Browsing by Author Papadaki, Maria

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)Citation
2016Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylationDos Remedios, Cristobal Guillermo; Bayliss, Christopher R.; El-Mezgueldi, Mohammed; Leung, Manching; Marston, Steve B.; Messer, Andrew; Papadaki, Maria; Redwood, Charles; Ward, Douglas G.; School of Medical Sciences: Bosch InstituteMutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation, Archives of Biochemistry and Biophysics, vol.601, N/A, 2016,pp 113-120
2016Mutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylationDos Remedios, Cristobal Guillermo; Bayliss, Christopher R.; El-Mezgueldi, Mohammed; Leung, Manching; Marston, Steve B.; Messer, Andrew; Papadaki, Maria; Redwood, Charles; Ward, Douglas G.; School of Medical Sciences: Bosch InstituteMutations in troponin T associated with Hypertrophic Cardiomyopathy increase Ca2+-sensitivity and suppress the modulation of Ca2+-sensitivity by troponin I phosphorylation, Archives of Biochemistry and Biophysics, vol.601, N/A, 2016,pp 113-120
2015TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotypeClarke, Nigel; Bolduc, Veronique; Dastgir, Jahannaz; de Winter, Josine Marieke; Donkervoort, Sandra; et al, Various; Gibbons, Melissa A; Hu, Ying; Kirschner, Janbernd; Neu, Matthae B; Papadaki, Maria; Yang, Michelle L; Childrens Hospital Westmead: Paediatrics & Child HealthTPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype, Annals of Neurology, vol.78, 6, 2015,pp 982-994