Search | IOVS | ARVO Journals

Showing 1 – 17 of 17

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract June 2023

Exploring the onset of retinal degeneration in Joubert Syndrome using retinal organoids

Kae Whiting; Emma Dyke; Marina Moya Molina; Sylvia Van Beersum; Thomas Theil; Majlinda Lako; Nael Nadif Kasri; Ronald Roepman

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5075.

ARVO Annual Meeting Abstract June 2021

Dissecting the disease mechanism of Leber congenital amaurosis type 5 (LCA5) using retinal affinity proteomics

Siebren Faber; Stef Letteboer; Alejandro Garanto; Katrin Junger; Tina Beyer; Jean Bennett; Marius Ueffing; Rob W.J. Collin; Karsten Boldt; Ronald Roepman

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):3077.

ARVO Annual Meeting Abstract June 2020

Dissecting the function of IQCB1/NPHP5, associated with retinal ciliopathies, by targeting its endogenous interactome

Ideke J.C. Lamers; Filine van den Bosch; Kim Klarenaar; Lisa Elze; Marius Ueffing; Karsten Boldt; Ronald Roepman

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):4008.

ARVO Annual Meeting Abstract July 2018

Delivery and deployment of a ciliary actin dynamics module by PCARE drives the neogenesis of phototransductive membrane disks

Rob W J Collin; Julio Cesar Corral Serrano; Jeroen van Reeuwijk; Anita DM Hoogendoorn; Renate AA Ruigrok; Adem Yildirim; Stef JF Letteboer; Lonneke Duijkers; Sanae Sakami; Krzysztof Palczewski; Karsten Boldt; Uwe Wolfrum; Marius Ueffing; Alex Garanto; Ronald Roepman

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4979.

ARVO Annual Meeting Abstract September 2016

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity

Anneke I Den Hollander; Nicole T.M. Saksens; Mark P Krebs; Elfride De Baere; Frans P Cremers; Camiel J F Boon; Ronald Roepman; Bart Peter Leroy; Neal S Peachey; Carel C B Hoyng; Patsy M Nishina

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12)

ARVO Annual Meeting Abstract June 2015

Investigating the role of C2orf71 in the pathogenesis of retinitis pigmentosa

JC Corral Serrano; Stef Letteboer; Alex Garanto; Ronald Roepman; Rob W.J. Collin

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):4643.

ARVO Annual Meeting Abstract June 2015

Interactome analysis reveals that FAM161A is a component of the Golgi-centrosomal network

Pietro Farinelli; Silvio Alessandro Di Gioia; Stef Letteboer; Ronald Roepman; Dror Sharon; Yvan Arsenijevic; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5505.

ARVO Annual Meeting Abstract April 2014

Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis

Uwe Wolfrum; Barbara Knapp; Pia Jores; Ronald Roepman; Hannie Kremer; Erwin vanWijk; Katharina Bauss

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6016.

ARVO Annual Meeting Abstract April 2014

The Mouse Homolog of the Human LCA3 Gene, Spata7, Plays a Critical Role in Cilium Structural Maintenance and Protein Trafficking in Photoreceptor Cells

Rui Chen; Aiden Eblimit; Yiyun Chen; Minh Nguyen; Julian Esteve-Rudd; Lin Gan; Samuel M Wu; David S Williams; Ronald Roepman; Graeme Mardon

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):6315.

ARVO Annual Meeting Abstract March 2012

Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal Recessive Cone-Rod Dystrophy and Retinitis Pigmentosa with Early Macular Involvement

Alejandro Estrada Cuzcano; Kornelia Neveling; Susanne Kohl; Dror Sharon; Ygal Rotenstreich; Ronald Roepman; Hans Scheffer; Anneke I. Den Hollander; B J. Klevering; Frans P. Cremers

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1730.

ARVO Annual Meeting Abstract March 2012

FAM161A, Associated With Autosomal Recessive Retinitis Pigmentosa, Localizes At The Level Of The Photoreceptor Cilium And Interacts With Proteins Involved In Ciliopathies

Silvio Alessandro Di Gioia; Corinne Kostic; Stef J.F. Letteboer; Lisette Hetterschijt; Yvan Arsenijevic; Ronald Roepman; Carlo Rivolta

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1732.

ARVO Annual Meeting Abstract March 2012

The USH1G Protein SANS Collaborates With Cytoplasmic Dynein Motor Components In Mammalian Photoreceptor Cells

Nasrin Sorusch; Nora Overlack; Andrea Kunz; Erwin van Wijk; Katharina Bauss; Tina Maerker; Ronald Roepman; Hannie Kremer; Uwe Wolfrum

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):2579.

