Terminology for early pregnancy loss must be changed

Por Hutchon, David J R, Cooper, Sandra
Publicado em 1998

Membrane Repair: Mechanisms and Pathophysiology

Por Cooper, Sandra T., McNeil, Paul L.
Publicado no Physiol Rev (2015)

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 em 1998

Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins

Por Lek, Angela, Lek, Monkol, North, Kathryn N, Cooper, Sandra T
Publicado em 2010

Farmacologia na prática da enfermagem /

Por Clayton, Bruce D., Stock, Yvonne N., Cooper, Sandra E.
Publicado em 2012.

A Novel Function for Hydroxyproline Oxidase in Apoptosis through Generation of Reactive Oxygen Species

Por Cooper, Sandra K., Pandhare, Jui, Donald, Steven P., Phang, James M.
Publicado em 2008

Regulation and Function of Proline Oxidase under Nutrient Stress

Por Pandhare, Jui, Cooper, Sandra K., Donald, Steven P., Phang, James M.
Publicado em 2009

The Effects of Disease Models of Nuclear Actin Polymerization on the Nucleus

Por Serebryannyy, Leonid A., Yuen, Michaela, Parilla, Megan, Cooper, Sandra T., de Lanerolle, Primal
Publicado no Front Physiol (2016)

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 em 2006

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 no Acta Neuropathol Commun (2016)

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 em 2010

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 em 2014

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 no Invest Ophthalmol Vis Sci (2015)

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 em 2008

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 em 2013

Mutation of the Mitochondrial Tyrosyl-tRNA Synthetase Gene, YARS2, Causes Myopathy, Lactic Acidosis, and Sideroblastic Anemia—MLASA Syndrome

Por Riley, Lisa G., Cooper, Sandra, Hickey, Peter, Rudinger-Thirion, Joëlle, McKenzie, Matthew, Compton, Alison, Lim, Sze Chern, Thorburn, David, Ryan, Michael T., Giegé, Richard, Bahlo, Melanie, Christodoulou, John
Publicado em 2010

Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factor

Por Lemckert, Frances A., Bournazos, Adam, Eckert, Daniel M., Kenzler, Manuel, Hawkes, Joanne M., Butler, Tanya L., Ceely, Bradley, North, Kathryn N., Winlaw, David S., Egan, Jonathan R., Cooper, Sandra T.
Publicado no Cardiovasc Res (2016)

Mutations in Contactin-1, a Neural Adhesion and Neuromuscular Junction Protein, Cause a Familial Form of Lethal Congenital Myopathy

Por Compton, Alison G., Albrecht, Douglas E., Seto, Jane T., Cooper, Sandra T., Ilkovski, Biljana, Jones, Kristi J., Challis, Daniel, Mowat, David, Ranscht, Barbara, Bahlo, Melanie, Froehner, Stanley C., North, Kathryn N.
Publicado em 2008

LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure

Por Riley, Lisa G., Rudinger-Thirion, Joëlle, Schmitz-Abe, Klaus, Thorburn, David R., Davis, Ryan L., Teo, Juliana, Arbuckle, Susan, Cooper, Sandra T., Campagna, Dean R., Frugier, Magali, Markianos, Kyriacos, Sue, Carolyn M., Fleming, Mark D., Christodoulou, John
Publicado no JIMD Rep (2015)

Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene

Por Ilkovski, Biljana, Cooper, Sandra T., Nowak, Kristen, Ryan, Monique M., Yang, Nan, Schnell, Christina, Durling, Hayley J., Roddick, Laurence G., Wilkinson, Ian, Kornberg, Andrew J., Collins, Kevin J., Wallace, Geoff, Gunning, Peter, Hardeman, Edna C., Laing, Nigel G., North, Kathryn N.
Publicado em 2001