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Erwin van Wijk

Showing results (21-30 of 82) with videos related to

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Human Molecular Genetics|November 23, 2005
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2Jan Reiners, Erwin van Wijk, Tina Märker, et al.
International Journal of Molecular Sciences|November 11, 2022
Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in <i>USH2A</i>Janine Reurink, Jaap Oostrik, Marco Aben, et al.
Molecular Therapy. Nucleic Acids|April 5, 2021
AON-based degradation of c.151C>T mutant <i>COCH</i> transcripts associated with dominantly inherited hearing impairment DFNA9Erik de Vrieze, Jorge Cañas Martín, Jolien Peijnenborg, et al.
Pflugers Archiv : European Journal of Physiology|November 13, 2018
SLC41A1 is essential for magnesium homeostasis in vivoFrancisco J Arjona, Femke Latta, Sami G Mohammed, et al.
Human Molecular Genetics|October 2, 2007
A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cellsTina Maerker, Erwin van Wijk, Nora Overlack, et al.
HGG Advances|September 1, 2023
<i>USH2A</i> variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoidsCarla Sanjurjo-Soriano, Carla Jimenez-Medina, Nejla Erkilic, et al.
Investigative Ophthalmology & Visual Science|February 26, 2020
Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal VasculatureDyah W Karjosukarso, Zaheer Ali, Theo A Peters, et al.
American Journal of Human Genetics|March 12, 2004
Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type IIErwin van Wijk, Ronald J E Pennings, Heleen te Brinke, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 17, 2004
A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairmentMartijn H Kemperman, Els M R De Leenheer, Patrick L M Huygen, et al.
Cilia|January 29, 2013
The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitoticallyFerry Fj Kersten, Erwin van Wijk, Lisette Hetterschijt, et al.
Pageof 9

Showing results (21-30 of 82) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|November 23, 2005
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2Jan Reiners, Erwin van Wijk, Tina Märker, et al.
International Journal of Molecular Sciences|November 11, 2022
Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in <i>USH2A</i>Janine Reurink, Jaap Oostrik, Marco Aben, et al.
Molecular Therapy. Nucleic Acids|April 5, 2021
AON-based degradation of c.151C>T mutant <i>COCH</i> transcripts associated with dominantly inherited hearing impairment DFNA9Erik de Vrieze, Jorge Cañas Martín, Jolien Peijnenborg, et al.
Pflugers Archiv : European Journal of Physiology|November 13, 2018
SLC41A1 is essential for magnesium homeostasis in vivoFrancisco J Arjona, Femke Latta, Sami G Mohammed, et al.
Human Molecular Genetics|October 2, 2007
A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cellsTina Maerker, Erwin van Wijk, Nora Overlack, et al.
HGG Advances|September 1, 2023
<i>USH2A</i> variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoidsCarla Sanjurjo-Soriano, Carla Jimenez-Medina, Nejla Erkilic, et al.
Investigative Ophthalmology & Visual Science|February 26, 2020
Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal VasculatureDyah W Karjosukarso, Zaheer Ali, Theo A Peters, et al.
American Journal of Human Genetics|March 12, 2004
Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type IIErwin van Wijk, Ronald J E Pennings, Heleen te Brinke, et al.
Archives of Otolaryngology--Head & Neck Surgery|March 17, 2004
A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairmentMartijn H Kemperman, Els M R De Leenheer, Patrick L M Huygen, et al.
Cilia|January 29, 2013
The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitoticallyFerry Fj Kersten, Erwin van Wijk, Lisette Hetterschijt, et al.
Pageof 9