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Here, there, and everywhere: The importance of ER membrane contact sites

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s10545-017-0076-9openalex-snapshot

Functional characterisation of peroxisomal β‐oxidation disorders in fibroblasts using lipidomics

inferredcites →https://doi.org/10.1016/0143-4160(86)90026-6openalex-snapshot

A model for receptor-regulated calcium entry

inferredcites →https://doi.org/10.1016/b978-0-12-820552-5.00021-8openalex-snapshot

Hereditary Spastic Paraplegia

inferredcites →https://doi.org/10.1016/b978-0-444-64076-5.00041-7openalex-snapshot

Hereditary spastic paraplegia

inferredcites →https://doi.org/10.1016/j.cell.2008.08.006openalex-snapshot

Structural and Mechanistic Insights into STIM1-Mediated Initiation of Store-Operated Calcium Entry

inferredcites →https://doi.org/10.1016/j.cell.2009.02.014openalex-snapshot

STIM1 Clusters and Activates CRAC Channels via Direct Binding of a Cytosolic Domain to Orai1

inferredcites →https://doi.org/10.1016/j.cell.2010.06.007openalex-snapshot

Essential Regulation of Cell Bioenergetics by Constitutive InsP3 Receptor Ca2+ Transfer to Mitochondria

inferredcites →https://doi.org/10.1016/j.cell.2010.12.034openalex-snapshot

Osh Proteins Regulate Phosphoinositide Metabolism at ER-Plasma Membrane Contact Sites

inferredcites →https://doi.org/10.1016/j.cell.2012.01.055openalex-snapshot

SARAF Inactivates the Store Operated Calcium Entry Machinery to Prevent Excess Calcium Refilling

inferredcites →https://doi.org/10.1016/j.cell.2012.02.035openalex-snapshot

Mitochondria: In Sickness and in Health

inferredcites →https://doi.org/10.1016/j.cell.2013.05.026openalex-snapshot

PI(4,5)P2-Dependent and Ca2+-Regulated ER-PM Interactions Mediated by the Extended Synaptotagmins

inferredcites →https://doi.org/10.1016/j.cell.2013.09.056openalex-snapshot

A Four-Step Cycle Driven by PI(4)P Hydrolysis Directs Sterol/PI(4)P Exchange by the ER-Golgi Tether OSBP

inferredcites →https://doi.org/10.1016/j.cell.2014.10.023openalex-snapshot

ER Contact Sites Define the Position and Timing of Endosome Fission

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.celrep.2015.06.022openalex-snapshot

Lam6 Regulates the Extent of Contacts between Organelles

inferredcites →https://doi.org/10.1016/j.cmet.2014.01.002openalex-snapshot

Peroxisomes: A Nexus for Lipid Metabolism and Cellular Signaling

inferredcites →https://doi.org/10.1016/j.cub.2005.05.055openalex-snapshot

STIM Is a Ca2+ Sensor Essential for Ca2+-Store-Depletion-Triggered Ca2+ Influx

inferredcites →https://doi.org/10.1016/j.cub.2006.08.085openalex-snapshot

CRACM1 Multimers Form the Ion-Selective Pore of the CRAC Channel

inferredcites →https://doi.org/10.1016/j.cub.2013.05.015openalex-snapshot

Local Cytoskeletal and Organelle Interactions Impact Molecular-Motor-Driven Early Endosomal Trafficking

inferredcites →https://doi.org/10.1016/j.devcel.2012.11.004openalex-snapshot

ER-to-Plasma Membrane Tethering Proteins Regulate Cell Signaling and ER Morphology

inferredcites →https://doi.org/10.1016/j.devcel.2014.06.006openalex-snapshot

Cellular Metabolism Regulates Contact Sites between Vacuoles and Mitochondria

inferredcites →https://doi.org/10.1016/j.devcel.2014.06.007openalex-snapshot

A Dynamic Interface between Vacuoles and Mitochondria in Yeast

inferredcites →https://doi.org/10.1016/j.devcel.2015.04.028openalex-snapshot

Phosphatidylinositol-Phosphatidic Acid Exchange by Nir2 at ER-PM Contact Sites Maintains Phosphoinositide Signaling Competence

inferredcites →https://doi.org/10.1016/j.str.2013.11.011openalex-snapshot

Structure and Ca2+-Binding Properties of the Tandem C2 Domains of E-Syt2

inferredcites →https://doi.org/10.1016/s0021-9258(19)39106-9openalex-snapshot

Phospholipid synthesis in a membrane fraction associated with mitochondria.

inferredcites →https://doi.org/10.1016/s1097-2765(00)80391-3openalex-snapshot

C. elegans Dynamin-Related Protein DRP-1 Controls Severing of the Mitochondrial Outer Membrane

inferredcites →https://doi.org/10.1038/13014openalex-snapshot

The dynamin-related GTPase Dnm1 regulates mitochondrial fission in yeast

inferredcites →https://doi.org/10.1038/emboj.2011.198openalex-snapshot

Human MIEF1 recruits Drp1 to mitochondrial outer membranes and promotes mitochondrial fusion rather than fission

inferredcites →https://doi.org/10.1038/emboj.2013.170openalex-snapshot

An ER‐peroxisome tether exerts peroxisome population control in yeast

inferredcites →https://doi.org/10.1038/embor.2011.54openalex-snapshot

MiD49 and MiD51, new components of the mitochondrial fission machinery

inferredcites →https://doi.org/10.1038/embor.2013.113openalex-snapshot

The phosphatidylinositol‐transfer protein Nir2 binds phosphatidic acid and positively regulates phosphoinositide signalling

inferredcites →https://doi.org/10.1038/nature02188openalex-snapshot

Molecular machinery for non-vesicular trafficking of ceramide

inferredcites →https://doi.org/10.1038/nature04702openalex-snapshot

A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function

inferredcites →https://doi.org/10.1038/nature05108openalex-snapshot

Molecular identification of the CRAC channel by altered ion selectivity in a mutant of Orai

inferredcites →https://doi.org/10.1038/nature05122openalex-snapshot

Orai1 is an essential pore subunit of the CRAC channel

inferredcites →https://doi.org/10.1038/nature07534openalex-snapshot

Mitofusin 2 tethers endoplasmic reticulum to mitochondria

inferredcites →https://doi.org/10.1038/nature10230openalex-snapshot

A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1038/nature10234openalex-snapshot

Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1038/nature13269openalex-snapshot

