On the public citation graph
Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7–RILP–p150Glued and late endosome positioning
0 signed · 750 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/andp.19484370105openalex-snapshot
Zwischenmolekulare Energiewanderung und Fluoreszenz
inferredcites →https://doi.org/10.1002/ijc.2910350302openalex-snapshot
Biochemical characterization and cellular localization of a formalin‐resistant melanoma‐associated antigen reacting with monoclonal antibody NKI/C‐3
inferredcites →https://doi.org/10.1006/bbrc.1998.9876openalex-snapshot
Molecular Cloning and Characterization of Mammalian Homologues of Vesicle-Associated Membrane Protein-Associated (VAMP-Associated) Proteins
inferredcites →https://doi.org/10.1016/0076-6879(83)98152-1openalex-snapshot
[19] Receptor-mediated endocytosis of low-density lipoprotein in cultured cells
inferredcites →https://doi.org/10.1016/j.bbalip.2004.08.009openalex-snapshot
Lipid and cholesterol trafficking in NPC
inferredcites →https://doi.org/10.1016/j.cell.2005.02.017openalex-snapshot
Modulation of Receptor Recycling and Degradation by the Endosomal Kinesin KIF16B
inferredcites →https://doi.org/10.1016/j.cellsig.2006.04.006openalex-snapshot
Cellular mechanism of U18666A-mediated apoptosis in cultured murine cortical neurons: Bridging Niemann–Pick disease type C and Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.immuni.2005.01.006openalex-snapshot
Spatial Separation of HLA-DM/HLA-DR Interactions within MIIC and Phagosome-Induced Immune Escape
inferredcites →https://doi.org/10.1016/s0006-3495(04)74307-6openalex-snapshot
Correcting Confocal Acquisition to Optimize Imaging of Fluorescence Resonance Energy Transfer by Sensitized Emission
inferredcites →https://doi.org/10.1016/s0021-9258(18)80136-3openalex-snapshot
The intracellular transport of low density lipoprotein-derived cholesterol is inhibited in Chinese hamster ovary cells cultured with 3-β-[2-(diethylamino)ethoxy]androst-5-en-17-one
inferredcites →https://doi.org/10.1016/s0021-9258(18)98391-2openalex-snapshot
Interaction with newly synthesized and retained proteins in the endoplasmic reticulum suggests a chaperone function for human integral membrane protein IP90 (calnexin)
inferredcites →https://doi.org/10.1016/s0091-679x(08)61599-xopenalex-snapshot
Chapter 1 Lysed Chromatophores: A Model System for the Study of Bidirectional Organelle Transport
inferredcites →https://doi.org/10.1016/s0960-9822(00)00289-xopenalex-snapshot
Mobilization of late-endosomal cholesterol is inhibited by Rab guanine nucleotide dissociation inhibitor
inferredcites →https://doi.org/10.1016/s0960-9822(01)00531-0openalex-snapshot
The Rab7 effector protein RILP controls lysosomal transport by inducing the recruitment of dynein-dynactin motors
inferredcites →https://doi.org/10.1016/s0960-9822(99)80117-1openalex-snapshot
Simultaneous detection of multiple green fluorescent proteins in live cells by fluorescence lifetime imaging microscopy
inferredcites →https://doi.org/10.1016/s0962-8924(01)02147-xopenalex-snapshot
Rab GTPases: specifying and deciphering organelle identity and function
inferredcites →https://doi.org/10.1016/s0962-8924(98)01410-xopenalex-snapshot
Fluorescence lifetime imaging microscopy: spatial resolution of biochemical processes in the cell
inferredcites →https://doi.org/10.1038/10084openalex-snapshot
Late endosomal membranes rich in lysobisphosphatidic acid regulate cholesterol transport
inferredcites →https://doi.org/10.1038/346864a0openalex-snapshot
Radial extension of macrophage tubular lysosomes supported by kinesin
inferredcites →https://doi.org/10.1038/35008103openalex-snapshot
The major substrates for TAP in vivo are derived from newly synthesized proteins
inferredcites →https://doi.org/10.1038/emboj.2008.133openalex-snapshot
Huntingtin phosphorylation acts as a molecular switch for anterograde/retrograde transport in neurons
inferredcites →https://doi.org/10.1038/nature03571openalex-snapshot
Genome-wide analysis of human kinases in clathrin- and caveolae/raft-mediated endocytosis
inferredcites →https://doi.org/10.1038/nature03923openalex-snapshot
Structural mechanism for sterol sensing and transport by OSBP-related proteins
inferredcites →https://doi.org/10.1038/nature04399openalex-snapshot
Role of cholesterol and lipid organization in disease
inferredcites →https://doi.org/10.1038/nrm1591openalex-snapshot
Lipid traffic: floppy drives and a superhighway
inferredcites →https://doi.org/10.1038/nrm2336openalex-snapshot
Cellular cholesterol trafficking and compartmentalization
inferredcites →https://doi.org/10.1042/0264-6021:3500001openalex-snapshot
Signal-dependent membrane targeting by pleckstrin homology (PH) domains
inferredcites →https://doi.org/10.1042/bj20030358openalex-snapshot
Monitoring conformational changes of proteins in cells by fluorescence lifetime imaging microscopy
inferredcites →https://doi.org/10.1042/bj20070176openalex-snapshot
The mammalian oxysterol-binding protein-related proteins (ORPs) bind 25-hydroxycholesterol in an evolutionarily conserved pocket
inferredcites →https://doi.org/10.1074/jbc.273.7.4266openalex-snapshot
Evidence for a Cholesterol Transport Pathway from Lysosomes to Endoplasmic Reticulum That Is Independent of the Plasma Membrane
inferredcites →https://doi.org/10.1074/jbc.m201191200openalex-snapshot
Vesicle-associated Membrane Protein-associated Protein-A (VAP-A) Interacts with the Oxysterol-binding Protein to Modify Export from the Endoplasmic Reticulum
inferredcites →https://doi.org/10.1074/jbc.m314160200openalex-snapshot
The ABCA1 Transporter Modulates Late Endocytic Trafficking
inferredcites →https://doi.org/10.1074/jbc.m500147200openalex-snapshot
A Highly Conserved Binding Site in Vesicle-associated Membrane Protein-associated Protein (VAP) for the FFAT Motif of Lipid-binding Proteins
inferredcites →https://doi.org/10.1074/jbc.m603215200openalex-snapshot
Roles of Endogenously Synthesized Sterols in the Endocytic Pathway
inferredcites →https://doi.org/10.1083/jcb.108.5.1625openalex-snapshot
The intracellular transport of low density lipoprotein-derived cholesterol is defective in Niemann-Pick type C fibroblasts.
