201 related articles for article (PubMed ID: 31587092)
1. ESCRT-III-associated proteins and spastin inhibit protrudin-dependent polarised membrane traffic.
Connell JW; Allison RJ; Rodger CE; Pearson G; Zlamalova E; Reid E
Cell Mol Life Sci; 2020 Jul; 77(13):2641-2658. PubMed ID: 31587092
[TBL] [Abstract][Full Text] [Related]
2. An ESCRT-spastin interaction promotes fission of recycling tubules from the endosome.
Allison R; Lumb JH; Fassier C; Connell JW; Ten Martin D; Seaman MN; Hazan J; Reid E
J Cell Biol; 2013 Aug; 202(3):527-43. PubMed ID: 23897888
[TBL] [Abstract][Full Text] [Related]
3. Friction-driven membrane scission by the human ESCRT-III proteins CHMP1B and IST1.
Cada AK; Pavlin MR; Castillo JP; Tong AB; Larsen KP; Ren X; Yokom AL; Tsai FC; Shiah JV; Bassereau PM; Bustamante CJ; Hurley JH
Proc Natl Acad Sci U S A; 2022 Jul; 119(29):e2204536119. PubMed ID: 35858336
[TBL] [Abstract][Full Text] [Related]
4. The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.
Reid E; Connell J; Edwards TL; Duley S; Brown SE; Sanderson CM
Hum Mol Genet; 2005 Jan; 14(1):19-38. PubMed ID: 15537668
[TBL] [Abstract][Full Text] [Related]
5. The AAA ATPase spastin links microtubule severing to membrane modelling.
Lumb JH; Connell JW; Allison R; Reid E
Biochim Biophys Acta; 2012 Jan; 1823(1):192-7. PubMed ID: 21888932
[TBL] [Abstract][Full Text] [Related]
6. Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III.
Chang CL; Weigel AV; Ioannou MS; Pasolli HA; Xu CS; Peale DR; Shtengel G; Freeman M; Hess HF; Blackstone C; Lippincott-Schwartz J
J Cell Biol; 2019 Aug; 218(8):2583-2599. PubMed ID: 31227594
[TBL] [Abstract][Full Text] [Related]
7. Spastin is required for human immunodeficiency virus-1 efficient replication through cooperation with the endosomal sorting complex required for transport (ESCRT) protein.
Shen W; Liu C; Hu Y; Ding Q; Feng J; Liu Z; Kong X
Virol Sin; 2023 Jun; 38(3):448-458. PubMed ID: 37172824
[TBL] [Abstract][Full Text] [Related]
8. Spastin MIT Domain Disease-Associated Mutations Disrupt Lysosomal Function.
Allison R; Edgar JR; Reid E
Front Neurosci; 2019; 13():1179. PubMed ID: 31787869
[TBL] [Abstract][Full Text] [Related]
9. Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing.
Vietri M; Schink KO; Campsteijn C; Wegner CS; Schultz SW; Christ L; Thoresen SB; Brech A; Raiborg C; Stenmark H
Nature; 2015 Jun; 522(7555):231-5. PubMed ID: 26040712
[TBL] [Abstract][Full Text] [Related]
10. The enhanced association between mutant CHMP2B and spastin is a novel pathological link between frontotemporal dementia and hereditary spastic paraplegias.
Chen Y; Krishnan G; Parsi S; Pons M; Nikolaki V; Cao L; Xu Z; Gao FB
Acta Neuropathol Commun; 2022 Nov; 10(1):169. PubMed ID: 36414997
[TBL] [Abstract][Full Text] [Related]
11. Missense mutation of SPAST protein (I344K) results in loss of ATPase activity and prolonged the half-life, implicated in autosomal dominant hereditary spastic paraplegia.
Lim JH; Kang HM; Jung HR; Kim DS; Noh KH; Chang TK; Kim BJ; Sung DH; Cho HS; Chung KS; Kim NS; Jung CR
Biochim Biophys Acta Mol Basis Dis; 2018 Oct; 1864(10):3221-3233. PubMed ID: 30006150
[TBL] [Abstract][Full Text] [Related]
12. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics.
Errico A; Ballabio A; Rugarli EI
Hum Mol Genet; 2002 Jan; 11(2):153-63. PubMed ID: 11809724
[TBL] [Abstract][Full Text] [Related]
13. Hereditary spastic paraplegia SPG4: what is known and not known about the disease.
Solowska JM; Baas PW
Brain; 2015 Sep; 138(Pt 9):2471-84. PubMed ID: 26094131
[TBL] [Abstract][Full Text] [Related]
14. Defects in ER-endosome contacts impact lysosome function in hereditary spastic paraplegia.
Allison R; Edgar JR; Pearson G; Rizo T; Newton T; Günther S; Berner F; Hague J; Connell JW; Winkler J; Lippincott-Schwartz J; Beetz C; Winner B; Reid E
J Cell Biol; 2017 May; 216(5):1337-1355. PubMed ID: 28389476
[TBL] [Abstract][Full Text] [Related]
15. A newly identified NES sequence present in spastin regulates its subcellular localization and microtubule severing activity.
Sakoe K; Shioda N; Matsuura T
Biochim Biophys Acta Mol Cell Res; 2021 Jan; 1868(1):118862. PubMed ID: 32979422
[TBL] [Abstract][Full Text] [Related]
16. Resolving ESCRT-III Spirals at the Intercellular Bridge of Dividing Cells Using 3D STORM.
Goliand I; Adar-Levor S; Segal I; Nachmias D; Dadosh T; Kozlov MM; Elia N
Cell Rep; 2018 Aug; 24(7):1756-1764. PubMed ID: 30110633
[TBL] [Abstract][Full Text] [Related]
17. Role of spastin and protrudin in neurite outgrowth.
Zhang C; Li D; Ma Y; Yan J; Yang B; Li P; Yu A; Lu C; Ma X
J Cell Biochem; 2012 Jul; 113(7):2296-307. PubMed ID: 22573551
[TBL] [Abstract][Full Text] [Related]
18. Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing.
Evans KJ; Gomes ER; Reisenweber SM; Gundersen GG; Lauring BP
J Cell Biol; 2005 Feb; 168(4):599-606. PubMed ID: 15716377
[TBL] [Abstract][Full Text] [Related]
19. Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network.
Park SH; Zhu PP; Parker RL; Blackstone C
J Clin Invest; 2010 Apr; 120(4):1097-110. PubMed ID: 20200447
[TBL] [Abstract][Full Text] [Related]
20. Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.
Kasher PR; De Vos KJ; Wharton SB; Manser C; Bennett EJ; Bingley M; Wood JD; Milner R; McDermott CJ; Miller CC; Shaw PJ; Grierson AJ
J Neurochem; 2009 Jul; 110(1):34-44. PubMed ID: 19453301
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