Structure of a lipid-bound extended synaptotagmin indicates a role in lipid transfer

inferredcites →https://doi.org/10.1038/nature14359openalex-snapshot

Repeated ER–endosome contacts promote endosome translocation and neurite outgrowth

inferredcites →https://doi.org/10.1038/nature15249openalex-snapshot

Gating machinery of InsP3R channels revealed by electron cryomicroscopy

inferredcites →https://doi.org/10.1038/nature20555openalex-snapshot

Multiple dynamin family members collaborate to drive mitochondrial division

inferredcites →https://doi.org/10.1038/nature22369openalex-snapshot

Applying systems-level spectral imaging and analysis to reveal the organelle interactome

inferredcites →https://doi.org/10.1038/ncb1842openalex-snapshot

SOAR and the polybasic STIM1 domains gate and regulate Orai channels

inferredcites →https://doi.org/10.1038/ncb2026openalex-snapshot

Membrane contacts between endosomes and ER provide sites for PTP1B–epidermal growth factor receptor interaction

inferredcites →https://doi.org/10.1038/ncb2045openalex-snapshot

A novel EF-hand protein, CRACR2A, is a cytosolic Ca2+ sensor that stabilizes CRAC channels in T cells

inferredcites →https://doi.org/10.1038/ncb3234openalex-snapshot

Proteomic mapping of ER–PM junctions identifies STIMATE as a regulator of Ca2+ influx

inferredcites →https://doi.org/10.1038/ncb3339openalex-snapshot

Control of plasma membrane lipid homeostasis by the extended synaptotagmins

inferredcites →https://doi.org/10.1038/ncomms15754openalex-snapshot

Constriction of the mitochondrial inner compartment is a priming event for mitochondrial division

inferredcites →https://doi.org/10.1038/ng585openalex-snapshot

Identification of the gene altered in Berardinelli–Seip congenital lipodystrophy on chromosome 11q13

inferredcites →https://doi.org/10.1038/nrm.2015.8openalex-snapshot

Structure and function of ER membrane contact sites with other organelles

inferredcites →https://doi.org/10.1038/nsmb.2625openalex-snapshot

Initial activation of STIM1, the regulator of store-operated calcium entry

inferredcites →https://doi.org/10.1038/sj.emboj.7600135openalex-snapshot

Implication of ZW10 in membrane trafficking between the endoplasmic reticulum and Golgi

inferredcites →https://doi.org/10.1038/srep30777openalex-snapshot

A phospholipid transfer function of ER-mitochondria encounter structure revealed in vitro

inferredcites →https://doi.org/10.1073/pnas.0603161103openalex-snapshot

Genome-wide RNAi screen of Ca 2+ influx identifies genes that regulate Ca 2+ release-activated Ca 2+ channel activity

inferredcites →https://doi.org/10.1073/pnas.0611725104openalex-snapshot

E-Syts, a family of membranous Ca 2+ -sensor proteins with multiple C 2 domains

inferredcites →https://doi.org/10.1073/pnas.0704154104openalex-snapshot

The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology

inferredcites →https://doi.org/10.1073/pnas.0911280106openalex-snapshot

STIM1-induced precortical and cortical subdomains of the endoplasmic reticulum

inferredcites →https://doi.org/10.1073/pnas.1118947109openalex-snapshot

Structural and mechanistic insights into the activation of Stromal interaction molecule 1 (STIM1)

inferredcites →https://doi.org/10.1073/pnas.1200667109openalex-snapshot

Junctate is a Ca 2 + -sensing structural component of Orai1 and stromal interaction molecule 1 (STIM1)

inferredcites →https://doi.org/10.1073/pnas.1422363112openalex-snapshot

Conserved SMP domains of the ERMES complex bind phospholipids and mediate tether assembly

inferredcites →https://doi.org/10.1073/pnas.1503191112openalex-snapshot

Three-dimensional architecture of extended synaptotagmin-mediated endoplasmic reticulum–plasma membrane contact sites

inferredcites →https://doi.org/10.1073/pnas.1521924112openalex-snapshot

TMEM110 regulates the maintenance and remodeling of mammalian ER–plasma membrane junctions competent for STIM–ORAI signaling

inferredcites →https://doi.org/10.1073/pnas.1524229113openalex-snapshot

Junctophilin-4, a component of the endoplasmic reticulum–plasma membrane junctions, regulates Ca 2+ dynamics in T cells

inferredcites →https://doi.org/10.1073/pnas.1701078114openalex-snapshot

Contacts between the endoplasmic reticulum and other membranes in neurons

inferredcites →https://doi.org/10.1073/pnas.1715592114openalex-snapshot

Crystal structures of Mmm1 and Mdm12–Mmm1 reveal mechanistic insight into phospholipid trafficking at ER-mitochondria contact sites

inferredcites →https://doi.org/10.1073/pnas.1719709115openalex-snapshot

Structural basis of sterol recognition and nonvesicular transport by lipid transfer proteins anchored at membrane contact sites

inferredcites →https://doi.org/10.1074/jbc.274.31.21913openalex-snapshot

The II-III Loop of the Skeletal Muscle Dihydropyridine Receptor Is Responsible for the Bi-directional Coupling with the Ryanodine Receptor

inferredcites →https://doi.org/10.1074/jbc.m409566200openalex-snapshot

Differential Regulation of Endoplasmic Reticulum Structure through VAP-Nir Protein Interaction

inferredcites →https://doi.org/10.1074/jbc.m605032200openalex-snapshot

Efficient Trafficking of Ceramide from the Endoplasmic Reticulum to the Golgi Apparatus Requires a VAMP-associated Protein-interacting FFAT Motif of CERT

inferredcites →https://doi.org/10.1080/15384101.2017.1314422openalex-snapshot

Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations

inferredcites →https://doi.org/10.1083/jcb.143.2.351openalex-snapshot

A Human Dynamin-related Protein Controls the Distribution of Mitochondria

inferredcites →https://doi.org/10.1083/jcb.200205091openalex-snapshot

Recombinant expression of the voltage-dependent anion channel enhances the transfer of Ca2+ microdomains to mitochondria

inferredcites →https://doi.org/10.1083/jcb.200211046openalex-snapshot

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

inferredcites →https://doi.org/10.1083/jcb.200502019openalex-snapshot

STIM1, an essential and conserved component of store-operated Ca2 + channel function

inferredcites →https://doi.org/10.1083/jcb.200608073openalex-snapshot

Chaperone-mediated coupling of endoplasmic reticulum and mitochondrial Ca2+ channels

inferredcites →https://doi.org/10.1083/jcb.200711136openalex-snapshot

Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast

inferredcites →https://doi.org/10.1083/jcb.200811005openalex-snapshot

Cholesterol sensor ORP1L contacts the ER protein VAP to control Rab7–RILP–p150Glued and late endosome positioning