inferredcites →https://doi.org/10.1083/jcb.119.6.1589openalex-snapshot
Directional instability of microtubule transport in the presence of kinesin and dynein, two opposite polarity motor proteins.
inferredcites →https://doi.org/10.1083/jcb.131.4.1039openalex-snapshot
Point mutation of adenosine triphosphate-binding motif generated rigor kinesin that selectively blocks anterograde lysosome membrane transport.
inferredcites →https://doi.org/10.1083/jcb.139.2.469openalex-snapshot
Overexpression of the Dynamitin (p50) Subunit of the Dynactin Complex Disrupts Dynein-dependent Maintenance of Membrane Organelle Distribution
inferredcites →https://doi.org/10.1083/jcb.200210066openalex-snapshot
Dynactin is required for bidirectional organelle transport
inferredcites →https://doi.org/10.1083/jcb.200606077openalex-snapshot
Activation of endosomal dynein motors by stepwise assembly of Rab7–RILP–p150Glued, ORP1L, and the receptor βlll spectrin
inferredcites →https://doi.org/10.1091/mbc.e03-08-0614openalex-snapshot
Dynein-mediated Vesicle Transport Controls Intracellular Salmonella Replication
inferredcites →https://doi.org/10.1091/mbc.e05-03-0189openalex-snapshot
The Oxysterol-binding Protein Homologue ORP1L Interacts with Rab7 and Alters Functional Properties of Late Endocytic Compartments
inferredcites →https://doi.org/10.1093/emboj/21.6.1289openalex-snapshot
Late endosome motility depends on lipids via the small GTPase Rab7
inferredcites →https://doi.org/10.1093/emboj/cdg201openalex-snapshot
A conserved ER targeting motif in three families of lipid binding proteins and in Opi1p binds VAP
inferredcites →https://doi.org/10.1096/fj.04-2714fjeopenalex-snapshot
Protein transduction of Rab9 in Niemann‐Pick C cells reduces cholesterol storage
inferredcites →https://doi.org/10.1097/00041433-200306000-00006openalex-snapshot
Fast flip-flop of cholesterol and fatty acids in membranes: implications for membrane transport proteins
inferredcites →https://doi.org/10.1111/j.1600-0854.2005.00336.xopenalex-snapshot
Rab Proteins, Connecting Transport and Vesicle Fusion
inferredcites →https://doi.org/10.1111/j.1600-0854.2005.00347.xopenalex-snapshot
Kinesin‐2 is a Motor for Late Endosomes and Lysosomes
inferredcites →https://doi.org/10.1111/j.1600-0854.2006.00419.xopenalex-snapshot
Morphogenesis of the Endoplasmic Reticulum: Beyond Active Membrane Expansion
inferredcites →https://doi.org/10.1126/science.277.5323.228openalex-snapshot
Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis
inferredcites →https://doi.org/10.1126/science.279.5350.580openalex-snapshot
Interaction of a Golgi-Associated Kinesin-Like Protein with Rab6
inferredcites →https://doi.org/10.1128/jvi.79.21.13473-13482.2005openalex-snapshot
Human VAP-B Is Involved in Hepatitis C Virus Replication through Interaction with NS5A and NS5B
inferredcites →https://doi.org/10.1159/000112179openalex-snapshot
Type C Niemann-Pick Disease: Use of Hydrophobic Amines to Study Defective Cholesterol Transport
inferredcites →https://doi.org/10.1182/blood.v90.3.1255openalex-snapshot
Human Monocytes and Neutrophils Store Transforming Growth Factor-α in a Subpopulation of Cytoplasmic Granules
inferredcites →https://doi.org/10.1242/jcs.112.6.785openalex-snapshot
Opposing motor activities of dynein and kinesin determine retention and transport of MHC class II-containing compartments
inferredcites →https://doi.org/10.1371/journal.pone.0000851openalex-snapshot
Late Endosomal Cholesterol Accumulation Leads to Impaired Intra-Endosomal Trafficking
inferredcites →https://doi.org/10.1523/jneurosci.2661-07.2007openalex-snapshot
Motor Neuron Disease-Associated Mutant Vesicle-Associated Membrane Protein-Associated Protein (VAP) B Recruits Wild-Type VAPs into Endoplasmic Reticulum-Derived Tubular Aggregates
inferredcites →https://doi.org/10.1529/biophysj.106.099366openalex-snapshot
Cholesterol Level Regulates Endosome Motility via Rab Proteins
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4767188openalex-extracted
Hydrophilic Polymeric Fluorescent Probes Based on Benzothiadiazole Constructed for Real-Time Monitoring of Lipid Droplet Levels in Cells
inferred← citeshttps://doi.org/10.1002/1873-3468.13639openalex-snapshot
Illuminating the membrane contact sites between the endoplasmic reticulum and the trans‐Golgi network
inferred← citeshttps://doi.org/10.1002/1873-3468.13777openalex-snapshot
Role of cytoplasmic dynein and kinesins in adenovirus transport
inferred← citeshttps://doi.org/10.1002/2211-5463.13605openalex-snapshot
Glycosphingolipids within membrane contact sites influence their function as signaling hubs in neurodegenerative diseases
