The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Vps35 in cooperation with LRRK2 regulates synaptic vesicle endocytosis through the endosomal pathway in Drosophila
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The retromer complex regulates pre-synaptic vesicle release.
“recent studies which have demonstrated the role of the retromer complex system in the regulation of pre-synaptic vesicle release [22, 23]”
From Retromer Stabilization Improves Cognitive Function and Synaptic Plasticity in a Mouse Model of Down Syndrome (2023) · cites this paper as [22]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Ultrafast endocytosis at mouse hippocampal synapses
Watanabe, S., Rost, B. R., Camacho-Pérez, M., Davis, M. W., Söhl-Kielczynski, B., Rosenmund, C., & Jorgensen, E. M. (2013) · Nature · doi:10.1038/nature12809 · Cited by 607
Endophilin marks and controls a clathrin-independent endocytic pathway
Boucrot, E., Ferreira, A. P. A., Almeida-Souza, L., Debard, S., Vallis, Y., Howard, G., Bertot, L., Sauvonnet, N., & McMahon, H. T. (2015) · Nature · doi:10.1038/nature14067 · Cited by 542
Clathrin regenerates synaptic vesicles from endosomes
Watanabe, S., Trimbuch, T., Camacho-Pérez, M., Rost, B. R., Brokowski, B., Söhl-Kielczynski, B., Felies, A., Davis, M. W., Rosenmund, C., & Jorgensen, E. M. (2014) · Nature · doi:10.1038/nature13846 · Cited by 333
Flagged first, then by citations
Research works printed but not linked: 50
- 2011, VPS35 mutations in Parkinson disease, Am. J. Hum. Genet, 89, 162, 10.1016/j.ajhg.2011.06.001 · DOI · Paper page
- 2011, A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease, Am. J. Hum. Genet, 89, 168, 10.1016/j.ajhg.2011.06.008 · DOI · Paper page
- 2007, Functional architecture of the retromer cargo-recognition complex, Nature, 449, 1063, 10.1038/nature06216 · DOI · Paper page
- 2001, Vps26p, a component of retromer, directs the interactions of Vps35p in endosome-to-Golgi retrieval, Mol. Biol. Cell, 12, 3242, 10.1091/mbc.12.10.3242 · DOI
- 1999, Distinct domains within Vps35p mediate the retrieval of two different cargo proteins from the yeast prevacuolar/endosomal compartment, Mol. Biol. Cell, 10, 875, 10.1091/mbc.10.4.875 · DOI
- 2009, A FAM21-containing WASH complex regulates retromer-dependent sorting, Dev. Cell, 17, 699, 10.1016/j.devcel.2009.09.009 · DOI · Paper page
- 2014, Mutation in VPS35 associated with Parkinson's disease impairs WASH complex association and inhibits autophagy, Nat. Ccommun, 5, 3828, 10.1038/ncomms4828 · DOI · Paper page
- 2014, Retromer binding to FAM21 and the WASH complex is perturbed by the Parkinson disease-linked VPS35(D620N) mutation, Curr. Biol, 24, 1670, 10.1016/j.cub.2014.06.024 · DOI · Paper page
- 2006, Localization of LRRK2 to membranous and vesicular structures in mammalian brain, Ann. Neurol, 60, 557, 10.1002/ana.21019 · DOI
- 2013, LRRK2 affects vesicle trafficking, neurotransmitter extracellular level and membrane receptor localization, PLoS One, 8, e77198, 10.1371/journal.pone.0077198 · DOI
- 2013, RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk, Neuron, 77, 425, 10.1016/j.neuron.2012.11.033 · DOI · Paper page
- 2014, Leucine-rich repeat kinase 2 regulates Sec16A at ER exit sites to allow ER-Golgi export, EMBO J, 33, 2314, 10.15252/embj.201487807 · DOI
