Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development
Thomas-Jinu, Swapna, Gordon, Patricia M., Fielding, Triona, Taylor, Richard, Smith, Bradley N., Snowden, Victoria, Blanc, Eric, Vance, Caroline, Topp, Simon, Wong, Chun-Hao, Bielen, Holger, Williams, Kelly L., McCann, Emily P., Nicholson, Garth A., Pan-Vazquez, Alejandro, Fox, Archa H., Bond, Charles S., Talbot, William S., Blair, Ian P., Shaw, Christopher E., Houart, Corinne
Published in Neuron (Cambridge, Mass.) (19.04.2017)
Published in Neuron (Cambridge, Mass.) (19.04.2017)
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Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development
Thomas-Jinu, Swapna, Gordon, Patricia M., Fielding, Triona, Taylor, Richard, Smith, Bradley N., Snowden, Victoria, Blanc, Eric, Vance, Caroline, Topp, Simon, Wong, Chun-Hao, Bielen, Holger, Williams, Kelly L., McCann, Emily P., Nicholson, Garth A., Pan-Vazquez, Alejandro, Fox, Archa H., Bond, Charles S., Talbot, William S., Blair, Ian P., Shaw, Christopher E., Houart, Corinne
Published in Neuron (Cambridge, Mass.) (17.05.2017)
Published in Neuron (Cambridge, Mass.) (17.05.2017)
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Novel mutations support a role for Profilin 1 in the pathogenesis of ALS
Smith, Bradley N, Vance, Caroline, Scotter, Emma L, Troakes, Claire, Wong, Chun Hao, Topp, Simon, Maekawa, Satomi, King, Andrew, Mitchell, Jacqueline C, Lund, Karan, Al-Chalabi, Ammar, Ticozzi, Nicola, Silani, Vincenzo, Sapp, Peter, Brown, Robert H, Landers, John E, Al-Sarraj, Safa, Shaw, Christopher E
Published in Neurobiology of aging (01.03.2015)
Published in Neurobiology of aging (01.03.2015)
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C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissue
Scotter, Emma L., Smyth, Leon, Bailey, James W.T., Wong, Chun-Hao, de Majo, Martina, Vance, Caroline A., Synek, Beth J., Turner, Clinton, Pereira, Jennifer, Charleston, Alison, Waldvogel, Henry J., Curtis, Maurice A., Dragunow, Mike, Shaw, Christopher E., Smith, Bradley N., Faull, Richard L.M.
Published in Neurobiology of aging (01.01.2017)
Published in Neurobiology of aging (01.01.2017)
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Genome-scale requirements for dynein-based trafficking revealed by a high-content arrayed CRISPR screen
Wong, Chun Hao, Wingett, Steven W, Qian, Chen, Taliaferro, J Matthew, Ross-Thriepland, Douglas, Bullock, Simon L
Published in bioRxiv (01.03.2023)
Published in bioRxiv (01.03.2023)
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Genome-scale requirements for dynein-based transport revealed by a high-content arrayed CRISPR screen
Wong, Chun Hao, Wingett, Steven W, Qian, Chen, Hunter, Morag Rose, Taliaferro, J Matthew, Ross-Thriepland, Douglas, Bullock, Simon L
Published in The Journal of cell biology (06.05.2024)
Published in The Journal of cell biology (06.05.2024)
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ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
de Majo, Martina, Topp, Simon D., Smith, Bradley N., Nishimura, Agnes L., Chen, Han-Jou, Gkazi, Athina Soragia, Miller, Jack, Wong, Chun Hao, Vance, Caroline, Baas, Frank, ten Asbroek, Anneloor L.M.A., Kenna, Kevin P., Ticozzi, Nicola, Redondo, Alberto Garcia, Esteban-Pérez, Jesús, Tiloca, Cinzia, Verde, Federico, Duga, Stefano, Morrison, Karen E., Shaw, Pamela J., Kirby, Janine, Turner, Martin R., Talbot, Kevin, Hardiman, Orla, Glass, Jonathan D., de Belleroche, Jacqueline, Gellera, Cinzia, Ratti, Antonia, Al-Chalabi, Ammar, Brown, Robert H., Silani, Vincenzo, Landers, John E., Shaw, Christopher E.
Published in Neurobiology of aging (01.11.2018)
Published in Neurobiology of aging (01.11.2018)
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A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decay
Gotkine, Marc, de Majo, Martina, Wong, Chun Hao, Topp, Simon D., Michaelson-Cohen, Rachel, Epsztejn-Litman, Silvina, Eiges, Rachel, Y, Yossef Lerner, Kanaan, Moein, Shaked, Hagar Mor, Alahmady, Nada, Vance, Caroline, Newhouse, Stephen J., Breen, Gerome, Nishimura, Agnes L., Shaw, Christopher E., Smith, Bradley N.
Published in Neurobiology of aging (01.10.2021)
Published in Neurobiology of aging (01.10.2021)
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The CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients
Wong, Chun Hao, Topp, Simon, Gkazi, Athina Soragia, Troakes, Claire, Miller, Jack W, de Majo, Martina, Kirby, Janine, Shaw, Pamela J, Morrison, Karen E, de Belleroche, Jacqueline, Vance, Caroline A, Al-Chalabi, Ammar, Al-Sarraj, Safa, Shaw, Christopher E, Smith, Bradley N
Published in Neurobiology of aging (01.10.2015)
Published in Neurobiology of aging (01.10.2015)
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