inferred← citeshttps://doi.org/10.1002/9781118342312.ch1openalex-snapshot
Cholesterol Trafficking and Distribution between Cellular Membranes
inferred← citeshttps://doi.org/10.1002/9781119436812.ch13openalex-snapshot
Organelle–Organelle Contacts
inferred← citeshttps://doi.org/10.1002/advs.202206095openalex-snapshot
A Review of Extracellular Vesicles in COVID‐19 Diagnosis, Treatment, and Prevention
inferred← citeshttps://doi.org/10.1002/bies.201500095openalex-snapshot
ER contact sites direct late endosome transport
inferred← citeshttps://doi.org/10.1002/bies.202200111openalex-snapshot
Endolysosomal cholesterol export: More than just NPC1
inferred← citeshttps://doi.org/10.1002/bies.202300052openalex-snapshot
JNK‐interacting protein 4 is a central molecule for lysosomal retrograde trafficking
inferred← citeshttps://doi.org/10.1002/cdt3.123openalex-snapshot
Molecular regulation of calcium‐sensing receptor (CaSR)‐mediated signaling
inferred← citeshttps://doi.org/10.1002/cm.21226openalex-snapshot
Emerging roles of sumoylation in the regulation of actin, microtubules, intermediate filaments, and septins
inferred← citeshttps://doi.org/10.1002/cphy.c210046openalex-snapshot
Extracellular Vesicles in Hepatobiliary Health and Disease
inferred← citeshttps://doi.org/10.1002/dneu.22560openalex-snapshot
The axonal endoplasmic reticulum: One organelle—many functions in development, maintenance, and plasticity
inferred← citeshttps://doi.org/10.1002/dvdy.22202openalex-snapshot
Sperm and oocyte communication mechanisms controlling C. elegans fertility
inferred← citeshttps://doi.org/10.1002/ejlt.201200044openalex-snapshot
Oxysterol‐binding proteins–emerging roles in cell regulation
inferred← citeshttps://doi.org/10.1002/glia.24580openalex-snapshot
Lysosomal cholesterol accumulation in aged astrocytes impairs cholesterol delivery to neurons and can be rescued by cannabinoids
inferred← citeshttps://doi.org/10.1002/iub.1737openalex-snapshot
The role of lipids in host–pathogen interactions
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2023.tb00263.xopenalex-snapshot
Extracellular Vesicles in Hepatobiliary Health and Disease
inferred← citeshttps://doi.org/10.1002/jev2.12132openalex-snapshot
Itraconazole inhibits nuclear delivery of extracellular vesicle cargo by disrupting the entry of late endosomes into the nucleoplasmic reticulum
inferred← citeshttps://doi.org/10.1002/jev2.12382openalex-snapshot
High‐fat diets: You are what you eat….your extracellular vesicles too!
inferred← citeshttps://doi.org/10.1002/jev2.70223openalex-snapshot
Myofibroblast‐Derived Extracellular Vesicles Drive Profibrotic Cascade Amplification in Pulmonary Fibrosis via the Nestin‐Rab7 Axis
inferred← citeshttps://doi.org/10.1002/med.21623openalex-snapshot
Tumor‐derived exosomes (TDEs): How to avoid the sting in the tail
inferred← citeshttps://doi.org/10.1002/pmic.201800265openalex-snapshot
Global Profiling of PknG Interactions Using a Human Proteome Microarray Reveals Novel Connections with CypA
inferred← citeshttps://doi.org/10.1002/pmic.202300099openalex-snapshot
Analysis of small EV proteomes reveals unique functional protein networks regulated by VAP‐A
inferred← citeshttps://doi.org/10.1002/wsbm.1505openalex-snapshot
Dynamic organization of intracellular organelle networks
inferred← citeshttps://doi.org/10.1007/978-1-4939-2569-8_28openalex-snapshot
Quantitative Bead-Based Flow Cytometry for Assaying Rab7 GTPase Interaction with the Rab-Interacting Lysosomal Protein (RILP) Effector Protein
inferred← citeshttps://doi.org/10.1007/978-1-4939-6934-0_6openalex-snapshot
Quantitative Co-Localization and Pattern Analysis of Endo-Lysosomal Cargo in Subcellular Image Cytometry and Validation on Synthetic Image Sets
inferred← citeshttps://doi.org/10.1007/978-1-62703-218-6_36openalex-snapshot
Studying MHC Class II Transport in Dendritic Cells
inferred← citeshttps://doi.org/10.1007/978-3-031-21547-6_1openalex-snapshot
PI(4,5)P2 and Cholesterol: Synthesis, Regulation, and Functions
inferred← citeshttps://doi.org/10.1007/978-3-031-21547-6_12openalex-snapshot
Roles of Phosphatidylinositol 4-Phosphorylation in Non-vesicular Cholesterol Trafficking
inferred← citeshttps://doi.org/10.1007/978-3-031-21547-6_15openalex-snapshot
Ca2+ and Annexins – Emerging Players for Sensing and Transferring Cholesterol and Phosphoinositides via Membrane Contact Sites
inferred← citeshttps://doi.org/10.1007/978-3-319-13939-5_13openalex-snapshot
Autophagic Pathology and Calcium Deregulation in Neurodegeneration
