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8. Concurrent AFG3L2 and SPG7 mutations associated with syndromic parkinsonism and optic atrophy with aberrant OPA1 processing and mitochondrial network fragmentation. Magri S; Fracasso V; Plumari M; Alfei E; Ghezzi D; Gellera C; Rusmini P; Poletti A; Di Bella D; Elia AE; Pantaleoni C; Taroni F Hum Mutat; 2018 Dec; 39(12):2060-2071. PubMed ID: 30252181 [TBL] [Abstract][Full Text] [Related]
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11. The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Nolden M; Ehses S; Koppen M; Bernacchia A; Rugarli EI; Langer T Cell; 2005 Oct; 123(2):277-89. PubMed ID: 16239145 [TBL] [Abstract][Full Text] [Related]
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13. The formation of respiratory chain complexes in mitochondria is under the proteolytic control of the m-AAA protease. Arlt H; Steglich G; Perryman R; Guiard B; Neupert W; Langer T EMBO J; 1998 Aug; 17(16):4837-47. PubMed ID: 9707443 [TBL] [Abstract][Full Text] [Related]
14. Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease. Lee S; Augustin S; Tatsuta T; Gerdes F; Langer T; Tsai FT J Biol Chem; 2011 Feb; 286(6):4404-11. PubMed ID: 21147776 [TBL] [Abstract][Full Text] [Related]
15. m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria. Tatsuta T; Augustin S; Nolden M; Friedrichs B; Langer T EMBO J; 2007 Jan; 26(2):325-35. PubMed ID: 17245427 [TBL] [Abstract][Full Text] [Related]
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18. OPA1 cleavage depends on decreased mitochondrial ATP level and bivalent metals. Baricault L; Ségui B; Guégand L; Olichon A; Valette A; Larminat F; Lenaers G Exp Cell Res; 2007 Oct; 313(17):3800-8. PubMed ID: 17826766 [TBL] [Abstract][Full Text] [Related]
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