- 2014, LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity, Hum. Mol. Genet, 23, 6779, 10.1093/hmg/ddu395 · DOI · Paper page
- 2008, Phosphorylation of 4E-BP by LRRK2 affects the maintenance of dopaminergic neurons in Drosophila, EMBO J, 27, 2432, 10.1038/emboj.2008.163 · DOI
- 2014, Novel ethyl methanesulfonate (EMS)-induced null alleles of the Drosophila homolog of LRRK2 reveal a crucial role in endolysosomal functions and autophagy in vivo, Dis. Model Mech, 7, 1351, 10.1242/dmm.017020 · DOI
- 2015, The Parkinson's Disease-Associated Protein Kinase LRRK2 Modulates Notch Signaling through the Endosomal Pathway, PLoS Genet, 11, e1005503, 10.1371/journal.pgen.1005503 · DOI
- 2008, LRRK2 regulates synaptic vesicle endocytosis, Exp. Cell Res, 314, 2055, 10.1016/j.yexcr.2008.02.015 · DOI
- 2010, LRRK2 kinase regulates synaptic morphology through distinct substrates at the presynaptic and postsynaptic compartments of the Drosophila neuromuscular junction. J, Neurosci, 30, 16959, 10.1523/JNEUROSCI.1807-10.2010 · DOI
- 2011, LRRK2 controls synaptic vesicle storage and mobilization within the recycling pool, J. Neurosci, 31, 2225, 10.1523/JNEUROSCI.3730-10.2011 · DOI
- 2012, LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosis, Neuron, 75, 1008, 10.1016/j.neuron.2012.08.022 · DOI · Paper page
- 2015, LRRK2 functions in synaptic vesicle endocytosis through a kinase-dependent mechanism, J. Cell Sci, 128, 541, 10.1242/jcs.158196 · DOI · Paper page
- 2014, LRRK2 regulates synaptogenesis and dopamine receptor activation through modulation of PKA activity, Nat. Neurosci, 17, 367, 10.1038/nn.3636 · DOI
- 2014, Vacuolar protein sorting 35 (Vps35) rescues locomotor deficits and shortened lifespan in Drosophila expressing a Parkinson's disease mutant of Leucine-Rich Repeat Kinase 2 (LRRK2), Mol. Neurodegener, 9, 23, 10.1186/1750-1326-9-23 · DOI
- 2014, Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease, Proc. Natl Acad. Sci. USA, 111, 2626, 10.1073/pnas.1318306111 · DOI · Paper page
- 2008, Wingless secretion requires endosome-to-Golgi retrieval of Wntless/Evi/Sprinter by the retromer complex, Nat. Cell Biol, 10, 170, 10.1038/ncb1678 · DOI
- 2007, Drosophila Vps35 function is necessary for normal endocytic trafficking and actin cytoskeleton organisation, J. Cell Sci, 120, 4367, 10.1242/jcs.012336 · DOI · Paper page
- 2014, PINK1-mediated phosphorylation of Parkin boosts Parkin activity in Drosophila, PLoS Genet, 10, e1004391, 10.1371/journal.pgen.1004391 · DOI
- 2003, Role of Drosophila Rab5 during endosomal trafficking at the synapse and evoked neurotransmitter release, J. Cell Biol, 161, 609, 10.1083/jcb.200211087 · DOI
- 2015, An early endosome regulator, Rab5b, is an LRRK2 kinase substrate, J. Biochem, 157, 485, 10.1093/jb/mvv005 · DOI
- 2003, An essential role of Rab5 in uniformity of synaptic vesicle size, J. Cell Sci, 116, 3583, 10.1242/jcs.00676 · DOI
- 2002, Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release, Cell, 109, 101, 10.1016/S0092-8674(02)00688-8 · DOI
- 2012, Identification of a dopamine pathway that regulates sleep and arousal in Drosophila, Nat. Neurosci, 15, 1516, 10.1038/nn.3238 · DOI
- 2015, VPS35 pathogenic mutations confer no dominant toxicity but partial loss of function in Drosophila and genetically interact with parkin, Hum. Mol. Genet, 24, 6106, 10.1093/hmg/ddv322 · DOI
