Related references
Note: Only part of the references are listed.Lysosome Function and Dysfunction in Hereditary Spastic Paraplegias
Daisy Edmison et al.
BRAIN SCIENCES (2021)
The Vps13 Family of Lipid Transporters and Its Role at Membrane Contact Sites
Samantha Katarzyna Dziurdzik et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2021)
Astroglial ER-mitochondria calcium transfer mediates endocannabinoid-dependent synaptic integration
Roman Serrat et al.
CELL REPORTS (2021)
Mitochondria Endoplasmic Reticulum Contact Sites (MERCs): Proximity Ligation Assay as a Tool to Study Organelle Interaction
Sara Benhammouda et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)
Dysregulation of mitochondria-lysosome contacts by GBA1 dysfunction in dopaminergic neuronal models of Parkinson's disease
Soojin Kim et al.
NATURE COMMUNICATIONS (2021)
VPS13D interacts with VCP/p97 and negatively regulates endoplasmic reticulum-mitochondria interactions
Yuanjiao Du et al.
MOLECULAR BIOLOGY OF THE CELL (2021)
ER - lysosome contacts at a pre-axonal region regulate axonal lysosome availability
Nazmiye Ozkan et al.
NATURE COMMUNICATIONS (2021)
Lysosomes as dynamic regulators of cell and organismal homeostasis
Andrea Ballabio et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2020)
A VPS13D spastic ataxia mutation disrupts the conserved adaptor-binding site in yeast Vps13
Samantha K. Dziurdzik et al.
HUMAN MOLECULAR GENETICS (2020)
Mitochondria-Endoplasmic Reticulum Contacts in Reactive Astrocytes Promote Vascular Remodeling
Jana Goebel et al.
CELL METABOLISM (2020)
Split-TurboID enables contact-dependent proximity labeling in cells
Kelvin F. Cho et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Contact-ID, a tool for profiling organelle contact sites, reveals regulatory proteins of mitochondrial-associated membrane formation
Chulhwan Kwak et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Current and Emerging Approaches for Studying Inter-Organelle Membrane Contact Sites
Xue Huang et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)
The Alzheimer's disease-associated C99 fragment of APP regulates cellular cholesterol trafficking
Jorge Montesinos et al.
EMBO JOURNAL (2020)
Mitochondria-lysosome contacts regulate mitochondrial Ca2+ dynamics via lysosomal TRPML1
Wesley Peng et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
PDZD8 interacts with Protrudin and Rab7 at ER-late endosome membrane contact sites associated with mitochondria
Yael Elbaz-Alon et al.
NATURE COMMUNICATIONS (2020)
Mitochondria-lysosome membrane contacts are defective in GDAP1-related Charcot-Marie-Tooth disease
Lara Cantarero et al.
HUMAN MOLECULAR GENETICS (2020)
Cerebellar ataxia disease-associated Snx14 promotes lipid droplet growth at ER-droplet contacts
Sanchari Datta et al.
JOURNAL OF CELL BIOLOGY (2019)
Coming together to define membrane contact sites
Luca Scorrano et al.
NATURE COMMUNICATIONS (2019)
Lipid exchange at ER-mitochondria contact sites: a puzzle falling into place with quite a few pieces missing
Carmelina Petrungaro et al.
CURRENT OPINION IN CELL BIOLOGY (2019)
A molecular rheostat: Kv2.1 currents maintain or suppress repetitive firing in motoneurons
Shannon H. Romer et al.
JOURNAL OF PHYSIOLOGY-LONDON (2019)
The ER-Localized Protein DFCP1 Modulates ER-Lipid Droplet Contact Formation
Dongfang Li et al.
CELL REPORTS (2019)
Mutations in RHOT1 Disrupt Endoplasmic Reticulum-Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's Disease
Dajana Grossmann et al.
ANTIOXIDANTS & REDOX SIGNALING (2019)
Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III
Chi-Lun Chang et al.
JOURNAL OF CELL BIOLOGY (2019)
Lysosomal Regulation of Inter-mitochondrial Contact Fate and Motility in Charcot-Marie-Tooth Type 2
Yvette C. Wong et al.
