea Tóth, Holger Thiele, et al.
The American Journal of Tropical Medicine and Hygiene|March 18, 2005
Immunogenicity and safety of BERNA-YF compared with two other 17D yellow fever vaccines in a phase 3 clinical trialMarkus Pfister, Oliver Kürsteiner, Helene Hilfiker, et al.
Journal of Applied Genetics|January 7, 2015
A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairmentMohamed Ahamed Hassan, Aftab Ali Shah, Elzbieta Szmida, et al.
Human Mutation|July 12, 2002
Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairmentSusan Kupka, Simone Braun, Susanne Aberle, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma casesKathrin Riemann, Karl Sotlar, Susan Kupka, et al.
The European Journal of Neuroscience|January 19, 2007
Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the ratNicola Schug, Claudia Braig, Ulrike Zimmermann, et al.
European Radiology|February 11, 2011
Feasibility of simultaneous PET/MR imaging in the head and upper neck areaAndreas Boss, Lars Stegger, Sotirios Bisdas, et al.
Journal of Applied Genetics|August 13, 2004
Analysis of candidate genes for genotypic diagnosis in the long QT syndromeBirgit Haack, Susan Kupka, Margret Ebauer, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 5, 2014
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signalingMegan Ealy, Nicole C Meyer, Johnny Cruz Corchado, et al.
Disease Models & Mechanisms|February 10, 2010
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutationAnping Xia, Simon S Gao, Tao Yuan, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Molecular Medicine (Cambridge, Mass.)|December 13, 2002
A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10Markus Pfister, Tímea Tóth, Holger Thiele, et al.
The American Journal of Tropical Medicine and Hygiene|March 18, 2005
Immunogenicity and safety of BERNA-YF compared with two other 17D yellow fever vaccines in a phase 3 clinical trialMarkus Pfister, Oliver Kürsteiner, Helene Hilfiker, et al.
Journal of Applied Genetics|January 7, 2015
A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairmentMohamed Ahamed Hassan, Aftab Ali Shah, Elzbieta Szmida, et al.
Human Mutation|July 12, 2002
Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairmentSusan Kupka, Simone Braun, Susanne Aberle, et al.
Cancer Genetics and Cytogenetics|April 7, 2004
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma casesKathrin Riemann, Karl Sotlar, Susan Kupka, et al.
The European Journal of Neuroscience|January 19, 2007
Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the ratNicola Schug, Claudia Braig, Ulrike Zimmermann, et al.
European Radiology|February 11, 2011
Feasibility of simultaneous PET/MR imaging in the head and upper neck areaAndreas Boss, Lars Stegger, Sotirios Bisdas, et al.
Journal of Applied Genetics|August 13, 2004
Analysis of candidate genes for genotypic diagnosis in the long QT syndromeBirgit Haack, Susan Kupka, Margret Ebauer, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 5, 2014
Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signalingMegan Ealy, Nicole C Meyer, Johnny Cruz Corchado, et al.
Disease Models & Mechanisms|February 10, 2010
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutationAnping Xia, Simon S Gao, Tao Yuan, et al.
Pageof 6