![Ronald Roepman [Session Chair] Radboud University Nijmegen Medical Centre, ... - bio-jackson-sm](http://www.yasni.info/show_image.php?name=Ronald+Roepman&ref=http%3A%2F%2Fwww.visionresearch-conference.elsevier.com%2Fresources%2Fimage%2Fbio-jackson-sm.jpg&refurl=http%3A%2F%2Fwww.visionresearch-conference.elsevier.com%2Fconference-speakers.html&width=36&height=50&showads=1&lc=en-us&lg=en&rg=us&rip=us "Ronald Roepman [Session Chair] Radboud University Nijmegen Medical Centre, ...")
1
0
0
News
Google News - Ronald Roepman - Aktuell
news.google.com
Mit Google News kannst du zum Thema Ronald Roepman vollständige Artikel lesen, Videos ansehen und in Tausenden von Titeln stöbern.
WN - roepman
wn.com
Ronald Roepman appointed Professor of Molecular Biology of Ciliopathies (Radboud Universiteit) · noodls (Source: Radboud Universiteit) Ronald ...
CILIA International Conference - the Ciliopathy Alliance!
www.ciliopathyalliance.org
The next meeting - Cilia will be organised in Amsterdam from 4 to 7 October 2016, under the supervision of Ronald Roepman, chair of Oct - 9 Oct
CILIA CONFERENCE
Network Profiles
LinkedIn: Ronald Roepman | LinkedIn
Bekijk het professionele profiel van Ronald Roepman op LinkedIn. LinkedIn is het grootste zakelijke netwerk ter wereld en stelt professionals als Ronald ...
LinkedIn: Ronald Roepman - Nederland | LinkedIn
Ronald Roepman-- Location Nijmegen Area, Netherlands Industry Hospital & Health Care
Ronald Roepman PhD - Radboudumc
www.radboudumc.nl
Looking for information on Ronald Roepman PhD? Read more about this Radboudumc employee.
Interests
Research team enlightens the reasons for severe blindness ...
www.eurekalert.org
Coordinated by the geneticist Ronald Roepman from Nijemegen, an important step has now been made in this direction by an international ...
Gene Responsible For Blindness In Infants And Children Identified
www.sciencedaily.com
"Our main research goal is to identify all the genes responsible for congenital blindness in children and then ... Frans Cremers and Ronald Roepman from the
De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
download.cell.com
Peer Arts, Bart van Lier, Marloes Steehouwer, Jeroen van Reeuwijk, Sarina G. Kant, Ronald Roepman, Nine V.A.M. Knoers, Joris A. Veltman, and Han G. Brunner ...
Scientists gain new insights into 'antenna' of human cells ...
www.sciencedaily.com
Professor Ronald Roepman, of the Radboud University Medical Center, Nijmegen, added: "We confirmed that each of the genes on the list ...
Education
Functional proteomics [electronic resource] : methods and protocols /...
catalog.princeton.edu
Free-flow electrophoresis of the human urinary proteome / Mikkel Nissum and Robert Wildgruber -- Versatile screening for binary protein-protein interactions by yeast two-hybrid mating / Stef J.F. Letteboer and Ronald Roepman -- Native fractionation : isolation of native membrane-bound protein complexes from porcine rod ...
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy...
kclpure.kcl.ac.uk
... Wicking and Valerie Cormier-Daire and Ronald Roepman and Mitchison, {Hannah M} and Witman, {George B} and UK10K and Metrustry, {Sarah Jane}",.
Projects
Syscilia: Institute for Ophthalmic Research Tuebingen
www.eye-tuebingen.de
Ronald Roepman, Radboud University Nijmegen Medical Centre, The Netherlands (Coordinator); H. Kremer, Radboud University Nijmegen Medical Centre, ...
Books & Literature
Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and...
biblio.ugent.be
... SOPHIE WALRAEDT UGent, Sandro Banfi, Francesca Simonelli, Frans PM Cremers, Camiel JF Boon, Ronald Roepman, Bart Leroy UGent, ...
NINL and DZANK1 Co-function in Vesicle PLOS Genetics
journals.plos.org
Ronald Roepman. Affiliations Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, the Netherlands, ...
Subcellular Proteomics: From Cell Deconstruction to System...
books.google.de
This volume summarizes the new developments that made subcellular proteomics a rapidly expanding area. It examines the different levels of subcellular...
Cilia: Structure and Motility - Google Books
books.google.de
... University of Leeds, Leeds LS29JT, United Kingdom Ronald Roepman (143), Department of Human Genetics, Radboud University Nijmegen Medical Centre, ...
