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Erwin van Wijk

Showing results (51-60 of 82) with videos related to

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Experimental Eye Research|May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafishMargo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Molecular Therapy. Nucleic Acids|November 2, 2016
Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic MutationRadulfus Wn Slijkerman, Christel Vaché, Margo Dona, et al.
Human Molecular Genetics|June 23, 2007
MPP1 links the Usher protein network and the Crumbs protein complex in the retinaIlse Gosens, Erwin van Wijk, Ferry F J Kersten, et al.
Human Molecular Genetics|January 26, 2006
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1Erwin van Wijk, Bert van der Zwaag, Theo Peters, et al.
Communications Biology|June 4, 2021
Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafishWim H Quint, Kirke C D Tadema, Erik de Vrieze, et al.
Scientific Reports|October 7, 2016
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrumMaleeha Maria, Ideke J C Lamers, Miriam Schmidts, et al.
American Journal of Human Genetics|July 15, 2014
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophySusanne Roosing, Ideke J C Lamers, Erik de Vrieze, et al.
Plos Genetics|October 21, 2015
The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle TraffickingRuxandra Bachmann-Gagescu, Margo Dona, Lisette Hetterschijt, et al.
Genome Research|March 4, 2025
Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approachesMerel Stemerdink, Tabea Riepe, Nick Zomer, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsCelia Zazo Seco, Arnaud P Giese, Sobia Shafique, et al.
Pageof 9

Showing results (51-60 of 82) with videos related to

Sort By:
Pageof 9
Experimental Eye Research|May 20, 2018
Usherin defects lead to early-onset retinal dysfunction in zebrafishMargo Dona, Ralph Slijkerman, Kimberly Lerner, et al.
Molecular Therapy. Nucleic Acids|November 2, 2016
Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic MutationRadulfus Wn Slijkerman, Christel Vaché, Margo Dona, et al.
Human Molecular Genetics|June 23, 2007
MPP1 links the Usher protein network and the Crumbs protein complex in the retinaIlse Gosens, Erwin van Wijk, Ferry F J Kersten, et al.
Human Molecular Genetics|January 26, 2006
The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1Erwin van Wijk, Bert van der Zwaag, Theo Peters, et al.
Communications Biology|June 4, 2021
Loss of Gap Junction Delta-2 (GJD2) gene orthologs leads to refractive error in zebrafishWim H Quint, Kirke C D Tadema, Erik de Vrieze, et al.
Scientific Reports|October 7, 2016
Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrumMaleeha Maria, Ideke J C Lamers, Miriam Schmidts, et al.
American Journal of Human Genetics|July 15, 2014
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophySusanne Roosing, Ideke J C Lamers, Erik de Vrieze, et al.
Plos Genetics|October 21, 2015
The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle TraffickingRuxandra Bachmann-Gagescu, Margo Dona, Lisette Hetterschijt, et al.
Genome Research|March 4, 2025
Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approachesMerel Stemerdink, Tabea Riepe, Nick Zomer, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsCelia Zazo Seco, Arnaud P Giese, Sobia Shafique, et al.
Pageof 9