Natasha Kraeva

An <i>Ryr1</i> ^{<i>I4895T</i>} mutation abolishes Ca ²⁺ release channel function and delays development in homozygous offspring of a mutant mouse line

Elena Zvaritch, Frederic Depreux, Natasha Kraeva et al. · Proceedings of the National Academy of Sciences · 2007 · 80 citations · Full text

Ca ²⁺ dysregulation in <i> Ryr1 ^I4895T/wt </i> mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Elena Zvaritch, Natasha Kraeva, Éric Bombardier et al. · Proceedings of the National Academy of Sciences · 2009 · 72 citations · Full text

Ryanodine receptor type 1 gene mutations found in the Canadian malignant hyperthermia population

Natasha Kraeva, Sheila Riazi, Julian Loke et al. · Canadian Journal of Anesthesia/Journal canadien d anesthésie · 2011 · 52 citations · Full text

Molecular Biology, Pathology, Gene Mutations

Exome analysis identifies <scp>B</scp>rody myopathy in a family diagnosed with malignant hyperthermia susceptibility

Nyamkhishig Sambuughin, Elena Zvaritch, Natasha Kraeva et al. · Molecular Genetics & Genomic Medicine · 2014 · 23 citations · Full text

Muscle Function, Exome Analysis Identifies, Pathology +22

Genetic variation and cognitive dysfunction one year after cardiac surgery

Alastair G. Stewart, Rita Katznelson, Natasha Kraeva et al. · Anaesthesia · 2013 · 11 citations · Full text