Related Documents
EBSCOhost | | C14ORF179 encoding IFT43 is mutated in...
web.a.ebscohost.com
Ronald Roepman. 1,2,3. ABSTRACT. Background Sensenbrenner syndrome is a heterogeneous ciliopathy that is characterised by skeletal and ectodermal ...
CC2D2A Is Mutated in Joubert Syndrome and Interacts with ...
depts.washington.edu
Nine V.A.M. Knoers,8 Phillip F. Chance,1 Ronald Roepman,8 Cecilia B. Moens, 19. Ian A. Glass,1 and Dan Doherty1,*. Joubert syndrome and related disorders ...
OASIS
www.abstractsonline.com
Silvio Alessandro Di Gioia 1, Corinne Kostic 2, Stef J.F. Letteboer 3, Lisette Hetterschijt 3, Yvan Arsenijevic 2, Ronald Roepman 3, Carlo Rivolta 1.
Scientific Publications
DFG - GEPRIS - Professor Dr. Ronald Roepman, Ph.D.
gepris.dfg.de
Professor Dr. Ronald Roepman, Ph.D., Department of Human Genetics, Geert Grooteplein 10, GA Nijmegen, Niederlande.
Methods in Cell Biology | Cilia: Structure and Motility |...
www.sciencedirect.com
Karsten Boldt, Jeroen van Reeuwijk, Christian Johannes Gloeckner, Marius Ueffing, Ronald Roepman. Pages : Download PDF. Chapter preview.
OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with...
www.ncbi.nlm.nih.gov
OFD1 Is Mutated in X-Linked Joubert Syndrome and Interacts with LCA5- Encoded Lebercilin. Karlien L.M. Coene,1,2,9 Ronald Roepman,1,2,9,∗ Dan Doherty,4 ...
The more we know, the more we have to discover: an exciting future...
ciliajournal.biomedcentral.com
The Cilia conference was organised by four European networks: the Ciliopathy Alliance, the Groupement de Recherche CIL, the Nordic Cilia and Centrosome...
Publications
Publications Authored by Ronald Roepman | PubFacts
www.pubfacts.com
Publications Authored by Ronald Roepman
Versatile Screening for Binary Protein-Protein Interactions by ...
link.springer.com
Versatile Screening for Binary Protein-Protein Interactions by Yeast Two-Hybrid Mating. Authors; Authors and affiliations. Stef J. F. Letteboer; Ronald Roepman.
The SYSCILIA gold standard (SCGSv1) of known BioMedSearch
www.biomedsearch.com
de la Sante et de la Recherche Medicale, Paris, France), Ronald Roepman. (Radboud University Medical Centre, Nijmegen, The Netherlands), ...
Reports & Statements
Evidence for RPGRIP1 gene as risk factor for primary open angle ...
www.nature.com
Authors: Lorena Fernández-Martínez, Stef Letteboer, Christian Y Mardin, Nicole Weisschuh, Eugen Gramer, Bernhard HF Weber, Bernd Rautenstrauss, Paulo A Ferreira, Friedrich E Kruse, André Reis, Ronald Roepman & Francesca Pasutto.
DYX1C1 is required for axonemal dynein assembly and ciliary motility...
www.nature.com
Heymut Omran, Joseph LoTurco and colleagues show that mutations in the dyslexia susceptibility candidate gene DYX1C1 cause primary ciliary dyskinesia. Their...
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy...
www.nature.com
Severe congenital development defects such as Jeune syndrome can result from the malfunction of primary cilia and dynein. Here Schmidts et al. report unique...
Miscellaneous
ronald roepman | LinkedIn
www.linkedin.com
View ronald roepman's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like ronald roepman discover inside
Ronald Roepman | Publons
publons.com
View Ronald Roepman's profile on Publons with 131 publications.
Ronald Roepman Archieven - Vox magazine
www.voxweb.nl
Onderzoekers van de afdeling Antropogenetica van het UMC St Radboud hebben ontdekt dat een defecte transportband in lichtgevoelige cellen erfelijke…
Dr Ronald ROEPMAN - Orphanet
www.orpha.net
Afdeling Genetica; Radboudumc - Radboud universitair medisch centrum; Geert Grooteplein-Zuid 10; GA NIJMEGEN; NETHERLANDS; More information ...