inferredcites →https://doi.org/10.1083/jcb.200907074openalex-snapshot

Membrane expansion alleviates endoplasmic reticulum stress independently of the unfolded protein response

inferredcites →https://doi.org/10.1083/jcb.201007152openalex-snapshot

Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells

inferredcites →https://doi.org/10.1083/jcb.201011039openalex-snapshot

A 3D analysis of yeast ER structure reveals how ER domains are organized by membrane curvature

inferredcites →https://doi.org/10.1083/jcb.201104062openalex-snapshot

Osh4p exchanges sterols for phosphatidylinositol 4-phosphate between lipid bilayers

inferredcites →https://doi.org/10.1083/jcb.201201139openalex-snapshot

The FATP1–DGAT2 complex facilitates lipid droplet expansion at the ER–lipid droplet interface

inferredcites →https://doi.org/10.1083/jcb.201502033openalex-snapshot

Ltc1 is an ER-localized sterol transporter and a component of ER–mitochondria and ER–vacuole contacts

inferredcites →https://doi.org/10.1083/jcb.201502070openalex-snapshot

The seipin complex Fld1/Ldb16 stabilizes ER–lipid droplet contact sites

inferredcites →https://doi.org/10.1083/jcb.201502105openalex-snapshot

ER–mitochondrial junctions can be bypassed by dominant mutations in the endosomal protein Vps13

inferredcites →https://doi.org/10.1083/jcb.201606059openalex-snapshot

An inducible ER–Golgi tether facilitates ceramide transport to alleviate lipotoxicity

inferredcites →https://doi.org/10.1083/jcb.201607055openalex-snapshot

ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER

inferredcites →https://doi.org/10.1083/jcb.201608128openalex-snapshot

VAPs and ACBD5 tether peroxisomes to the ER for peroxisome maintenance and lipid homeostasis

inferredcites →https://doi.org/10.1083/jcb.201609033openalex-snapshot

Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia

inferredcites →https://doi.org/10.1083/jcb.201610055openalex-snapshot

Vps13-Mcp1 interact at vacuole–mitochondria interfaces and bypass ER–mitochondria contact sites

inferredcites →https://doi.org/10.1083/jcb.201704184openalex-snapshot

Rab18 promotes lipid droplet (LD) growth by tethering the ER to LDs through SNARE and NRZ interactions

inferredcites →https://doi.org/10.1086/504927openalex-snapshot

ZFYVE27 (SPG33), a Novel Spastin-Binding Protein, Is Mutated in Hereditary Spastic Paraplegia

inferredcites →https://doi.org/10.1091/mbc.e07-12-1287openalex-snapshot

The Novel Tail-anchored Membrane Protein Mff Controls Mitochondrial and Peroxisomal Fission in Mammalian Cells

inferredcites →https://doi.org/10.1091/mbc.e08-05-0498openalex-snapshot

Coordinated Lipid Transfer between the Endoplasmic Reticulum and the Golgi Complex Requires the VAP Proteins and Is Essential for Golgi-mediated Transport

inferredcites →https://doi.org/10.1091/mbc.e12-10-0733openalex-snapshot

Endoplasmic reticulum–endosome contact increases as endosomes traffic and mature

inferredcites →https://doi.org/10.1093/cvr/cvt025openalex-snapshot

Microarchitecture of the dyad

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/10.1111/j.1600-0854.2012.01352.xopenalex-snapshot

Gem1 and ERMES Do Not Directly Affect Phosphatidylserine Transport from ER to Mitochondria or Mitochondrial Inheritance

inferredcites →https://doi.org/10.1126/science.1127883openalex-snapshot

CRACM1 Is a Plasma Membrane Protein Essential for Store-Operated Ca 2+ Entry

inferredcites →https://doi.org/10.1126/science.1175088openalex-snapshot

An ER-Mitochondria Tethering Complex Revealed by a Synthetic Biology Screen

inferredcites →https://doi.org/10.1126/science.1207385openalex-snapshot

ER Tubules Mark Sites of Mitochondrial Division

inferredcites →https://doi.org/10.1126/science.1228360openalex-snapshot

An Actin-Dependent Step in Mitochondrial Fission Mediated by the ER-Associated Formin INF2

inferredcites →https://doi.org/10.1126/science.1228757openalex-snapshot

Crystal Structure of the Calcium Release–Activated Calcium Channel Orai

inferredcites →https://doi.org/10.1126/science.280.5370.1763openalex-snapshot

Close Contacts with the Endoplasmic Reticulum as Determinants of Mitochondrial Ca 2+ Responses

inferredcites →https://doi.org/10.1126/science.aab1370openalex-snapshot

PI4P/phosphatidylserine countertransport at ORP5- and ORP8-mediated ER–plasma membrane contacts

inferredcites →https://doi.org/10.1126/science.aaf5549openalex-snapshot

ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells

inferredcites →https://doi.org/10.1126/science.aah4701openalex-snapshot

Coupling organelle inheritance with mitosis to balance growth and differentiation

inferredcites →https://doi.org/10.1126/science.aah6171openalex-snapshot

Lipid transport by TMEM24 at ER–plasma membrane contacts regulates pulsatile insulin secretion

inferredcites →https://doi.org/10.1126/science.aan6009openalex-snapshot

ER-mitochondria tethering by PDZD8 regulates Ca 2+ dynamics in mammalian neurons

inferredcites →https://doi.org/10.1146/annurev-cellbio-100616-060608openalex-snapshot

Lipid Droplet Biogenesis

inferredcites →https://doi.org/10.1194/jlr.m037325openalex-snapshot

Cholesterol-binding molecules MLN64 and ORP1L mark distinct late endosomes with transporters ABCA3 and NPC1

inferredcites →https://doi.org/10.1242/jcs.076836openalex-snapshot

Lipid droplets are functionally connected to the endoplasmic reticulum in Saccharomyces cerevisiae

inferredcites →https://doi.org/10.1242/jcs.085118openalex-snapshot

A conserved membrane-binding domain targets proteins to organelle contact sites

inferredcites →https://doi.org/10.1242/jcs.121244openalex-snapshot

Mcp1 and Mcp2, two novel proteins involved in mitochondrial lipid homeostasis

inferredcites →https://doi.org/10.1242/jcs.137737openalex-snapshot

Size control of lipid droplets in budding yeast requires a collaboration of Fld1 and Ldb16

inferredcites →https://doi.org/10.1242/jcs.139295openalex-snapshot

STARD3/STARD3NL and VAP make a novel molecular tether between late endosomes and the ER