DEVELOPMENTAL CELL (2019)
Phagolysosome resolution requires contacts with the endoplasmic reticulum and phosphatidylinositol-4-phosphate signalling
Roni Levin-Konigsberg et al.
NATURE CELL BIOLOGY (2019)
PDZD8 mediates a Rab7-dependent interaction of the ER with late endosomes and lysosomes
Andres Guillen-Samander et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)
DJ-1 regulates the integrity and function of ER-mitochondria association through interaction with IP3R3-Grp75-VDAC1
Yi Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)
NPC1 regulates ER contacts with endocytic organelles to mediate cholesterol egress
D. Hoglinger et al.
NATURE COMMUNICATIONS (2019)
NeurodegenERation: The Central Role for ER Contacts in Neuronal Function and Axonopathy, Lessons From Hereditary Spastic Paraplegias and Related Diseases
Philippa C. Fowler et al.
FRONTIERS IN NEUROSCIENCE (2019)
Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons
Jean-Michel Cioni et al.
CELL (2019)
MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics
Delfina Larrea et al.
HUMAN MOLECULAR GENETICS (2019)
Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson's Disease
Maria Nguyen et al.
TRENDS IN NEUROSCIENCES (2019)
Variants in Miro1 Cause Alterations of ER-Mitochondria Contact Sites in Fibroblasts from Parkinson's Disease Patients
Clara Berenguer-Escuder et al.
JOURNAL OF CLINICAL MEDICINE (2019)
Recessive mutations in >VPS13D cause childhood onset movement disorders
Julie Gauthier et al.
ANNALS OF NEUROLOGY (2018)
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
Eunju Seong et al.
ANNALS OF NEUROLOGY (2018)
Tau localises within mitochondrial sub-compartments and its caspase cleavage affects ER-mitochondria interactions and cellular Ca2+ handling
Domenico Cieri et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2018)
Converging cellular themes for the hereditary spastic paraplegias
Craig Blackstone
CURRENT OPINION IN NEUROBIOLOGY (2018)
Rab18 promotes lipid droplet (LD) growth by tethering the ER to LDs through SNARE and NRZ interactions
Dijin Xu et al.
JOURNAL OF CELL BIOLOGY (2018)
Mitochondria-lysosome contacts regulate mitochondrial fission via RAB7 GTP hydrolysis
Yvette C. Wong et al.
NATURE (2018)
Kv2 potassium channels form endoplasmic reticulum/plasma membrane junctions via interaction with VAPA and VAPB
Ben Johnson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Single organelle dynamics linked to 3D structure by correlative live-cell imaging and 3D electron microscopy
Job Fermie et al.
TRAFFIC (2018)
Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact
Nadav Shai et al.
NATURE COMMUNICATIONS (2018)
Visualizing multiple inter-organelle contact sites using the organelle-targeted split-GFP system
Yuriko Kakimoto et al.
SCIENTIFIC REPORTS (2018)
VPS13A and VPS13C are lipid transport proteins differentially localized at ER contact sites
Nikit Kumar et al.
JOURNAL OF CELL BIOLOGY (2018)
Altered ER-mitochondria contact impacts mitochondria calcium homeostasis and contributes to neurodegeneration in vivo in disease models
Kyu-Sun Lee et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
LRRK2 and its substrate Rab GTPases are sequentially targeted onto stressed lysosomes and maintain their homeostasis
Tomoya Eguchi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)
Super-Resolution Tracking of Mitochondrial Dynamics with An Iridium(III) Luminophore
Qixin Chen et al.
SMALL (2018)
Localization and Processing of the Amyloid-β Protein Precursor in Mitochondria-Associated Membranes
Dolores Del Prete et al.
JOURNAL OF ALZHEIMERS DISEASE (2017)
Ascorbate peroxidase proximity labeling coupled with biochemical fractionation identifies promoters of endoplasmic reticulum-mitochondrial contacts
Il-Taeg Cho et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2017)
Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia
Rachel Allison et al.
JOURNAL OF CELL BIOLOGY (2017)
VAPs and ACBD5 tether peroxisomes to the ER for peroxisome maintenance and lipid homeostasis
Rong Hua et al.
JOURNAL OF CELL BIOLOGY (2017)
ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER
Joseph L. Costello et al.
