(Q43231821)

16 November 2017

title

Zebrafish Rpgr is required for normal retinal development and plays a role in dynein-based retrograde transport processes (English)

1 reference

16 November 2017

3

Philippe Gautier

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16 November 2017

6

E Elizabeth Patton

1 reference

16 November 2017

Xinhua Shu

1

1 reference

16 November 2017

Zhiqiang Zeng

2

1 reference

16 November 2017

Alan Lennon

4

1 reference

16 November 2017

Milica Gakovic

5

1 reference

16 November 2017

Alan F Wright

7

1 reference

16 November 2017

publication date

1 December 2009

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16 November 2017

published in

Human Molecular Genetics

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16 November 2017

volume

19

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16 November 2017

issue

4

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16 November 2017

page(s)

657-670

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

16 November 2017

1 reference

Inherited and orphan retinal diseases: phenotypes, genotypes, and probable treatment groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

On the heredity of retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RPGR mutation analysis and disease: an update.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Mutational hot spot within a new RPGR exon in X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Positional cloning of the gene for X-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Focus on Molecules: RPGR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Dominant X linked retinitis pigmentosa is frequently accounted for by truncating mutations in exon ORF15 of the RPGR gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

X-linked retinitis pigmentosa: RPGR mutations in most families with definite X linkage and clustering of mutations in a short sequence stretch of exon ORF15

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Mutations of RPGR in X-linked retinitis pigmentosa (RP3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

The human retinitis pigmentosa GTPase regulator gene variant database

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

The 1.7 A crystal structure of the regulator of chromosome condensation (RCC1) reveals a seven-bladed propeller

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RPGR ORF15 isoform co-localizes with RPGRIP1 at centrioles and basal bodies and interacts with nucleophosmin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Developmental and tissue expression of Xenopus laevis RPGR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

RPGR isoforms in photoreceptor connecting cilia and the transitional zone of motile cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Age-dependent disease expression determines remodeling of the retinal mosaic in carriers of RPGR exon ORF15 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Identification of zebrafish insertional mutants with defects in visual system development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Early eye morphogenesis in the zebrafish, Brachydanio rerio.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Retinal neurogenesis: the formation of the initial central patch of postmitotic cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

The development of vision in the zebrafish (Danio rerio).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

dazed gene is necessary for late cell type development and retinal cell maintenance in the zebrafish retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Loss of PINK1 function affects development and results in neurodegeneration in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

A rapid apoptosis assay measuring relative acridine orange fluorescence in zebrafish embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Pigment Cells: A Model for the Study of Organelle Transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Stages of embryonic development of the zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

21 January 2018

GeneWise and Genomewise

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Zebrafish comparative genomics and the origins of vertebrate chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Splitting pairs: the diverging fates of duplicated genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Prox1 function controls progenitor cell proliferation and horizontal cell genesis in the mammalian retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Requirement for math5 in the development of retinal ganglion cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Kif3a constrains beta-catenin-dependent Wnt signalling through dual ciliary and non-ciliary mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Cilia and developmental signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Zebrafish ift57, ift88, and ift172 intraflagellar transport mutants disrupt cilia but do not affect hedgehog signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Mouse Kif7/Costal2 is a cilia-associated protein that regulates Sonic hedgehog signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Regulatory dissociation of Tctex-1 light chain from dynein complex is essential for the apical delivery of rhodopsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

The cytoplasmic tail of rhodopsin acts as a novel apical sorting signal in polarized MDCK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Evidence that microtubules do not mediate opsin vesicle transport in photoreceptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Ciliary targeting motif VxPx directs assembly of a trafficking module through Arf4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

Identification and characterization of a novel RPGR isoform in human retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP533

21 January 2018

Identifiers

DOI

10.1093/HMG/DDP533

1 reference

16 November 2017

1 reference