Publications by authors named "Theo A Peters"

24Publications

Modeling ZNF408-Associated FEVR in Zebrafish Results in Abnormal Retinal Vasculature.

Authors:
Dyah W Karjosukarso Zaheer Ali Theo A Peters Jia Qi Cheng Zhang Anita D M Hoogendoorn Alejandro Garanto Erwin van Wijk Lasse D Jensen Rob W J Collin

Invest Ophthalmol Vis Sci 2020 02;61(2):39

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February 2020

Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish.

Authors:
Muriël Messchaert Margo Dona Sanne Broekman Theo A Peters Julio C Corral-Serrano Ralph W N Slijkerman Erwin van Wijk Rob W J Collin

PLoS One 2018 27;13(7):e0200789. Epub 2018 Jul 27.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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January 2019

C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish.

Authors:
Julio C Corral-Serrano Muriël Messchaert Margo Dona Theo A Peters Leonie M Kamminga Erwin van Wijk Rob W J Collin

Sci Rep 2018 06 26;8(1):9675. Epub 2018 Jun 26.

Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.

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June 2018

Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation.

Authors:
Radulfus Wn Slijkerman Christel Vaché Margo Dona Gema García-García Mireille Claustres Lisette Hetterschijt Theo A Peters Bas P Hartel Ronald Je Pennings José M Millan Elena Aller Alejandro Garanto Rob Wj Collin Hannie Kremer Anne-Françoise Roux Erwin Van Wijk

Mol Ther Nucleic Acids 2016 Nov 1;5(10):e381. Epub 2016 Nov 1.

Department of Otorhinolaryngology, Radboudumc, Nijmegen, the Netherlands.

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November 2016

NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish.

Authors:
Margo Dona Ruxandra Bachmann-Gagescu Yves Texier Grischa Toedt Lisette Hetterschijt Edith L Tonnaer Theo A Peters Sylvia E C van Beersum Judith G M Bergboer Nicola Horn Erik de Vrieze Ralph W N Slijkerman Jeroen van Reeuwijk Gert Flik Jan E Keunen Marius Ueffing Toby J Gibson Ronald Roepman Karsten Boldt Hannie Kremer Erwin van Wijk

PLoS Genet 2015 Oct 20;11(10):e1005574. Epub 2015 Oct 20.

Department of Otorhinolaryngology, Radboud University Medical Centre, Nijmegen, the Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, the Netherlands.

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October 2015

Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy.

Authors:
Susanne Roosing Ideke J C Lamers Erik de Vrieze L Ingeborgh van den Born Stanley Lambertus Heleen H Arts Theo A Peters Carel B Hoyng Hannie Kremer Lisette Hetterschijt Stef J F Letteboer Erwin van Wijk Ronald Roepman Anneke I den Hollander Frans P M Cremers

Am J Hum Genet 2014 Aug 10;95(2):131-42. Epub 2014 Jul 10.

Department of Human Genetics, Radboud University Medical Center, PO Box 9101, 6500 HB Nijmegen, the Netherlands; Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, PO Box 9101, 6500 HB Nijmegen, the Netherlands. Electronic address:

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August 2014

Unexpected CEP290 mRNA splicing in a humanized knock-in mouse model for Leber congenital amaurosis.

Authors:
Alejandro Garanto Sylvia E C van Beersum Theo A Peters Ronald Roepman Frans P M Cremers Rob W J Collin

PLoS One 2013 6;8(11):e79369. Epub 2013 Nov 6.

Department of Human Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands ; Institute for Genetic and Metabolic Disease, Radboud University Medical Centre, Nijmegen, The Netherlands.

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August 2014

Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy.

Authors:
Susanne Roosing Klaus Rohrschneider Avigail Beryozkin Dror Sharon Nicole Weisschuh Jennifer Staller Susanne Kohl Lina Zelinger Theo A Peters Kornelia Neveling Tim M Strom L Ingeborgh van den Born Carel B Hoyng Caroline C W Klaver Ronald Roepman Bernd Wissinger Eyal Banin Frans P M Cremers Anneke I den Hollander

Am J Hum Genet 2013 Jul 6;93(1):110-7. Epub 2013 Jun 6.

Department of Human Genetics, Radboud University Medical Centre, 6500 HB Nijmegen, the Netherlands.

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July 2013

The mitotic spindle protein SPAG5/Astrin connects to the Usher protein network postmitotically.