JOURNAL OF CELL BIOLOGY (2017)
Applying systems-level spectral imaging and analysis to reveal the organelle interactome
Alex M. Valm et al.
NATURE (2017)
Newly born peroxisomes are a hybrid of mitochondrial and ER-derived pre-peroxisomes
Ayumu Sugiura et al.
NATURE (2017)
Rapid immunopurification of mitochondria for metabolite profiling and absolute quantification of matrix metabolites
Walter W. Chen et al.
NATURE PROTOCOLS (2017)
Contacts between the endoplasmic reticulum and other membranes in neurons
Yumei Wu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)
Lysosomal metabolomics reveals V-ATPase- and mTOR-dependent regulation of amino acid efflux from lysosomes
Monther Abu-Remaileh et al.
SCIENCE (2017)
ER-mitochondria tethering by PDZD8 regulates Ca2+ dynamics in mammalian neurons
Yusuke Hirabayahi et al.
SCIENCE (2017)
Cell-permeable organic fluorescent probes for live-cell long-term super-resolution imaging reveal lysosome-mitochondrion interactions
Yubing Han et al.
NATURE COMMUNICATIONS (2017)
High resolution structural evidence suggests the Sarcoplasmic Reticulum forms microdomains with Acidic Stores (lysosomes) in the heart
Daniel Aston et al.
SCIENTIFIC REPORTS (2017)
PINK1 and BECN1 relocalize at mitochondria-associated membranes during mitophagy and promote ER-mitochondria tethering and autophagosome formation
Vania Gelmetti et al.
AUTOPHAGY (2017)
Mitochondria and Lysosomes: Discovering Bonds
Kiran Todkar et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2017)
α-Synuclein binds to the ER-mitochondria tethering protein VAPB to disrupt Ca2+ homeostasis and mitochondrial ATP production
Sebastien Paillusson et al.
ACTA NEUROPATHOLOGICA (2017)
The endoplasmic reticulum: structure, function and response to cellular signaling
Dianne S. Schwarz et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2016)
ApoE4 upregulates the activity of mitochondria-associated ER membranes
Marc D. Tambini et al.
EMBO REPORTS (2016)
Loss of VPS1 3C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Suzanne Lesage et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Evidence for the involvement of lipid rafts localized at the ER-mitochondria associated membranes in autophagosome formation
Tina Garofalo et al.
AUTOPHAGY (2016)
Signalling at membrane contact sites: two membranes come together to handle second messengers
Tim P. Levine et al.
CURRENT OPINION IN CELL BIOLOGY (2016)
Polo Kinase Phosphorylates Miro to Control ER-Mitochondria Contact Sites and Mitochondrial Ca2+ Homeostasis in Neural Stem Cell Development
Seongsoo Lee et al.
DEVELOPMENTAL CELL (2016)
A Tether is a Tether is a Tether: Tethering at Membrane Contact Sites
Michel Eisenberg-Bord et al.
DEVELOPMENTAL CELL (2016)
Annexin A1 Tethers Membrane Contact Sites that Mediate ER to Endosome Cholesterol Transport
Emily R. Eden et al.
DEVELOPMENTAL CELL (2016)
Seipin regulates ER-lipid droplet contacts and cargo delivery
Veijo T. Salo et al.
EMBO JOURNAL (2016)
Mitochondria-associated membrane collapse is a common pathomechanism in SIGMAR1- and SOD1-linked ALS
Seiji Watanabe et al.
EMBO MOLECULAR MEDICINE (2016)
DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease
Young Bin Hong et al.
HUMAN MUTATION (2016)
There's Something Wrong with my MAM; the ER-Mitochondria Axis and Neurodegenerative Diseases
Sebastien Paillusson et al.
TRENDS IN NEUROSCIENCES (2016)
Mutations in the Human AAA plus Chaperone p97 and Related Diseases
Wai Kwan Tang et al.
FRONTIERS IN MOLECULAR BIOSCIENCES (2016)
Hereditary spastic paraplegia-linked REEP1 modulates endoplasmic reticulum/mitochondria contacts
Youngshin Lim et al.
