RPGRIP1s with distinct neuronal localization and biochemical properties associate selectively with RanBP2 in amacrine neurons (Q44521176)

3 December 2017

RPGRIP1s with distinct neuronal localization and biochemical properties associate selectively with RanBP2 in amacrine neurons (English)

1 reference

3 December 2017

5

1 reference

3 December 2017

P Castagnet

1

1 reference

3 December 2017

T Mavlyutov

series ordinal

2

1 reference

3 December 2017

Y Cai

series ordinal

3

1 reference

3 December 2017

F Zhong

series ordinal

4

1 reference

3 December 2017

1 August 2003

1 reference

3 December 2017

Human Molecular Genetics

1 reference

3 December 2017

12

1 reference

3 December 2017

15

1 reference

3 December 2017

1847-1863

1 reference

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

3 December 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

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%2FDDG202

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%2FDDG202

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%2FDDG202

Identification of a gene disrupted by a microdeletion in a patient with X-linked retinitis pigmentosa (XLRP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

X-linked cone-rod dystrophy (locus COD1): identification of mutations in RPGR exon ORF15

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Mutations in the RPGR gene cause X-linked cone dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

X-linked recessive atrophic macular degeneration from RPGR mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

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%2FDDG202

DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

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%2FDDG202

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Identification of a novel protein interacting with RPGR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Retinitis pigmentosa GTPase regulator (RPGRr)-interacting protein is stably associated with the photoreceptor ciliary axoneme and anchors RPGR to the connecting cilium

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Null RPGRIP1 alleles in patients with Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Classification of congenital and early onset retinitis pigmentosa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Molecular genetics of Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Identification and characterization of a nuclear pore complex protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

A nuclear pore complex protein that contains zinc finger motifs, binds DNA, and faces the nucleoplasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Nup358, a cytoplasmically exposed nucleoporin with peptide repeats, Ran-GTP binding sites, zinc fingers, a cyclophilin A homologous domain, and a leucine-rich region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Nuclear pore complex glycoproteins contain cytoplasmically disposed O-linked N-acetylglucosamine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Monoclonal antibodies identify a group of nuclear pore complex glycoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Retina-specifically expressed novel subtypes of bovine cyclophilin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

A giant nucleopore protein that binds Ran/TC4

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

RanGTP targets p97 to RanBP2, a filamentous protein localized at the cytoplasmic periphery of the nuclear pore complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Identification of RanBP2- and kinesin-mediated transport pathways with restricted neuronal and subcellular localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

The zinc finger cluster domain of RanBP2 is a specific docking site for the nuclear export factor, exportin-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

The docking of kinesins, KIF5B and KIF5C, to Ran-binding protein 2 (RanBP2) is mediated via a novel RanBP2 domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

The fundamental plan of the retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Amacrine-signaled loss of intrinsic axon growth ability by retinal ganglion cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Cell differentiation in the retina of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Bilateral retinal and brain tumors in transgenic mice expressing simian virus 40 large T antigen under control of the human interphotoreceptor retinoid-binding protein promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Photo-oxidative stress down-modulates the activity of nuclear factor-kappaB via involvement of caspase-1, leading to apoptosis of photoreceptor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Retina-derived microglial cells induce photoreceptor cell death in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

High hyperopia in Leber's congenital amaurosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Mental retardation in amaurosis congenita of Leber.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

The retinitis pigmentosa GTPase regulator (RPGR)- interacting protein: subserving RPGR function and participating in disk morphogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Transport between the cell nucleus and the cytoplasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Transport of proteins and RNAs in and out of the nucleus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

GTP hydrolysis links initiation and termination of nuclear import on the nucleoporin nup358

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

A RIP tide in neuronal signal transduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

Site-specific photocrosslinking to probe interactions of Arf1 with proteins involved in budding of COPI vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

The cyclophilin-like domain mediates the association of Ran-binding protein 2 with subunits of the 19 S regulatory complex of the proteasome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG202

21 January 2018

Identifiers

DOI

10.1093/HMG/DDG202

1 reference

3 December 2017

1 reference