Browsing by Author Marston, Steven

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Issue DateTitleAuthor(s)Citation
2013Familial dilated cardiomyopathy mutations uncouple troponin l phosphorylation from changes in myofibrillar Ca2+ sensitivitydos Remedios, Cristobal; Leung, Man-Ching; Marston, Steven; McNamara, Elyshia; Memo, Massimiliano; Messer, Andrew; Morimoto, Sachio; Nowak, Kristen; Ravenscroft, Gianina; Ward, Douglas; Zhang, Lianfeng; School of Medical Sciences: Bosch InstituteFamilial dilated cardiomyopathy mutations uncouple troponin l phosphorylation from changes in myofibrillar Ca2+ sensitivity, Cardiovascular Research, vol.99, 1, 2013,pp 65-73
2013GSK3β phosphorylates newly identified site in the proline-alanine-rich region of cardiac myosin-binding protein C and alters cross-bridge cycling kinetics in human: Short communicationDos Remedios, Cristobal Guillermo; Boontje, Nicky M.; Carrier, Lucie; Demmers, Jeroen; Kuster, Diederik; Marston, Steven; Najafi, Aref; Paalberends, Rosalie; Redwood, Charles; Sadayappan, Sakthivel; Sequeira, Vasco; van der Velden, Jolanda; Wijnker, Paul; School of Medical Sciences: Bosch InstituteGSK3β phosphorylates newly identified site in the proline-alanine-rich region of cardiac myosin-binding protein C and alters cross-bridge cycling kinetics in human: Short communication, Circulation Research, vol.112, 4, 2013,pp 633-639
2006Investigating the pathogenesis of ACTA1-related congenital fibre type disproportionClarke, Nigel; Ilkovski, B; North, Kathryn; Feng, Juan-Juan; Marston, Steven; Nonaka, I; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child HealthInvestigating the pathogenesis of ACTA1-related congenital fibre type disproportion, Neuromuscular Disorders, vol.16,(Supplement 1),2006,pp s61-s61
2013K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivityClarke, Nigel; Ilkovski, B; Jeffries, Cy; Kreissl, Michaela; Mokbel, Nancy; North, Kathryn; Trewhella, Jill; Yang, Nan; Echaniz-Laguna, Andoni; Gronholm, Mikaela; Laing, Nigel G; Lehtokari, Vilma-Lotta; Lemola, Elina; Marcorelles, Pascale; Marston, Steven; Marttila, Minttu; McNamara, Elyshia; Memo, Massimiliano; Menard, Dominique; Monnier, Nicole; Nowak, Kristen J; Ottenheijm, Coen; Ravenscroft, Gianina; Reimann, Jens; Vainzof, Mariz; Wallgren-Pettersson, Carina; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Childrens Medical Research Ins; Molecular Bioscience; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child Health; Molecular Bioscience; Children's Hospital Westmead: Paediatrics & Child HealthK7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity, Brain, vol.136, 2, 2013,pp 494-507
2014Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathiesClarke, Nigel; Barnerias, C; Beggs, Alan H.; Bertini, E; Ceyhan-Birsoy, Ozge; Cintas, Pascal; et al, Various; Gerard, Marion; Lehtokari, Vilma-Lotta; Marston, Steven; Marttila, Minttu; Nyman, Tuula; Childrens Hospital Westmead: Paediatrics & Child HealthMutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies, Human Mutation, vol.35, 7, 2014,pp 779-790
2013Myofibrillar Ca(2+) sensitivity is uncoupled from troponin l phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin Tdos Remedios, Cristobal; Bayliss, Christopher; Copeland, O'Neal; Gallon, Clare; Jacques, Adam; Leung, Man-Ching; Marston, Steven; McKenna, William J; Messer, Andrew; Redwood, Charles; Ward, Douglas; School of Medical Sciences: Bosch InstituteMyofibrillar Ca(2+) sensitivity is uncoupled from troponin l phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T, Cardiovascular Research, vol.97, 3, 2013,pp 500-508
2010Normal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathyDos Remedios, Cristobal Guillermo; Adams, Kim; Avkiran, Metin; Bardswell, Sonia C; Ehler, Elizabeth; Hoskins, Anita C; Jacques, Adam; Jalilzadeh, Shapour; Kentish, Jonathon C; Marston, Steven; McKenna, William J; Redwood, Charles; Tsang, Victor; Watkins, Hugh; School of Medical Sciences: Bosch InstituteNormal passive viscoelasticity but abnormal myofibrillar force generation in human hypertrophic cardiomyopathy, Journal of Molecular and Cellular Cardiology, vol.49, 5, 2010,pp 737-745
2015OBSCN Mutations Associated with Dilated Cardiomyopathy and HaploinsufficiencyDos Remedios, Cristobal Guillermo; Choi, Onjee; Copeland, O'Neal; Ehler, Elisabeth; Knöll, Ralph; Marston, Steven; Messer, Andrew; Montgiraud, Cecile; Munster, Alex B; School of Medical Sciences: Bosch InstituteOBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency, PloS One, vol.10, 9, 2015,pp 1-10
2007The pathogenesis of ACTA1-related congenital fiber type disproportionClarke, Nigel; Cooper, Sandra; Ilkovski, B; North, Kathryn; Feng, Juan-Juan; Marston, Steven; Nonaka, Ikuya; Robinson, Phillip James; Valova, Valentina A; Children's Hospital Westmead: Paediatrics & Child Health; Western Clinical School: Medicine (Westmead); Children's Hospital Westmead: Childrens Medical Research Ins; Children's Hospital Westmead: Paediatrics & Child HealthThe pathogenesis of ACTA1-related congenital fiber type disproportion, Annals of Neurology, vol.61,(6),2007,pp 552-561
2017The Sydney Heart Bank: improving translational research while eliminating or reducing the use of animal models of human heart diseaseDos Remedios, Cristobal Guillermo; Lal, Sean; Li, Amy; McNamara, James; Bezzina, Connie; Cooke, Roger; Ehler, Elisabeth; et al, Various; Granzier, Henk; Keogh, Anne M; Knoll, R; Macdonald, Peter S.; Marston, Steven; Stelzer, Julian; School of Medical Sciences: Bosch Institute; School of Medical Sciences: Anatomy & Histology; School of Medical Sciences: Bosch Institute; School of Medical Sciences: Anatomy & HistologyThe Sydney Heart Bank: improving translational research while eliminating or reducing the use of animal models of human heart disease, Biophysical Reviews, vol.9, 4, 2017,pp 431-441