ANNALS OF NEUROLOGY (2015)
Calcium signaling at ER membrane contact sites
Thomas Burgoyne et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2015)
Cholesterol Transport through Lysosome-Peroxisome Membrane Contacts
Bei-Bei Chu et al.
CELL (2015)
Membrane contact sites, gateways for lipid homeostasis
Sujoy Lahiri et al.
CURRENT OPINION IN CELL BIOLOGY (2015)
Mdm l/Snx 13 is a novel ER-endolysosomal interorganelle tethering protein
W. Mike Henne et al.
JOURNAL OF CELL BIOLOGY (2015)
Repeated ER-endosome contacts promote endosome translocation and neurite outgrowth
Camilla Raiborg et al.
NATURE (2015)
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction
Naiara Akizu et al.
NATURE GENETICS (2015)
The Roles of PINK1, Parkin, and Mitochondrial Fidelity in Parkinson's Disease
Alicia M. Pickrell et al.
NEURON (2015)
Chorein Sensitive Dopamine Release from Pheochromocytoma (PC12) Cells
Sabina Honisch et al.
NEUROSIGNALS (2015)
TDP-43 Proteinopathy and ALS: Insights into Disease Mechanisms and Therapeutic Targets
Emma L. Scotter et al.
NEUROTHERAPEUTICS (2015)
PI4P/phosphatidylserine countertransport at ORP5-and ORP8-mediated ER-plasma membrane contacts
Jeeyun Chung et al.
SCIENCE (2015)
Identification and characterization of essential genes in the human genome
Tim Wang et al.
SCIENCE (2015)
De novo KCNB1 mutations in infantile epilepsy inhibit repetitive neuronal firing
Hirotomo Saitsu et al.
SCIENTIFIC REPORTS (2015)
Cohen Syndrome-associated Protein COH1 Physically and Functionally Interacts with the Small GTPase RAB6 at the Golgi Complex and Directs Neurite Outgrowth
Wenke Seifert et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
Disturbed mitochondrial dynamics and neurodegenerative disorders
Florence Burte et al.
NATURE REVIEWS NEUROLOGY (2015)
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
Anna C. Thomas et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2014)
Pharmacological stimulation of sigma-1 receptors has neurorestorative effects in experimental parkinsonism
Veronica Francardo et al.
BRAIN (2014)
ER Contact Sites Define the Position and Timing of Endosome Fission
Ashley A. Rowland et al.
CELL (2014)
Charcot-Marie-Tooth disease and pathways to molecular based therapies
T. Harel et al.
CLINICAL GENETICS (2014)
A close-up view of membrane contact sites between the endoplasmic reticulum and the endolysosomal system: From yeast to man
Carina Hoenscher et al.
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY (2014)
A Dynamic Interface between Vacuoles and Mitochondria in Yeast
Yael Elbaz-Alon et al.
DEVELOPMENTAL CELL (2014)
Cellular Metabolism Regulates Contact Sites between Vacuoles and Mitochondria
Canna Hoenscher et al.
DEVELOPMENTAL CELL (2014)
Protrudin Regulates Endoplasmic Reticulum Morphology and Function Associated with the Pathogenesis of Hereditary Spastic Paraplegia
Yutaka Hashimoto et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2014)
Bridging the gap: Membrane contact sites in signaling, metabolism, and organelle dynamics
William A. Prinz
JOURNAL OF CELL BIOLOGY (2014)
Spastic paraplegia proteins spastizin and spatacsin mediate autophagic lysosome reformation
Jaerak Chang et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
alpha-Synuclein Is Localized to Mitochondria-Associated ER Membranes
Cristina Guardia-Laguarta et al.
JOURNAL OF NEUROSCIENCE (2014)
Mitochondrial form and function
Jonathan R. Friedman et al.
NATURE (2014)
Neuroprotective effects of the Sigma-1 receptor (SIR) agonist PRE-084, in a mouse model of moter neuron disease not linked to SOD1 mutation
Marco Peviani et al.
NEUROBIOLOGY OF DISEASE (2014)
ER-mitochondria associations are regulated by the VAPB-PTPIP51 interaction and are disrupted by ALS/FTD-associated TDP-43
Radu Stoica et al.
NATURE COMMUNICATIONS (2014)
Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success
Vincent Timmerman et al.
