Related references
Note: Only part of the references are listed.iPSC modeling of severe aplastic anemia reveals impaired differentiation and telomere shortening in blood progenitors
Dario Melguizo-Sanchis et al.
CELL DEATH & DISEASE (2018)
Primary Cilium-Mediated Retinal Pigment Epithelium Maturation Is Disrupted in Ciliopathy Patient Cells
Helen Louise May-Simera et al.
CELL REPORTS (2018)
In Vivo Applications of CRISPR-Based Genome Editing in the Retina
Wenhan Yu et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2018)
The Output of Protein-Coding Genes Shifts to Circular RNAs When the Pre-mRNA Processing Machinery Is Limiting
Dongming Liang et al.
MOLECULAR CELL (2017)
Towards optimisation of induced pluripotent cell culture: Extracellular acidification results in growth arrest of iPSC prior to nutrient exhaustion
Anja Wilmes et al.
TOXICOLOGY IN VITRO (2017)
High prevalence of mutations affecting the splicing process in a Spanish cohort with autosomal dominant retinitis pigmentosa
Maitane Ezquerra-Inchausti et al.
SCIENTIFIC REPORTS (2017)
Pan-retinal characterisation of Light Responses from Ganglion Cells in the Developing Mouse Retina
Gerrit Hilgen et al.
SCIENTIFIC REPORTS (2017)
Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors
Jie Zhu et al.
CELL RESEARCH (2017)
Harnessing the Potential of Human Pluripotent Stem Cells and Gene Editing for the Treatment of Retinal Degeneration
Patrick Ovando-Roche et al.
CURRENT STEM CELL REPORTS (2017)
2016 update of the PRIDE database and its related tools
Juan Antonio Vizcaino et al.
NUCLEIC ACIDS RESEARCH (2016)
The Perseus computational platform for comprehensive analysis of (prote)omics data
Stefka Tyanova et al.
NATURE METHODS (2016)
The Musashi 1 Controls the Splicing of Photoreceptor-Specific Exons in the Vertebrate Retina
Daniel Murphy et al.
PLOS GENETICS (2016)
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
Gabrielle Wheway et al.
NATURE CELL BIOLOGY (2015)
IGF-1 Signaling Plays an Important Role in the Formation of Three-Dimensional Laminated Neural Retina and Other Ocular Structures From Human Embryonic Stem Cells
Carla B. Mellough et al.
STEM CELLS (2015)
Generation of a ciliary margin-like stem cell niche from self-organizing human retinal tissue
Atsushi Kuwahara et al.
NATURE COMMUNICATIONS (2015)
Spike Detection for Large Neural Populations Using High Density Multielectrode Arrays
Jens-Oliver Muthmann et al.
FRONTIERS IN NEUROINFORMATICS (2015)
HTSeq-a Python framework to work with high-throughput sequencing data
Simon Anders et al.
BIOINFORMATICS (2015)
PRPF8 defects cause missplicing in myeloid malignancies
A. Kurtovic-Kozaric et al.
LEUKEMIA (2015)
Segmentation of the Clustered Cells with Optimized Boundary Detection in Negative Phase Contrast Images
Yuliang Wang et al.
PLOS ONE (2015)
Mutations in Pre-mRNA Processing Factors 3, 8, and 31 Cause Dysfunction of the Retinal Pigment Epithelium
Michael H. Farkas et al.
AMERICAN JOURNAL OF PATHOLOGY (2014)
PRPF4 mutations cause autosomal dominant retinitis pigmentosa
Xue Chen et al.
HUMAN MOLECULAR GENETICS (2014)
Genome engineering using the CRISPR-Cas9 system
F. Ann Ran et al.
NATURE PROTOCOLS (2013)
Functional Analysis of Serially Expanded Human iPS Cell-Derived RPE Cultures
Ruchira Singh et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2013)
clusterProfiler: an R Package for Comparing Biological Themes Among Gene Clusters
Guangchuang Yu et al.
OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY (2012)
CNOT3 Is a Modifier of PRPF31 Mutations in Retinitis Pigmentosa with Incomplete Penetrance
Giulia Venturini et al.
PLOS GENETICS (2012)
A Missense Mutation in PRPF6 Causes Impairment of pre-mRNA Splicing and Autosomal-Dominant Retinitis Pigmentosa
Goranka Tanackovic et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
PRPF mutations are associated with generalized defects in spliceosome formation and pre-mRNA splicing in patients with retinitis pigmentosa
Goranka Tanackovic et al.
HUMAN MOLECULAR GENETICS (2011)
Human Induced Pluripotent Stem-Derived Retinal Pigment Epithelium (RPE) Cells Exhibit Ion Transport, Membrane Potential, Polarized Vascular Endothelial Growth Factor Secretion, and Gene Expression Pattern Similar to Native RPE
Maria Kokkinaki et al.
STEM CELLS (2011)
Three Gene-Targeted Mouse Models of RNA Splicing Factor RP Show Late-Onset RPE and Retinal Degeneration
John J. Graziotto et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)
Metadata matters: access to image data in the real world
Melissa Linkert et al.
JOURNAL OF CELL BIOLOGY (2010)
Enhancing Serial Block-Face Scanning Electron Microscopy to Enable High Resolution 3-D Nanohistology of Cells and Tissues
TJ Deerinck et al.
MICROSCOPY AND MICROANALYSIS (2010)
The Cellular Expression of Antiangiogenic Factors in Fetal Primate Macula
Peter Kozulin et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
Autosomal-Dominant Retinitis Pigmentosa Caused by a Mutation in SNRNP200, a Gene Required for Unwinding of U4/U6 snRNAs
Chen Zhao et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Nesprin-2 interacts with meckelin and mediates ciliogenesis via remodelling of the actin cytoskeleton
Helen R. Dawe et al.
JOURNAL OF CELL SCIENCE (2009)
PRPF31 Alternative Splicing and Expression in Human Retina
Goranka Tanackovic et al.
OPHTHALMIC GENETICS (2009)
Protective Effects of Human iPS-Derived Retinal Pigment Epithelium Cell Transplantation in the Retinal Dystrophic Rat
Amanda-Jayne Carr et al.
PLOS ONE (2009)
Study of Gene-Targeted Mouse Models of Splicing Factor Gene Prpf31 Implicated in Human Autosomal Dominant Retinitis Pigmentosa (RP)
Kinga Bujakowska et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)
Endogenous VEGF Is Required for Visual Function: Evidence for a Survival Role on Muller Cells and Photoreceptors
Magali Saint-Geniez et al.
PLOS ONE (2008)
Decreased levels of the RNA splicing factor Prpf3 in mice and zebrafish do not cause photoreceptor degeneration
John J. Graziotto et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2008)
Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells
Antonella Comitato et al.
HUMAN MOLECULAR GENETICS (2007)
Prevalence of disease-causing mutations in families with autosomal dominant retinitis pigmentosa: A screen of known genes in 200 families
Lori S. Sullivan et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Pigment epithelium-derived factor in the monkey retinal pigment epithelium and interphotoreceptor matrix: apical secretion and distribution
SP Becerra et al.
EXPERIMENTAL EYE RESEARCH (2004)
Segmentation and tracking of migrating cells in videomicroscopy with parametric active contours:: A tool for cell-based drug testing
C Zimmer et al.
IEEE TRANSACTIONS ON MEDICAL IMAGING (2002)
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosa
TJ Keen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2002)
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
CF Chakarova et al.
HUMAN MOLECULAR GENETICS (2002)
A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13.4 (RP11)
EN Vithana et al.
MOLECULAR CELL (2001)
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
AB McKie et al.
HUMAN MOLECULAR GENETICS (2001)
PAP-1, a novel target protein of phosphorylation by Pim-1 kinase
H Maita et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2000)