Patrik Verstreken - Publications

Affiliations: 
Katholieke Universiteit Leuven, Leuven, Vlaanderen, Belgium 
Area:
neurotransmitter release, endocytosis

67 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Lambert E, Saha O, Soares Landeira B, Melo de Farias AR, Hermant X, Carrier A, Pelletier A, Gadaut J, Davoine L, Dupont C, Amouyel P, Bonnefond A, Lafont F, Abdelfettah F, Verstreken P, et al. The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects. Acta Neuropathologica Communications. 10: 4. PMID 34998435 DOI: 10.1186/s40478-021-01285-5  0.597
2021 Thues C, Valadas JS, Deaulmerie L, Geens A, Chouhan AK, Duran-Romaña R, Schymkowitz J, Rousseau F, Bartusel M, Rehimi R, Rada-Iglesias A, Verstreken P, Van Esch H. MAPRE2 mutations result in altered human cranial neural crest migration, underlying craniofacial malformations in CSC-KT syndrome. Scientific Reports. 11: 4976. PMID 33654163 DOI: 10.1038/s41598-021-83771-3  0.736
2021 Klionsky DJ, Abdel-Aziz AK, Abdelfatah S, Abdellatif M, Abdoli A, Abel S, Abeliovich H, Abildgaard MH, Abudu YP, Acevedo-Arozena A, Adamopoulos IE, Adeli K, Adolph TE, Adornetto A, Aflaki E, ... ... Verstreken P, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition). Autophagy. 1-382. PMID 33634751 DOI: 10.1080/15548627.2020.1797280  0.673
2021 Largo-Barrientos P, Apóstolo N, Creemers E, Callaerts-Vegh Z, Swerts J, Davies C, McInnes J, Wierda K, De Strooper B, Spires-Jones T, de Wit J, Uytterhoeven V, Verstreken P. Lowering Synaptogyrin-3 expression rescues Tau-induced memory defects and synaptic loss in the presence of microglial activation. Neuron. PMID 33472038 DOI: 10.1016/j.neuron.2020.12.016  0.369
2020 Cascalho A, Foroozandeh J, Hennebel L, Swerts J, Klein C, Rous S, Dominguez Gonzalez B, Pisani A, Meringolo M, Gallego SF, Verstreken P, Seibler P, Goodchild RE. Excess Lipin enzyme activity contributes to TOR1A recessive disease and DYT-TOR1A dystonia. Brain : a Journal of Neurology. 143: 1746-1765. PMID 32516804 DOI: 10.1093/brain/awaa139  0.304
2019 Lüthy K, Mei D, Fischer B, De Fusco M, Swerts J, Paesmans J, Parrini E, Lubarr N, Meijer IA, Mackenzie KM, Lee WT, Cittaro D, Aridon P, Schoovaerts N, Versées W, ... Verstreken P, et al. TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model. Brain : a Journal of Neurology. PMID 31257402 DOI: 10.1093/brain/awz175  0.41
2018 Lauwers E, Wang YC, Gallardo R, Van der Kant R, Michiels E, Swerts J, Baatsen P, Zaiter SS, McAlpine SR, Gounko NV, Rousseau F, Schymkowitz J, Verstreken P. Hsp90 Mediates Membrane Deformation and Exosome Release. Molecular Cell. 71: 689-702.e9. PMID 30193096 DOI: 10.1016/J.Molcel.2018.07.016  0.345
2018 Valadas JS, Esposito G, Vandekerkhove D, Miskiewicz K, Deaulmerie L, Raitano S, Seibler P, Klein C, Verstreken P. ER Lipid Defects in Neuropeptidergic Neurons Impair Sleep Patterns in Parkinson's Disease. Neuron. PMID 29887339 DOI: 10.1016/j.neuron.2018.05.022  0.332
2018 Cornelissen T, Vilain S, Vints K, Gounko N, Verstreken P, Vandenberghe W. Deficiency of parkin and PINK1 impairs age-dependent mitophagy in . Elife. 7. PMID 29809156 DOI: 10.7554/Elife.35878  0.677
2018 McInnes J, Wierda K, Snellinx A, Bounti L, Wang YC, Stancu IC, Apóstolo N, Gevaert K, Dewachter I, Spires-Jones TL, De Strooper B, De Wit J, Zhou L, Verstreken P. Synaptogyrin-3 Mediates Presynaptic Dysfunction Induced by Tau. Neuron. PMID 29398363 DOI: 10.1016/J.Neuron.2018.01.022  0.428