Genes (2014)
Chorein, the protein responsible for chorea-acanthocytosis, interacts with β-adducin and β-actin
Nari Shiokawa et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2013)
Enhanced parkin levels favor ER-mitochondria crosstalk and guarantee Ca2+ transfer to sustain cell bioenergetics
Tito Cali et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2013)
A Four-Step Cycle Driven by PI(4)P Hydrolysis Directs Sterol/PI(4)P Exchange by the ER-Golgi Tether OSBP
Bruno Mesmin et al.
CELL (2013)
PI(4,5) P2-Dependent and Ca2+-Regulated ER-PM Interactions Mediated by the Extended Synaptotagmins
Francesca Giordano et al.
CELL (2013)
The Parkinson disease-related protein DJ-1 counteracts mitochondrial impairment induced by the tumour suppressor protein p53 by enhancing endoplasmic reticulum-mitochondria tethering
Denis Ottolini et al.
HUMAN MOLECULAR GENETICS (2013)
Mutation for Nonsyndromic Mental Retardation in the trans-2-Enoyl-CoA Reductase TER Gene Involved in Fatty Acid Elongation Impairs the Enzyme Activity and Stability, Leading to Change in Sphingolipid Profile
Kensuke Abe et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Fis1 acts as a mitochondrial recruitment factor for TBC1D15 that is involved in regulation of mitochondrial morphology
Kenta Onoue et al.
JOURNAL OF CELL SCIENCE (2013)
A new seipin-associated neurodegenerative syndrome
Encarna Guillen-Navarro et al.
JOURNAL OF MEDICAL GENETICS (2013)
Endoplasmic reticulum-endosome contact increases as endosomes traffic and mature
Jonathan R. Friedman et al.
MOLECULAR BIOLOGY OF THE CELL (2013)
Neuronal vulnerability, pathogenesis, and Parkinson's disease
David Sulzer et al.
MOVEMENT DISORDERS (2013)
Autophagosomes form at ER-mitochondria contact sites
Maho Hamasaki et al.
NATURE (2013)
Modulation of the endoplasmic reticulum-mitochondria interface in Alzheimer's disease and related models
Louise Hedskog et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Endoplasmic reticulum-associated mitochondria-cortex tether functions in the distribution and inheritance of mitochondria
Laura L. Lackner et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
An Actin-Dependent Step in Mitochondrial Fission Mediated by the ER-Associated Formin INF2
Farida Korobova et al.
SCIENCE (2013)
Upregulated function of mitochondria-associated ER membranes in Alzheimer disease
Estela Area-Gomez et al.
EMBO JOURNAL (2012)
Characterization of inclusion bodies with cytoprotective properties formed by seipinopathy-linked mutant seipin
Daisuke Ito et al.
HUMAN MOLECULAR GENETICS (2012)
VAPB interacts with the mitochondrial protein PTPIP51 to regulate calcium homeostasis
Kurt J. De Vos et al.
HUMAN MOLECULAR GENETICS (2012)
α-Synuclein Controls Mitochondrial Calcium Homeostasis by Enhancing Endoplasmic Reticulum-Mitochondria Interactions
Tito Cali et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
The FATP1-DGAT2 complex facilitates lipid droplet expansion at the ER-lipid droplet interface
Ningyi Xu et al.
JOURNAL OF CELL BIOLOGY (2012)
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12
Gladys Montenegro et al.
JOURNAL OF CLINICAL INVESTIGATION (2012)
Kv2.1 cell surface clusters are insertion platforms for ion channel delivery to the plasma membrane
Emily Deutsch et al.
MOLECULAR BIOLOGY OF THE CELL (2012)
TDP-43: gumming up neurons through protein-protein and protein-RNA interactions
Emanuele Buratti et al.
TRENDS IN BIOCHEMICAL SCIENCES (2012)
Genetics of Parkinson's Disease
Christine Klein et al.
COLD SPRING HARBOR PERSPECTIVES IN MEDICINE (2012)
Molecular Genetics of Charcot-Marie-Tooth Disease: From Genes to Genomes
H. Azzedine et al.
MOLECULAR SYNDROMOLOGY (2012)
Loss-of-Function Mutations in RAB18 Cause Warburg Micro Syndrome
Danai Bem et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis
Amr Al-Saif et al.
