Moss KR - Search Results

1

Dysregulation of mRNA Localization and Translation in Genetic Disease.

Wang ET, Taliaferro JM, Lee JA, Sudhakaran IP, Rossoll W, Gross C, Moss KR, Bassell GJ. Wang ET, et al. Among authors: moss kr. J Neurosci. 2016 Nov 9;36(45):11418-11426. doi: 10.1523/JNEUROSCI.2352-16.2016. J Neurosci. 2016. PMID: 27911744 Free PMC article. Review.

2

Fragile X mental retardation protein recognizes a G quadruplex structure within the survival motor neuron domain containing 1 mRNA 5'-UTR.

McAninch DS, Heinaman AM, Lang CN, Moss KR, Bassell GJ, Rita Mihailescu M, Evans TL. McAninch DS, et al. Among authors: moss kr. Mol Biosyst. 2017 Jul 25;13(8):1448-1457. doi: 10.1039/c7mb00070g. Mol Biosyst. 2017. PMID: 28612854 Free PMC article.

3

FMRP - G-quadruplex mRNA - miR-125a interactions: Implications for miR-125a mediated translation regulation of PSD-95 mRNA.

DeMarco B, Stefanovic S, Williams A, Moss KR, Anderson BR, Bassell GJ, Mihailescu MR. DeMarco B, et al. Among authors: moss kr. PLoS One. 2019 May 21;14(5):e0217275. doi: 10.1371/journal.pone.0217275. eCollection 2019. PLoS One. 2019. PMID: 31112584 Free PMC article.

4

New evidence for secondary axonal degeneration in demyelinating neuropathies.

Moss KR, Bopp TS, Johnson AE, Höke A. Moss KR, et al. Neurosci Lett. 2021 Jan 23;744:135595. doi: 10.1016/j.neulet.2020.135595. Epub 2020 Dec 24. Neurosci Lett. 2021. PMID: 33359733 Free PMC article. Review.

5

Targeting the programmed axon degeneration pathway as a potential therapeutic for Charcot-Marie-Tooth disease.

Moss KR, Höke A. Moss KR, et al. Brain Res. 2020 Jan 15;1727:146539. doi: 10.1016/j.brainres.2019.146539. Epub 2019 Nov 2. Brain Res. 2020. PMID: 31689415 Free PMC article. Review.

6

SARM1 knockout does not rescue neuromuscular phenotypes in a Charcot-Marie-Tooth disease Type 1A mouse model.

Moss KR, Johnson AE, Bopp TS, Yu AT, Perry K, Chung T, Höke A. Moss KR, et al. J Peripher Nerv Syst. 2022 Mar;27(1):58-66. doi: 10.1111/jns.12483. Epub 2022 Feb 13. J Peripher Nerv Syst. 2022. PMID: 35137510 Free PMC article.

7

Schwann Cells in Neuromuscular Disorders: A Spotlight on Amyotrophic Lateral Sclerosis.

Moss KR, Saxena S. Moss KR, et al. Cells. 2025 Jan 3;14(1):47. doi: 10.3390/cells14010047. Cells. 2025. PMID: 39791748 Free PMC article. Review.

8

hESC- and hiPSC-derived Schwann cells are molecularly comparable and functionally equivalent.

Moss KR, Mi R, Kawaguchi R, Ehmsen JT, Shi Q, Vargas PI, Mukherjee-Clavin B, Lee G, Höke A. Moss KR, et al. iScience. 2024 Apr 30;27(6):109855. doi: 10.1016/j.isci.2024.109855. eCollection 2024 Jun 21. iScience. 2024. PMID: 38770143 Free PMC article.

9

Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes.

Hildebrandt RP, Moss KR, Janusz-Kaminska A, Knudson LA, Denes LT, Saxena T, Boggupalli DP, Li Z, Lin K, Bassell GJ, Wang ET. Hildebrandt RP, et al. Among authors: moss kr. Nat Commun. 2023 Jun 9;14(1):3427. doi: 10.1038/s41467-023-38923-6. Nat Commun. 2023. PMID: 37296096 Free PMC article.

10

A comparative study of admissions to two public sector regional secure units and one independent medium-secure psychiatric hospital.

Moss KR. Moss KR. Med Sci Law. 2000 Jul;40(3):216-22. doi: 10.1177/002580240004000305. Med Sci Law. 2000. PMID: 10976183

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