2018 Bademosi AT, Steeves J, Karunanithi S, Zalucki OH, Gormal RS, Liu S, Lauwers E, Verstreken P, Anggono V, Meunier FA, van Swinderen B. Trapping of Syntaxin1a in Presynaptic Nanoclusters by a Clinically Relevant General Anesthetic. Cell Reports. 22: 427-440. PMID 29320738 DOI: 10.1016/j.celrep.2017.12.054  0.37
2018 Cornelissen T, Vilain S, Vints K, Gounko N, Verstreken P, Vandenberghe W. Author response: Deficiency of parkin and PINK1 impairs age-dependent mitophagy in Drosophila Elife. DOI: 10.7554/Elife.35878.015  0.677
2017 Zhou L, McInnes J, Wierda K, Holt M, Herrmann AG, Jackson RJ, Wang YC, Swerts J, Beyens J, Miskiewicz K, Vilain S, Dewachter I, Moechars D, De Strooper B, Spires-Jones TL, ... ... Verstreken P, et al. Tau association with synaptic vesicles causes presynaptic dysfunction. Nature Communications. 8: 15295. PMID 28492240 DOI: 10.1038/Ncomms15295  0.761
2017 Vanhauwaert R, Kuenen S, Masius R, Bademosi A, Manetsberger J, Schoovaerts N, Bounti L, Gontcharenko S, Swerts J, Vilain S, Picillo M, Barone P, Munshi ST, de Vrij FM, Kushner SA, ... ... Verstreken P, et al. The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals. The Embo Journal. PMID 28331029 DOI: 10.15252/Embj.201695773  0.776
2017 Vos M, Geens A, Böhm C, Deaulmerie L, Swerts J, Rossi M, Craessaerts K, Leites EP, Seibler P, Rakovic A, Lohnau T, De Strooper B, Fendt SM, Morais VA, Klein C, ... Verstreken P, et al. Cardiolipin promotes electron transport between ubiquinone and complex I to rescue PINK1 deficiency. The Journal of Cell Biology. PMID 28137779 DOI: 10.1083/jcb.201511044  0.34
2017 Bademosi AT, Lauwers E, Padmanabhan P, Odierna L, Chai YJ, Papadopulos A, Goodhill GJ, Verstreken P, van Swinderen B, Meunier FA. In vivo single-molecule imaging of syntaxin1A reveals polyphosphoinositide- and activity-dependent trapping in presynaptic nanoclusters. Nature Communications. 8: 13660. PMID 28045048 DOI: 10.1038/Ncomms13660  0.385
2016 Lorendeau D, Rinaldi G, Boon R, Spincemaille P, Metzger K, Jäger C, Christen S, Dong X, Kuenen S, Voordeckers K, Verstreken P, Cassiman D, Vermeersch P, Verfaillie C, Hiller K, et al. Dual loss of succinate dehydrogenase (SDH) and complex I activity is necessary to recapitulate the metabolic phenotype of SDH mutant tumors. Metabolic Engineering. PMID 27847310 DOI: 10.1016/J.Ymben.2016.11.005  0.303
2016 Murdoch JD, Rostosky CM, Gowrisankaran S, Arora AS, Soukup SF, Vidal R, Capece V, Freytag S, Fischer A, Verstreken P, Bonn S, Raimundo N, Milosevic I. Endophilin-A Deficiency Induces the Foxo3a-Fbxo32 Network in the Brain and Causes Dysregulation of Autophagy and the Ubiquitin-Proteasome System. Cell Reports. PMID 27720640 DOI: 10.1016/J.Celrep.2016.09.058  0.412
2016 Soukup SF, Kuenen S, Vanhauwaert R, Manetsberger J, Hernández-Díaz S, Swerts J, Schoovaerts N, Vilain S, Gounko NV, Vints K, Geens A, De Strooper B, Verstreken P. A LRRK2-Dependent EndophilinA Phosphoswitch Is Critical for Macroautophagy at Presynaptic Terminals. Neuron. PMID 27720484 DOI: 10.1016/J.Neuron.2016.09.037  0.677
2016 Fischer B, Lüthy K, Paesmans J, De Koninck C, Maes I, Swerts J, Kuenen S, Uytterhoeven V, Verstreken P, Versées W. Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic function. Nature Structural & Molecular Biology. PMID 27669036 DOI: 10.1038/nsmb.3297  0.405
