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Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution

Cell reports (Cambridge), 2018-05, Vol.23 (6), p.1742-1753

2018

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

Nature (London), 2009-08, Vol.460 (7258), p.978-983

2009

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Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion

The Journal of cell biology, 2014-02, Vol.204 (3), p.303-312

2014

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In vivo Analysis of CRISPR/Cas9 Induced Atlastin Pathological Mutations in Drosophila

Frontiers in neuroscience, 2020-10, Vol.14, p.547746-547746

2020

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

Journal of cell science, 2016-04, Vol.129 (8), p.1635-1648

2016

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Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon

Nature communications, 2019-11, Vol.10 (1), p.5327-11, Article 5327

2019

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ER Morphology in the Pathogenesis of Hereditary Spastic Paraplegia

Cells (Basel, Switzerland), 2021-10, Vol.10 (11), p.2870

2021

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Spastin binds to lipid droplets and affects lipid metabolism

PLoS genetics, 2015-04, Vol.11 (4), p.e1005149-e1005149

2015

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Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca2+ Handling

Frontiers in physiology, 2019-12, Vol.10, p.1544-1544

2019

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Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain

Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (27), p.11133-11138

2011

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The Hereditary Spastic Paraplegia Gene, spastin, Regulates Microtubule Stability to Modulate Synaptic Structure and Function

Current biology, 2004-07, Vol.14 (13), p.1135-1147

2004

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GTP-dependent packing of a three-helix bundle is required for atlastin-mediated fusion

Proceedings of the National Academy of Sciences - PNAS, 2011-09, Vol.108 (39), p.16283-16288

2011

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Balancing ER dynamics: shaping, bending, severing, and mending membranes

Current opinion in cell biology, 2011-08, Vol.23 (4), p.435-442

2011

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Proteasome dysfunction induces excessive proteome instability and loss of mitostasis that can be mitigated by enhancing mitochondrial fusion or autophagy

Autophagy, 2019-10, Vol.15 (10), p.1757-1773

2019

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Lozenge is expressed in pluripotent precursor cells and patterns multiple cell types in the Drosophila eye through the control of cell-specific transcription factors

Development (Cambridge), 1998-09, Vol.125 (18), p.3681-3687

1998

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Natural Selection Favors a Newly Derived Timeless Allele in Drosophila melanogaster

Science (American Association for the Advancement of Science), 2007-06, Vol.316 (5833), p.1895-1898

2007

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Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastine

The Journal of clinical investigation, 2005-11, Vol.115 (11), p.3026-3034

2005

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Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca 2+ Handling

Frontiers in physiology, 2019, Vol.10, p.1544

2019

Volltextzugriff (PDF)

Fusing a lasting relationship between ER tubules

Trends in cell biology, 2011-07, Vol.21 (7), p.416-423

2011

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The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function

Brain (London, England : 1878), 2006-07, Vol.129 (7), p.1710-1719

2006

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Defhc1.1, a homologue of the juvenile myoclonic gene EFHC1, modulates architecture and basal activity of the neuromuscular junction in Drosophila

Human molecular genetics, 2011-11, Vol.20 (21), p.4248-4257

2011

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Spastin Binds to Lipid Droplets and Affects Lipid Metabolism: e1005149

PLoS genetics, 2015-04, Vol.11 (4)

2015

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Transgenic fruit-flies expressing a FRET-based sensor for in vivo imaging of cAMP dynamics

Cellular signalling, 2007-11, Vol.19 (11), p.2296-2303

2007

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Myoclonin1/EFHC1 disease mechanisms in JME

Epilepsia (Copenhagen), 2010-12, Vol.51 (s5), p.74-74

2010

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Manipulation of Mitochondria Dynamics Reveals Separate Roles for Form and Function in Mitochondria Distribution

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

Reduction of endoplasmic reticulum stress attenuates the defects caused by Drosophila mitofusin depletion

In vivo Analysis of CRISPR/Cas9 Induced Atlastin Pathological Mutations in Drosophila

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

Dynamic constriction and fission of endoplasmic reticulum membranes by reticulon

ER Morphology in the Pathogenesis of Hereditary Spastic Paraplegia

Spastin binds to lipid droplets and affects lipid metabolism

Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca2+ Handling

Membrane fusion by the GTPase atlastin requires a conserved C-terminal cytoplasmic tail and dimerization through the middle domain

The Hereditary Spastic Paraplegia Gene, spastin, Regulates Microtubule Stability to Modulate Synaptic Structure and Function

EFHC1 variants in juvenile myoclonic epilepsy: reanalysis according to NHGRI and ACMG guidelines for assigning disease causality

GTP-dependent packing of a three-helix bundle is required for atlastin-mediated fusion

Balancing ER dynamics: shaping, bending, severing, and mending membranes

Proteasome dysfunction induces excessive proteome instability and loss of mitostasis that can be mitigated by enhancing mitochondrial fusion or autophagy

Lozenge is expressed in pluripotent precursor cells and patterns multiple cell types in the Drosophila eye through the control of cell-specific transcription factors

Natural Selection Favors a Newly Derived Timeless Allele in Drosophila melanogaster

Disease-related phenotypes in a Drosophila model of hereditary spastic paraplegia are ameliorated by treatment with vinblastine

Microtubules Stabilization by Mutant Spastin Affects ER Morphology and Ca 2+ Handling

Fusing a lasting relationship between ER tubules

The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function

Defhc1.1, a homologue of the juvenile myoclonic gene EFHC1, modulates architecture and basal activity of the neuromuscular junction in Drosophila

Spastin Binds to Lipid Droplets and Affects Lipid Metabolism: e1005149

Transgenic fruit-flies expressing a FRET-based sensor for in vivo imaging of cAMP dynamics

Myoclonin1/EFHC1 disease mechanisms in JME

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