نتائج البحث - Shor, Oded
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Novel RyR2 Mutation (G3118R) Is Associated With Autosomal Recessive Ventricular Fibrillation and Sudden Death: Clinical, Functional, and Computational Analysis حسب Shauer, Ayelet, Shor, Oded, Wei, Jinhong, Elitzur, Yair, Kucherenko, Nataly, Wang, Ruiwu, Chen, S. R. Wayne, Einav, Yulia, Luria, David
منشور في 2021نص -
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Phosphatidylinositol (4,5)Bisphosphate Inhibits K(+)-Efflux Channel Activity in NT1 Tobacco Cultured Cells حسب Ma, Xiaohong, Shor, Oded, Diminshtein, Sofia, Yu, Ling, Im, Yang Ju, Perera, Imara, Lomax, Aaron, Boss, Wendy F., Moran, Nava
منشور في 2009نص -
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Paroxysmal slow wave events predict epilepsy following a first seizure حسب Zelig, Daniel, Goldberg, Ilan, Shor, Oded, Ben Dor, Shira, Yaniv‐Rosenfeld, Amit, Milikovsky, Dan Z., Ofer, Jonathan, Imtiaz, Hamza, Friedman, Alon, Benninger, Felix
منشور في 2021نص -
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Mild Phenotype of Wolfram Syndrome Associated With a Common Pathogenic Variant Is Predicted by a Structural Model of Wolframin حسب Wilf-Yarkoni, Adi, Shor, Oded, Fellner, Avi, Hellmann, Mark Andrew, Pras, Elon, Yonath, Hagit, Shkedi-Rafid, Shiri, Basel-Salmon, Lina, Bazak, Lili, Eliahou, Ruth, Greenbaum, Lior, Stiebel-Kalish, Hadas, Benninger, Felix, Goldberg, Yael
منشور في 2021نص -
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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy حسب Helbig, Ingo, Lopez-Hernandez, Tania, Shor, Oded, Galer, Peter, Ganesan, Shiva, Pendziwiat, Manuela, Rademacher, Annika, Ellis, Colin A., Hümpfer, Nadja, Schwarz, Niklas, Seiffert, Simone, Peeden, Joseph, Shen, Joseph, Štěrbová, Katalin, Hammer, Trine Bjørg, Møller, Rikke S., Shinde, Deepali N., Tang, Sha, Smith, Lacey, Poduri, Annapurna, Krause, Roland, Benninger, Felix, Helbig, Katherine L., Haucke, Volker, Weber, Yvonne G.
منشور في 2019نص