DrosophilaAtlastin in motor neurons is required for locomotion and presynaptic function

The effects of ER morphology on synaptic structure and function inDrosophila melanogaster

(2016) James B. Summerville et al.   JOURNAL OF CELL SCIENCE

Beneficial effects of rapamycin in aDrosophilamodel for hereditary spastic paraplegia

(2016) Shiyu Xu et al.   JOURNAL OF CELL SCIENCE

Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting

(2015) S. Klebe et al.   REVUE NEUROLOGIQUE

ER network homeostasis is critical for plant endosome streaming and endocytosis

(2015) Giovanni Stefano et al.   Cell Discovery

dAcsl, the Drosophila Ortholog of Acyl-CoA Synthetase Long-Chain Family Member 3 and 4, Inhibits Synapse Growth by Attenuating Bone Morphogenetic Protein Signaling via Endocytic Recycling

(2014) Z. Liu et al.   JOURNAL OF NEUROSCIENCE

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

(2014) G. Novarino et al.   SCIENCE

Spartin Regulates Synaptic Growth and Neuronal Survival by Inhibiting BMP-Mediated Microtubule Stabilization

(2013) Minyeop Nahm et al.   NEURON

Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure

(2013) C. Beetz et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The axonal endoplasmic reticulum and protein trafficking: Cellular bootlegging south of the soma

(2013) Carolina González et al.   SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY

Cellular Pathways of Hereditary Spastic Paraplegia

(2012) Craig Blackstone   Annual Review of Neuroscience

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

(2012) N. C. O'Sullivan et al.   HUMAN MOLECULAR GENETICS

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

(2012) Gladys Montenegro et al.   JOURNAL OF CLINICAL INVESTIGATION

Analysis of Synaptic Growth and Function in Drosophila with an Extended Larval Stage

(2012) D. L. Miller et al.   JOURNAL OF NEUROSCIENCE

Drosophila Acyl-CoA Synthetase Long-Chain Family Member 4 Regulates Axonal Transport of Synaptic Vesicles and Is Required for Synaptic Development and Transmission

(2011) Z. Liu et al.   JOURNAL OF NEUROSCIENCE

Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I

(2010) Christian Guelly et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia

(2010) DS McCorquodale et al.   CLINICAL GENETICS

Sec24-Dependent Secretion Drives Cell-Autonomous Expansion of Tracheal Tubes in Drosophila

(2010) Dominique Förster et al.   CURRENT BIOLOGY

Mixed Microtubules Steer Dynein-Driven Cargo Transport into Dendrites

(2010) Lukas C. Kapitein et al.   CURRENT BIOLOGY

Functional conservation of human Spastin in a Drosophila model of autosomal dominant-hereditary spastic paraplegia

(2010) Fang Du et al.   HUMAN MOLECULAR GENETICS

The nonsense-mediated decay pathway maintains synapse architecture and synaptic vesicle cycle efficacy

(2010) A. A. Long et al.   JOURNAL OF CELL SCIENCE

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

(2010) Seong H. Park et al.   JOURNAL OF CLINICAL INVESTIGATION

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

(2010) Coralie Fassier et al.   NATURE NEUROSCIENCE

A Class of Dynamin-like GTPases Involved in the Generation of the Tubular ER Network

(2009) Junjie Hu et al.   CELL

Drosophila Atlastin regulates the stability of muscle microtubules and is required for synapse development

(2009) Mihye Lee et al.   DEVELOPMENTAL BIOLOGY

Genomic mapping and expression patterns of C380, OK6 and D42 enhancer trap lines in the larval nervous system of Drosophila

(2009) Subhabrata Sanyal   GENE EXPRESSION PATTERNS

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

(2009) Genny Orso et al.   NATURE

Membrane Proteins of the Endoplasmic Reticulum Induce High-Curvature Tubules

(2008) J. Hu et al.   SCIENCE

Loss of spastic paraplegia gene atlastin induces age-dependent death of dopaminergic neurons in Drosophila

(2006) Youngseok Lee et al.   NEUROBIOLOGY OF AGING