Rab18 and a Rab18 GEF complex are required for normal ER structure. (Q24298701)

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Language	Label	Description	Also known as
English	Rab18 and a Rab18 GEF complex are required for normal ER structure.	scientific article

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

title

Rab18 and a Rab18 GEF complex are required for normal ER structure. (English)

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stated in

Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

main subject

cell biology

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author

Francis A. Barr

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8

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author name string

Andreas Gerondopoulos

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1

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

Ricardo Nunes Bastos

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2

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

Shin-Ichiro Yoshimura

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3

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

Rachel Anderson

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4

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

Sarah Carpanini

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5

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

Irene Aligianis

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6

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

Mark T Handley

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7

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

language of work or name

English

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publication date

2 June 2014

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

published in

Journal of Cell Biology

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

volume

205

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

issue

5

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Europe PubMed Central

PubMed publication ID

24891604

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25 June 2017

page(s)

707-720

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Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

cites work

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Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans

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Rab10 GTPase regulates ER dynamics and morphology

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Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

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Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

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A class of dynamin-like GTPases involved in the generation of the tubular ER network

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Analysis of GTPase-activating proteins: Rab1 and Rab43 are key Rabs required to maintain a functional Golgi complex in human cells

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Specific Rab GTPase-activating proteins define the Shiga toxin and epidermal growth factor uptake pathways

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Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders

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Rab GTPase regulation of membrane identity

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BLOC-3 mutated in Hermansky-Pudlak syndrome is a Rab32/38 guanine nucleotide exchange factor

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Insights regarding guanine nucleotide exchange from the structure of a DENN-domain protein complexed with its Rab GTPase substrate

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Rab18 and Rab43 have key roles in ER-Golgi trafficking

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The reticulon and DP1/Yop1p proteins form immobile oligomers in the tubular endoplasmic reticulum

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Rab18 inhibits secretory activity in neuroendocrine cells by interacting with secretory granules

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Rab3 GTPase-activating protein regulates synaptic transmission and plasticity through the inactivation of Rab3

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Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

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Cloning and subcellular localization of novel rab proteins reveals polarized and cell type-specific expression

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Localization of Rab proteins to peroxisomes: a proteomics and immunofluorescence study

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RAB3GAP1, RAB3GAP2 and RAB18: disease genes in Micro and Martsolf syndromes.

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Cellular pathways of hereditary spastic paraplegia

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Sculpting the endomembrane system in deep time: high resolution phylogenetics of Rab GTPases

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The ER in 3D: a multifunctional dynamic membrane network

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27 September 2017

Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

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27 September 2017

Mechanisms determining the morphology of the peripheral ER

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27 September 2017

A genome-wide RNA interference screen identifies two novel components of the metazoan secretory pathway

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27 September 2017

Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin

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27 September 2017

Structure, exchange determinants, and family-wide rab specificity of the tandem helical bundle and Vps9 domains of Rabex-5.

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27 September 2017

Diversity and plasticity in Rab GTPase nucleotide release mechanism has consequences for Rab activation and inactivation

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30 May 2018

Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome

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30 May 2018

A Rab10-dependent mechanism for polarized basement membrane secretion during organ morphogenesis

1 reference

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PubMed Central

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30 May 2018

Sheets, ribbons and tubules - how organelles get their shape.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1083%2FJCB.201403026

retrieved

21 January 2018

Identifiers

DOI

10.1083/JCB.201403026

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

OpenCitations bibliographic resource ID

997886

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

997886

PMC publication ID

4050724

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

997886

PubMed publication ID

24891604

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24891604

retrieved

25 June 2017

ResearchGate publication ID

273426252

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