2016 Grillet M, Dominguez Gonzalez B, Sicart A, Pöttler M, Cascalho A, Billion K, Hernandez Diaz S, Swerts J, Naismith TV, Gounko NV, Verstreken P, Hanson PI, Goodchild RE. Torsins Are Essential Regulators of Cellular Lipid Metabolism. Developmental Cell. PMID 27453503 DOI: 10.1016/j.devcel.2016.06.017  0.314
2016 Lugtenberg D, Reijnders MR, Fenckova M, Bijlsma EK, Bernier R, van Bon BW, Smeets E, Vulto-van Silfhout AT, Bosch D, Eichler EE, Mefford HC, Carvill GL, Bongers EM, Schuurs-Hoeijmakers JH, Ruivenkamp CA, ... ... Verstreken P, et al. De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila. European Journal of Human Genetics : Ejhg. PMID 26757981 DOI: 10.1038/Ejhg.2015.282  0.349
2015 Uytterhoeven V, Lauwers E, Maes I, Miskiewicz K, Melo MN, Swerts J, Kuenen S, Wittocx R, Corthout N, Marrink SJ, Munck S, Verstreken P. Hsc70-4 Deforms Membranes to Promote Synaptic Protein Turnover by Endosomal Microautophagy. Neuron. 88: 735-48. PMID 26590345 DOI: 10.1016/J.Neuron.2015.10.012  0.472
2015 Dubos A, Castells-Nobau A, Meziane H, Oortveld MA, Houbaert X, Iacono G, Martin C, Mittelhaeuser C, Lalanne V, Kramer JM, Bhukel A, Quentin C, Slabbert J, Verstreken P, Sigrist SJ, et al. Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration. Human Molecular Genetics. PMID 26376863 DOI: 10.1093/hmg/ddv380  0.379
2014 Vilain S, Vanhauwaert R, Maes I, Schoovaerts N, Zhou L, Soukup S, da Cunha R, Lauwers E, Fiers M, Verstreken P. Fast and efficient Drosophila melanogaster gene knock-ins using MiMIC transposons. G3 (Bethesda, Md.). 4: 2381-7. PMID 25298537 DOI: 10.1534/G3.114.014803  0.677
2014 Miskiewicz K, Jose LE, Yeshaw WM, Valadas JS, Swerts J, Munck S, Feiguin F, Dermaut B, Verstreken P. HDAC6 is a Bruchpilot deacetylase that facilitates neurotransmitter release. Cell Reports. 8: 94-102. PMID 24981865 DOI: 10.1016/j.celrep.2014.05.051  0.604
2014 Morais VA, Haddad D, Craessaerts K, De Bock PJ, Swerts J, Vilain S, Aerts L, Overbergh L, Grünewald A, Seibler P, Klein C, Gevaert K, Verstreken P, De Strooper B. PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling. Science (New York, N.Y.). 344: 203-7. PMID 24652937 DOI: 10.1126/Science.1249161  0.724
2014 Vandewalle J, Langen M, Zschaetzsch M, Nijhof B, Kramer JM, Brems H, Bauters M, Lauwers E, Srahna M, Marynen P, Verstreken P, Schenck A, Hassan BA, Froyen G. Correction: Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability (PLoS ONE (2013) 8, 11 (e81791) DOI: 10.1371/journal.pone.0081791) Plos One. 9. DOI: 10.1371/annotation/5a4ac42e-a148-4a89-b148-e47de0d72d16  0.511
2013 Vandewalle J, Langen M, Zschätzsch M, Zschaetzsch M, Nijhof B, Kramer JM, Brems H, Bauters M, Lauwers E, Srahna M, Marynen P, Verstreken P, Schenck A, Hassan BA, Froyen G. Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability. Plos One. 8: e81791. PMID 24303071 DOI: 10.1371/journal.pone.0081791  0.614
2013 Oortveld MA, Keerthikumar S, Oti M, Nijhof B, Fernandes AC, Kochinke K, Castells-Nobau A, van Engelen E, Ellenkamp T, Eshuis L, Galy A, van Bokhoven H, Habermann B, Brunner HG, Zweier C, ... Verstreken P, et al. Human intellectual disability genes form conserved functional modules in Drosophila. Plos Genetics. 9: e1003911. PMID 24204314 DOI: 10.1371/Journal.Pgen.1003911  0.34