inferredcites →https://doi.org/10.1242/jcs.185165openalex-snapshot

Cooperative and independent roles of the Drp1 adaptors Mff, MiD49 and MiD51 in mitochondrial fission

inferredcites →https://doi.org/10.1385/cbb:39:3:279openalex-snapshot

The Voltage-Dependent Anion Channel: Characterization, Modulation, and Role in Mitochondrial Function in Cell Life and Death

inferredcites →https://doi.org/10.15252/embj.201591565openalex-snapshot

Triggered Ca2+ influx is required for extended synaptotagmin 1‐induced ER‐plasma membrane tethering

inferredcites →https://doi.org/10.15252/embj.201695170openalex-snapshot

Seipin regulates ER–lipid droplet contacts and cargo delivery

inferredcites →https://doi.org/10.15252/embj.201798002openalex-snapshot

Molecular basis for sterol transport by StART‐like lipid transfer domains

inferredcites →https://doi.org/10.15252/embr.201642706openalex-snapshot

Crystal structure of Mdm12 reveals the architecture and dynamic organization of the ERMES complex

inferredcites →https://doi.org/10.3389/fphys.2015.00420openalex-snapshot

Critical Role of Intracellular RyR1 Calcium Release Channels in Skeletal Muscle Function and Disease

inferredcites →https://doi.org/10.7554/elife.00422openalex-snapshot

ER-associated mitochondrial division links the distribution of mitochondria and mitochondrial DNA in yeast

inferredcites →https://doi.org/10.7554/elife.01607openalex-snapshot

Arf1/COPI machinery acts directly on lipid droplets and enables their connection to the ER for protein targeting

inferredcites →https://doi.org/10.7554/elife.07253openalex-snapshot

A new family of StART domain proteins at membrane contact sites has a role in ER-PM sterol transport

inferredcites →https://doi.org/10.7554/elife.08828openalex-snapshot

A mitochondria-anchored isoform of the actin-nucleating spire protein regulates mitochondrial division

inferredcites →https://doi.org/10.7554/elife.16582openalex-snapshot

Seipin is required for converting nascent to mature lipid droplets

inferredcites →https://doi.org/10.7554/elife.31019openalex-snapshot

GRAM domain proteins specialize functionally distinct ER-PM contact sites in human cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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High-Throughput Super-Resolution Single Particle Trajectory Analysis Reconstructs Organelle Dynamics and Membrane Re-Organization

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Intricacies of Lipid Supply in Autophagic Membrane Expansion

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Identification and Characterization of Plant Exclusive Smp-Domain Proteins at Er-Chloroplast and Er-Tgn Membrane Contact Sites

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Peroxisomes undergo morphological changes in a light‐dependent manner with proximity to the nucleus

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Remodelling of mitochondrial function by import of specific lipids at multiple membrane‐contact sites

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Spatial organization of phosphoinositide signaling

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Intercompartmental communication in senescence

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Plant Endoplasmic Reticulum

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Remodeling of Membrane Shape and Topology by Curvature Elasticity and Membrane Tension

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Polarity‐selective Transfer of Lipophilic Cargoes From Lipid Droplets (Oleosomes) to Lipid Bilayers

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Metamaterial‐Assisted Illumination Nanoscopy with Exceptional Axial Resolution

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Lipid Droplet‐Derived Biomimetic Nanocarriers for the Enhancement of Porcine Intermuscular Fat Content

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Pericentrosomal Redistribution of the Endoplasmic Reticulum Ensures Organelle Symmetric Inheritance and Mitotic Progression

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ATL2 Recruits TRAK1 to Promote Mitochondrial Transport at ER–Mitochondria Contact Sites

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Mechanically Regulated Secretion: How Physical Forces Instruct the Secretory Pathway and Remodel the Secretome

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Lipid Droplet–Mitochondria Interactions: From Molecular Components to Spatial Aggregation Manipulation

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Programmable DNA Nanocages Enable Adaptive Spatiotemporal Organization of Biomimetic Organelle Networks

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Programmable DNA Nanocages Enable Adaptive Spatiotemporal Organization of Biomimetic Organelle Networks

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Are endoplasmic reticulum subdomains shaped by asymmetric distribution of phospholipids? Evidence from a C. elegans model system

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Controlling contacts—Molecular mechanisms to regulate organelle membrane tethering

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PAQR proteins and the evolution of a superpower: Eating all kinds of fats

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Ion‐ and Temperature‐Programmable Reconfiguration of Subcompartments in Synthetic Cells

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Interplay between endoplasmic reticulum membrane contacts and actomyosin cytoskeleton

inferred← citeshttps://doi.org/10.1002/cpz1.71openalex-snapshot

Optogenetic Tools for Manipulating Protein Subcellular Localization and Intracellular Signaling at Organelle Contact Sites

inferred← citeshttps://doi.org/10.1002/cpz1.842openalex-snapshot

Immunofluorescence Microscopy

inferred← citeshttps://doi.org/10.1002/ctm2.1441openalex-snapshot

Application of synthetic lipid droplets in metabolic diseases

inferred← citeshttps://doi.org/10.1002/iid3.647openalex-snapshot

The mitochondrial associated endoplasmic reticulum membranes: A platform for the pathogenesis of inflammation‐mediated metabolic diseases

inferred← citeshttps://doi.org/10.1002/jcp.30928openalex-snapshot

Lysosome signaling in cell survival and programmed cell death for cellular homeostasis

inferred← citeshttps://doi.org/10.1002/jcp.70187openalex-snapshot

Cell Membrane Biogenesis: A Matter of Survival. Its Role in Renal Epithelia Restitution After Calcium Oxalate Injury

inferred← citeshttps://doi.org/10.1002/jimd.12083openalex-snapshot

Organelle interplay—peroxisome interactions in health and disease

inferred← citeshttps://doi.org/10.1002/mco2.70379openalex-snapshot

Mitochondria‐Associated Endoplasmic Reticulum Membranes in Health and Diseases

inferred← citeshttps://doi.org/10.1002/rth2.12260openalex-snapshot

3D ultrastructural analysis of α‐granule, dense granule, mitochondria, and canalicular system arrangement in resting human platelets

inferred← citeshttps://doi.org/10.1002/wsbm.1505openalex-snapshot

Dynamic organization of intracellular organelle networks

inferred← citeshttps://doi.org/10.1002/wsbm.1612openalex-snapshot

Membrane contact sites orchestrate cholesterol homeostasis that is central to vascular aging

