(Q47070588)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

title

ER-shaping proteins are required for ER and mitochondrial network organization in motor neurons (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

ADP-ribosylation factor-like 6 interacting protein 1 Dmel_CG10326

4 April 2020

main subject

1 reference

Dynamin related protein 1 Dmel_CG3210

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Niamh O'Sullivan

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

author name string

Philippa C Fowler

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

publication date

11 May 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

volume

25

1 reference

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4 April 2020

issue

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

page(s)

2827-2837

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

Membrane-shaping disorders: a common pathway in axon degeneration

4 April 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Cellular pathways of hereditary spastic paraplegia

21 January 2018

1 reference

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Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms

21 January 2018

1 reference

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Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

A class of membrane proteins shaping the tubular endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Arl6IP1 has the ability to shape the mammalian ER membrane in a reticulon-like fashion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Membrane proteins of the endoplasmic reticulum induce high-curvature tubules

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders

21 January 2018

1 reference

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D. melanogaster, mitochondria and neurodegeneration: small model organism, big discoveries.

21 January 2018

1 reference

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A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The leucine zipper motif of the Drosophila AF10 homologue can inhibit PRE-mediated repression: implications for leukemogenic activity of human MLL-AF10 fusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The Drosophila fragile X mental retardation gene regulates sleep need

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Reticulon-like-1, the Drosophila orthologue of the hereditary spastic paraplegia gene reticulon 2, is required for organization of endoplasmic reticulum and of distal motor axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

An intimate liaison: spatial organization of the endoplasmic reticulum-mitochondria relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

wishful thinking encodes a BMP type II receptor that regulates synaptic growth in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

ER tubules mark sites of mitochondrial division

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Dnm1 forms spirals that are structurally tailored to fit mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Mito-Morphosis: Mitochondrial Fusion, Fission, and Cristae Remodeling as Key Mediators of Cellular Function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The effects of ER morphology on synaptic structure and function in Drosophila melanogaster

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Tau promotes neurodegeneration via DRP1 mislocalization in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The PINK1/Parkin pathway regulates mitochondrial morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

The PINK1-Parkin pathway is involved in the regulation of mitochondrial remodeling process.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Different expression levels of spartin cause broad spectrum of cellular consequences in human neuroblastoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Absence of alsin function leads to corticospinal motor neuron vulnerability via novel disease mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Unique function of Kinesin Kif5A in localization of mitochondria in axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Mitochondrial fission protein Drp1 regulates mitochondrial transport and dendritic arborization in cerebellar Purkinje cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

In vivo analysis of proteomes and interactomes using Parallel Affinity Capture (iPAC) coupled to mass spectrometry

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDW139

21 January 2018

Identifiers

DOI

10.1093/HMG/DDW139

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27170313%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

1 reference