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Journal of Cell Science|May 6, 2025
The role of mitochondrial mRNA translation in cellular communicationEleonora Zilio, Tim Schlegel, Marta Zaninello, et al.
Experimental Cell Research|July 20, 2005
Spastin subcellular localization is regulated through usage of different translation start sites and active export from the nucleusPamela Claudiani, Elena Riano, Alessia Errico, et al.
The European Journal of Neuroscience|July 20, 2005
UMODL1/Olfactorin is an extracellular membrane-bound molecule with a restricted spatial expression in olfactory and vomeronasal neuronsElia Di Schiavi, Elena Riano, Babett Heye, et al.
Molecular and Cellular Biology|November 15, 2006
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegiaMirko Koppen, Metodi D Metodiev, Giorgio Casari, et al.
Cell|October 22, 2005
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondriaMark Nolden, Sarah Ehses, Mirko Koppen, et al.
BMC Genetics|October 13, 2006
Functional dissection of the Drosophila Kallmann's syndrome protein DmKal-1Davide Andrenacci, Maria R Grimaldi, Vittorio Panetta, et al.
The Journal of Clinical Investigation|December 17, 2005
Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegiaMarinella Pirozzi, Angelo Quattrini, Gennaro Andolfi, et al.
The EMBO Journal|March 10, 2020
CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagyDavid Pla-Martín, Désirée Schatton, Janica L Wiederstein, et al.
Plos Genetics|December 3, 2016
The Mitochondrial m-AAA Protease Prevents Demyelination and Hair GreyingShuaiyu Wang, Julie Jacquemyn, Sara Murru, et al.
Archives of Neurology|June 24, 2004
Hereditary spastic paraplegia: clinical genetic study of 15 familiesAntonio Orlacchio, Toshitaka Kawarai, Antonio Totaro, et al.
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