inferred← citeshttps://doi.org/10.1007/5584_2025_852openalex-snapshot

Crosstalk Between Phase-Separated Membraneless Condensates and Membrane-Bound Organelles in Cellular Function and Disease

inferred← citeshttps://doi.org/10.1007/978-1-0716-1270-5_22openalex-snapshot

Isolation of Mitochondria-Associated ER Membranes (MAMs), Synaptic MAMs, and Glycosphingolipid Enriched Microdomains (GEMs) from Brain Tissues and Neuronal Cells

inferred← citeshttps://doi.org/10.1007/978-1-0716-2863-8_11openalex-snapshot

Quantitative Analysis of the Endoplasmic Reticulum-Associated Proteins Using ER-Localizable Reactive Molecules

inferred← citeshttps://doi.org/10.1007/978-1-0716-4318-1_15openalex-snapshot

DNA-Assisted Assays for Studying Lipid Transfer Between Membranes

inferred← citeshttps://doi.org/10.1007/978-1-0716-4318-1_2openalex-snapshot

Measurement of ORP10-Mediated Lipid Countertransport at ER-Endosome Membrane Contact Sites via a Chemically Induced Dimerization Strategy

inferred← citeshttps://doi.org/10.1007/978-1-4939-2257-4_3openalex-snapshot

Isolation of Mitochondria-Associated ER Membranes (MAMs) and Glycosphingolipid-Enriched Microdomains (GEMs) from Brain Tissues and Neuronal Cells

inferred← citeshttps://doi.org/10.1007/978-3-030-12457-1_29openalex-snapshot

ER-Mitochondria Calcium Transfer, Organelle Contacts and Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.1007/978-3-030-34025-4_1openalex-snapshot

Metabolic Remodeling as a Way of Adapting to Tumor Microenvironment (TME), a Job of Several Holders

inferred← citeshttps://doi.org/10.1007/978-3-030-38266-7_8openalex-snapshot

The Ubiquitin System in Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1007/978-3-031-62036-2_1openalex-snapshot

Organelle Communication with the Nucleus

inferred← citeshttps://doi.org/10.1007/978-3-031-94744-5_6openalex-snapshot

Divide Et Impera: How Cellular Integration and Control Are Established Through the Division of the Intracellular Space

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/s00018-020-03523-wopenalex-snapshot

A central role of the endoplasmic reticulum in the cell emerges from its functional contact sites with multiple organelles

inferred← citeshttps://doi.org/10.1007/s00018-022-04426-8openalex-snapshot

Surface cholesterol-enriched domains specifically promote invasion of breast cancer cell lines by controlling invadopodia and extracellular matrix degradation

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/s00018-026-06191-4openalex-snapshot

Peroxisome calcium uptake is dependent on ER-peroxisome membrane contact

inferred← citeshttps://doi.org/10.1007/s00204-024-03719-0openalex-snapshot

The interactions of subcellular organelles in pulmonary fibrosis induced by carbon black nanoparticles: a comprehensive review

inferred← citeshttps://doi.org/10.1007/s00299-021-02799-xopenalex-snapshot

Phytosterol metabolism in plant positive-strand RNA virus replication

inferred← citeshttps://doi.org/10.1007/s00418-019-01829-wopenalex-snapshot

Selective autophagy of cytosolic protein aggregates involves ribosome-free rough endoplasmic reticulum

inferred← citeshttps://doi.org/10.1007/s00709-021-01667-5openalex-snapshot

Gland cell responses to feeding in Drosera capensis, a carnivorous plant

inferred← citeshttps://doi.org/10.1007/s11033-023-08517-yopenalex-snapshot

Molecular characterization of wild-type and HSAN2B-linked FAM134B

inferred← citeshttps://doi.org/10.1007/s11064-021-03438-3openalex-snapshot

The CACNA1A Mutant Disrupts Lysosome Calcium Homeostasis in Cerebellar Neurons and the Resulting Endo-Lysosomal Fusion Defect Can be Improved by Calcium Modulation

inferred← citeshttps://doi.org/10.1007/s11095-022-03216-yopenalex-snapshot

A Novel Fluoro-Pyrazine-Bridged Donor-Accepter-Donor Fluorescent Probe for Lipid Droplet-Specific Imaging in Diverse Cells and Superoxide Anion Generation

inferred← citeshttps://doi.org/10.1007/s11427-023-2443-9openalex-snapshot

Stay in touch with the endoplasmic reticulum

inferred← citeshttps://doi.org/10.1007/s11427-025-3248-3openalex-snapshot

Organelle-specific fluorescent probes for live imaging at the nanoscale

inferred← citeshttps://doi.org/10.1007/s12200-023-00090-3openalex-snapshot

Organic fluorescent probes for live-cell super-resolution imaging

inferred← citeshttps://doi.org/10.1007/s12551-018-0479-3openalex-snapshot

Molecular mechanisms of contractile-ring constriction and membrane trafficking in cytokinesis

inferred← citeshttps://doi.org/10.1007/s40242-021-1191-6openalex-snapshot

Conventional Molecular and Novel Structural Mechanistic Insights into Orderly Organelle Interactions

inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.00010-1openalex-snapshot

Mature eosinophils: General morphology

inferred← citeshttps://doi.org/10.1016/b978-0-12-813755-0.09990-1openalex-snapshot

References

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/bs.apcsb.2021.02.007openalex-snapshot

Apoptotic signals at the endoplasmic reticulum-mitochondria interface

inferred← citeshttps://doi.org/10.1016/j.addr.2021.05.030openalex-snapshot

Understanding the interactions between inorganic-based nanomaterials and biological membranes

inferred← citeshttps://doi.org/10.1016/j.addr.2023.115025openalex-snapshot

Targeted to neuronal organelles for CNS drug development

inferred← citeshttps://doi.org/10.1016/j.ajpath.2022.12.002openalex-snapshot

Mitochondria and Endoplasmic Reticulum Stress in Retinal Organoids from Patients with Vision Loss

inferred← citeshttps://doi.org/10.1016/j.aquaculture.2023.740538openalex-snapshot

Effects of quercetin and hydroxytyrosol supplementation in a high-fat diet on growth, lipid metabolism, and mitochondrial function in spotted seabass (Lateolabrax maculatus)

inferred← citeshttps://doi.org/10.1016/j.bbalip.2019.04.007openalex-snapshot

SMP domain proteins in membrane lipid dynamics

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.2019.07.001openalex-snapshot

Specialized ER membrane domains for lipid metabolism and transport

inferred← citeshttps://doi.org/10.1016/j.bbalip.2021.158990openalex-snapshot

Sec14 family of lipid transfer proteins in yeasts

inferred← citeshttps://doi.org/10.1016/j.bbalip.2022.159219openalex-snapshot

Palmitate and thapsigargin have contrasting effects on ER membrane lipid composition and ER proteostasis in neuronal cells

