(Q40565472)

21 September 2017

title

Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology (English)

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21 September 2017

Guohua Zhao

1

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21 September 2017

Peng-Peng Zhu

2

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21 September 2017

Benoît Renvoisé

3

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21 September 2017

Lymarie Maldonado-Báez

4

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21 September 2017

Seong Hee Park

5

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21 September 2017

Craig Blackstone

6

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21 September 2017

language of work or name

English

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publication date

23 September 2016

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Experimental Cell Research

21 September 2017

published in

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21 September 2017

volume

349

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21 September 2017

issue

1

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21 September 2017

page(s)

32-44

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Cellular pathways of hereditary spastic paraplegia

21 September 2017

cites work

1 reference

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

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

7 January 2021

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Atlastin GTPases are required for Golgi apparatus and ER morphogenesis

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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ROOT HAIR DEFECTIVE3 family of dynamin-like GTPases mediates homotypic endoplasmic reticulum fusion and is essential for Arabidopsis development

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2016.09.015

ER - the key to the highway

7 January 2021

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Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

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A novel missense mutation confirms ATL3 as a gene for hereditary sensory neuropathy type 1.

7 January 2021

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Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I.

7 January 2021

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

7 January 2021

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Untangling the web: mechanisms underlying ER network formation

7 January 2021

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A conserved role for atlastin GTPases in regulating lipid droplet size

7 January 2021

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Functional mutation analysis provides evidence for a role of REEP1 in lipid droplet biology

7 January 2021

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Spastin binds to lipid droplets and affects lipid metabolism

7 January 2021

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

7 January 2021

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Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A.

7 January 2021

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ER stress signaling requires RHD3, a functionally conserved ER-shaping GTPase

7 January 2021

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RNA-guided human genome engineering via Cas9

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Prolonged induction activates Cebpα independent adipogenesis in NIH/3T3 cells

7 January 2021

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

7 January 2021

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Rab10 GTPase regulates ER dynamics and morphology

7 January 2021

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Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.

7 January 2021

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Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling

7 January 2021

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The human lipodystrophy gene BSCL2/seipin may be essential for normal adipocyte differentiation

7 January 2021

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ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering

7 January 2021

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In Arabidopsis, the spatial and dynamic organization of the endoplasmic reticulum and Golgi apparatus is influenced by the integrity of the C-terminal domain of RHD3, a non-essential GTPase

7 January 2021

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Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis

7 January 2021

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Arabidopsis RHD3 mediates the generation of the tubular ER network and is required for Golgi distribution and motility in plant cells.

7 January 2021

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Atlastin-1, the dynamin-like GTPase responsible for spastic paraplegia SPG3A, remodels lipid membranes and may form tubules and vesicles in the endoplasmic reticulum

7 January 2021

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Adipogenesis: from stem cell to adipocyte

7 January 2021

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Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway

7 January 2021

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Spartin regulates synaptic growth and neuronal survival by inhibiting BMP-mediated microtubule stabilization

7 January 2021

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The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling

7 January 2021

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Drosophila spichthyin inhibits BMP signaling and regulates synaptic growth and axonal microtubules

7 January 2021

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Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking

7 January 2021

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Neuronal endoplasmic reticulum stress in axon injury and neurodegeneration

7 January 2021

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Phosphorylation of the C Terminus of RHD3 Has a Critical Role in Homotypic ER Membrane Fusion in Arabidopsis

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2016.09.015

The endoplasmic reticulum exerts control over organelle streaming during cell expansion

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2016.09.015

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YEXCR.2016.09.015

ER network formation and membrane fusion by atlastin1/SPG3A disease variants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2016.09.015

10.1016/J.YEXCR.2016.09.015

7 January 2021

Identifiers

DOI

1 reference

21 September 2017

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