ARVO Annual Meeting Abstract March 2012

Dissecting the sub-structure of the intraflagellar transport complex B

Karsten Boldt; Yves Texier; Jeroen van Reeuwijk; Dorus M. Mans; Ronald Roepman; Marius Ueffing

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):765.

ARVO Annual Meeting Abstract April 2011

The Ush1g Protein Sans Interacts With The Vesicular Traffic Associated Protein Magi2

Katharina Baub; Tina Maerker; Erwin v.Wijk; Ferry Kersten; Ronald Roepman; Hannie Kremer; Uwe Wolfrum

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):49.

Biochemistry and Molecular Biology May 2010

Association of Whirlin with Ca v 1.3 (α 1D ) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network

PDF

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
TAGS: photoreceptors, proteins, retina
Invest. Ophthalmol. Vis. Sci.. 2010; 51(5):2338-2346. https://doi.org/10.1167/iovs.09-4650

Retina March 2006

Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

PDF

Suzanne Yzer; Bart P. Leroy; Elfride De Baere; Thomy J. de Ravel; Marijke N. Zonneveld; Krysta Voesenek; Ulrich Kellner; Jose P. Martinez Ciriano; Jan-Tjeerd H. N. de Faber; Klaus Rohrschneider; Ronald Roepman; Anneke I. den Hollander; Johannes R. Cruysberg; Françoise Meire; Ingele Casteels; Norka G. van Moll-Ramirez; Rando Allikmets; L. Ingeborgh van den Born; Frans P. M. Cremers
TAGS: genotype, leber's amaurosis, mutation, phenotype, genes, ophthalmoscopy, eye
Invest. Ophthalmol. Vis. Sci.. 2006; 47(3):1167-1176. https://doi.org/10.1167/iovs.05-0848

Retinal Cell Biology June 2005

MPP5 Recruits MPP4 to the CRB1 Complex in Photoreceptors

PDF

Albena Kantardzhieva; Ilse Gosens; Svetlana Alexeeva; Ingrid M. Punte; Inge Versteeg; Elmar Krieger; Carla A. Neefjes-Mol; Anneke I. den Hollander; Stef J. F. Letteboer; Jan Klooster; Frans P. M. Cremers; Ronald Roepman; Jan Wijnholds
TAGS: photoreceptors, proteins, retina, mice, yeast one/two-hybrid system, antibodies, yeasts
Invest. Ophthalmol. Vis. Sci.. 2005; 46(6):2192-2201. https://doi.org/10.1167/iovs.04-1417

NARROW

Content Type

Journal

Article Type

Topics

Tags

Specify Date Range

Exploring the onset of retinal degeneration in Joubert Syndrome using retinal organoids

Dissecting the disease mechanism of Leber congenital amaurosis type 5 (LCA5) using retinal affinity proteomics

Dissecting the function of IQCB1/NPHP5, associated with retinal ciliopathies, by targeting its endogenous interactome

Delivery and deployment of a ciliary actin dynamics module by PCARE drives the neogenesis of phototransductive membrane disks

Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity

Investigating the role of C2orf71 in the pathogenesis of retinitis pigmentosa

Interactome analysis reveals that FAM161A is a component of the Golgi-centrosomal network

Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis

The Mouse Homolog of the Human LCA3 Gene, Spata7, Plays a Critical Role in Cilium Structural Maintenance and Protein Trafficking in Photoreceptor Cells

Mutations in C8orf37, Encoding a Ciliary Protein, are Associated with Autosomal Recessive Cone-Rod Dystrophy and Retinitis Pigmentosa with Early Macular Involvement

FAM161A, Associated With Autosomal Recessive Retinitis Pigmentosa, Localizes At The Level Of The Photoreceptor Cilium And Interacts With Proteins Involved In Ciliopathies

The USH1G Protein SANS Collaborates With Cytoplasmic Dynein Motor Components In Mammalian Photoreceptor Cells

Dissecting the sub-structure of the intraflagellar transport complex B

The Ush1g Protein Sans Interacts With The Vesicular Traffic Associated Protein Magi2

Association of Whirlin with Ca v 1.3 (α 1D ) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network

Microarray-Based Mutation Detection and Phenotypic Characterization of Patients with Leber Congenital Amaurosis

MPP5 Recruits MPP4 to the CRB1 Complex in Photoreceptors

To View More...

You must be signed into an individual account to use this feature.