| Q34283635 | A complete set of SNAREs in yeast |
| Q27930648 | A genome-wide immunodetection screen in S. cerevisiae uncovers novel genes involved in lysosomal vacuole function and morphology |
| Q33228605 | A genome-wide visual screen reveals a role for sphingolipids and ergosterol in cell surface delivery in yeast |
| Q34223018 | A lipid-anchored SNARE supports membrane fusion |
| Q46629478 | A novel immunodetection screen for vacuolar defects identifies a unique allele of VPS35 in S. cerevisiae |
| Q37491866 | A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion. |
| Q33763601 | A sorting nexin PpAtg24 regulates vacuolar membrane dynamics during pexophagy via binding to phosphatidylinositol-3-phosphate |
| Q30596706 | Actin cytoskeletal reorganizations and coreceptor-mediated activation of rac during human immunodeficiency virus-induced cell fusion |
| Q35197991 | Actin remodeling to facilitate membrane fusion |
| Q34698090 | Amino acids regulate retrieval of the yeast general amino acid permease from the vacuolar targeting pathway |
| Q41003511 | Analysis of a novel calcium auxotrophy in Aspergillus nidulans. |
| Q37663089 | Autophagy in the fission yeast Schizosaccharomyces pombe. |
| Q43101127 | Avt5p is required for vacuolar uptake of amino acids in the fission yeast Schizosaccharomyces pombe |
| Q30159716 | Bem1p is a positive regulator of the homotypic fusion of yeast vacuoles |
| Q44394257 | Biochemical characterization of the vacuolar palmitoyl acyltransferase. |
| Q36498417 | Bioengineered yeast-derived vacuoles with enhanced tissue-penetrating ability for targeted cancer therapy |
| Q43151943 | Candida albicans VAC8 is required for vacuolar inheritance and normal hyphal branching. |
| Q39538510 | Cdc42p is activated during vacuole membrane fusion in a sterol-dependent subreaction of priming |
| Q27938436 | Diacylglycerol and its formation by phospholipase C regulate Rab- and SNARE-dependent yeast vacuole fusion |
| Q34979915 | Emerging roles of presynaptic proteins in Ca++-triggered exocytosis |
| Q40070000 | Enhanced membrane fusion in sterol-enriched vacuoles bypasses the Vrp1p requirement |
| Q40028306 | Enhancing effects on vacuole-targeting fungicidal activity of amphotericin B |
| Q36321097 | Generation of nonidentical compartments in vesicular transport systems |
| Q34850406 | Genome-wide identification, phylogeny and expression profile of vesicle fusion components in Verticillium dahliae |
| Q27932357 | HOPS prevents the disassembly of trans-SNARE complexes by Sec17p/Sec18p during membrane fusion |
| Q42280237 | Hermansky-Pudlak syndrome protein complexes associate with phosphatidylinositol 4-kinase type II alpha in neuronal and non-neuronal cells. |
| Q36322950 | Hierarchy of protein assembly at the vertex ring domain for yeast vacuole docking and fusion |
| Q30409393 | In vitro assay using engineered yeast vacuoles for neuronal SNARE-mediated membrane fusion. |
| Q49034414 | In vitro fusion of plant Golgi membranes can be influenced by divalent cations |
| Q41812787 | Interaction of SNAREs with ArfGAPs precedes recruitment of Sec18p/NSF. |
| Q35197977 | Involvement of LMA1 and GATE-16 family members in intracellular membrane dynamics |
| Q45287569 | Ion regulation of homotypic vacuole fusion in Saccharomyces cerevisiae |
| Q33232474 | Loss of the homotypic fusion and vacuole protein sorting or golgi-associated retrograde protein vesicle tethering complexes results in gentamicin sensitivity in the yeast Saccharomyces cerevisiae |
| Q33715200 | Mechanisms of organelle biogenesis govern stochastic fluctuations in organelle abundance |
| Q26269942 | Membrane fusion as a team effort |
| Q46108311 | Merging cultures in the study of membrane traffic |
| Q34545756 | Mitochondrial dynamics in mammals |
| Q38344916 | Natamycin inhibits vacuole fusion at the priming phase via a specific interaction with ergosterol |
| Q42531466 | One SNARE complex is sufficient for membrane fusion |
| Q27333856 | Organelle acidification negatively regulates vacuole membrane fusion in vivo. |
| Q33402655 | Phylogeny of the SNARE vesicle fusion machinery yields insights into the conservation of the secretory pathway in fungi |
