Barmada SJ - Search Results

1

Overexpression of a conserved HSP40 chaperone reduces toxicity of several neurodegenerative disease proteins.

Park SK, Arslan F, Kanneganti V, Barmada SJ, Purushothaman P, Verma SC, Liebman SW. Park SK, et al. Among authors: barmada sj. Prion. 2018 Jan 2;12(1):16-22. doi: 10.1080/19336896.2017.1423185. Epub 2018 Jan 31. Prion. 2018. PMID: 29308690 Free PMC article.

2

Counter-regulation of RNA stability by UPF1 and TDP43.

Gomez N, Hsieh C, Li X, Dykstra M, Waksmacki J, Altheim C, Bechar Y, Klim J, Zaepfel B, Rothstein J, Tank EE, Barmada SJ. Gomez N, et al. Among authors: barmada sj. bioRxiv [Preprint]. 2024 Feb 15:2024.01.31.578310. doi: 10.1101/2024.01.31.578310. bioRxiv. 2024. PMID: 38352350 Free PMC article. Preprint.

3

AAGGG repeat expansions trigger RFC1-independent synaptic dysregulation in human CANVAS Neurons.

Maltby CJ, Krans A, Grudzien SJ, Palacios Y, Muiños J, Suárez A, Asher M, Khurana V, Barmada SJ, Dijkstra AA, Todd PK. Maltby CJ, et al. Among authors: barmada sj. bioRxiv [Preprint]. 2023 Dec 14:2023.12.13.571345. doi: 10.1101/2023.12.13.571345. bioRxiv. 2023. PMID: 38168171 Free PMC article. Preprint.

4

Overexpression of the essential Sis1 chaperone reduces TDP-43 effects on toxicity and proteolysis.

Park SK, Hong JY, Arslan F, Kanneganti V, Patel B, Tietsort A, Tank EMH, Li X, Barmada SJ, Liebman SW. Park SK, et al. Among authors: barmada sj. PLoS Genet. 2017 May 22;13(5):e1006805. doi: 10.1371/journal.pgen.1006805. eCollection 2017 May. PLoS Genet. 2017. PMID: 28531192 Free PMC article.

5

RNA Degradation in Neurodegenerative Disease.

Weskamp K, Barmada SJ. Weskamp K, et al. Among authors: barmada sj. Adv Neurobiol. 2018;20:103-142. doi: 10.1007/978-3-319-89689-2_5. Adv Neurobiol. 2018. PMID: 29916018 Free PMC article. Review.

6

An Intramolecular Salt Bridge Linking TDP43 RNA Binding, Protein Stability, and TDP43-Dependent Neurodegeneration.

Flores BN, Li X, Malik AM, Martinez J, Beg AA, Barmada SJ. Flores BN, et al. Among authors: barmada sj. Cell Rep. 2019 Apr 23;27(4):1133-1150.e8. doi: 10.1016/j.celrep.2019.03.093. Cell Rep. 2019. PMID: 31018129 Free PMC article.

7

Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.

Barmada SJ. Barmada SJ. Neurotherapeutics. 2015 Apr;12(2):340-51. doi: 10.1007/s13311-015-0340-3. Neurotherapeutics. 2015. PMID: 25689976 Free PMC article. Review.

8

TDP43 and RNA instability in amyotrophic lateral sclerosis.

Weskamp K, Barmada SJ. Weskamp K, et al. Among authors: barmada sj. Brain Res. 2018 Aug 15;1693(Pt A):67-74. doi: 10.1016/j.brainres.2018.01.015. Epub 2018 Jan 31. Brain Res. 2018. PMID: 29395044 Free PMC article. Review.

9

TDP43 nuclear export and neurodegeneration in models of amyotrophic lateral sclerosis and frontotemporal dementia.

Archbold HC, Jackson KL, Arora A, Weskamp K, Tank EM, Li X, Miguez R, Dayton RD, Tamir S, Klein RL, Barmada SJ. Archbold HC, et al. Among authors: barmada sj. Sci Rep. 2018 Mar 15;8(1):4606. doi: 10.1038/s41598-018-22858-w. Sci Rep. 2018. PMID: 29545601 Free PMC article.

10

Matrin 3-dependent neurotoxicity is modified by nucleic acid binding and nucleocytoplasmic localization.

Malik AM, Miguez RA, Li X, Ho YS, Feldman EL, Barmada SJ. Malik AM, et al. Among authors: barmada sj. Elife. 2018 Jul 17;7:e35977. doi: 10.7554/eLife.35977. Elife. 2018. PMID: 30015619 Free PMC article.

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