inferred← citeshttps://doi.org/10.1007/978-3-319-26974-0_18openalex-snapshot
Modulation of Calcium Entry by the Endo-lysosomal System
inferred← citeshttps://doi.org/10.1007/978-3-319-57732-6_15openalex-snapshot
The Role of Mitochondria in the Activation/Maintenance of SOCE: Membrane Contact Sites as Signaling Hubs Sustaining Store-Operated Ca2+ Entry
inferred← citeshttps://doi.org/10.1007/978-3-319-96704-2_2openalex-snapshot
Integration of the Endocytic System into the Network of Cellular Functions
inferred← citeshttps://doi.org/10.1007/978-3-319-96704-2_9openalex-snapshot
EGFR Trafficking in Physiology and Cancer
inferred← citeshttps://doi.org/10.1007/978-90-481-8622-8_6openalex-snapshot
Oxysterol-Binding Proteins
inferred← citeshttps://doi.org/10.1007/978-981-10-4567-7_10openalex-snapshot
Discovery and Roles of ER-Endolysosomal Contact Sites in Disease
inferred← citeshttps://doi.org/10.1007/978-981-10-4567-7_16openalex-snapshot
Hijacking of Membrane Contact Sites by Intracellular Bacterial Pathogens
inferred← citeshttps://doi.org/10.1007/978-981-99-8365-0_2openalex-snapshot
Biogenesis and Functions of Extracellular Vesicles
inferred← citeshttps://doi.org/10.1007/s00018-010-0470-zopenalex-snapshot
Sterol binding by OSBP-related protein 1L regulates late endosome motility and function
inferred← citeshttps://doi.org/10.1007/s00018-011-0913-1openalex-snapshot
Neuronal ceroid lipofuscinosis protein CLN3 interacts with motor proteins and modifies location of late endosomal compartments
inferred← citeshttps://doi.org/10.1007/s00018-014-1786-xopenalex-snapshot
Ligand-dependent localization and function of ORP–VAP complexes at membrane contact sites
inferred← citeshttps://doi.org/10.1007/s00018-018-2795-yopenalex-snapshot
Bridging the molecular and biological functions of the oxysterol-binding protein family
inferred← citeshttps://doi.org/10.1007/s00018-019-03330-yopenalex-snapshot
Annexin A6 modulates TBC1D15/Rab7/StARD3 axis to control endosomal cholesterol export in NPC1 cells
inferred← citeshttps://doi.org/10.1007/s00018-020-03604-wopenalex-snapshot
ORP/Osh mediate cross-talk between ER-plasma membrane contact site components and plasma membrane SNAREs
inferred← citeshttps://doi.org/10.1007/s00018-025-05830-6openalex-snapshot
The complex web of membrane contact sites in brain aging and neurodegeneration
inferred← citeshttps://doi.org/10.1007/s10565-016-9376-3openalex-snapshot
Look who’s talking—the crosstalk between oxidative stress and autophagy supports exosomal-dependent release of HCV particles
inferred← citeshttps://doi.org/10.1007/s11427-023-2443-9openalex-snapshot
Stay in touch with the endoplasmic reticulum
inferred← citeshttps://doi.org/10.1007/s13238-018-0523-xopenalex-snapshot
Release and uptake mechanisms of vesicular Ca2+ stores
inferred← citeshttps://doi.org/10.1007/s43630-025-00785-wopenalex-snapshot
Hydrophilic polymeric fluorescent probes based on benzothiadiazole constructed for real-time monitoring of lipid droplet levels in cells
inferred← citeshttps://doi.org/10.1016/b978-0-12-407178-0.00003-xopenalex-snapshot
Signaling Endosomes and Growth Cone Motility in Axon Regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-800186-8.00004-3openalex-snapshot
Unselective Disposal of Cellular Aggregates
inferred← citeshttps://doi.org/10.1016/b978-0-12-801043-3.00003-0openalex-snapshot
The Nucleus-Vacuole Junction in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1016/b978-0-12-809470-9.00010-2openalex-snapshot
Impacts of virus-mediated manipulation of host Dynein
inferred← citeshttps://doi.org/10.1016/b978-0-12-816053-4.00003-1openalex-snapshot
Exosomes, microvesicles, and their friends in solid tumors
inferred← citeshttps://doi.org/10.1016/b978-0-12-819460-7.00082-7openalex-snapshot
Membrane organization | Topography and Functions of Membrane Contact Sites
inferred← citeshttps://doi.org/10.1016/b978-0-12-824048-9.00019-5openalex-snapshot
Inter- and intra-membrane lipid transport
inferred← citeshttps://doi.org/10.1016/b978-0-323-85857-1.00038-9openalex-snapshot
Niemann-Pick type C disease (NPC)
inferred← citeshttps://doi.org/10.1016/b978-0-323-90142-0.00007-4openalex-snapshot
Mechanism of autophagosome–lysosome fusion in autophagy
inferred← citeshttps://doi.org/10.1016/bs.abl.2018.05.002openalex-snapshot
Mechanisms of Lipid Sorting in the Endosomal Pathway
inferred← citeshttps://doi.org/10.1016/bs.ircmb.2015.09.006openalex-snapshot
OSBP-Related Protein Family: Mediators of Lipid Transport and Signaling at Membrane Contact Sites
inferred← citeshttps://doi.org/10.1016/j.abb.2011.08.012openalex-snapshot
