PubMed (GeneRIF) for id: 1639

Year	Number of Results
2001	1
2003	2
2004	3
2005	1
2006	2
2007	7
2008	5
2009	6
2010	6
2011	3
2012	9
2013	5
2014	8
2015	6
2016	5
2017	3
2018	1
2019	2
2020	4
2021	4
2022	2
2023	1
2024	1

1

Wild-Type DCTN1 Suppresses the Aggregation of DCTN1 Mutants Associated with Perry Disease.

Fukui Y, Shirakawa H, Kaneko S, Nagayasu K. Fukui Y, et al. Biol Pharm Bull. 2024;47(1):253-258. doi: 10.1248/bpb.b23-00828. Biol Pharm Bull. 2024. PMID: 38267040 Free article.

2

Perry syndrome: Novel DCTN1 mutation in a large kindred and first observation of prodromal disease.

Dulski J, Koga S, Prudencio M, Tipton PW, Ali S, Strongosky AJ, Rose JH, Parrales ZA, Dunmore JA, Jansen-West K, Petrucelli L, Dickson DW, Wszolek ZK. Dulski J, et al. Parkinsonism Relat Disord. 2023 Jul;112:105481. doi: 10.1016/j.parkreldis.2023.105481. Epub 2023 Jun 13. Parkinsonism Relat Disord. 2023. PMID: 37336025

3

Perry disease in an Argentine family due to the DCTN1 p.G67D variant.

Silva E, Itzcovich T, Niikado M, Caride A, Fernández E, Vázquez JC, Romorini L, Marazita M, Sevlever G, Martinetto H, Surace EI. Silva E, et al. Parkinsonism Relat Disord. 2022 Apr;97:63-64. doi: 10.1016/j.parkreldis.2022.03.009. Epub 2022 Mar 21. Parkinsonism Relat Disord. 2022. PMID: 35325666 No abstract available.

4

An identical DCTN1 mutation in two Chinese siblings manifest as dHMN and ALS respectively: a case report.

He J, Yu W, Liu X, Fan D. He J, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb;23(1-2):149-153. doi: 10.1080/21678421.2021.1918722. Epub 2021 Oct 7. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34615428

5

DCTN1 Binds to TDP-43 and Regulates TDP-43 Aggregation.

Deshimaru M, Kinoshita-Kawada M, Kubota K, Watanabe T, Tanaka Y, Hirano S, Ishidate F, Hiramoto M, Ishikawa M, Uehara Y, Okano H, Hirose S, Fujioka S, Iwasaki K, Yuasa-Kawada J, Mishima T, Tsuboi Y. Deshimaru M, et al. Int J Mol Sci. 2021 Apr 13;22(8):3985. doi: 10.3390/ijms22083985. Int J Mol Sci. 2021. PMID: 33924373 Free PMC article.

6

Study on the Prognostic Values of Dynactin Genes in Low-Grade Glioma.

Su X, Li H, Chen S, Qin C. Su X, et al. Technol Cancer Res Treat. 2021 Jan-Dec;20:15330338211010143. doi: 10.1177/15330338211010143. Technol Cancer Res Treat. 2021. PMID: 33896271 Free PMC article.

7

Septin 7 is a centrosomal protein that ensures S phase entry and microtubule nucleation by maintaining the abundance of p150^glued.

Chen TY, Lin TC, Kuo PL, Chen ZR, Cheng HL, Chao YY, Syu JS, Lu FI, Wang CY. Chen TY, et al. J Cell Physiol. 2021 Apr;236(4):2706-2724. doi: 10.1002/jcp.30037. Epub 2020 Sep 1. J Cell Physiol. 2021. PMID: 32869310

8

DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB.

Procopio R, Gagliardi M, D'Amelio M, Brighina L, Nicoletti G, Morelli M, Bonapace G, Quattrone A, Annesi G. Procopio R, et al. Neurobiol Aging. 2020 Sep;93:143.e5-143.e7. doi: 10.1016/j.neurobiolaging.2020.04.006. Epub 2020 Apr 15. Neurobiol Aging. 2020. PMID: 32402491

9

A Novel Cosegregating DCTN1 Splice Site Variant in a Family with Bipolar Disorder May Hold the Key to Understanding the Etiology.

Hallen A, Cooper AJL. Hallen A, et al. Genes (Basel). 2020 Apr 18;11(4):446. doi: 10.3390/genes11040446. Genes (Basel). 2020. PMID: 32325768 Free PMC article.

10

Autophagy and Ubiquitin-Proteasome System Coordinate to Regulate the Protein Quality Control of Neurodegenerative Disease-Associated DCTN1.

Wang N, Ma Q, Peng P, Yu Y, Xu S, Wang G, Ying Z, Wang H. Wang N, et al. Neurotox Res. 2020 Jan;37(1):48-57. doi: 10.1007/s12640-019-00113-y. Epub 2019 Oct 25. Neurotox Res. 2020. PMID: 31654383

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