2013 Frank CA, Wang X, Collins CA, Rodal AA, Yuan Q, Verstreken P, Dickman DK. New approaches for studying synaptic development, function, and plasticity using Drosophila as a model system. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 17560-8. PMID 24198346 DOI: 10.1523/Jneurosci.3261-13.2013  0.412
2013 Haddad DM, Vilain S, Vos M, Esposito G, Matta S, Kalscheuer VM, Craessaerts K, Leyssen M, Nascimento RM, Vianna-Morgante AM, De Strooper B, Van Esch H, Morais VA, Verstreken P. Mutations in the intellectual disability gene Ube2a cause neuronal dysfunction and impair parkin-dependent mitophagy. Molecular Cell. 50: 831-43. PMID 23685073 DOI: 10.1016/J.Molcel.2013.04.012  0.737
2013 Esposito G, Vos M, Vilain S, Swerts J, De Sousa Valadas J, Van Meensel S, Schaap O, Verstreken P. Aconitase causes iron toxicity in Drosophila pink1 mutants. Plos Genetics. 9: e1003478. PMID 23637640 DOI: 10.1371/Journal.Pgen.1003478  0.677
2013 van Bon BW, Oortveld MA, Nijtmans LG, Fenckova M, Nijhof B, Besseling J, Vos M, Kramer JM, de Leeuw N, Castells-Nobau A, Asztalos L, Viragh E, Ruiter M, Hofmann F, Eshuis L, ... ... Verstreken P, et al. CEP89 is required for mitochondrial metabolism and neuronal function in man and fly. Human Molecular Genetics. 22: 3138-51. PMID 23575228 DOI: 10.1093/Hmg/Ddt170  0.397
2013 Khuong TM, Habets RL, Kuenen S, Witkowska A, Kasprowicz J, Swerts J, Jahn R, van den Bogaart G, Verstreken P. Synaptic PI(3,4,5)P3 is required for Syntaxin1A clustering and neurotransmitter release. Neuron. 77: 1097-108. PMID 23522045 DOI: 10.1016/j.neuron.2013.01.025  0.408
2012 Volders K, Scholz S, Slabbaert JR, Nagel AC, Verstreken P, Creemers JW, Callaerts P, Schwärzel M. Drosophila rugose is a functional homolog of mammalian Neurobeachin and affects synaptic architecture, brain morphology, and associative learning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 15193-204. PMID 23100440 DOI: 10.1523/JNEUROSCI.6424-11.2012  0.432
2012 Matta S, Van Kolen K, da Cunha R, van den Bogaart G, Mandemakers W, Miskiewicz K, De Bock PJ, Morais VA, Vilain S, Haddad D, Delbroek L, Swerts J, Chávez-Gutiérrez L, Esposito G, Daneels G, ... ... Verstreken P, et al. LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosis. Neuron. 75: 1008-21. PMID 22998870 DOI: 10.1016/J.Neuron.2012.08.022  0.749
2012 Vos M, Esposito G, Edirisinghe JN, Vilain S, Haddad DM, Slabbaert JR, Van Meensel S, Schaap O, De Strooper B, Meganathan R, Morais VA, Verstreken P. Vitamin K2 is a mitochondrial electron carrier that rescues pink1 deficiency. Science (New York, N.Y.). 336: 1306-10. PMID 22582012 DOI: 10.1126/Science.1218632  0.671
2012 Vilain S, Esposito G, Haddad D, Schaap O, Dobreva MP, Vos M, Van Meensel S, Morais VA, De Strooper B, Verstreken P. The yeast complex I equivalent NADH dehydrogenase rescues pink1 mutants. Plos Genetics. 8: e1002456. PMID 22242018 DOI: 10.1371/Journal.Pgen.1002456  0.677
2009 Morais VA, Verstreken P, Roethig A, Smet J, Snellinx A, Vanbrabant M, Haddad D, Frezza C, Mandemakers W, Vogt-Weisenhorn D, Van Coster R, Wurst W, Scorrano L, De Strooper B. Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function. Embo Molecular Medicine. 1: 99-111. PMID 20049710 DOI: 10.1002/Emmm.200900006  0.411
2009 Verstreken P, Ohyama T, Haueter C, Habets RL, Lin YQ, Swan LE, Ly CV, Venken KJ, De Camilli P, Bellen HJ. Tweek, an evolutionarily conserved protein, is required for synaptic vesicle recycling. Neuron. 63: 203-15. PMID 19640479 DOI: 10.1016/J.Neuron.2009.06.017  0.83
