Cahir J O'Kane - Publications

Affiliations: 
Department of Genetics University of Cambridge, Cambridge, England, United Kingdom 

14 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
2023 Smith G, Sweeney ST, O'Kane CJ, Prokop A. How neurons maintain their axons long-term: an integrated view of axon biology and pathology. Frontiers in Neuroscience. 17: 1236815. PMID 37564364 DOI: 10.3389/fnins.2023.1236815  0.417
2023 Pérez-Moreno JJ, Smith RC, Oliva MK, Gallo F, Ojha S, Müller KH, O'Kane CJ. Drosophila SPG12 ortholog, reticulon-like 1, governs presynaptic ER organization and Ca2+ dynamics. The Journal of Cell Biology. 222. PMID 36952540 DOI: 10.1083/jcb.202112101  0.681
2020 Oliva MK, Pérez-Moreno JJ, O'Shaughnessy J, Wardill TJ, O'Kane CJ. Endoplasmic Reticulum Lumenal Indicators in Reveal Effects of HSP-Related Mutations on Endoplasmic Reticulum Calcium Dynamics. Frontiers in Neuroscience. 14: 816. PMID 32903680 DOI: 10.3389/fnins.2020.00816  0.692
2020 Öztürk Z, O'Kane CJ, Pérez-Moreno JJ. Axonal Endoplasmic Reticulum Dynamics and Its Roles in Neurodegeneration. Frontiers in Neuroscience. 14: 48. PMID 32116502 DOI: 10.3389/fnins.2020.00048  0.664
2019 Pérez-Moreno JJ, O'Kane CJ. Drivers Specific for Type Ib and Type Is Motor Neurons in . G3 (Bethesda, Md.). 9: 453-462. PMID 30530644 DOI: 10.1534/g3.118.200809  0.635
2017 Yalçın B, Zhao L, Stofanko M, O'Sullivan NC, Kang ZH, Roost A, Thomas MR, Zaessinger S, Blard O, Patto AL, Sohail A, Baena V, Terasaki M, O'Kane CJ. Modeling of axonal endoplasmic reticulum network by spastic paraplegia proteins. Elife. 6. PMID 28742022 DOI: 10.7554/Elife.23882  0.478
2014 Masuda-Nakagawa LM, Ito K, Awasaki T, O'Kane CJ. A single GABAergic neuron mediates feedback of odor-evoked signals in the mushroom body of larval Drosophila. Frontiers in Neural Circuits. 8: 35. PMID 24782716 DOI: 10.3389/fncir.2014.00035  0.318
2012 O'Sullivan NC, Jahn TR, Reid E, O'Kane CJ. Reticulon-like-1, the Drosophila orthologue of the hereditary spastic paraplegia gene reticulon 2, is required for organization of endoplasmic reticulum and of distal motor axons. Human Molecular Genetics. 21: 3356-65. PMID 22543973 DOI: 10.1093/hmg/dds167  0.453
2009 Tsang HT, Edwards TL, Wang X, Connell JW, Davies RJ, Durrington HJ, O'Kane CJ, Luzio JP, Reid E. The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling. Human Molecular Genetics. 18: 3805-21. PMID 19620182 DOI: 10.1093/hmg/ddp324  0.306
2008 Wang X, O'Kane CJ. Hereditary spastic paraplegia genes in Drosophila: dissecting their roles in axonal degeneration and intracellular traffic. Seb Experimental Biology Series. 60: 161-82. PMID 18309792  0.319
2007 Koh TW, Korolchuk VI, Wairkar YP, Jiao W, Evergren E, Pan H, Zhou Y, Venken KJ, Shupliakov O, Robinson IM, O'Kane CJ, Bellen HJ. Eps15 and Dap160 control synaptic vesicle membrane retrieval and synapse development. The Journal of Cell Biology. 178: 309-22. PMID 17620409 DOI: 10.1083/jcb.200701030  0.472
2005 Ravikumar B, Acevedo-Arozena A, Imarisio S, Berger Z, Vacher C, O'Kane CJ, Brown SD, Rubinsztein DC. Dynein mutations impair autophagic clearance of aggregate-prone proteins. Nature Genetics. 37: 771-6. PMID 15980862 DOI: 10.1038/Ng1591  0.302
2004 Ryder E, Blows F, Ashburner M, Bautista-Llacer R, Coulson D, Drummond J, Webster J, Gubb D, Gunton N, Johnson G, O'Kane CJ, Huen D, Sharma P, Asztalos Z, Baisch H, et al. The DrosDel collection: a set of P-element insertions for generating custom chromosomal aberrations in Drosophila melanogaster. Genetics. 167: 797-813. PMID 15238529 DOI: 10.1534/Genetics.104.026658  0.448
2002 Bhattacharya S, Stewart BA, Niemeyer BA, Burgess RW, McCabe BD, Lin P, Boulianne G, O'Kane CJ, Schwarz TL. Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability. Proceedings of the National Academy of Sciences of the United States of America. 99: 13867-72. PMID 12364587 DOI: 10.1073/pnas.202335999  0.314
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