Molecular pathways for intracellular cholesterol accumulation: Common pathogenic mechanisms in Niemann–Pick disease Type C and cystic fibrosis
inferred← citeshttps://doi.org/10.1016/j.antiviral.2017.01.008openalex-snapshot
Uncovering oxysterol-binding protein (OSBP) as a target of the anti-enteroviral compound TTP-8307
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2016.04.005openalex-snapshot
A loss-of-function variant in OSBPL1A predisposes to low plasma HDL cholesterol levels and impaired cholesterol efflux capacity
inferred← citeshttps://doi.org/10.1016/j.bbalip.2015.02.012openalex-snapshot
Effects of 5α-cholestan-3-one on the synaptic vesicle cycle at the mouse neuromuscular junction
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.01.020openalex-snapshot
The formation and function of ER-endosome membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.02.001openalex-snapshot
Lipid transfer and metabolism across the endolysosomal–mitochondrial boundary
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.02.009openalex-snapshot
VAP, a Versatile Access Point for the Endoplasmic Reticulum: Review and analysis of FFAT-like motifs in the VAPome
inferred← citeshttps://doi.org/10.1016/j.bbalip.2016.02.024openalex-snapshot
The counterflow transport of sterols and PI4P
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.04.013openalex-snapshot
Vesicular and non-vesicular lipid export from the ER to the secretory pathway
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.05.011openalex-snapshot
Bis(monoacylglycero)phosphate regulates oxysterol binding protein-related protein 11 dependent sterol trafficking
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.06.016openalex-snapshot
Faraway, so close! Functions of Endoplasmic reticulum–Endosome contacts
inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.158544openalex-snapshot
ER morphology and endo-lysosomal crosstalk: Functions and disease implications
inferred← citeshttps://doi.org/10.1016/j.bbalip.2021.159107openalex-snapshot
Phosphoinositide transport and metabolism at membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbalip.2025.159673openalex-snapshot
Phosphoinositides as regulators of membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.10.030openalex-snapshot
Identifying protein partners of CLN8, an ER-resident protein involved in neuronal ceroid lipofuscinosis
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.11.018openalex-snapshot
Maturation of autophagosomes and endosomes: A key role for Rab7
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.01.028openalex-snapshot
Organization and function of membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2013.06.004openalex-snapshot
The endoplasmic reticulum and junctional membrane communication during calcium signaling
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2015.01.022openalex-snapshot
Calcium signaling at ER membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.04.007openalex-snapshot
The ER phagosome connection in the era of membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2017.05.018openalex-snapshot
ER-plasma membrane junctions: Why and how do we study them?
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2018.02.011openalex-snapshot
Rab7a modulates ER stress and ER morphology
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2019.02.006openalex-snapshot
DENN domain-containing protein FAM45A regulates the homeostasis of late/multivesicular endosomes
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2025.119896openalex-snapshot
The multiple facets of Rab proteins modulating the cellular distribution of cholesterol from the late endosomal compartment
inferred← citeshttps://doi.org/10.1016/j.bbamem.2015.05.010openalex-snapshot
How cholesterol interacts with proteins and lipids during its intracellular transport
inferred← citeshttps://doi.org/10.1016/j.bbcan.2022.188776openalex-snapshot
Role of exosomes in lung cancer: A comprehensive insight from immunomodulation to theragnostic applications
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.12.002openalex-snapshot
A vertebrate model for the study of lipid binding/transfer protein function: Conservation of OSBP-related proteins between zebrafish and human
inferred← citeshttps://doi.org/10.1016/j.bbrc.2014.04.102openalex-snapshot
First evidence of pathogenicity of V234I mutation of hVAPB found in Amyotrophic Lateral Sclerosis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150232openalex-snapshot
Structure of GDP-bound Rab7 Q67L in complex with ORP1L
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.02.016openalex-snapshot
