Rojo M, Legros F, Chateau D, Lombès A (April 2002). "Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo". Journal of Cell Science. 115 (Pt 8): 1663–74. doi:10.1242/jcs.115.8.1663. PMID11950885.
Santel A, Frank S, Gaume B, Herrler M, Youle RJ, Fuller MT (July 2003). "Mitofusin-1 protein is a generally expressed mediator of mitochondrial fusion in mammalian cells". Journal of Cell Science. 116 (Pt 13): 2763–74. doi:10.1242/jcs.00479. PMID12759376. S2CID6661619.
Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, et al. (February 2006). "Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2". Annals of Neurology. 59 (2): 276–81. doi:10.1002/ana.20797. PMID16437557. S2CID30679835.
Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, et al. (November 2008). "Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations". Journal of Neuropathology and Experimental Neurology. 67 (11): 1097–102. doi:10.1097/nen.0b013e31818b6cbc. PMID18957892. S2CID16302093.
Milane L, Trivedi M, Singh A, Talekar M, Amiji M (June 2015). "Mitochondrial biology, targets, and drug delivery". Journal of Controlled Release. 207: 40–58. doi:10.1016/j.jconrel.2015.03.036. PMID25841699.
Rojo M, Legros F, Chateau D, Lombès A (April 2002). "Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo". Journal of Cell Science. 115 (Pt 8): 1663–74. doi:10.1242/jcs.115.8.1663. PMID11950885.
Santel A, Frank S, Gaume B, Herrler M, Youle RJ, Fuller MT (July 2003). "Mitofusin-1 protein is a generally expressed mediator of mitochondrial fusion in mammalian cells". Journal of Cell Science. 116 (Pt 13): 2763–74. doi:10.1242/jcs.00479. PMID12759376. S2CID6661619.
Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, et al. (February 2006). "Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2". Annals of Neurology. 59 (2): 276–81. doi:10.1002/ana.20797. PMID16437557. S2CID30679835.
Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, et al. (November 2008). "Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations". Journal of Neuropathology and Experimental Neurology. 67 (11): 1097–102. doi:10.1097/nen.0b013e31818b6cbc. PMID18957892. S2CID16302093.
Zorzano A, Sebastián D, Segalés J, Palacín M (September 2009). "The molecular machinery of mitochondrial fusion and fission: An opportunity for drug discovery?". Current Opinion in Drug Discovery & Development. 12 (5): 597–606. PMID19736619.
Milane L, Trivedi M, Singh A, Talekar M, Amiji M (June 2015). "Mitochondrial biology, targets, and drug delivery". Journal of Controlled Release. 207: 40–58. doi:10.1016/j.jconrel.2015.03.036. PMID25841699.
ncbi.nlm.nih.gov
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Santel A, Frank S, Gaume B, Herrler M, Youle RJ, Fuller MT (July 2003). "Mitofusin-1 protein is a generally expressed mediator of mitochondrial fusion in mammalian cells". Journal of Cell Science. 116 (Pt 13): 2763–74. doi:10.1242/jcs.00479. PMID12759376. S2CID6661619.
Züchner S, De Jonghe P, Jordanova A, Claeys KG, Guergueltcheva V, Cherninkova S, et al. (February 2006). "Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2". Annals of Neurology. 59 (2): 276–81. doi:10.1002/ana.20797. PMID16437557. S2CID30679835.
Vallat JM, Ouvrier RA, Pollard JD, Magdelaine C, Zhu D, Nicholson GA, et al. (November 2008). "Histopathological findings in hereditary motor and sensory neuropathy of axonal type with onset in early childhood associated with mitofusin 2 mutations". Journal of Neuropathology and Experimental Neurology. 67 (11): 1097–102. doi:10.1097/nen.0b013e31818b6cbc. PMID18957892. S2CID16302093.