A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia

por Tavasoli, Mahtab, Feridooni, Tiam, Feridooni, Hirad, Sokolenko, Stanislav, Mishra, Abhishek, Lefsay, Abir, Srinivassane, Sadish, Reid, Sarah Anne, Rowsell, Joyce, Praest, Molly, MacKinnon, Alexandra, Mammoliti, Melissa, Maloney, Ashley Alyssa, Moraca, Marina, Uaesoontrachoon, Kitipong, Nagaraju, Kanneboyina, Hoffman, Eric P., Pasumarthi, Kishore B.S., McMaster, Christopher R.
Publicado 2022

Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism

por Tavasoli, Mahtab, Lahire, Sarah, Sokolenko, Stanislav, Novorolsky, Robyn, Reid, Sarah Anne, Lefsay, Abir, Otley, Meredith O. C., Uaesoontrachoon, Kitipong, Rowsell, Joyce, Srinivassane, Sadish, Praest, Molly, MacKinnon, Alexandra, Mammoliti, Melissa Stella, Maloney, Ashley Alyssa, Moraca, Marina, Pedro Fernandez-Murray, J., McKenna, Meagan, Sinal, Christopher J., Nagaraju, Kanneboyina, Robertson, George S., Hoffman, Eric P., McMaster, Christopher R.
Publicado 2022