Oxysterol-binding proteins: Functions in cell regulation beyond lipid metabolism
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.02.029openalex-snapshot
Oxysterols in cancer cell proliferation and death
inferred← citeshttps://doi.org/10.1016/j.bcp.2013.03.012openalex-snapshot
Similar pyruvate kinase modifications in glioblastoma cells by 7β-hydroxycholesterol and glutamine withdrawal
inferred← citeshttps://doi.org/10.1016/j.bcp.2017.11.018openalex-snapshot
ATP-binding cassette transporter-2 (ABCA2) as a therapeutic target
inferred← citeshttps://doi.org/10.1016/j.bcp.2021.114455openalex-snapshot
The emerging roles of OSBP-related proteins in cancer: Impacts through phosphoinositide metabolism and protein–protein interactions
inferred← citeshttps://doi.org/10.1016/j.bcp.2025.117323openalex-snapshot
CAMK2G in subcellular Ca2+ homeostasis: Molecular mechanisms and therapeutic targeting
inferred← citeshttps://doi.org/10.1016/j.biocel.2011.10.012openalex-snapshot
Endoplasmic reticulum: ER stress regulates mitochondrial bioenergetics
inferred← citeshttps://doi.org/10.1016/j.biochi.2016.08.001openalex-snapshot
Running up that hill: How to create cellular lipid gradients by lipid counter-flows
inferred← citeshttps://doi.org/10.1016/j.biochi.2018.12.013openalex-snapshot
ORP2 interacts with phosphoinositides and controls the subcellular distribution of cholesterol
inferred← citeshttps://doi.org/10.1016/j.biochi.2026.10.004openalex-snapshot
Organelle Localization and Trafficking of Ether Lipids: Current Evidence and Open Questions
inferred← citeshttps://doi.org/10.1016/j.ccr.2020.213577openalex-snapshot
Fluorescent probes for the imaging of lipid droplets in live cells
inferred← citeshttps://doi.org/10.1016/j.ccr.2023.215337openalex-snapshot
Emerging designs of aggregation-induced emission luminogens for lipid droplets imaging
inferred← citeshttps://doi.org/10.1016/j.ceb.2010.04.008openalex-snapshot
Linking molecular motors to membrane cargo
inferred← citeshttps://doi.org/10.1016/j.ceb.2010.05.004openalex-snapshot
Cholesterol, the central lipid of mammalian cells
inferred← citeshttps://doi.org/10.1016/j.ceb.2011.04.006openalex-snapshot
Lipid transfer and signaling at organelle contact sites: the tip of the iceberg
inferred← citeshttps://doi.org/10.1016/j.ceb.2015.04.001openalex-snapshot
Endoplasmic reticulum–Golgi complex membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.ceb.2015.04.002openalex-snapshot
Novel mechanisms of intracellular cholesterol transport: oxysterol-binding proteins and membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.09.005openalex-snapshot
Lipid - Motor Interactions: Soap Opera or Symphony?
inferred← citeshttps://doi.org/10.1016/j.ceb.2017.01.008openalex-snapshot
Moving and positioning the endolysosomal system
inferred← citeshttps://doi.org/10.1016/j.ceb.2018.04.003openalex-snapshot
Formation and maturation of autophagosomes in higher eukaryotes: a social network
inferred← citeshttps://doi.org/10.1016/j.ceb.2018.06.002openalex-snapshot
Mechanisms of cellular cholesterol compartmentalization: recent insights
inferred← citeshttps://doi.org/10.1016/j.ceb.2019.02.010openalex-snapshot
Motor–cargo adaptors at the organelle–cytoskeleton interface
inferred← citeshttps://doi.org/10.1016/j.ceb.2019.02.011openalex-snapshot
And three’s a party: lysosomes, lipid droplets, and the ER in lipid trafficking and cell homeostasis
inferred← citeshttps://doi.org/10.1016/j.ceb.2021.03.004openalex-snapshot
Regulation and physiology of membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102155openalex-snapshot
Endosome biogenesis is controlled by ER and the cytoskeleton at tripartite junctions
inferred← citeshttps://doi.org/10.1016/j.ceb.2026.102641openalex-snapshot
Bridging the gap between organelles: Membrane contact sites as regulator of endocytic dynamics
inferred← citeshttps://doi.org/10.1016/j.ceb.2026.102677openalex-snapshot
Rabs in the driving seat: Coordinating vesicular traffic and membrane contact site dynamics
inferred← citeshttps://doi.org/10.1016/j.ceca.2015.03.006openalex-snapshot
Coupling acidic organelles with the ER through Ca2+ microdomains at membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.ceca.2019.02.003openalex-snapshot
Getting close. Lysosome-ER contact sites tailor Ca2+ signals
inferred← citeshttps://doi.org/10.1016/j.ceca.2022.102658openalex-snapshot
The evolution of organellar calcium mapping technologies
inferred← citeshttps://doi.org/10.1016/j.cell.2010.11.031openalex-snapshot
Lipid Trafficking sans Vesicles: Where, Why, How?
