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Tau Promotes Neurodegeneration via DRP1 Mislocalization In Vivo

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Expression of Mfn2, the Charcot-Marie-Tooth Neuropathy Type 2A Gene, in Human Skeletal Muscle

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Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

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Mitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity

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Mitofusin-2 Maintains Mitochondrial Structure and Contributes to Stress-Induced Permeability Transition in Cardiac Myocytes

Papanicolaou, K. N., Khairallah, R. J., Ngoh, G. A., Chikando, A. C., Luptak, I., O’Shea, K. M., Riley, D. D., Lugus, J. J., Colucci, W. S., Lederer, W. J., et al. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.00911-10 · Cited by 371

Mitochondrial loss, dysfunction and altered dynamics in Huntington's disease

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Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Zuchner, S. L., Jonghe, P. D., Jordanova, A., Claeys, K. G., Guergueltcheva, V., Cherninkova, S., Hamilton, S. R., Stavern, G. P. V., Krajewski, K. M., Stajich, J. M., et al. (2006) · Annals of Neurology · doi:10.1002/ana.20797 · Cited by 357

Mitochondrial GTPase mitofusin 2 mutation in Charcot?Marie?Tooth neuropathy type 2A

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Mitochondrial fusion protein mutated in CMT2A

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Clinical and Genetic Characteristics in Patients of Charcot-Marie-Tooth type 2A with Mitofusin 2 (MFN2) Mutations

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Mitofusin 2 (MFN2) �쑀�쟾�옄 �룎�뿰蹂��씠媛� �엳�뒗 Charcot-Marie-Tooth 2A �솚�옄�뱾�쓽 �엫�긽 諛� �쑀�쟾�븰�쟻 �듅�꽦

源��꽭�썕, 源��듅誘�, & �꽑�슦�씪�궓 (2006) · YUHSpace (Yonsei University Medical Library)

Mitochondrial GTPase mitofusin 2 mutations in Korean patients with Charcot‐Marie‐Tooth neuropathy type 2

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