The European Vision Awardee 2010: Dr. Ronald Roepman: European Vision...
www.europeanvisioninstitute.org
The European Vision Institute EEIG proudly presents the winner of the European Vision Award 2010: Dr. Ronald Roepman Radboud University Nijmegen Medical Centre
14th Vision Research Conference Retina Ciliopathies: From Genes to...
webvision.med.utah.edu
Ronald Roepman, Radboud University Nijmegen Medical Centre, The Netherlands. Session 7 Animal models of retinal ciliopathies Chair: Tiansen Li, NEI, United States
Citations to Disruption of intraflagellar protein transport in JCI
www.jci.org
Karsten Boldt, … , Ronald Roepman, Marius Ueffing. Karsten Boldt, … , Ronald Roepman, Marius Ueffing. Published June 1, 2011; First published May 23, 2011
CCDC151 mutations cause primary ciliary dyskinesia by disruption of...
www.semanticscholar.org
... Ian M. Carr, Christopher O'Callaghan, Eduardo Moya, Eddie M.K. Chung,. UK10K, Eamonn Sheridan, Kim G. Nielsen, Ronald Roepman, Kerstin Bartscherer,.
An siRNA-based functional genomics screen for the identification of...
pure.qub.ac.uk
... G.} and Uwe Wolfrum and Beales, {Philip L.} and Toby Gibson and Dan Doherty and Mitchison, {Hannah M.} and Ronald Roepman and Johnson, {Colin A.}",.
ALUMNI
www.ferreira-lab.org
Indulekha CL, PhD ( ); Postdoctoral fellow, University of North Carolina, Chapel Hill. • Emdadul Haque, PhD ( ); Research Scientist, Syngenta Biotechnology. Past Graduate Student Ph.D. Trainees: • Ronald Roepman, Ph.D. ( ); Associate Professor, Department of Human Genetics, Univ.
MPP5 Recruits MPP4 to the CRB1 Complex in Photoreceptors | IOVS |...
iovs.arvojournals.org
Ronald Roepman. University Medical Centre Nijmegen, Nijmegen, The Netherlands; and the. Jan Wijnholds MPP5 Recruits MPP4 to the CRB1 Complex in Photoreceptors.
JCI - Disruption of intraflagellar protein transport in photoreceptor...
www.jci.org
Or to: Ronald Roepman, Department of Human Genetics (855), Radboud University Nijmegen Medical Centre, P.O. Box 9101, HB Nijmegen, Netherlands.
Association of Whirlin with Cav1.3 (α1D) Channels in Photoreceptors,...
iovs.arvojournals.org
Uwe Wolfrum,7 Jan E. E. Keunen,3 Ronald Roepman,1,4,11 and Hannie Kremer2,4,5,11. PURPOSE. Usher syndrome is the most common form of hered-.
Ciliopathies with Skeletal Anomalies and Renal Insufficiency due to...
research.rug.nl
... Helge Boman and Eyvind Rodahl and Veltman, {Joris A.} and Knappskog, {Per M.} and Knoers, {Nine V. A. M.} and Ronald Roepman and Arts, {Heleen H.}",.
OPUS FAU | Mutations in PIK3C2A cause syndromic short stature,...
opus4.kobv.de
... André Reis, Nadine N. Hauer, Emilio Hirsch, Ronald Roepman, Rolph Pfundt, Christian T. Thiel, Michael S. Wiesener, Mariam G. Aslanyan, ...
A G-protein activation cascade from Arl13B to Arl3 and implications...
elifesciences.org
The ciliary G-protein Arl13B – which is often mutated in Joubert syndrome – is the Guanine nucleotide exchange factor for the G-protein Arl3 and exclusively...
Disease gene identification with exome sequencing - PDF
docplayer.net
... de Vries, Nine Knoers Molecular Genetics Heleen Arts, Ronald Roepman Next generation sequencing team Genomic Disorders Group: Alexander Hoischen, ...
SPATA7 maintains a novel photoreceptor-specific zone in the ...jcb.rupress.org › early › › jcb › tab-article-info
rupress.org
... Jain,3; Yumei Li,2; Jun Qin,3; Paul Overbeek,1; Ronald Roepman,4,5; Graeme Mardon,1,6; Theodore G. Wensel,3 and; Rui Chen1,2,3⇑.
Saudi Journal of Kidney Diseases and Transplantation (SJKDT): Table...
www.sjkdt.org
... Heijden,Hester Y. Kroes,Elly Ippel,Annelien J. A. Schulp,Koen L. van Gassen,Iris A. L. M. van Rooij,Rachel H. Giles,Philip L. Beales,Ronald Roepman,Heleen ...
Roepman Makelaardij: groot netwerk en goede waardering | Delft op...
www.delftopzondag.nl
Het zijn bijzondere tijden op de woningmarkt, merkt Roepman Makelaardij. Zelden was het voor woningzoekenden zó belangrijk om een goede ervaren aankoopmakelaar...
Related search requests for Ronald Roepman
| Peter Swoboda Marius Ueffing André Reis | Karsten Boldt |
People Forename "Ronald" (37693) Name "Roepman" (1) |
sorted by relevance / date