Resultados de procura - Cooper, Sandra T
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Development and Evaluation of a PCR-Based Assay for Detection of Haemobartonella felis in Cats and Differentiation of H. felis from Related Bacteria by Restriction Fragment Length... por Messick, Joanne B., Berent, Linda M., Cooper, Sandra K.
Publicado 1998Text -
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Eating habits and attitudes among 10-year-old children of mothers with eating disorders: Longitudinal study por Stein, Alan, Woolley, Helen, Cooper, Sandra, Winterbottom, Jonathan, Fairburn, Christopher G., Cortina-Borja, Mario
Publicado 2006Text -
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Limited proteolysis as a tool to probe the tertiary conformation of dysferlin and structural consequences of patient missense variant L344P por Woolger, Natalie, Bournazos, Adam, Sophocleous, Reece A., Evesson, Frances J., Lek, Angela, Driemer, Birgit, Sutton, R. Bryan, Cooper, Sandra T.
Publicado 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... por Sinmaz, Nese, Tea, Fiona, Pilli, Deepti, Zou, Alicia, Amatoury, Mazen, Nguyen, Tina, Merheb, Vera, Ramanathan, Sudarshini, Cooper, Sandra T., Dale, Russell C., Brilot, Fabienne
Publicado 2016Text -
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Reduced Plasma Membrane Expression of Dysferlin Mutants Is Attributed to Accelerated Endocytosis via a Syntaxin-4-associated Pathway por 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.
Publicado 2010Text -
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Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient por 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.
Publicado 2014Text -
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Ornithine-δ-Aminotransferase Inhibits Neurogenesis During Xenopus Embryonic Development por Peng, Ying, Cooper, Sandra K., Li, Yi, Mei, Jay M., Qiu, Shuwei, Borchert, Gregory L., Donald, Steven P., Kung, Hsiang-fu, Phang, James M.
Publicado 2015Text -
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Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling por 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.
Publicado 2017Text -
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Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy por 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.
Publicado 2008Text -
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Phenotypic variability and identification of novel YARS2 mutations in YARS2 mitochondrial myopathy, lactic acidosis and sideroblastic anaemia por 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
Publicado 2013Text -
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Calpains, Cleaved Mini-Dysferlin(C72), and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair por 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.
Publicado 2013Text -
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Alternate Splicing of Dysferlin C2A Confers Ca(2+)-Dependent and Ca(2+)-Independent Binding for Membrane Repair por 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
Publicado 2013Text -
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Neonatal-lethal dilated cardiomyopathy due to a homozygous LMOD2 donor splice-site variant por 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.
Publicado 2022Text