2009 Choi CM, Vilain S, Langen M, Van Kelst S, De Geest N, Yan J, Verstreken P, Hassan BA. Conditional mutagenesis in Drosophila. Science (New York, N.Y.). 324: 54. PMID 19342580 DOI: 10.1126/Science.1168275  0.758
2009 Simpson CL, Lemmens R, Miskiewicz K, Broom WJ, Hansen VK, van Vught PW, Landers JE, Sapp P, Van Den Bosch L, Knight J, Neale BM, Turner MR, Veldink JH, Ophoff RA, Tripathi VB, ... ... Verstreken P, et al. Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. Human Molecular Genetics. 18: 472-81. PMID 18996918 DOI: 10.1093/Hmg/Ddn375  0.335
2008 Venken KJ, Kasprowicz J, Kuenen S, Yan J, Hassan BA, Verstreken P. Recombineering-mediated tagging of Drosophila genomic constructs for in vivo localization and acute protein inactivation. Nucleic Acids Research. 36: e114. PMID 18676454 DOI: 10.1093/nar/gkn486  0.726
2008 Ly CV, Yao CK, Verstreken P, Ohyama T, Bellen HJ. straightjacket is required for the synaptic stabilization of cacophony, a voltage-gated calcium channel alpha1 subunit. The Journal of Cell Biology. 181: 157-70. PMID 18391075 DOI: 10.1083/Jcb.200712152  0.815
2008 Verstreken P, Ohyama T, Bellen HJ. FM 1-43 labeling of synaptic vesicle pools at the Drosophila neuromuscular junction. Methods in Molecular Biology (Clifton, N.J.). 440: 349-69. PMID 18369958 DOI: 10.1007/978-1-59745-178-9_26  0.78
2008 Romero E, Cha GH, Verstreken P, Ly CV, Hughes RE, Bellen HJ, Botas J. Suppression of neurodegeneration and increased neurotransmission caused by expanded full-length huntingtin accumulating in the cytoplasm. Neuron. 57: 27-40. PMID 18184562 DOI: 10.1016/J.Neuron.2007.11.025  0.741
2007 Ohyama T, Verstreken P, Ly CV, Rosenmund T, Rajan A, Tien AC, Haueter C, Schulze KL, Bellen HJ. Huntingtin-interacting protein 14, a palmitoyl transferase required for exocytosis and targeting of CSP to synaptic vesicles. The Journal of Cell Biology. 179: 1481-96. PMID 18158335 DOI: 10.1083/Jcb.200710061  0.787
2006 Zhai RG, Cao Y, Hiesinger PR, Zhou Y, Mehta SQ, Schulze KL, Verstreken P, Bellen HJ. Drosophila NMNAT maintains neural integrity independent of its NAD synthesis activity. Plos Biology. 4: e416. PMID 17132048 DOI: 10.1371/journal.pbio.0040416  0.789
2006 Hiesinger PR, Zhai RG, Zhou Y, Koh TW, Mehta SQ, Schulze KL, Cao Y, Verstreken P, Clandinin TR, Fischbach KF, Meinertzhagen IA, Bellen HJ. Activity-independent prespecification of synaptic partners in the visual map of Drosophila. Current Biology : Cb. 16: 1835-43. PMID 16979562 DOI: 10.1016/j.cub.2006.07.047  0.816
2006 Ly CV, Verstreken P. Mitochondria at the synapse. The Neuroscientist : a Review Journal Bringing Neurobiology, Neurology and Psychiatry. 12: 291-9. PMID 16840705 DOI: 10.1177/1073858406287661  0.654
2005 Verstreken P, Ly CV, Venken KJ, Koh TW, Zhou Y, Bellen HJ. Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions. Neuron. 47: 365-78. PMID 16055061 DOI: 10.1016/J.Neuron.2005.06.018  0.823
2005 Dermaut B, Norga KK, Kania A, Verstreken P, Pan H, Zhou Y, Callaerts P, Bellen HJ. Aberrant lysosomal carbohydrate storage accompanies endocytic defects and neurodegeneration in Drosophila benchwarmer. The Journal of Cell Biology. 170: 127-39. PMID 15998804 DOI: 10.1083/Jcb.200412001  0.816
2005 Hiesinger PR, Fayyazuddin A, Mehta SQ, Rosenmund T, Schulze KL, Zhai RG, Verstreken P, Cao Y, Zhou Y, Kunz J, Bellen HJ. The v-ATPase V0 subunit a1 is required for a late step in synaptic vesicle exocytosis in Drosophila. Cell. 121: 607-20. PMID 15907473 DOI: 10.1016/J.Cell.2005.03.012  0.785
