34831058 31827426 35260846 27400686 27834214 35178161 30582188 31319884 30575981 32653673 33991504 34273246 33963840 30938443 34750982 29431050 26779612 36609661 26521126 34890791 32965492 30982635 35762418 28674981 33289081 29161404 31802140 2786446 - Search Results

Year	Number of Results
2015	1
2016	6
2017	2
2018	6
2019	8
2020	5
2021	10
2022	7
2023	1

1

The Cytotoxicity and Clearance of Mutant Huntingtin and Other Misfolded Proteins.

Folger A, Wang Y. Folger A, et al. Cells. 2021 Oct 21;10(11):2835. doi: 10.3390/cells10112835. Cells. 2021. PMID: 34831058 Free PMC article. Review.

2

Transcriptomic Characterization of the Human Insular Cortex and Claustrum.

Ibrahim C, Le Foll B, French L. Ibrahim C, et al. Front Neuroanat. 2019 Nov 27;13:94. doi: 10.3389/fnana.2019.00094. eCollection 2019. Front Neuroanat. 2019. PMID: 31827426 Free PMC article.

3

Modelling amyotrophic lateral sclerosis in rodents.

Todd TW, Petrucelli L. Todd TW, et al. Nat Rev Neurosci. 2022 Apr;23(4):231-251. doi: 10.1038/s41583-022-00564-x. Epub 2022 Mar 8. Nat Rev Neurosci. 2022. PMID: 35260846 Review.

4

From animal models to human disease: a genetic approach for personalized medicine in ALS.

Picher-Martel V, Valdmanis PN, Gould PV, Julien JP, Dupré N. Picher-Martel V, et al. Acta Neuropathol Commun. 2016 Jul 11;4(1):70. doi: 10.1186/s40478-016-0340-5. Acta Neuropathol Commun. 2016. PMID: 27400686 Free PMC article. Review.

5

Motor neuron disease, TDP-43 pathology, and memory deficits in mice expressing ALS-FTD-linked UBQLN2 mutations.

Le NT, Chang L, Kovlyagina I, Georgiou P, Safren N, Braunstein KE, Kvarta MD, Van Dyke AM, LeGates TA, Philips T, Morrison BM, Thompson SM, Puche AC, Gould TD, Rothstein JD, Wong PC, Monteiro MJ. Le NT, et al. Proc Natl Acad Sci U S A. 2016 Nov 22;113(47):E7580-E7589. doi: 10.1073/pnas.1608432113. Epub 2016 Nov 9. Proc Natl Acad Sci U S A. 2016. PMID: 27834214 Free PMC article.

6

MPO/HOCl Facilitates Apoptosis and Ferroptosis in the SOD1^G93A Motor Neuron of Amyotrophic Lateral Sclerosis.

Peng J, Pan J, Mo J, Peng Y. Peng J, et al. Oxid Med Cell Longev. 2022 Feb 7;2022:8217663. doi: 10.1155/2022/8217663. eCollection 2022. Oxid Med Cell Longev. 2022. PMID: 35178161 Free PMC article.

7

Review: Modelling the pathology and behaviour of frontotemporal dementia.

Solomon DA, Mitchell JC, Salcher-Konrad MT, Vance CA, Mizielinska S. Solomon DA, et al. Neuropathol Appl Neurobiol. 2019 Feb;45(1):58-80. doi: 10.1111/nan.12536. Neuropathol Appl Neurobiol. 2019. PMID: 30582188 Review.

8

Key role of UBQLN2 in pathogenesis of amyotrophic lateral sclerosis and frontotemporal dementia.

Renaud L, Picher-Martel V, Codron P, Julien JP. Renaud L, et al. Acta Neuropathol Commun. 2019 Jul 18;7(1):103. doi: 10.1186/s40478-019-0758-7. Acta Neuropathol Commun. 2019. PMID: 31319884 Free PMC article. Review.

9

Review: Molecular pathology of frontotemporal lobar degenerations.

Borroni B, Alberici A, Buratti E. Borroni B, et al. Neuropathol Appl Neurobiol. 2019 Feb;45(1):41-57. doi: 10.1111/nan.12534. Neuropathol Appl Neurobiol. 2019. PMID: 30575981 Review.

10

Modeling UBQLN2-mediated neurodegenerative disease in mice: Shared and divergent properties of wild type and mutant UBQLN2 in phase separation, subcellular localization, altered proteostasis pathways, and selective cytotoxicity.

Sharkey LM, Sandoval-Pistorius SS, Moore SJ, Gerson JE, Komlo R, Fischer S, Negron-Rios KY, Crowley EV, Padron F, Patel R, Murphy GG, Paulson HL. Sharkey LM, et al. Neurobiol Dis. 2020 Sep;143:105016. doi: 10.1016/j.nbd.2020.105016. Epub 2020 Jul 10. Neurobiol Dis. 2020. PMID: 32653673 Free PMC article.

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