Authors:
Ferry Fj Kersten Erwin van Wijk Lisette Hetterschijt Katharina Bauβ Theo A Peters Mariam G Aslanyan Bert van der Zwaag Uwe Wolfrum Jan Ee Keunen Ronald Roepman Hannie Kremer

Cilia 2012 Apr 25;1(1). Epub 2012 Apr 25.

Department of Human Genetics, Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, The Netherlands.

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April 2012

Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome.

Authors:
Monique C M Balemans Nael Nadif Kasri Maksym V Kopanitsa Nurudeen O Afinowi Ger Ramakers Theo A Peters Andy J Beynon Sanne M Janssen Rik C J van Summeren Jorine M Eeftens Nathalie Eikelenboom Marco Benevento Makoto Tachibana Yoichi Shinkai Tjitske Kleefstra Hans van Bokhoven Catharina E E M Van der Zee

Hum Mol Genet 2013 Mar 21;22(5):852-66. Epub 2012 Nov 21.

Department of Human Genetics, Nijmegen Centre for Molecular Life Sciences, Nijmegen, the Netherlands.

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March 2013

Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss.

Authors:
Kemal O Yariz Duygu Duman Celia Zazo Seco Julia Dallman Mingqian Huang Theo A Peters Asli Sirmaci Na Lu Margit Schraders Isaac Skromne Jaap Oostrik Oscar Diaz-Horta Juan I Young Suna Tokgoz-Yilmaz Ozlem Konukseven Hashem Shahin Lisette Hetterschijt Moien Kanaan Anne M M Oonk Yvonne J K Edwards Huawei Li Semra Atalay Susan Blanton Alexandra A Desmidt Xue-Zhong Liu Ronald J E Pennings Zhongmin Lu Zheng-Yi Chen Hannie Kremer Mustafa Tekin

Am J Hum Genet 2012 11;91(5):872-82

John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

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November 2012

The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase.

Authors:
Karlien L M Coene Dorus A Mans Karsten Boldt C Johannes Gloeckner Jeroen van Reeuwijk Emine Bolat Susanne Roosing Stef J F Letteboer Theo A Peters Frans P M Cremers Marius Ueffing Ronald Roepman

Hum Mol Genet 2011 Sep 17;20(18):3592-605. Epub 2011 Jun 17.

Department of Human Genetics (855), Radboud University Nijmegen Medical Centre, PO Box9101, 6500 HB Nijmegen, The Netherlands.

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September 2011

Flow of energy in the outer retina in darkness and in light.

Authors:
Jonathan D Linton Lars C Holzhausen Norbert Babai Hongman Song Kiyoharu J Miyagishima George W Stearns Ken Lindsay Junhua Wei Andrei O Chertov Theo A Peters Romeo Caffe Helma Pluk Mathias W Seeliger Naoyuki Tanimoto Kimberly Fong Laura Bolton Denise L T Kuok Ian R Sweet Theodore M Bartoletti Roxana A Radu Gabriel H Travis Willam N Zagotta Ellen Townes-Anderson Ed Parker Catharina E E M Van der Zee Alapakkam P Sampath Maxim Sokolov Wallace B Thoreson James B Hurley

Proc Natl Acad Sci U S A 2010 May 5;107(19):8599-604. Epub 2010 May 5.

Department of Biochemistry, University of Washington, Seattle, WA 98195, USA.

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May 2010

Neurofilament localization and phosphorylation in the developing inner ear of the rat.

Authors:
Edith L G M Tonnaer Theo A Peters Jo H A J Curfs

Hear Res 2010 Aug 27;267(1-2):27-35. Epub 2010 Apr 27.

Radboud University Nijmegen Medical Center, Department of Otorhinolaryngology, Head & Neck Surgery, Donders Institute for Brain, Cognition and Behaviour, Center for Neuroscience, Philips van Leydenlaan 15, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.

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August 2010

Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein network.

Authors:
Ferry F J Kersten Erwin van Wijk Jeroen van Reeuwijk Bert van der Zwaag Tina Märker Theo A Peters Nicholas Katsanis Uwe Wolfrum Jan E E Keunen Ronald Roepman Hannie Kremer

Invest Ophthalmol Vis Sci 2010 May 3;51(5):2338-46. Epub 2009 Dec 3.

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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May 2010

ATP8B1 is essential for maintaining normal hearing.