ANNALS OF NEUROLOGY (2011)
Fis1 and Bap31 bridge the mitochondria-ER interface to establish a platform for apoptosis induction
Ryota Iwasawa et al.
EMBO JOURNAL (2011)
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13
Minal Caliskan et al.
HUMAN MOLECULAR GENETICS (2011)
Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients
Miguel Mitne-Neto et al.
HUMAN MOLECULAR GENETICS (2011)
REEP1 Mutations in SPG31: Frequency, Mutational Spectrum, and Potential Association with Mitochondrial Morpho-Functional Dysfunction
Cyril Goizet et al.
HUMAN MUTATION (2011)
Increased ER-mitochondrial coupling promotes mitochondrial respiration and bioenergetics during early phases of ER stress
Roberto Bravo et al.
JOURNAL OF CELL SCIENCE (2011)
Perilipin 5, a lipid droplet-associated protein, provides physical and metabolic linkage to mitochondria
Hong Wang et al.
JOURNAL OF LIPID RESEARCH (2011)
INF2 Mutations in Charcot-Marie-Tooth Disease with Glomerulopathy
Olivia Boyer et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Presenilin 2 modulates endoplasmic reticulum (ER)-mitochondria interactions and Ca2+ cross-talk
Enrico Zampese et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
ER Tubules Mark Sites of Mitochondrial Division
Jonathan R. Friedman et al.
SCIENCE (2011)
The Mon1-Ccz1 Complex Is the GEF of the Late Endosomal Rab7 Homolog Ypt7
Mirjana Nordmann et al.
CURRENT BIOLOGY (2010)
FYCO1 is a Rab7 effector that binds to LC3 and PI3P to mediate microtubule plus end-directed vesicle transport
Serhiy Pankiv et al.
JOURNAL OF CELL BIOLOGY (2010)
Genetics of Alzheimer Disease
Lynn M. Bekris et al.
JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY (2010)
Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism
Paul P. Van Veldhoven
JOURNAL OF LIPID RESEARCH (2010)
The Micro-Architecture of Mitochondria at Active Zones: Electron Tomography Reveals Novel Anchoring Scaffolds and Cristae Structured for High-Rate Metabolism
Guy A. Perkins et al.
JOURNAL OF NEUROSCIENCE (2010)
Ca2+ Hot Spots on the Mitochondrial Surface Are Generated by Ca2+ Mobilization from Stores, but Not by Activation of Store-Operated Ca2+ Channels
Marta Giacomello et al.
MOLECULAR CELL (2010)
Imaging Interorganelle Contacts and Local Calcium Dynamics at the ER-Mitochondrial Interface
Gyoergy Csordas et al.
MOLECULAR CELL (2010)
Membrane contacts between endosomes and ER provide sites for PTP1B-epidermal growth factor receptor interaction
Emily R. Eden et al.
NATURE CELL BIOLOGY (2010)
PINK1 Is Selectively Stabilized on Impaired Mitochondria to Activate Parkin
Derek P. Narendra et al.
PLOS BIOLOGY (2010)
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
Juliane Neumann et al.
BRAIN (2009)
Lipid Droplets Finally Get a Little R-E-S-P-E-C-T
Robert V. Farese et al.
CELL (2009)
Deletions in the VPS13B(COH1) Gene as a Cause of Cohen Syndrome
I. Balikova et al.
HUMAN MUTATION (2009)
The Endoplasmic Reticulum Enzyme DGAT2 Is Found in Mitochondria-associated Membranes and Has a Mitochondrial Targeting Signal That Promotes Its Association with Mitochondria
Scot J. Stone et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Promotion of Neurite Extension by Protrudin Requires Its Interaction with Vesicle-associated Membrane Protein-associated Protein
Shotaro Saita et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7-RILP-p150Glued and late endosome positioning
Nuno Rocha et al.
JOURNAL OF CELL BIOLOGY (2009)
Increased Association Between Rough Endoplasmic Reticulum Membranes and Mitochondria in Transgenic Mice That Express P301 L Tau
Sebastien Perreault et al.
