Rugarli E - Search Results

1

Fam134c and Fam134b shape axonal endoplasmic reticulum architecture in vivo.

Iavarone F, Zaninello M, Perrone M, Monaco M, Barth E, Gaedke F, Pizzo MT, Di Lorenzo G, Desiderio V, Sommella E, Merciai F, Salviati E, Campiglia P, Luongo L, De Leonibus E, Rugarli E, Settembre C. Iavarone F, et al. Among authors: rugarli e. EMBO Rep. 2024 Aug;25(8):3651-3677. doi: 10.1038/s44319-024-00213-7. Epub 2024 Jul 22. EMBO Rep. 2024. PMID: 39039299 Free PMC article.

2

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. Mancuso G, et al. Among authors: rugarli ei. PLoS One. 2012;7(5):e36337. doi: 10.1371/journal.pone.0036337. Epub 2012 May 1. PLoS One. 2012. PMID: 22563492 Free PMC article.

3

Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.

Sprenger HG, Wani G, Hesseling A, König T, Patron M, MacVicar T, Ahola S, Wai T, Barth E, Rugarli EI, Bergami M, Langer T. Sprenger HG, et al. Among authors: rugarli ei. EMBO Mol Med. 2019 Jan;11(1):e9288. doi: 10.15252/emmm.201809288. EMBO Mol Med. 2019. PMID: 30389680 Free PMC article.

4

CLUH maintains functional mitochondria and translation in motoneuronal axons and prevents peripheral neuropathy.

Zaninello M, Schlegel T, Nolte H, Pirzada M, Savino E, Barth E, Klein I, Wüstenberg H, Uddin T, Wolff L, Wirth B, Lehmann HC, Cioni JM, Langer T, Rugarli EI. Zaninello M, et al. Among authors: rugarli ei. Sci Adv. 2024 May 31;10(22):eadn2050. doi: 10.1126/sciadv.adn2050. Epub 2024 May 29. Sci Adv. 2024. PMID: 38809982 Free PMC article.

5

The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying.

Wang S, Jacquemyn J, Murru S, Martinelli P, Barth E, Langer T, Niessen CM, Rugarli EI. Wang S, et al. Among authors: rugarli ei. PLoS Genet. 2016 Dec 2;12(12):e1006463. doi: 10.1371/journal.pgen.1006463. eCollection 2016 Dec. PLoS Genet. 2016. PMID: 27911893 Free PMC article.

6

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. Montoro-Gámez C, et al. Among authors: rugarli ei. Brain. 2023 Oct 3;146(10):4117-4131. doi: 10.1093/brain/awad136. Brain. 2023. PMID: 37086482

7

Astrocyte-specific deletion of the mitochondrial m-AAA protease reveals glial contribution to neurodegeneration.

Murru S, Hess S, Barth E, Almajan ER, Schatton D, Hermans S, Brodesser S, Langer T, Kloppenburg P, Rugarli EI. Murru S, et al. Among authors: rugarli ei. Glia. 2019 Aug;67(8):1526-1541. doi: 10.1002/glia.23626. Epub 2019 Apr 16. Glia. 2019. PMID: 30989755 Free PMC article.

8

AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival.

Almajan ER, Richter R, Paeger L, Martinelli P, Barth E, Decker T, Larsson NG, Kloppenburg P, Langer T, Rugarli EI. Almajan ER, et al. Among authors: rugarli ei. J Clin Invest. 2012 Nov;122(11):4048-58. doi: 10.1172/JCI64604. Epub 2012 Oct 8. J Clin Invest. 2012. PMID: 23041622 Free PMC article.

9

CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins.

Gao J, Schatton D, Martinelli P, Hansen H, Pla-Martin D, Barth E, Becker C, Altmueller J, Frommolt P, Sardiello M, Rugarli EI. Gao J, et al. Among authors: rugarli ei. J Cell Biol. 2014 Oct 27;207(2):213-23. doi: 10.1083/jcb.201403129. J Cell Biol. 2014. PMID: 25349259 Free PMC article.

10

Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation.

Kondadi AK, Wang S, Montagner S, Kladt N, Korwitz A, Martinelli P, Herholz D, Baker MJ, Schauss AC, Langer T, Rugarli EI. Kondadi AK, et al. EMBO J. 2014 May 2;33(9):1011-26. doi: 10.1002/embj.201387009. Epub 2014 Mar 28. EMBO J. 2014. PMID: 24681487 Free PMC article.

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