Authors:
Janneke M Stapelbroek Theo A Peters Denis H A van Beurden Jo H A J Curfs Anneke Joosten Andy J Beynon Bibian M van Leeuwen Lieke M van der Velden Laura Bull Ronald P Oude Elferink Bert A van Zanten Leo W J Klomp Roderick H J Houwen

Proc Natl Acad Sci U S A 2009 Jun 28;106(24):9709-14. Epub 2009 May 28.

Department of Pediatric Gastroenterology, University Medical Center Utrecht, Utrecht, The Netherlands.

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June 2009

Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein.

Authors:
Erwin van Wijk Ferry F J Kersten Aileen Kartono Dorus A Mans Kim Brandwijk Stef J F Letteboer Theo A Peters Tina Märker Xiumin Yan Cor W R J Cremers Frans P M Cremers Uwe Wolfrum Ronald Roepman Hannie Kremer

Hum Mol Genet 2009 Jan 30;18(1):51-64. Epub 2008 Sep 30.

Department of Otorhinolaryngology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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January 2009

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome.

Authors:
Heleen H Arts Dan Doherty Sylvia E C van Beersum Melissa A Parisi Stef J F Letteboer Nicholas T Gorden Theo A Peters Tina Märker Krysta Voesenek Aileen Kartono Hamit Ozyurek Federico M Farin Hester Y Kroes Uwe Wolfrum Han G Brunner Frans P M Cremers Ian A Glass Nine V A M Knoers Ronald Roepman

Nat Genet 2007 Jul 10;39(7):882-8. Epub 2007 Jun 10.

Department of Human Genetics, Radboud University Nijmegen Medical Centre and Nijmegen Centre for Molecular Life Sciences, 6500 HB Nijmegen, The Netherlands.

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July 2007

Kidney failure in mice lacking the tetraspanin CD151.

Authors:
Norman Sachs Maaike Kreft Marius A van den Bergh Weerman Andy J Beynon Theo A Peters Jan J Weening Arnoud Sonnenberg

J Cell Biol 2006 Oct 2;175(1):33-9. Epub 2006 Oct 2.

Division of Cell Biology, The Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.

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October 2006

No evidence of hearing loss in pseudohypoaldosteronism type 1 patients.

Authors:
Theo A Peters Elena Levtchenko Cor W R J Cremers Jo H A J Curfs Leo A H Monnens

Acta Otolaryngol 2006 Mar;126(3):237-9

Department of Otorhinolaryngology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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March 2006

Identification of a rat model for usher syndrome type 1B by N-ethyl-N-nitrosourea mutagenesis-driven forward genetics.

Authors:
Bart M G Smits Theo A Peters Joram D Mul Huib J Croes Jack A M Fransen Andy J Beynon Victor Guryev Ronald H A Plasterk Edwin Cuppen

Genetics 2005 Aug 18;170(4):1887-96. Epub 2005 Jun 18.

Hubrecht Laboratory, Centre for Biomedical Genetics, 3584 CT Utrecht, The Netherlands.

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August 2005

Genetic disorders of transporters/channels in the inner ear and their relation to the kidney.

Authors:
Theo A Peters Leo A H Monnens Cor W R J Cremers Jo H A J Curfs

Pediatr Nephrol 2004 Nov 9;19(11):1194-201. Epub 2004 Sep 9.

Department of Otorhinolaryngology, University Medical Center Nijmegen, Philips van Leydenlaan 15, 6525 EX Nijmegen, The Netherlands.

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November 2004

Changes in ultrastructural characteristics of endolymphatic sac ribosome-rich cells of the rat during development.

Authors:
Theo A Peters Edith L G M Tonnaer Wim Kuijpers Jo H A J Curfs

Hear Res 2003 Feb;176(1-2):94-104

Department of Otorhinolaryngology, University Medical Center St Radboud, Philips van Leydenlaan 15, 6500 HB Nijmegen, The Netherlands.

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February 2003

Differences in endolymphatic sac mitochondria-rich cells indicate specific functions.

Authors:
Theo A Peters Edith L G M Tonnaer Wim Kuijpers Cor W R J Cremers Jo H A J Curfs

Laryngoscope 2002 Mar;112(3):534-41

Department of Otorhinolaryngology, University Medical Center St Radboud, Nijmegen, The Netherlands.

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March 2002