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Erwin van Wijk

Showing results (41-50 of 82) with videos related to

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Ear and Hearing|September 26, 2014
Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrumAnne Marthe Maria Oonk, Ramon A C van Huet, Joop M Leijendeckers, et al.
Oncotarget|October 1, 2016
In vivo phage display screening for tumor vascular targets in glioblastoma identifies a llama nanobody against dynactin-1-p150GluedSanne A M van Lith, Ilse Roodink, Joost J C Verhoeff, et al.
Ophthalmology Science|June 19, 2023
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2aJessie M Hendricks, Juriaan R Metz, Hedwig M Velde, et al.
Molecular Vision|March 31, 2010
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse originElena Aller, Teresa Jaijo, Erwin van Wijk, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 26, 2022
Dawn and dusk peaks of outer segment phagocytosis, and visual cycle function require Rab28Ailís L Moran, Stephen P Carter, Joanna J Kaylor, et al.
Molecular Therapy. Nucleic Acids|December 4, 2024
Exploring non-coding variants and evaluation of antisense oligonucleotides for splicing redirection in Usher syndromeBelén García-Bohórquez, Pilar Barberán-Martínez, Elena Aller, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2ADirk H Wijn, Mirthe L A Fehrmann, Sybren M M Robijn, et al.
Hearing Research|June 19, 2016
A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIaBas P Hartel, Maria Löfgren, Patrick L M Huygen, et al.
Plos Genetics|April 5, 2014
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemiaFrancisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, et al.
Human Molecular Genetics|October 2, 2008
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like proteinErwin van Wijk, Ferry F J Kersten, Aileen Kartono, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Ear and Hearing|September 26, 2014
Nonsyndromic hearing loss caused by USH1G mutations: widening the USH1G disease spectrumAnne Marthe Maria Oonk, Ramon A C van Huet, Joop M Leijendeckers, et al.
Oncotarget|October 1, 2016
In vivo phage display screening for tumor vascular targets in glioblastoma identifies a llama nanobody against dynactin-1-p150GluedSanne A M van Lith, Ilse Roodink, Joost J C Verhoeff, et al.
Ophthalmology Science|June 19, 2023
Evaluation of Sleep Quality and Fatigue in Patients with Usher Syndrome Type 2aJessie M Hendricks, Juriaan R Metz, Hedwig M Velde, et al.
Molecular Vision|March 31, 2010
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse originElena Aller, Teresa Jaijo, Erwin van Wijk, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 26, 2022
Dawn and dusk peaks of outer segment phagocytosis, and visual cycle function require Rab28Ailís L Moran, Stephen P Carter, Joanna J Kaylor, et al.
Molecular Therapy. Nucleic Acids|December 4, 2024
Exploring non-coding variants and evaluation of antisense oligonucleotides for splicing redirection in Usher syndromeBelén García-Bohórquez, Pilar Barberán-Martínez, Elena Aller, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2ADirk H Wijn, Mirthe L A Fehrmann, Sybren M M Robijn, et al.
Hearing Research|June 19, 2016
A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIaBas P Hartel, Maria Löfgren, Patrick L M Huygen, et al.
Plos Genetics|April 5, 2014
CNNM2 mutations cause impaired brain development and seizures in patients with hypomagnesemiaFrancisco J Arjona, Jeroen H F de Baaij, Karl P Schlingmann, et al.
Human Molecular Genetics|October 2, 2008
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like proteinErwin van Wijk, Ferry F J Kersten, Aileen Kartono, et al.
Pageof 9