Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations
Konopka, Anna, Whelan, Donna R., Jamali, Md Shafi, Perri, Emma, Shahheydari, Hamideh, Toth, Reka P., Parakh, Sonam, Robinson, Tina, Cheong, Alison, Mehta, Prachi, Vidal, Marta, Ragagnin, Audrey M. G., Khizhnyak, Ivan, Jagaraj, Cyril J., Galper, Jasmin, Grima, Natalie, Deva, Anand, Shadfar, Sina, Nicholson, Garth A., Yang, Shu, Cutts, Suzanne M., Horejsi, Zuzana, Bell, Toby D. M., Walker, Adam K., Blair, Ian P., Atkin, Julie D.
Published in Molecular neurodegeneration (09.09.2020)
Published in Molecular neurodegeneration (09.09.2020)
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Journal Article
ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis
Parakh, Sonam, Jagaraj, Cyril J, Vidal, Marta, Ragagnin, Audrey M G, Perri, Emma R, Konopka, Anna, Toth, Reka P, Galper, Jasmin, Blair, Ian P, Thomas, Colleen J, Walker, Adam K, Yang, Shu, Spencer, Damian M, Atkin, Julie D
Published in Human molecular genetics (15.04.2018)
Published in Human molecular genetics (15.04.2018)
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Journal Article
Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum
Shahheydari, Hamideh, Ragagnin, Audrey, Walker, Adam K, Toth, Reka P, Vidal, Marta, Jagaraj, Cyril J, Perri, Emma R, Konopka, Anna, Sultana, Jessica M, Atkin, Julie D
Published in Frontiers in molecular neuroscience (10.05.2017)
Published in Frontiers in molecular neuroscience (10.05.2017)
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Rab1-dependent ER–Golgi transport dysfunction is a common pathogenic mechanism in SOD1, TDP-43 and FUS-associated ALS
Soo, Kai Y., Halloran, Mark, Sundaramoorthy, Vinod, Parakh, Sonam, Toth, Reka P., Southam, Katherine A., McLean, Catriona A., Lock, Peter, King, Anna, Farg, Manal A., Atkin, Julie D.
Published in Acta neuropathologica (01.11.2015)
Published in Acta neuropathologica (01.11.2015)
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