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2009)
The role of ZFYVE27/protrudin in hereditary spastic paraplegia
Monica Martignoni et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13
D. K. Nolan et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Functional characterization of Rab7 mutant proteins associated with Charcot-Marie-Tooth type 2B disease
Maria Rita Spinosa et al.
JOURNAL OF NEUROSCIENCE (2008)
The subcellular distribution of calnexin is mediated by PACS-2
Nathan Myhill et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Coordinated lipid transfer between the endoplasmic reticulum and the Golgi complex requires the VAP proteins and is essential for Golgi-mediated transport
Diego Peretti et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Role of SERCA1 Truncated Isoform in the Proapoptotic Calcium Transfer from ER to Mitochondria during ER Stress
Mounia Chami et al.
MOLECULAR CELL (2008)
Mitofusin 2 tethers endoplasmic reticulum to mitochondria
Olga Martins de Brito et al.
NATURE (2008)
Sigma-1 receptor chaperones at the ER-Mitochondrion interface regulate Ca2+ signaling and cell survival
Teruo Hayashi et al.
CELL (2007)
ITPR2 as a susceptibility gene in sporadic arnyotrophic lateral sclerosis: a genorne-wide association study
Michael A. van Es et al.
LANCET NEUROLOGY (2007)
Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates
Eva Teuling et al.
JOURNAL OF NEUROSCIENCE (2007)
Regulated ATP release from astrocytes through lysosome exocytosis
Zhijun Zhang et al.
NATURE CELL BIOLOGY (2007)
Live-cell imaging reveals sequential oligomerization and local plasma membrane targeting of stromal interaction molecule 1 after Ca2+ store depletion
Jen Liou et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Mitochondrial aberrations in mucolipidosis type IV
John J. Jennings et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Chaperone-mediated coupling of endoplasmic reticulum and mitochondrial Ca2+ channels
Gyorgy Szabadkai et al.
JOURNAL OF CELL BIOLOGY (2006)
Characterization of amyotrophic lateral sclerosis-linked P56S mutation of vesicle-associated membrane protein-associated protein B (VAPB/ALS8)
Kohsuke Kanekura et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
ALS:: A disease of motor neurons and their nonneuronal neighbors
Sverine Boillee et al.
NEURON (2006)
ZFYVE27 (SPG33), a novel spastin-binding protein, is mutated in hereditary spastic paraplegia
Ashraf U. Mannan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Mitochondrial dynamics and Ca2+ signaling
G. Szabadkai et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2006)
A class of membrane proteins shaping the tubular endoplasmic reticulum
GK Voeltz et al.
CELL (2006)
Targeting of Tsc13p to nucleus-vacuole junctions: A role for very-long-chain fatty acids in the biogenesis of microautophagic vesicles
E Kvam et al.
MOLECULAR BIOLOGY OF THE CELL (2005)
Neuroprotective effects of sigma-I receptor agonists against beta-amyloid-induced toxicity
A Marrazzo et al.
NEUROREPORT (2005)
Rab18 localizes to lipid droplets and induces their close apposition to the endoplasmic reticulum-derived membrane
S Ozeki et al.
JOURNAL OF CELL SCIENCE (2005)
PACS-2 controls endoplasmic reticulum-mitochondria communication and Bid-mediated apoptosis
T Simmen et al.
EMBO JOURNAL (2005)
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome
C Windpassinger et al.
NATURE GENETICS (2004)
Analysis of the human VPS13 gene family
A Velayos-Baeza et al.
GENOMICS (2004)
A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis
AL Nishimura et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Involvement of the endoplasmic reticulum in peroxisome formation
HJ Geuze et al.
MOLECULAR BIOLOGY OF THE CELL (2003)
The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors
I Jordens et al.
CURRENT BIOLOGY (2001)
The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis
S Ueno et al.
NATURE GENETICS (2001)
A conserved sorting-associated protein is mutant in chorea-acanthocytosis
L Rampoldi et al.
NATURE GENETICS (2001)
Tsc13p is required for fatty acid elongation and localizes to a novel structure at the nuclear-vacuolar interface in Saccharomyces cerevisiae
SD Kohlwein et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel
M Sun et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
