Axonal Charcot–Marie–Tooth disease patient-derived motor neurons demonstrate disease-specific phenotypes including abnormal electrophysiological properties
Saporta, Mario A., Dang, Vu, Volfson, Dmitri, Zou, Bende, Xie, Xinmin (Simon), Adebola, Adijat, Liem, Ronald K., Shy, Michael, Dimos, John T.
Published in Experimental neurology (01.01.2015)
Published in Experimental neurology (01.01.2015)
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A Molecular Network for the Transport of the TI-VAMP/VAMP7 Vesicles from Cell Center to Periphery
Burgo, Andrea, Proux-Gillardeaux, Véronique, Sotirakis, Emmanuel, Bun, Philippe, Casano, Alessandra, Verraes, Agathe, Liem, Ronald K.H., Formstecher, Etienne, Coppey-Moisan, Maïté, Galli, Thierry
Published in Developmental cell (17.07.2012)
Published in Developmental cell (17.07.2012)
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BPAG1a and b associate with EB1 and EB3 and modulate vesicular transport, Golgi apparatus structure, and cell migration in C2.7 myoblasts
Poliakova, Kseniia, Adebola, Adijat, Leung, Conrad L, Favre, Bertrand, Liem, Ronald K H, Schepens, Isabelle, Borradori, Luca
Published in PloS one (22.09.2014)
Published in PloS one (22.09.2014)
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Neurofilaments Form a Highly Stable Stationary Cytoskeleton after Reaching a Critical Level in Axons
Yuan, Aidong, Sasaki, Takahiro, Rao, Mala V, Kumar, Asok, Kanumuri, Vivek, Dunlop, David S, Liem, Ronald K, Nixon, Ralph A
Published in The Journal of neuroscience (09.09.2009)
Published in The Journal of neuroscience (09.09.2009)
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Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype
Adebola, Adijat A, Di Castri, Theo, He, Chui-Zhen, Salvatierra, Laura A, Zhao, Jian, Brown, Kristy, Lin, Chyuan-Sheng, Worman, Howard J, Liem, Ronald K H
Published in Human molecular genetics (15.04.2015)
Published in Human molecular genetics (15.04.2015)
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Plakins: Goliaths that link cell junctions and the cytoskeleton
Liem, Ronald K. H, Jefferson, Julius J, Leung, Conrad L
Published in Nature reviews. Molecular cell biology (01.07.2004)
Published in Nature reviews. Molecular cell biology (01.07.2004)
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Alpha-internexin is structurally and functionally associated with the neurofilament triplet proteins in the mature CNS
Yuan, Aidong, Rao, Mala V, Sasaki, Takahiro, Chen, Yuanxin, Kumar, Asok, Veeranna, Liem, Ronald K H, Eyer, Joel, Peterson, Alan C, Julien, Jean-Pierre, Nixon, Ralph A
Published in The Journal of neuroscience (27.09.2006)
Published in The Journal of neuroscience (27.09.2006)
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The role of microtubule actin cross-linking factor 1 (MACF1) in the Wnt signaling pathway
Chen, Hui-Jye, Lin, Chung-Ming, Lin, Chyuan-Sheng, Perez-Olle, Raul, Leung, Conrad L, Liem, Ronald K H
Published in Genes & development (15.07.2006)
Published in Genes & development (15.07.2006)
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Mutations in the neurofilament light gene linked to Charcot‐Marie‐Tooth disease cause defects in transport
Pérez‐Ollé, Raül, López‐Toledano, Miguel A., Goryunov, Dmitry, Cabrera‐Poch, Noemi, Stefanis, Leonidas, Brown, Kristy, Liem, Ronald K. H.
Published in Journal of neurochemistry (01.05.2005)
Published in Journal of neurochemistry (01.05.2005)
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Nervous-tissue-specific elimination of microtubule-actin crosslinking factor 1a results in multiple developmental defects in the mouse brain
Goryunov, Dmitry, He, Cui-Zhen, Lin, Chyuan-Sheng, Leung, Conrad L., Liem, Ronald K.H.
Published in Molecular and cellular neuroscience (01.05.2010)
Published in Molecular and cellular neuroscience (01.05.2010)
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Microtubule actin crosslinking factor 1b: a novel plakin that localizes to the Golgi complex
Lin, Chung-Ming, Chen, Hui-Jye, Leung, Conrad L, Parry, David A D, Liem, Ronald K H
Published in Journal of cell science (15.08.2005)
Published in Journal of cell science (15.08.2005)
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Multiple disease‐linked myotubularin mutations cause NFL assembly defects in cultured cells and disrupt myotubularin dimerization
Goryunov, Dmitry, Nightingale, Andrew, Bornfleth, Lorelei, Leung, Conrad, Liem, Ronald K. H.
Published in Journal of neurochemistry (01.03.2008)
Published in Journal of neurochemistry (01.03.2008)
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