2005 Mehta SQ, Hiesinger PR, Beronja S, Zhai RG, Schulze KL, Verstreken P, Cao Y, Zhou Y, Tepass U, Crair MC, Bellen HJ. Mutations in Drosophila sec15 reveal a function in neuronal targeting for a subset of exocyst components. Neuron. 46: 219-32. PMID 15848801 DOI: 10.1016/j.neuron.2005.02.029  0.795
2004 Koh TW, Verstreken P, Bellen HJ. Dap160/intersectin acts as a stabilizing scaffold required for synaptic development and vesicle endocytosis. Neuron. 43: 193-205. PMID 15260956 DOI: 10.1016/J.Neuron.2004.06.029  0.792
2004 Pesah Y, Pham T, Burgess H, Middlebrooks B, Verstreken P, Zhou Y, Harding M, Bellen H, Mardon G. Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress. Development (Cambridge, England). 131: 2183-94. PMID 15073152 DOI: 10.1242/dev.01095  0.66
2003 Fabian-Fine R, Verstreken P, Hiesinger PR, Horne JA, Kostyleva R, Zhou Y, Bellen HJ, Meinertzhagen IA. Endophilin promotes a late step in endocytosis at glial invaginations in Drosophila photoreceptor terminals. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 10732-44. PMID 14627659 DOI: 10.1523/Jneurosci.23-33-10732.2003  0.825
2003 Verstreken P, Koh TW, Schulze KL, Zhai RG, Hiesinger PR, Zhou Y, Mehta SQ, Cao Y, Roos J, Bellen HJ. Synaptojanin is recruited by endophilin to promote synaptic vesicle uncoating. Neuron. 40: 733-48. PMID 14622578 DOI: 10.1016/S0896-6273(03)00644-5  0.824
2003 Zhai RG, Hiesinger PR, Koh TW, Verstreken P, Schulze KL, Cao Y, Jafar-Nejad H, Norga KK, Pan H, Bayat V, Greenbaum MP, Bellen HJ. Mapping Drosophila mutations with molecularly defined P element insertions. Proceedings of the National Academy of Sciences of the United States of America. 100: 10860-5. PMID 12960394 DOI: 10.1073/Pnas.1832753100  0.726
2002 Kango-Singh M, Nolo R, Tao C, Verstreken P, Hiesinger PR, Bellen HJ, Halder G. Shar-pei mediates cell proliferation arrest during imaginal disc growth in Drosophila. Development (Cambridge, England). 129: 5719-30. PMID 12421711 DOI: 10.1242/Dev.00168  0.753
2002 Kjaerulff O, Verstreken P, Bellen HJ. Synaptic vesicle retrieval: still time for a kiss. Nature Cell Biology. 4: E245-8. PMID 12415277 DOI: 10.1038/ncb1102-e245  0.829
2002 Verstreken P, Bellen HJ. Meaningless minis? Mechanisms of neurotransmitter-receptor clustering. Trends in Neurosciences. 25: 383-5. PMID 12127745 DOI: 10.1016/S0166-2236(02)02197-5  0.644
2002 Morales J, Hiesinger PR, Schroeder AJ, Kume K, Verstreken P, Jackson FR, Nelson DL, Hassan BA. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain. Neuron. 34: 961-72. PMID 12086643 DOI: 10.1016/S0896-6273(02)00731-6  0.752
2002 Verstreken P, Kjaerulff O, Lloyd TE, Atkinson R, Zhou Y, Meinertzhagen IA, Bellen HJ. Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release. Cell. 109: 101-12. PMID 11955450 DOI: 10.1016/S0092-8674(02)00688-8  0.83
2001 Verstreken P, Bellen HJ. Neuroscience. The meaning of a mini. Science (New York, N.Y.). 293: 443-4. PMID 11463902 DOI: 10.1126/science.1063293  0.717
2000 Lloyd TE, Verstreken P, Ostrin EJ, Phillippi A, Lichtarge O, Bellen HJ. A genome-wide search for synaptic vesicle cycle proteins in Drosophila. Neuron. 26: 45-50. PMID 10798391 DOI: 10.1016/S0896-6273(00)81136-8  0.76
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