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118800openalex-snapshot

Maintaining social contacts: The physiological relevance of organelle interactions

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2020.118825openalex-snapshot

A cell cycle checkpoint for the endoplasmic reticulum

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119073openalex-snapshot

TorsinA folding and N-linked glycosylation are sensitive to redox homeostasis

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2021.119099openalex-snapshot

Keeping zombies alive: The ER-mitochondria Ca2+ transfer in cellular senescence

inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119475openalex-snapshot

Phosphatidylinositol 4,5-bisphosphate and calcium at ER-PM junctions — Complex interplay of simple messengers

inferred← citeshttps://doi.org/10.1016/j.bbamem.2024.184308openalex-snapshot

Coordinated regulation of phosphatidylinositol 4-phosphate and phosphatidylserine levels by Osh4p and Osh5p is an essential regulatory mechanism in autophagy

inferred← citeshttps://doi.org/10.1016/j.bbamem.2024.184365openalex-snapshot

Proposed dual membrane contact with full-length Osh4

inferred← citeshttps://doi.org/10.1016/j.bbamem.2025.184484openalex-snapshot

Tubulation of membrane sheets by curvature-inducing proteins

inferred← citeshttps://doi.org/10.1016/j.bbr.2025.115775openalex-snapshot

DJ-1 in Parkinson's disease: Its important role at endoplasmic reticulum–mitochondria contact sites

inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.10.073openalex-snapshot

Stasimon/Tmem41b localizes to mitochondria-associated ER membranes and is essential for mouse embryonic development

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2023.10.017openalex-snapshot

Enhancing drug penetration in solid tumors via nanomedicine: Evaluation models, strategies and perspectives

inferred← citeshttps://doi.org/10.1016/j.bioactmat.2025.02.040openalex-snapshot

Organelle-oriented nanomedicines in tumor therapy: Targeting, escaping, or collaborating?

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109437openalex-snapshot

A mitochondria-targeting glutathione fluorescent probe reveals distinct mitochondria-endoplasmic reticulum contact between disulfidptosis and ferroptosis

inferred← citeshttps://doi.org/10.1016/j.biopha.2021.112012openalex-snapshot

Mechanistic insight into high-fat diet-induced metabolic inflammation in the arcuate nucleus of the hypothalamus

inferred← citeshttps://doi.org/10.1016/j.bpj.2023.06.010openalex-snapshot

Extracting nanoscale membrane morphology from single-molecule localizations

inferred← citeshttps://doi.org/10.1016/j.bpj.2023.06.022openalex-snapshot

Endoplasmic reticulum network heterogeneity guides diffusive transport and kinetics

inferred← citeshttps://doi.org/10.1016/j.cbpa.2022.102262openalex-snapshot

Chemo- and opto-genetic tools for dissecting the role of membrane contact sites in living cells: Recent advances and limitations

inferred← citeshttps://doi.org/10.1016/j.ceb.2018.11.002openalex-snapshot

Moving out but keeping in touch: contacts between endoplasmic reticulum and lipid droplets

inferred← citeshttps://doi.org/10.1016/j.ceb.2019.03.018openalex-snapshot

Lipid droplet biogenesis

inferred← citeshttps://doi.org/10.1016/j.ceb.2021.01.010openalex-snapshot

Interorganelle communication and membrane shaping in the early secretory pathway

inferred← citeshttps://doi.org/10.1016/j.ceb.2021.02.004openalex-snapshot

Organelle distribution in neurons: Logistics behind polarized transport

inferred← citeshttps://doi.org/10.1016/j.ceb.2023.102212openalex-snapshot

Piecing together the structural organisation of lipid exchange at membrane contact sites

inferred← citeshttps://doi.org/10.1016/j.ceb.2024.102357openalex-snapshot

Endoplasmic reticulum – condensate interactions in protein synthesis and secretion

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.2019.02.003openalex-snapshot

Getting close. Lysosome-ER contact sites tailor Ca2+ signals

inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102179openalex-snapshot

The role of mitochondria in shaping odor responses in Drosophila melanogaster olfactory sensory neurons

inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102249openalex-snapshot

Getting intimate: Lysosomes and ER rendezvous to control autophagy

inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102343openalex-snapshot

Mitochondria Associated Membranes (MAMs): Architecture and physiopathological role

inferred← citeshttps://doi.org/10.1016/j.ceca.2020.102345openalex-snapshot

Recent studies on NCLX in health and diseases

inferred← citeshttps://doi.org/10.1016/j.ceca.2024.102875openalex-snapshot

The tether function of the anoctamins

inferred← citeshttps://doi.org/10.1016/j.cell.2019.12.005openalex-snapshot

Local Fatty Acid Channeling into Phospholipid Synthesis Drives Phagophore Expansion during Autophagy

inferred← citeshttps://doi.org/10.1016/j.cell.2021.08.001openalex-snapshot

Dual film-like organelles enable spatial separation of orthogonal eukaryotic translation

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.2022.111583openalex-snapshot

ER-mitochondrial contact protein Miga regulates autophagy through Atg14 and Uvrag

inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114592openalex-snapshot

VAP-mediated membrane-tethering mechanisms implicate ER-PM contact function in pH homeostasis

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115411openalex-snapshot

Multi-platform omics analysis of Nipah virus infection reveals viral glycoprotein modulation of mitochondria

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115483openalex-snapshot

PDZD8 promotes autophagy at ER-lysosome membrane contact sites to regulate activity-dependent synaptic growth

inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117537openalex-snapshot

Cholesterol transfer proteins promote Atg-independent ER clearance by lysosomes

inferred← citeshttps://doi.org/10.1016/j.cels.2025.101429openalex-snapshot

Anomaly detection for high-content image-based phenotypic cell profiling

inferred← citeshttps://doi.org/10.1016/j.chembiol.2025.02.003openalex-snapshot

Mechanisms and functions of lysosomal lipid homeostasis

inferred← citeshttps://doi.org/10.1016/j.cjca.2023.10.012openalex-snapshot

Oxidative Stress and Endoplasmic Reticular Stress Interplay in the Vasculopathy of Hypertension

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.cophys.2020.08.007openalex-snapshot

