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

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scientific article

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

Statements

instance of

scholarly article

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title

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

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main subject

cell biology

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author name string

Andreas Gerondopoulos

series ordinal

1

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Ricardo Nunes Bastos

series ordinal

2

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Shin-Ichiro Yoshimura

series ordinal

3

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Rachel Anderson

series ordinal

4

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Sarah Carpanini

series ordinal

5

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Irene Aligianis

series ordinal

6

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Mark T Handley

series ordinal

7

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Francis A Barr

series ordinal

8

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original language of film or TV show

English

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publication date

9 June 2014

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published in

Journal of Cell Biology

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volume

205

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issue

5

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page(s)

707-20

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cites work

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia

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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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Rab18 binds to hepatitis C virus NS5A and promotes interaction between sites of viral replication and lipid droplets

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RabGEFs are a major determinant for specific Rab membrane targeting

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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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Family-wide characterization of the DENN domain Rab GDP-GTP exchange factors

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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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Structural basis for Rab GTPase activation by VPS9 domain exchange factors

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Mutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndrome

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Subdomain-specific localization of CLIMP-63 (p63) in the endoplasmic reticulum is mediated by its luminal alpha-helical segment

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Molecular cloning and characterization of the noncatalytic subunit of the Rab3 subfamily-specific GTPase-activating protein

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Isolation and characterization of a GTPase activating protein specific for the Rab3 subfamily of small G proteins

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Identifiers

DOI

10.1083/JCB.201403026

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OpenCitations bibliographic resource ID

997886

1 reference

stated in

OpenCitations Corpus

PMC publication ID

4050724

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PubMed publication ID

24891604

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