PubMed (GeneRIF) for id: 6683

Year	Number of Results
2001	1
2002	6
2003	6
2004	6
2005	10
2006	11
2007	16
2008	13
2009	13
2010	11
2011	9
2012	10
2013	11
2014	12
2015	8
2016	8
2017	3
2018	6
2019	10
2020	8
2021	6
2022	6
2023	7
2024	0

1

A novel truncated variant in SPAST results in spastin accumulation and defects in microtubule dynamics.

Wang J, Wu Y, Dong H, Ji Y, Zhang L, Liu Y, Liu Y, Gao X, Jia Y, Wang X. Wang J, et al. BMC Med Genomics. 2023 Dec 8;16(1):321. doi: 10.1186/s12920-023-01759-6. BMC Med Genomics. 2023. PMID: 38066582 Free PMC article.

2

Identification of c.1495C > T mutation in SPAST gene in a family of Han Chinese with hereditary spastic paraplegia.

Chen X, Li X, Tan Y, Yang D, Lu L, Deng Y, Xu R. Chen X, et al. Neurosci Lett. 2023 Aug 24;812:137399. doi: 10.1016/j.neulet.2023.137399. Epub 2023 Jul 19. Neurosci Lett. 2023. PMID: 37473796

3

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. Shen W, et al. Virol Sin. 2023 Jun;38(3):448-458. doi: 10.1016/j.virs.2023.05.006. Epub 2023 May 11. Virol Sin. 2023. PMID: 37172824 Free PMC article.

4

A novel missense mutation in SPAST causes hereditary spastic paraplegia in male members of a family: A case report.

Wang XC, Liu RH, Wang T, Wang Y, Jiang Y, Chen DD, Wang XY, Hou TS, Kong QX. Wang XC, et al. Mol Med Rep. 2023 Apr;27(4):79. doi: 10.3892/mmr.2023.12966. Epub 2023 Feb 24. Mol Med Rep. 2023. PMID: 36825575 Free PMC article.

5

Spastin Promotes the Migration and Invasion Capability of T98G Glioblastoma Cells by Interacting with Pin1 through Its Microtubule-Binding Domain.

Temizci B, Kucukvardar S, Karabay A. Temizci B, et al. Cells. 2023 Jan 27;12(3):427. doi: 10.3390/cells12030427. Cells. 2023. PMID: 36766769 Free PMC article.

6

Phosphorylation mutation impairs the promoting effect of spastin on neurite outgrowth without affecting its microtubule severing ability.

Zhang Y, He X, Zou J, Yang J, Ma A, Tan M. Zhang Y, et al. Eur J Histochem. 2023 Jan 12;67(1):3594. doi: 10.4081/ejh.2023.3594. Eur J Histochem. 2023. PMID: 36632786 Free PMC article.

7

Copy number variations in SPAST and ATL1 are rare among Brazilians.

Fussiger H, Pereira BLDS, Padilha JPD, Donis KC; Rare-Genomes Project Consortium; Siebert M, Brusius-Facchin AC, Baldo G, Saute JAM. Fussiger H, et al. Clin Genet. 2023 May;103(5):580-584. doi: 10.1111/cge.14280. Epub 2023 Jan 15. Clin Genet. 2023. PMID: 36537231

8

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. Chen Y, et al. Acta Neuropathol Commun. 2022 Nov 22;10(1):169. doi: 10.1186/s40478-022-01476-8. Acta Neuropathol Commun. 2022. PMID: 36414997 Free PMC article.

9

Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST.

Mo A, Saffari A, Kellner M, Döbler-Neumann M, Jordan C, Srivastava S, Zhang B, Sahin M, Fink JK, Smith L, Posey JE, Alter KE, Toro C, Blackstone C, Soldatos AG, Christie M, Schüle R, Ebrahimi-Fakhari D. Mo A, et al. Mov Disord. 2022 Dec;37(12):2440-2446. doi: 10.1002/mds.29225. Epub 2022 Sep 14. Mov Disord. 2022. PMID: 36103453 Free PMC article.

10

Genetic, structural and clinical analysis of spastic paraplegia 4.

Varghaei P, Estiar MA, Ashtiani S, Veyron S, Mufti K, Leveille E, Yu E, Spiegelman D, Rioux MF, Yoon G, Tarnopolsky M, Boycott KM, Dupre N, Suchowersky O, Trempe JF, Rouleau GA, Gan-Or Z. Varghaei P, et al. Parkinsonism Relat Disord. 2022 May;98:62-69. doi: 10.1016/j.parkreldis.2022.03.019. Epub 2022 Apr 16. Parkinsonism Relat Disord. 2022. PMID: 35487127

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

169 results

Results by year