Search Results - Cooper, Sandra T.
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Terminology for early pregnancy loss must be changed by Hutchon, David J R, Cooper, Sandra
Published 1998Text -
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Limited proteolysis as a tool to probe the tertiary conformation of dysferlin and structural consequences of patient missense variant L344P by Woolger, Natalie, Bournazos, Adam, Sophocleous, Reece A., Evesson, Frances J., Lek, Angela, Driemer, Birgit, Sutton, R. Bryan, Cooper, Sandra T.
Published 2017Text -
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Dopamine-2 receptor extracellular N-terminus regulates receptor surface availability and is the target of human pathogenic antibodies from children with movement and psychiatric di... by Sinmaz, Nese, Tea, Fiona, Pilli, Deepti, Zou, Alicia, Amatoury, Mazen, Nguyen, Tina, Merheb, Vera, Ramanathan, Sudarshini, Cooper, Sandra T., Dale, Russell C., Brilot, Fabienne
Published 2016Text -
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Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway by Evesson, Frances J., Peat, Rachel A., Lek, Angela, Brilot, Fabienne, Lo, Harriet P., Dale, Russell C., Parton, Robert G., North, Kathryn N., Cooper, Sandra T.
Published 2010Text -
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Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient by Miller, David K., Menezes, Minal J., Simons, Cas, Riley, Lisa G., Cooper, Sandra T., Grimmond, Sean M., Thorburn, David R., Christodoulou, John, Taft, Ryan J.
Published 2014Text -
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Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling by Piper, Ann-Katrin, Ross, Samuel E., Redpath, Gregory M., Lemckert, Frances A., Woolger, Natalie, Bournazos, Adam, Greer, Peter A., Sutton, Roger B., Cooper, Sandra T.
Published 2017Text -
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Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy by Ilkovski, Biljana, Mokbel, Nancy, Lewis, Raymond A., Walker, Kendall, Nowak, Kristen J., Domazetovska, Ana, Laing, Nigel G., Fowler, Velia M., North, Kathryn N., Cooper, Sandra T.
Published 2008Text -
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Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia by Riley, Lisa G, Menezes, Minal J, Rudinger-Thirion, Joëlle, Duff, Rachael, de Lonlay, Pascale, Rotig, Agnes, Tchan, Michel C, Davis, Mark, Cooper, Sandra T, Christodoulou, John
Published 2013Text -
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Calpains, Cleaved Mini-Dysferlin(C72), and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair by Lek, Angela, Evesson, Frances J., Lemckert, Frances A., Redpath, Gregory M. I., Lueders, Ann-Katrin, Turnbull, Lynne, Whitchurch, Cynthia B., North, Kathryn N., Cooper, Sandra T.
Published 2013Text -
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Alternate Splicing of Dysferlin C2A Confers Ca(2+)-Dependent and Ca(2+)-Independent Binding for Membrane Repair by Fuson, Kerry, Rice, Anne, Mahling, Ryan, Snow, Adam, Nayak, Kamakshi, Shanbhogue, Prajna, Meyer, Austin G., Redpath, Gregory M.I., Hinderliter, Anne, Cooper, Sandra T., Sutton, R. Bryan
Published 2013Text -
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Neonatal-lethal dilated cardiomyopathy due to a homozygous LMOD2 donor splice-site variant by Yuen, Michaela, Worgan, Lisa, Iwanski, Jessika, Pappas, Christopher T., Joshi, Himanshu, Churko, Jared M., Arbuckle, Susan, Kirk, Edwin P., Zhu, Ying, Roscioli, Tony, Gregorio, Carol C., Cooper, Sandra T.
Published 2022Text