Cotranscription of two RNA coding for the cell adhesion regulator and its variant in Reh leukemia cells.Molla A., Rouard-Talbot L., Block M.R.View abstractCategorySequencesSourceMGI: 2385906PubMedEurope PMCBiochim Biophys Acta 1315:6-8 (1996)Cited in1Mapped to9
Impaired flickering of the permeability transition pore causes SPG7 spastic paraplegia.Sambri I., Massa F., Gullo F., Meneghini S., Cassina L., Carraro M., Dina G., Quattrini A., Patanella L.[...], Casari G.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCEBioMedicine 61:103050-103050 (2020)Mapped to13
Alternative splicing of Spg7, a gene involved in hereditary spastic paraplegia, encodes a variant of paraplegin targeted to the endoplasmic reticulum.Mancuso G., Barth E., Crivello P., Rugarli E.I.View abstractCategorySubcellular LocationSourceMGI: 2385906PubMedEurope PMCPLoS ONE 7:E36337-E36337 (2012)Cited in2Mapped to12
Autocatalytic processing of m-AAA protease subunits in mitochondria.Koppen M., Bonn F., Ehses S., Langer T.View abstractCategoryFunctionSourceMGI: 2385906PubMedEurope PMCMol. Biol. Cell 20:4216-4224 (2009)Cited in3Mapped to21
Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.Martinelli P., La Mattina V., Bernacchia A., Magnoni R., Cerri F., Cox G., Quattrini A., Casari G., Rugarli E.I.View abstractCategoryFunctionSourceMGI: 2385906PubMedEurope PMCHum Mol Genet 18:2001-2013 (2009)Mapped to13
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia.Koppen M., Metodiev M.D., Casari G., Rugarli E.I., Langer T.View abstractCategoriesFunction, InteractionSourceMGI: 2385906PubMedEurope PMCMol. Cell. Biol. 27:758-767 (2007)Cited in4Mapped to19
Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia.Pirozzi M., Quattrini A., Andolfi G., Dina G., Malaguti M.C., Auricchio A., Rugarli E.I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCJ Clin Invest 116:202-208 (2006)Mapped to13
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria.Nolden M., Ehses S., Koppen M., Bernacchia A., Rugarli E.I., Langer T.View abstractCategoryFunctionSourceMGI: 2385906PubMedEurope PMCCell 123:277-289 (2005)Cited in6Mapped to11
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport.Ferreirinha F., Quattrini A., Pirozzi M., Valsecchi V., Dina G., Broccoli V., Auricchio A., Piemonte F., Tozzi G.[...], Rugarli E.I.View abstractCategoriesFunction, Phenotypes & VariantsSourceMGI: 2385906PubMedEurope PMCJ. Clin. Invest. 113:231-242 (2004)Cited in1Mapped to7