Phosphoinositides and calcium signaling; a marriage arranged at ER-PM contact sites

inferred← citeshttps://doi.org/10.1016/j.cophys.2020.08.013openalex-snapshot

The ER-mitochondria tether at the hub of Ca2+ signaling

inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100277openalex-snapshot

High-throughput super-resolution single-particle trajectory analysis reconstructs organelle dynamics and membrane reorganization

inferred← citeshttps://doi.org/10.1016/j.cub.2021.03.038openalex-snapshot

Multiple roles for actin in secretory and endocytic pathways

inferred← citeshttps://doi.org/10.1016/j.cub.2022.07.014openalex-snapshot

A polarized supercell produces specialized metabolites in cannabis trichomes

inferred← citeshttps://doi.org/10.1016/j.cub.2022.07.058openalex-snapshot

Dual control of formin-nucleated actin assembly by the chromatin and ER in mouse oocytes

inferred← citeshttps://doi.org/10.1016/j.cub.2026.07.066openalex-snapshot

BLTP2 bridges the ER and MVB for exosome biogenesis at SCAMP3-dependent ER contacts

inferred← citeshttps://doi.org/10.1016/j.cub.2026.09.021openalex-snapshot

Mitochondria-ER-lipid droplet crosstalk regulates metabolic adaptation to shear stress via VMP1

inferred← citeshttps://doi.org/10.1016/j.devcel.2019.10.018openalex-snapshot

Tricalbin-Mediated Contact Sites Control ER Curvature to Maintain Plasma Membrane Integrity

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.2021.05.002openalex-snapshot

Membrane contact site-dependent cholesterol transport regulates Na+/K+-ATPase polarization and spermiogenesis in Caenorhabditis elegans

inferred← citeshttps://doi.org/10.1016/j.devcel.2021.11.015openalex-snapshot

TAOK2 is an ER-localized kinase that catalyzes the dynamic tethering of ER to microtubules

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.2022.05.002openalex-snapshot

The ER ladder is a unique morphological feature of developing mammalian axons

inferred← citeshttps://doi.org/10.1016/j.devcel.2022.09.014openalex-snapshot

PITTching in for lysosome repair

inferred← citeshttps://doi.org/10.1016/j.devcel.2022.12.010openalex-snapshot

VAP-A intrinsically disordered regions enable versatile tethering at membrane contact sites

inferred← citeshttps://doi.org/10.1016/j.devcel.2023.03.002openalex-snapshot

Deregulation of ER-mitochondria contact formation and mitochondrial calcium homeostasis mediated by VDAC in fragile X syndrome

inferred← citeshttps://doi.org/10.1016/j.devcel.2024.05.005openalex-snapshot

Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions

inferred← citeshttps://doi.org/10.1016/j.devcel.2024.06.005openalex-snapshot

SigmaR1 shapes rough endoplasmic reticulum membrane sheets

inferred← citeshttps://doi.org/10.1016/j.ejcb.2021.151180openalex-snapshot

Specific subdomain localization of ER resident proteins and membrane contact sites resolved by electron microscopy

inferred← citeshttps://doi.org/10.1016/j.ejcb.2025.151490openalex-snapshot

Viral vaccines promote endoplasmic reticulum stress-induced unfolding protein response in teleost erythrocytes

inferred← citeshttps://doi.org/10.1016/j.ejphar.2021.174687openalex-snapshot

Trans-cinnamaldehyde suppresses microtubule detyrosination and alleviates cardiac hypertrophy

inferred← citeshttps://doi.org/10.1016/j.exer.2021.108793openalex-snapshot

Quantifying inter-organelle membrane contact sites using proximity ligation assay in fixed optic nerve sections

inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114883openalex-snapshot

Cold inducible RNA binding protein-regulated mitochondria associated endoplasmic reticulum membranes-mediated Ca2+ transport play a critical role in hypothermia cerebral resuscitation

inferred← citeshttps://doi.org/10.1016/j.fgb.2020.103338openalex-snapshot

An endoplasmic reticulum domain is associated with the polarized growing cells of Podospora anserina hyphae

inferred← citeshttps://doi.org/10.1016/j.intimp.2024.113510openalex-snapshot

SUCNR 1 promotes atherosclerosis by inducing endoplasmic reticulum stress mediated ER-mito crosstalk

inferred← citeshttps://doi.org/10.1016/j.isci.2021.102324openalex-snapshot

MitopatHs: A new logically-framed tool for visualizing multiple mitochondrial pathways

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.isci.2023.105965openalex-snapshot

Transcriptome, Proteome, and Protein Synthesis Within the Intracellular Cytomatrix

inferred← citeshttps://doi.org/10.1016/j.isci.2023.108386openalex-snapshot

Yeast lunapark regulates the formation of trans-Sey1p complexes for homotypic ER membrane fusion

inferred← citeshttps://doi.org/10.1016/j.isci.2024.109379openalex-snapshot

Mitochondria-ER contact sites expand during mitosis

inferred← citeshttps://doi.org/10.1016/j.isci.2024.110683openalex-snapshot

Spastin regulates ER-mitochondrial contact sites and mitochondrial homeostasis

inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101740openalex-snapshot

Inositol triphosphate–triggered calcium release from the endoplasmic reticulum induces lysosome biogenesis via TFEB/TFE3

inferred← citeshttps://doi.org/10.1016/j.jbc.2022.101935openalex-snapshot

The mammalian rhomboid protein RHBDL4 protects against endoplasmic reticulum stress by regulating the morphology and distribution of ER sheets

inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102423openalex-snapshot

Quantitative interactome proteomics identifies a proteostasis network for GABAA receptors

inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104799openalex-snapshot

AdipoR2 recruits protein interactors to promote fatty acid elongation and membrane fluidity

inferred← citeshttps://doi.org/10.1016/j.jbc.2024.107665openalex-snapshot

The tricalbin family of membrane contact site tethers is involved in the transcriptional responses of Saccharomyces cerevisiae to glucose

inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110410openalex-snapshot

Maintenance of proper phosphatidylinositol-4-phosphate level by Stt4 and Sac1 contributes to vesicular transport to and from the plasma membrane

inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113144openalex-snapshot

Quantitative FRET FLIM imaging reveals multiple interactions between proteins of the ESYT, ORP, and VAP families at the endoplasmic reticulum membrane

inferred← citeshttps://doi.org/10.1016/j.jbior.2023.101001openalex-snapshot

A new role for phosphoinositides in regulating mitochondrial dynamics

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.137514openalex-snapshot

Fluoride induces spermatocyte apoptosis by IP3R1/MCU-mediated mitochondrial calcium overload through MAMs

inferred← citeshttps://doi.org/10.1016/j.jid.2025.05.031openalex-snapshot

Through the Microscope Lens: Investigating the Mechanisms of Desmosome Disruption in Pemphigus

inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168691openalex-snapshot

Phospholipid Supply for Autophagosome Biogenesis

inferred← citeshttps://doi.org/10.1016/j.jnutbio.2025.110064openalex-snapshot

Transport of cholesterol to ovary via the Srb selective uptake pathway supports Star-mediated steroidogenesis in swimming crab (Portunus trituberculatus)

inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2025.113209openalex-snapshot

