33064315 29986938 23475610 31817338 25656065 28129109 32042922 33391478 28468937 24080146 22029574 30785719 32345615 23900071 23368766 22697423 29203801 26222336 23922830 22426394 24113586 23280835 34061233 23730296 21471218 28522961 25017368 2656361 - Search Results

Year	Number of Results
2010	4
2011	42
2012	48
2013	38
2014	27
2015	34
2016	27
2017	28
2018	33
2019	38
2020	31
2021	37
2022	26
2023	4

1

Mislocalisation of TDP-43 to the cytoplasm causes cortical hyperexcitability and reduced excitatory neurotransmission in the motor cortex.

Dyer MS, Reale LA, Lewis KE, Walker AK, Dickson TC, Woodhouse A, Blizzard CA. Dyer MS, et al. J Neurochem. 2021 May;157(4):1300-1315. doi: 10.1111/jnc.15214. Epub 2020 Nov 9. J Neurochem. 2021. PMID: 33064315 Free article.

2

Mitochondrial dysfunction and neurodegenerative proteinopathies: mechanisms and prospects for therapeutic intervention.

Briston T, Hicks AR. Briston T, et al. Biochem Soc Trans. 2018 Aug 20;46(4):829-842. doi: 10.1042/BST20180025. Epub 2018 Jul 9. Biochem Soc Trans. 2018. PMID: 29986938 Free PMC article. Review.

3

Overexpression of ALS-associated p.M337V human TDP-43 in mice worsens disease features compared to wild-type human TDP-43 mice.

Janssens J, Wils H, Kleinberger G, Joris G, Cuijt I, Ceuterick-de Groote C, Van Broeckhoven C, Kumar-Singh S. Janssens J, et al. Mol Neurobiol. 2013 Aug;48(1):22-35. doi: 10.1007/s12035-013-8427-5. Epub 2013 Mar 10. Mol Neurobiol. 2013. PMID: 23475610 Free PMC article.

4

Existing and Emerging Metabolomic Tools for ALS Research.

Germeys C, Vandoorne T, Bercier V, Van Den Bosch L. Germeys C, et al. Genes (Basel). 2019 Dec 5;10(12):1011. doi: 10.3390/genes10121011. Genes (Basel). 2019. PMID: 31817338 Free PMC article. Review.

5

From nucleation to widespread propagation: A prion-like concept for ALS.

Maniecka Z, Polymenidou M. Maniecka Z, et al. Virus Res. 2015 Sep 2;207:94-105. doi: 10.1016/j.virusres.2014.12.032. Epub 2015 Feb 2. Virus Res. 2015. PMID: 25656065 Free article. Review.

6

Motor-Coordinative and Cognitive Dysfunction Caused by Mutant TDP-43 Could Be Reversed by Inhibiting Its Mitochondrial Localization.

Wang W, Arakawa H, Wang L, Okolo O, Siedlak SL, Jiang Y, Gao J, Xie F, Petersen RB, Wang X. Wang W, et al. Mol Ther. 2017 Jan 4;25(1):127-139. doi: 10.1016/j.ymthe.2016.10.013. Epub 2017 Jan 4. Mol Ther. 2017. PMID: 28129109 Free PMC article.

7

Neuropathologic description of CHCHD10 mutated amyotrophic lateral sclerosis.

Keith JL, Swinkin E, Gao A, Alminawi S, Zhang M, McGoldrick P, McKeever P, Robertson J, Rogaeva E, Zinman L. Keith JL, et al. Neurol Genet. 2020 Jan 13;6(1):e394. doi: 10.1212/NXG.0000000000000394. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042922 Free PMC article.

8

TDP-43 proteinopathy impairs mRNP granule mediated postsynaptic translation and mRNA metabolism.

Wong CE, Jin LW, Chu YP, Wei WY, Ho PC, Tsai KJ. Wong CE, et al. Theranostics. 2021 Jan 1;11(1):330-345. doi: 10.7150/thno.51004. eCollection 2021. Theranostics. 2021. PMID: 33391478 Free PMC article.

9

RNA metabolism in neurodegenerative disease.

Liu EY, Cali CP, Lee EB. Liu EY, et al. Dis Model Mech. 2017 May 1;10(5):509-518. doi: 10.1242/dmm.028613. Dis Model Mech. 2017. PMID: 28468937 Free PMC article. Review.

10

A unique mouse model for investigating the properties of amyotrophic lateral sclerosis-associated protein TDP-43, by in utero electroporation.

Akamatsu M, Takuma H, Yamashita T, Okada T, Keino-Masu K, Ishii K, Kwak S, Masu M, Tamaoka A. Akamatsu M, et al. Neurosci Res. 2013 Dec;77(4):234-41. doi: 10.1016/j.neures.2013.09.009. Epub 2013 Sep 27. Neurosci Res. 2013. PMID: 24080146

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