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Erwin van Wijk

Showing results (31-40 of 82) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 28, 2006
Cochleovestibular and ocular features in a Dutch DFNA11 familyAnne M L C Bischoff, Ronald J E Pennings, Patrick L M Huygen, et al.
Investigative Ophthalmology & Visual Science|December 5, 2009
Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein networkFerry F J Kersten, Erwin van Wijk, Jeroen van Reeuwijk, et al.
Experimental Dermatology|August 1, 2014
Analysis of protein-protein interaction between late cornified envelope proteins and corneodesmosinJudith G M Bergboer, Maria G Dulak, Ivonne M J J van Vlijmen-Willems, et al.
Hearing Research|January 13, 2024
Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9Dorien Verdoodt, Erwin van Wijk, Sanne Broekman, et al.
Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic <i>COCH</i> Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-AnalysisSybren M M Robijn, Jeroen J Smits, Kadriye Sezer, et al.
American Journal of Human Genetics|March 30, 2010
Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunctionMargit Schraders, Jaap Oostrik, Patrick L M Huygen, et al.
Human Molecular Genetics|January 31, 2020
Clinical and preclinical therapeutic outcome metrics for USH2A-related diseaseMaria Toms, Adam M Dubis, Erik de Vrieze, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 8, 2021
Attitudes of Potential Participants Towards Potential Gene Therapy Trials in Autosomal Dominant Progressive Sensorineural Hearing LossCamille Levie, Julie Moyaert, Sebastien Janssens de Varebeke, et al.
Human Molecular Genetics|December 23, 2017
Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosaMonika Weisz Hubshman, Sanne Broekman, Erwin van Wijk, et al.
Human Genetics|June 29, 2004
Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)Mirjam W J Luijendijk, Erwin Van Wijk, Anne M L C Bischoff, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 28, 2006
Cochleovestibular and ocular features in a Dutch DFNA11 familyAnne M L C Bischoff, Ronald J E Pennings, Patrick L M Huygen, et al.
Investigative Ophthalmology & Visual Science|December 5, 2009
Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein networkFerry F J Kersten, Erwin van Wijk, Jeroen van Reeuwijk, et al.
Experimental Dermatology|August 1, 2014
Analysis of protein-protein interaction between late cornified envelope proteins and corneodesmosinJudith G M Bergboer, Maria G Dulak, Ivonne M J J van Vlijmen-Willems, et al.
Hearing Research|January 13, 2024
Rational design of a genomically humanized mouse model for dominantly inherited hearing loss, DFNA9Dorien Verdoodt, Erwin van Wijk, Sanne Broekman, et al.
Biomolecules|February 25, 2022
Genotype-Phenotype Correlations of Pathogenic <i>COCH</i> Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-AnalysisSybren M M Robijn, Jeroen J Smits, Kadriye Sezer, et al.
American Journal of Human Genetics|March 30, 2010
Mutations in PTPRQ are a cause of autosomal-recessive nonsyndromic hearing impairment DFNB84 and associated with vestibular dysfunctionMargit Schraders, Jaap Oostrik, Patrick L M Huygen, et al.
Human Molecular Genetics|January 31, 2020
Clinical and preclinical therapeutic outcome metrics for USH2A-related diseaseMaria Toms, Adam M Dubis, Erik de Vrieze, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 8, 2021
Attitudes of Potential Participants Towards Potential Gene Therapy Trials in Autosomal Dominant Progressive Sensorineural Hearing LossCamille Levie, Julie Moyaert, Sebastien Janssens de Varebeke, et al.
Human Molecular Genetics|December 23, 2017
Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosaMonika Weisz Hubshman, Sanne Broekman, Erwin van Wijk, et al.
Human Genetics|June 29, 2004
Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)Mirjam W J Luijendijk, Erwin Van Wijk, Anne M L C Bischoff, et al.
Pageof 9