Photobiomodulation mediates endoplasmic reticulum-mitochondria contact and ameliorates lipotoxicity in MASLD via Mfn2 upregulation

inferred← citeshttps://doi.org/10.1016/j.jtha.2024.11.016openalex-snapshot

Molecular basis of platelet granule defects

inferred← citeshttps://doi.org/10.1016/j.lfs.2026.124625openalex-snapshot

SARS-CoV-2 nucleocapsid protein drives pulmonary injury by enhancing GRP75-dependent ER–mitochondria tethering and reprogramming of alveolar macrophages

inferred← citeshttps://doi.org/10.1016/j.mam.2020.100922openalex-snapshot

Mitochondria orchestrate macrophage effector functions in atherosclerosis

inferred← citeshttps://doi.org/10.1016/j.mcn.2023.103822openalex-snapshot

Neuronal endoplasmic reticulum architecture and roles in axonal physiology

inferred← citeshttps://doi.org/10.1016/j.metabol.2026.156623openalex-snapshot

SEC62 at mitochondria-associated membranes drives MASH progression by suppressing ATAD3B-mediated mitochondrial quality control

inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103542openalex-snapshot

Mitochondrial proteome profiling of Leishmania tropica

inferred← citeshttps://doi.org/10.1016/j.micron.2025.103981openalex-snapshot

Morphometric analysis of axonal ultrastructure: Coordinated scaling of organelles and myelin

inferred← citeshttps://doi.org/10.1016/j.molcel.2019.09.011openalex-snapshot

MIGA2 Links Mitochondria, the ER, and Lipid Droplets and Promotes De Novo Lipogenesis in Adipocytes

inferred← citeshttps://doi.org/10.1016/j.molcel.2020.04.017openalex-snapshot

Ca2+ Fluxes and Cancer

inferred← citeshttps://doi.org/10.1016/j.molcel.2020.10.013openalex-snapshot

Drp1 Tubulates the ER in a GTPase-Independent Manner

inferred← citeshttps://doi.org/10.1016/j.molcel.2022.08.005openalex-snapshot

Life in lockdown: Orchestrating endoplasmic reticulum and lysosome homeostasis for quiescent cells

inferred← citeshttps://doi.org/10.1016/j.molcel.2025.12.006openalex-snapshot

Membrane-protein-mediated phase separation orchestrates organelle contact sites

inferred← citeshttps://doi.org/10.1016/j.molcel.2026.07.027openalex-snapshot

ER-liquid condensate contacts sequester FAM134B/C and RhoA to govern cell morphology

inferred← citeshttps://doi.org/10.1016/j.molmed.2019.09.012openalex-snapshot

Staying in Healthy Contact: How Peroxisomes Interact with Other Cell Organelles

inferred← citeshttps://doi.org/10.1016/j.molmet.2022.101481openalex-snapshot

Organelle transporters and inter-organelle communication as drivers of metabolic regulation and cellular homeostasis

inferred← citeshttps://doi.org/10.1016/j.neuron.2024.04.025openalex-snapshot

Friend or foe: The role of stress granule in neurodegenerative disease

inferred← citeshttps://doi.org/10.1016/j.nwnano.2024.100060openalex-snapshot

DNA origami-based nano-vaccines for cancer immunotherapy

inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102366openalex-snapshot

The making of a ring: Assembly and regulation of microtubule-associated proteins during preprophase band formation and division plane set-up

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2020.09.005openalex-snapshot

A mammalian system for high-resolution imaging of intact cells by cryo-electron tomography

inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2025.12.003openalex-snapshot

WATER roles in cells: Biological and biophysical perspectives

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2022.108274openalex-snapshot

Interplay between fat cells and immune cells in bone: Impact on malignant progression and therapeutic response

inferred← citeshttps://doi.org/10.1016/j.phrs.2023.106761openalex-snapshot

Mitochondria associated ER membranes and cerebral ischemia: Molecular mechanisms and therapeutic strategies

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.phrs.2026.108220openalex-snapshot

Mitochondria-lipid droplet communication remodels bioenergetic metabolism in cardiovascular diseases

inferred← citeshttps://doi.org/10.1016/j.plipres.2021.101141openalex-snapshot

Hello from the other side: Membrane contact of lipid droplets with other organelles and subsequent functional implications

inferred← citeshttps://doi.org/10.1016/j.plipres.2025.101372openalex-snapshot

The plant lipid contactome: emerging roles of inter-organelle contact sites in lipid metabolism

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2021.102157openalex-snapshot

HIV infection of astrocytes compromises inter-organelle interactions and inositol phosphate metabolism: A potential mechanism of bystander damage and viral reservoir survival

inferred← citeshttps://doi.org/10.1016/j.prp.2026.156513openalex-snapshot

Reduced mitochondrial Rab32 impairs mitochondria-endoplasmic reticulum contacts and inhibits apoptosis in hepatocellular carcinoma cells

inferred← citeshttps://doi.org/10.1016/j.pt.2025.12.009openalex-snapshot

A parasitic secretory relay rewires host ER contacts

inferred← citeshttps://doi.org/10.1016/j.radmp.2026.06.001openalex-snapshot

Fractionated low-dose ionizing radiation induces senescence of human cardiovascular endothelial cells through the mtROS-ERS-MQC axis

inferred← citeshttps://doi.org/10.1016/j.redox.2021.101919openalex-snapshot

Acetaldehyde Dehydrogenase 2 regulates HMG-CoA reductase stability and cholesterol synthesis in the liver

inferred← citeshttps://doi.org/10.1016/j.redox.2024.103170openalex-snapshot

Non-esterified fatty acid palmitate facilitates oxidative endoplasmic reticulum stress and apoptosis of β-cells by upregulating ERO-1α expression

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.161741openalex-snapshot

The key role of proteostasis at mitochondria-associated endoplasmic reticulum membrane in vanadium-induced nephrotoxicity using a proteomic strategy

inferred← citeshttps://doi.org/10.1016/j.semcancer.2020.03.010openalex-snapshot

Autophagy in cancer: Recent advances and future directions

inferred← citeshttps://doi.org/10.1016/j.semcancer.2024.12.002openalex-snapshot

Theoretical framework and emerging challenges of lipid metabolism in cancer

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