| Q27938479 | Piecemeal microautophagy of the nucleus requires the core macroautophagy genes. |
| Q35963470 | Plasmodium falciparum enolase complements yeast enolase functions and associates with the parasite food vacuole |
| Q27307839 | Prion Aggregates Are Recruited to the Insoluble Protein Deposit (IPOD) via Myosin 2-Based Vesicular Transport |
| Q39130182 | Rab7 may be a novel therapeutic target for neurologic diseases as a key regulator in autophagy. |
| Q24669620 | Rabring7, a novel Rab7 target protein with a RING finger motif |
| Q39121955 | Reversible, cooperative reactions of yeast vacuole docking |
| Q34669186 | Role of synaptotagmin in Ca2+-triggered exocytosis |
| Q36016989 | Role of the V-ATPase in regulation of the vacuolar fission-fusion equilibrium |
| Q30336208 | SNARE Protein Structure and Function |
| Q36992967 | SNARE function is not involved in early endosome docking |
| Q24310765 | SPE-39 family proteins interact with the HOPS complex and function in lysosomal delivery |
| Q42059939 | Saccharomyces cerevisiae Env7 is a novel serine/threonine kinase 16-related protein kinase and negatively regulates organelle fusion at the lysosomal vacuole |
| Q33967718 | Structural insights into the SNARE mechanism |
| Q28186873 | Structure and assembly of the yeast V-ATPase |
| Q27936381 | Svp1p defines a family of phosphatidylinositol 3,5-bisphosphate effectors |
| Q39868712 | Synergistic fungicidal activities of polymyxin B and ionophores, and their dependence on direct disruptive action of polymyxin B on fungal vacuole |
| Q34763978 | The AtC-VPS protein complex is localized to the tonoplast and the prevacuolar compartment in arabidopsis |
| Q41871988 | The MAP kinase Slt2 is involved in vacuolar function and actin remodeling in Saccharomyces cerevisiae mutants affected by endogenous oxidative stress |
| Q27939522 | The Mon1-Ccz1 GEF activates the Rab7 GTPase Ypt7 via a longin-fold-Rab interface and association with PI3P-positive membranes |
| Q36124956 | The Role of mVps18p in Clustering, Fusion, and Intracellular Localization of Late Endocytic Organelles |
| Q27934671 | The SNARE Ykt6 mediates protein palmitoylation during an early stage of homotypic vacuole fusion |
| Q36381446 | The Sec1p/Munc18 (SM) protein, Vps45p, cycles on and off membranes during vesicle transport |
| Q27967625 | The TRAPP complex: insights into its architecture and function |
| Q36333378 | The organization, structure, and inheritance of the ER in higher and lower eukaryotes |
| Q35210346 | The regulation of phagosome maturation in Dictyostelium |
| Q27933767 | The type 1 phosphatase Reg1p-Glc7p is required for the glucose-induced degradation of fructose-1,6-bisphosphatase in the vacuole |
| Q27938688 | The ubiquitin-proteasome system regulates membrane fusion of yeast vacuoles |
| Q36321361 | The vacuolar kinase Yck3 maintains organelle fragmentation by regulating the HOPS tethering complex |
| Q43252106 | The vacuole-targeting fungicidal activity of amphotericin B against the pathogenic fungus Candida albicans and its enhancement by allicin |
| Q46931449 | The vegetative vacuole proteome of Arabidopsis thaliana reveals predicted and unexpected proteins |
| Q27936905 | The yeast casein kinase Yck3p is palmitoylated, then sorted to the vacuolar membrane with AP-3-dependent recognition of a YXXPhi adaptin sorting signal |
| Q37266848 | The yeast lysosome-like vacuole: endpoint and crossroads |
| Q59079282 | Trans-SNARE pairing can precede a hemifusion intermediate in intracellular membrane fusion |
| Q36320585 | Transition from hemifusion to pore opening is rate limiting for vacuole membrane fusion |
| Q45245106 | Two fission yeast rab7 homologs, ypt7 and ypt71, play antagonistic roles in the regulation of vacuolar morphology. |
| Q35608147 | Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing |
| Q27938299 | Vam10p defines a Sec18p-independent step of priming that allows yeast vacuole tethering |
| Q35169800 | What is the role of SNARE proteins in membrane fusion? |
| Q27934032 | Yeast homotypic vacuole fusion requires the Ccz1-Mon1 complex during the tethering/docking stage |
| Q36323472 | deep-orange and carnation define distinct stages in late endosomal biogenesis in Drosophila melanogaster |