inferred← citeshttps://doi.org/10.1016/j.cell.2010.12.034openalex-snapshot
Osh Proteins Regulate Phosphoinositide Metabolism at ER-Plasma Membrane Contact Sites
inferred← citeshttps://doi.org/10.1016/j.cell.2011.03.023openalex-snapshot
A Genome-wide Multidimensional RNAi Screen Reveals Pathways Controlling MHC Class II Antigen Presentation
inferred← citeshttps://doi.org/10.1016/j.cell.2014.10.023openalex-snapshot
ER Contact Sites Define the Position and Timing of Endosome Fission
inferred← citeshttps://doi.org/10.1016/j.cell.2015.12.054openalex-snapshot
Dynein Clusters into Lipid Microdomains on Phagosomes to Drive Rapid Transport toward Lysosomes
inferred← citeshttps://doi.org/10.1016/j.cell.2016.05.078openalex-snapshot
An ER-Associated Pathway Defines Endosomal Architecture for Controlled Cargo Transport
inferred← citeshttps://doi.org/10.1016/j.cell.2016.06.037openalex-snapshot
Endosome-ER Contacts Control Actin Nucleation and Retromer Function through VAP-Dependent Regulation of PI4P
inferred← citeshttps://doi.org/10.1016/j.cell.2018.08.030openalex-snapshot
A Novel Class of ER Membrane Proteins Regulates ER-Associated Endosome Fission
inferred← citeshttps://doi.org/10.1016/j.cell.2023.11.040openalex-snapshot
Making the connection: How membrane contact sites have changed our view of organelle biology
inferred← citeshttps://doi.org/10.1016/j.cellsig.2010.09.012openalex-snapshot
Rab7: Role of its protein interaction cascades in endo-lysosomal traffic
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.01.052openalex-snapshot
An Endosomal NAADP-Sensitive Two-Pore Ca2+ Channel Regulates ER-Endosome Membrane Contact Sites to Control Growth Factor Signaling
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.05.028openalex-snapshot
Oxysterol-Binding Protein-Related Protein 1L Regulates Cholesterol Egress from the Endo-Lysosomal System
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.11.064openalex-snapshot
IP3 Receptors Preferentially Associate with ER-Lysosome Contact Sites and Selectively Deliver Ca2+ to Lysosomes
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108475openalex-snapshot
Human VAPome Analysis Reveals MOSPD1 and MOSPD3 as Membrane Contact Site Proteins Interacting with FFAT-Related FFNT Motifs
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108659openalex-snapshot
The ER-embedded UBE2J1/RNF26 ubiquitylation complex exerts spatiotemporal control over the endolysosomal pathway
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109451openalex-snapshot
RalA and PLD1 Promote Lipid Droplet Growth in Response to Nutrient Withdrawal
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111882openalex-snapshot
The lipid transporter ORP2 regulates synaptic neurotransmitter release via two distinct mechanisms
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112108openalex-snapshot
Assembly and disassembly dynamics of nonmuscle myosin II control endosomal fission
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112229openalex-snapshot
Interaction between PI3K and the VDAC2 channel tethers Ras-PI3K-positive endosomes to mitochondria and promotes endosome maturation
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.116053openalex-snapshot
RNF13 mediates pH- and Ca2+-dependent regulation of lysosomal positioning
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2011.03.002openalex-snapshot
Cytoplasmic oxysterol-binding proteins: sterol sensors or transporters?
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2016.02.003openalex-snapshot
Active membrane cholesterol as a physiological effector
inferred← citeshttps://doi.org/10.1016/j.chemphyslip.2020.105047openalex-snapshot
Niemann Pick C2 protein enables cholesterol transfer from endo-lysosomes to the plasma membrane for efflux by shedding of extracellular vesicles
inferred← citeshttps://doi.org/10.1016/j.chom.2014.10.003openalex-snapshot
Rhinovirus Uses a Phosphatidylinositol 4-Phosphate/Cholesterol Counter-Current for the Formation of Replication Compartments at the ER-Golgi Interface
inferred← citeshttps://doi.org/10.1016/j.coi.2010.11.002openalex-snapshot
Routes to manipulate MHC class II antigen presentation
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.06.002openalex-snapshot
IP3 receptors and their intimate liaisons
inferred← citeshttps://doi.org/10.1016/j.cophys.2020.08.002openalex-snapshot
Two-pore channels as master regulators of membrane trafficking and endocytic well-being
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2019.102825openalex-snapshot
The opportunistic effect of exosomes on Non-Hodgkin Lymphoma microenvironment modulation
inferred← citeshttps://doi.org/10.1016/j.cub.2018.03.002openalex-snapshot
The ER Contact Proteins VAPA/B Interact with Multiple Autophagy Proteins to Modulate Autophagosome Biogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2021.06.022openalex-snapshot
Retrofusion of intralumenal MVB membranes parallels viral infection and coexists with exosome release
inferred← citeshttps://doi.org/10.1016/j.cub.2024.08.026openalex-snapshot
Systems mapping of bidirectional endosomal transport through the crowded cell
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2023.06.004openalex-snapshot
Extracellular vesicles as mediators of cell-cell communication in ovarian cancer and beyond – A lipids focus
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.11.004openalex-snapshot
ER-to-Plasma Membrane Tethering Proteins Regulate Cell Signaling and ER Morphology
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.06.006openalex-snapshot
Cellular Metabolism Regulates Contact Sites between Vacuoles and Mitochondria
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.12.008openalex-snapshot
Close Encounter of the Third Kind: The ER Meets Endosomes at Fission Sites
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.05.005openalex-snapshot
Annexin A1 Tethers Membrane Contact Sites that Mediate ER to Endosome Cholesterol Transport
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.09.030openalex-snapshot
Lipids and Their Trafficking: An Integral Part of Cellular Organization
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.10.022openalex-snapshot
A Tether Is a Tether Is a Tether: Tethering at Membrane Contact Sites
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.12.014openalex-snapshot
Reticulon-3 Promotes Endosome Maturation at ER Membrane Contact Sites
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.03.032openalex-snapshot
