Viral targets of acylguanidines

Por Gazina, Elena V., Petrou, Steven
Publicado no Drug Discov Today (2012)

Core Protein Phosphorylation Modulates Pregenomic RNA Encapsidation to Different Extents in Human and Duck Hepatitis B Viruses

Por Gazina, Elena V., Fielding, James E., Lin, Bo, Anderson, David A.
Publicado em 2000

Differential Requirements for COPI Coats in Formation of Replication Complexes among Three Genera of Picornaviridae

Por Gazina, Elena V., Mackenzie, Jason M., Gorrell, Rebecca J., Anderson, David A.
Publicado em 2002

Amiloride Derivatives Inhibit Coxsackievirus B3 RNA Replication

Por Harrison, David N., Gazina, Elena V., Purcell, Damian F., Anderson, David A., Petrou, Steven
Publicado em 2008

Computational Analysis of Amiloride Analogue Inhibitors of Coxsackievirus B3 RNA Polymerase

Por Holien, Jessica K, Gazina, Elena V, Elliott, Robert W, Jarrott, Bevyn, Cameron, Craig E, Williams, Spencer J, Parker, Michael W, Petrou, Steven
Publicado no J Proteomics Bioinform (2014)

Amiloride Is a Competitive Inhibitor of Coxsackievirus B3 RNA Polymerase

Por Gazina, Elena V., Smidansky, Eric D., Holien, Jessica K., Harrison, David N., Cromer, Brett A., Arnold, Jamie J., Parker, Michael W., Cameron, Craig E., Petrou, Steven
Publicado em 2011

Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery

Por Delahaye-Duriez, Andree, Srivastava, Prashant, Shkura, Kirill, Langley, Sarah R., Laaniste, Liisi, Moreno-Moral, Aida, Danis, Bénédicte, Mazzuferi, Manuela, Foerch, Patrik, Gazina, Elena V., Richards, Kay, Petrou, Steven, Kaminski, Rafal M., Petretto, Enrico, Johnson, Michael R.
Publicado no Genome Biol (2016)

A targeted resequencing gene panel for focal epilepsy

Por Hildebrand, Michael S., Myers, Candace T., Carvill, Gemma L., Regan, Brigid M., Damiano, John A., Mullen, Saul A., Newton, Mark R., Nair, Umesh, Gazina, Elena V., Milligan, Carol J., Reid, Christopher A., Petrou, Steven, Scheffer, Ingrid E., Berkovic, Samuel F., Mefford, Heather C.
Publicado no Neurology (2016)

Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy

Por Corbett, Mark A., Bellows, Susannah T., Li, Melody, Carroll, Renée, Micallef, Silvana, Carvill, Gemma L., Myers, Candace T., Howell, Katherine B., Maljevic, Snezana, Lerche, Holger, Gazina, Elena V., Mefford, Heather C., Bahlo, Melanie, Berkovic, Samuel F., Petrou, Steven, Scheffer, Ingrid E., Gecz, Jozef
Publicado no Neurology (2016)

Development of a rapid functional assay that predicts GLUT1 disease severity

Por Zaman, Sasha M., Mullen, Saul A., Petrovski, Slavé, Maljevic, Snezana, Gazina, Elena V., Phillips, A. Marie, Jones, Gabriel Davis, Hildebrand, Michael S., Damiano, John, Auvin, Stéphane, Lerche, Holger, Weber, Yvonne G., Berkovic, Samuel F., Scheffer, Ingrid E., Reid, Christopher A., Petrou, Steven
Publicado no Neurol Genet (2018)

KCNT1 gain-of-function in two epilepsy phenotypes is reversed by quinidine

Por Milligan, Carol J., Li, Melody, Gazina, Elena V., Heron, Sarah E., Nair, Umesh, Trager, Chantel, Reid, Christopher A., Venkat, Anu, Younkin, Donald P., Dlugos, Dennis J., Petrovski, Slavé, Goldstein, David B., Dibbens, Leanne M., Scheffer, Ingrid E., Berkovic, Samuel F, Petrou, Steven
Publicado em 2014

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

Por Hildebrand, Michael S, Tankard, Rick, Gazina, Elena V, Damiano, John A, Lawrence, Kate M, Dahl, Hans-Henrik M, Regan, Brigid M, Shearer, Aiden Eliot, Smith, Richard J H, Marini, Carla, Guerrini, Renzo, Labate, Angelo, Gambardella, Antonio, Tinuper, Paolo, Lichetta, Laura, Baldassari, Sara, Bisulli, Francesca, Pippucci, Tommaso, Scheffer, Ingrid E, Reid, Christopher A, Petrou, Steven, Bahlo, Melanie, Berkovic, Samuel F
Publicado no Ann Clin Transl Neurol (2015)

GABRA1 and STXBP1: Novel genetic causes of Dravet syndrome

Por Carvill, Gemma L., Weckhuysen, Sarah, McMahon, Jacinta M., Hartmann, Corinna, Møller, Rikke S., Hjalgrim, Helle, Cook, Joseph, Geraghty, Eileen, O’Roak, Brian J., Petrou, Steve, Clarke, Alison, Gill, Deepak, Sadleir, Lynette G., Muhle, Hiltrud, von Spiczak, Sarah, Nikanorova, Marina, Hodgson, Bree L., Gazina, Elena V., Suls, Arvid, Shendure, Jay, Dibbens, Leanne M., De Jonghe, Peter, Helbig, Ingo, Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.
Publicado em 2014

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy

Por McTague, Amy, Nair, Umesh, Malhotra, Sony, Meyer, Esther, Trump, Natalie, Gazina, Elena V., Papandreou, Apostolos, Ngoh, Adeline, Ackermann, Sally, Ambegaonkar, Gautam, Appleton, Richard, Desurkar, Archana, Eltze, Christin, Kneen, Rachel, Kumar, Ajith V., Lascelles, Karine, Montgomery, Tara, Ramesh, Venkateswaran, Samanta, Rajib, Scott, Richard H., Tan, Jeen, Whitehouse, William, Poduri, Annapurna, Scheffer, Ingrid E., Chong, W.K. “Kling”, Cross, J. Helen, Topf, Maya, Petrou, Steven, Kurian, Manju A.
Publicado no Neurology (2018)