(Q24318948)

Zinc finger FYVE-type containing 27

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Atlastin GTPase 3

1 reference

Proceedings of the National Academy of Sciences of the United States of America

GOA release 2020-03-11

1

Jaerak Chang

0 references

author name string

Seongju Lee

series ordinal

2

0 references

Craig Blackstone

series ordinal

3

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language of work or name

English

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publication date

10 September 2013

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published in

0 references

volume

110

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issue

37

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page(s)

14954-9

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describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3773775/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Rab10 GTPase regulates ER dynamics and morphology

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MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis

19 March 2017

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

19 March 2017

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

19 March 2017

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

19 March 2017

1 reference

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Promotion of neurite extension by protrudin requires its interaction with vesicle-associated membrane protein-associated protein

19 March 2017

1 reference

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Atlastin GTPases are required for Golgi apparatus and ER morphogenesis

19 March 2017

1 reference

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Protrudin induces neurite formation by directional membrane trafficking

19 March 2017

1 reference

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Interaction of two hereditary spastic paraplegia gene products, spastin and atlastin, suggests a common pathway for axonal maintenance

19 March 2017

1 reference

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Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleus

19 March 2017

1 reference

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Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

19 March 2017

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A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

19 March 2017

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ER-to-plasma membrane tethering proteins regulate cell signaling and ER morphology

19 March 2017

1 reference

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ER network formation requires a balance of the dynamin-like GTPase Sey1p and the Lunapark family member Lnp1p

19 March 2017

1 reference

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The dynamin-like GTPase Sey1p mediates homotypic ER fusion in S. cerevisiae

19 March 2017

1 reference

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Osh proteins regulate phosphoinositide metabolism at ER-plasma membrane contact sites

19 March 2017

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Membrane proteins of the endoplasmic reticulum induce high-curvature tubules

19 March 2017

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A class of membrane proteins shaping the tubular endoplasmic reticulum

19 March 2017

1 reference

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Protrudin serves as an adaptor molecule that connects KIF5 and its cargoes in vesicular transport during process formation

19 March 2017

1 reference

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SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development

19 March 2017

1 reference

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Phosphoinositides differentially regulate protrudin localization through the FYVE domain

19 March 2017

1 reference

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ER-shaping proteins facilitate lipid exchange between the ER and mitochondria in S. cerevisiae

27 September 2017

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Role of spastin and protrudin in neurite outgrowth

27 September 2017

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Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance

27 September 2017

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Cellular pathways of hereditary spastic paraplegia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Genetics of hereditary spastic paraplegias

27 September 2017

1 reference

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Oligomerization of ZFYVE27 (Protrudin) is necessary to promote neurite extension

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Hereditary spastic paraplegias: membrane traffic and the motor pathway

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Mechanisms determining the morphology of the peripheral ER

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Further assembly required: construction and dynamics of the endoplasmic reticulum network

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

A role for Rab5 in structuring the endoplasmic reticulum

27 September 2017

1 reference

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ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

Rab10 joins the ER social network

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3773775

The role of ZFYVE27/protrudin in hereditary spastic paraplegia

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1307391110

Reticulon-4A (Nogo-A) redistributes protein disulfide isomerase to protect mice from SOD1-dependent amyotrophic lateral sclerosis

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.1307391110

A VAPB mutant linked to amyotrophic lateral sclerosis generates a novel form of organized smooth endoplasmic reticulum

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23969831

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A mutation in VAPB that causes amyotrophic lateral sclerosis also causes a nuclear envelope defect

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23969831