These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
182 related articles for article (PubMed ID: 16357941)
1. Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia. Pirozzi M; Quattrini A; Andolfi G; Dina G; Malaguti MC; Auricchio A; Rugarli EI J Clin Invest; 2006 Jan; 116(1):202-8. PubMed ID: 16357941 [TBL] [Abstract][Full Text] [Related]
2. 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; Gaeta L; Casari G; Ballabio A; Rugarli EI J Clin Invest; 2004 Jan; 113(2):231-42. PubMed ID: 14722615 [TBL] [Abstract][Full Text] [Related]
3. SARM1 deletion delays cerebellar but not spinal cord degeneration in an enhanced mouse model of SPG7 deficiency. Montoro-Gámez C; Nolte H; Molinié T; Evangelista G; Tröder SE; Barth E; Popovic M; Trifunovic A; Zevnik B; Langer T; Rugarli EI Brain; 2023 Oct; 146(10):4117-4131. PubMed ID: 37086482 [TBL] [Abstract][Full Text] [Related]
4. 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 EI PLoS One; 2012; 7(5):e36337. PubMed ID: 22563492 [TBL] [Abstract][Full Text] [Related]
5. 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; Carissimo A; Iuliano A; Santorelli F; Codazzi F; Grohovaz F; Bernardi P; Becchetti A; Casari G EBioMedicine; 2020 Nov; 61():103050. PubMed ID: 33045469 [TBL] [Abstract][Full Text] [Related]
6. Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Koppen M; Metodiev MD; Casari G; Rugarli EI; Langer T Mol Cell Biol; 2007 Jan; 27(2):758-67. PubMed ID: 17101804 [TBL] [Abstract][Full Text] [Related]
7. 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 EI Hum Mol Genet; 2009 Jun; 18(11):2001-13. PubMed ID: 19289403 [TBL] [Abstract][Full Text] [Related]
8. Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Casari G; De Fusco M; Ciarmatori S; Zeviani M; Mora M; Fernandez P; De Michele G; Filla A; Cocozza S; Marconi R; Dürr A; Fontaine B; Ballabio A Cell; 1998 Jun; 93(6):973-83. PubMed ID: 9635427 [TBL] [Abstract][Full Text] [Related]
9. A novel phenotype of hereditary spastic paraplegia type 7 associated with a compound heterozygous mutation in paraplegin. Mahoney CJ; Dharmadasa T; Huynh W; Halpern JP; Vucic S; Mowat D; Kiernan MC Muscle Nerve; 2020 Jul; 62(1):E44-E45. PubMed ID: 32270516 [No Abstract] [Full Text] [Related]
10. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. Atorino L; Silvestri L; Koppen M; Cassina L; Ballabio A; Marconi R; Langer T; Casari G J Cell Biol; 2003 Nov; 163(4):777-87. PubMed ID: 14623864 [TBL] [Abstract][Full Text] [Related]