- 2007, Dominant-negative behavior of mammalian Vps35 in yeast requires a conserved PRLYL motif involved in retromer assembly, Traffic, 8, 1829, 10.1111/j.1600-0854.2007.00658.x · DOI
- 2014, In vivo evidence of pathogenicity of VPS35 mutations in the Drosophila, Mol. Brain, 7, 73, 10.1186/s13041-014-0073-y · DOI
- 2015, Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N, Hum. Mol. Genet, 24, 1691, 10.1093/hmg/ddu582 · DOI · Paper page
- 2016, Impaired striatal dopamine release in homozygous Vps35 D620N knock-in mice, Hum. Mol. Genet, 25, 4507
- 2014, Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration, Hum. Mol. Genet, 23, 4621, 10.1093/hmg/ddu178 · DOI · Paper page
- 2011, Distinct yet overlapping roles of Rab GTPases on synaptic vesicles, Small GTPases, 2, 77, 10.4161/sgtp.2.2.15201 · DOI
- 2010, Quantitative analysis of synaptic vesicle Rabs uncovers distinct yet overlapping roles for Rab3a and Rab27b in Ca2+-triggered exocytosis, J. Neurosci, 30, 13441, 10.1523/JNEUROSCI.0907-10.2010 · DOI
- 2015, Regulation of vesicular trafficking by Parkinson's disease-associated genes, AIMS Mol. Sci, 2, 461, 10.3934/molsci.2015.4.461 · DOI
- 2016, Identification of TMEM230 mutations in familial Parkinson's disease, Nat. Genet, 48, 733, 10.1038/ng.3589 · DOI
- 2008, The retromer complex influences Wnt secretion by recycling wntless from endosomes to the trans-Golgi network, Dev. Cell, 14, 120, 10.1016/j.devcel.2007.12.003 · DOI
- 2012, Roles of the Drosophila LRRK2 homolog in Rab7-dependent lysosomal positioning, Hum. Mol. Genet, 21, 1350, 10.1093/hmg/ddr573 · DOI
- 2013, Loss of vesicular dopamine release precedes tauopathy in degenerative dopaminergic neurons in a Drosophila model expressing human tau, Acta Neuropathol, 125, 711, 10.1007/s00401-013-1105-x · DOI
- 2013, Tubular endocytosis drives remodelling of the apical surface during epithelial morphogenesis in Drosophila, Nat. Commun, 4, 2244, 10.1038/ncomms3244 · DOI
- 2000, Gradient formation of the TGF-beta homolog Dpp, Cell, 103, 981, 10.1016/S0092-8674(00)00200-2 · DOI
- 2013, Rab9 and retromer regulate retrograde trafficking of luminal protein required for epithelial tube length control, Nat. Commun, 4, 1358, 10.1038/ncomms2347 · DOI
- 2008, Human herpesvirus-6 induces MVB formation, and virus egress occurs by an exosomal release pathway, Traffic, 9, 1728, 10.1111/j.1600-0854.2008.00796.x · DOI
- 2000, Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity, J. Biol. Chem, 275, 35661, 10.1074/jbc.C000447200 · DOI
Cited by
Sorted by citations
Synaptic, Mitochondrial, and Lysosomal Dysfunction in Parkinson’s Disease
Nguyen, M., Wong, Y. C., Ysselstein, D., Severino, A., & Krainc, D. (2019) · Trends in Neurosciences · doi:10.1016/j.tins.2018.11.001 · Cited by 323
Curtis, M. E., Smith, T., Nenov, M., Blass, B. E., & Praticò, D. (2023) · Journal of Alzheimer's Disease · doi:10.3233/jad-230205 · Cited by 3
Metadata
- Authors
- Inoshita, T., Arano, T., Hosaka, Y., Meng, H., Umezaki, Y., Kosugi, S., Morimoto, T., Koike, M., Chang, H.-Y., Imai, Y., & Hattori, N.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2017-05-08
- Volume
- 26
- Issue
- 15
- Pages
- 2933-2948
- ISSN
- 0964-6906
- 1460-2083
- Cited by
- 119
- References
- 3
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review