Lipid-mediated motor-adaptor sequestration impairs axonal lysosome delivery leading to autophagic stress and dystrophy in Niemann-Pick type C
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.03.012openalex-snapshot
VAP-A and its binding partner CERT drive biogenesis of RNA-containing extracellular vesicles at ER membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.07.010openalex-snapshot
A condensates-to-VPS41-associated phagic vacuoles conversion pathway controls autophagy degradation in plants
inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104628openalex-snapshot
Juvenile CLN3 disease is a lysosomal cholesterol storage disorder: similarities with Niemann-Pick type C disease
inferred← citeshttps://doi.org/10.1016/j.ejcb.2023.151382openalex-snapshot
Target lysis by cholesterol extraction is a rate limiting step in the resolution of phagolysosomes
inferred← citeshttps://doi.org/10.1016/j.fsi.2019.04.306openalex-snapshot
Molecular cloning of the Rab7 effector RILP (Rab-interacting lysosomal protein) in Litopenaeus vannamei and preliminary analysis of its role in white spot syndrome virus infection
inferred← citeshttps://doi.org/10.1016/j.gendis.2022.03.021openalex-snapshot
The biogenesis and secretion of exosomes and multivesicular bodies (MVBs): Intercellular shuttles and implications in human diseases
inferred← citeshttps://doi.org/10.1016/j.immuni.2011.06.009openalex-snapshot
Lysosomal Trafficking, Antigen Presentation, and Microbial Killing Are Controlled by the Arf-like GTPase Arl8b
inferred← citeshttps://doi.org/10.1016/j.immuni.2020.11.003openalex-snapshot
The SPPL3-Defined Glycosphingolipid Repertoire Orchestrates HLA Class I-Mediated Immune Responses
inferred← citeshttps://doi.org/10.1016/j.isci.2022.105612openalex-snapshot
PDZD8-deficient mice accumulate cholesteryl esters in the brain as a result of impaired lipophagy
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.100421openalex-snapshot
Invisible leashes: The tethering VAPs from infectious diseases to neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.102883openalex-snapshot
Loss of small GTPase Rab7 activation in prion infection negatively affects a feedback loop regulating neuronal cholesterol metabolism
inferred← citeshttps://doi.org/10.1016/j.jbc.2024.105743openalex-snapshot
Impaired lysosomal acidity maintenance in acid lipase-deficient cells leads to defective autophagy
inferred← citeshttps://doi.org/10.1016/j.jbior.2020.100779openalex-snapshot
Deregulation of phosphatidylinositol-4-phosphate in the development of amyotrophic lateral sclerosis 8
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2014.12.007openalex-snapshot
Two-hybrid-based systems: Powerful tools for investigation of membrane traffic machineries
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.10.028openalex-snapshot
Autophagosome-Lysosome Fusion
inferred← citeshttps://doi.org/10.1016/j.jprot.2025.105557openalex-snapshot
The protein cargo of extracellular vesicles. Recent advances in lung cancer research
inferred← citeshttps://doi.org/10.1016/j.jsb.2016.05.003openalex-snapshot
Organelle remodeling at membrane contact sites
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2021.106040openalex-snapshot
Cholesterol transport in the late endocytic pathway: Roles of ORP family proteins
inferred← citeshttps://doi.org/10.1016/j.jsps.2017.04.029openalex-snapshot
TSA protects H9c2 cells against thapsigargin-induced apoptosis related to endoplasmic reticulum stress-mediated mitochondrial injury
inferred← citeshttps://doi.org/10.1016/j.molcel.2026.01.011openalex-snapshot
Lysosomes as hubs of metabolic sensing and cellular homeostasis
inferred← citeshttps://doi.org/10.1016/j.molmet.2020.101146openalex-snapshot
Function of the endolysosomal network in cholesterol homeostasis and metabolic-associated fatty liver disease (MAFLD)
inferred← citeshttps://doi.org/10.1016/j.molmet.2022.101545openalex-snapshot
Extracellular vesicles in β cell biology: Role of lipids in vesicle biogenesis, cargo, and intercellular signaling
inferred← citeshttps://doi.org/10.1016/j.nbd.2020.105142openalex-snapshot
Deregulation of signalling in genetic conditions affecting the lysosomal metabolism of cholesterol and galactosyl-sphingolipids
inferred← citeshttps://doi.org/10.1016/j.neuint.2024.105905openalex-snapshot
Calcium balance through mutual orchestrated inter-organelle communication: A pleiotropic target for combating Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.neuron.2022.04.020openalex-snapshot
Dysregulation of organelle membrane contact sites in neurological diseases
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2011.03.004openalex-snapshot
Cytoplasmic dynein in neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2021.108018openalex-snapshot
The new fate of internalized membrane receptors: Internalized activation
inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107149openalex-snapshot
ER-organelle contacts: A signaling hub for neurological diseases
inferred← citeshttps://doi.org/10.1016/j.plipres.2013.06.004openalex-snapshot
Oxysterol-binding proteins: Sterol and phosphoinositide sensors coordinating transport, signaling and metabolism
inferred← citeshttps://doi.org/10.1016/j.plipres.2015.10.004openalex-snapshot
The orchestra of lipid-transfer proteins at the crossroads between metabolism and signaling
inferred← citeshttps://doi.org/10.1016/j.plipres.2020.101071openalex-snapshot
The return of malonyl-CoA to the brain: Cognition and other stories
inferred← citeshttps://doi.org/10.1016/j.plipres.2022.101146openalex-snapshot
Coordination of inter-organelle communication and lipid fluxes by OSBP-related proteins
inferred← citeshttps://doi.org/10.1016/j.plipres.2023.101225openalex-snapshot
The Niemann-Pick type diseases – A synopsis of inborn errors in sphingolipid and cholesterol metabolism
inferred← citeshttps://doi.org/10.1016/j.semcdb.2014.03.034openalex-snapshot
Endosome maturation, transport and functions
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.05.015openalex-snapshot
Interorganellar calcium signaling in the regulation of cell metabolism: A cancer perspective
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.02.019openalex-snapshot
Molecular machinery regulating organelle dynamics during axon growth and guidance
showing the first 200 of 691 · page through all 691
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.