Lynch-Godrei A - Search Results

1

Disruption in the autophagic process underlies the sensory neuropathy in dystonia musculorum mice.

Ferrier A, De Repentigny Y, Lynch-Godrei A, Gibeault S, Eid W, Kuo D, Zha X, Kothary R. Ferrier A, et al. Autophagy. 2015;11(7):1025-36. doi: 10.1080/15548627.2015.1052207. Autophagy. 2015. PMID: 26043942 Free PMC article.

2

Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.

Ferrier A, Sato T, De Repentigny Y, Gibeault S, Bhanot K, O'Meara RW, Lynch-Godrei A, Kornfeld SF, Young KG, Kothary R. Ferrier A, et al. Hum Mol Genet. 2014 May 15;23(10):2694-710. doi: 10.1093/hmg/ddt663. Epub 2013 Dec 30. Hum Mol Genet. 2014. PMID: 24381311 Free PMC article.

3

Functional and Genetic Analysis of Neuronal Isoforms of BPAG1.

Lynch-Godrei A, Kothary R. Lynch-Godrei A, et al. Methods Enzymol. 2016;569:355-72. doi: 10.1016/bs.mie.2015.05.004. Epub 2015 Jun 1. Methods Enzymol. 2016. PMID: 26778567 Review.

4

Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS Myelination.

Kornfeld SF, Lynch-Godrei A, Bonin SR, Gibeault S, De Repentigny Y, Kothary R. Kornfeld SF, et al. Among authors: lynch godrei a. PLoS One. 2016 Feb 17;11(2):e0149201. doi: 10.1371/journal.pone.0149201. eCollection 2016. PLoS One. 2016. PMID: 26886550 Free PMC article.

5

Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.

Lynch-Godrei A, De Repentigny Y, Gagnon S, Trung MT, Kothary R. Lynch-Godrei A, et al. Hum Mol Genet. 2018 Oct 15;27(20):3598-3611. doi: 10.1093/hmg/ddy250. Hum Mol Genet. 2018. PMID: 29982604

6

Characterization of gastrointestinal pathologies in the dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.

Lynch-Godrei A, De Repentigny Y, Yaworski RA, Gagnon S, Butcher J, Manoogian J, Stintzi A, Kothary R. Lynch-Godrei A, et al. Neurogastroenterol Motil. 2020 Apr;32(4):e13773. doi: 10.1111/nmo.13773. Epub 2019 Dec 9. Neurogastroenterol Motil. 2020. PMID: 31814231

7

HSAN-VI: A spectrum disorder based on dystonin isoform expression.

Lynch-Godrei A, Kothary R. Lynch-Godrei A, et al. Neurol Genet. 2020 Jan 2;6(1):e389. doi: 10.1212/NXG.0000000000000389. eCollection 2020 Feb. Neurol Genet. 2020. PMID: 32042917 Free PMC article.

8

Dystonin loss-of-function leads to impaired autophagosome-endolysosome pathway dynamics.

Lynch-Godrei A, Repentigny Y, Ferrier A, Gagnon S, Kothary R. Lynch-Godrei A, et al. Biochem Cell Biol. 2021 Jun;99(3):364-373. doi: 10.1139/bcb-2020-0557. Epub 2020 Dec 21. Biochem Cell Biol. 2021. PMID: 33347391

9

Providing Home-Based Support for Children with Chronic Conditions in an Urban Slum: Experiences from a Community-Based Palliative Care Program in Bangladesh.

Chowdhury MK, Shopna K, Lynch-Godrei A, Jain M, Farheen N, Begum N, Ahmad N, Doherty M. Chowdhury MK, et al. Among authors: lynch godrei a. Glob Pediatr Health. 2021 Mar 24;8:2333794X21999155. doi: 10.1177/2333794X21999155. eCollection 2021. Glob Pediatr Health. 2021. PMID: 33816710 Free PMC article.

10

interRAI Pediatric Home Care (PEDS-HC) Assessment Tool: Evaluating Ontario Healthcare Workers' Experience.

Lynch-Godrei A, Doherty M, Vadeboncoeur C. Lynch-Godrei A, et al. Health Serv Insights. 2022 Mar 25;15:11786329221078124. doi: 10.1177/11786329221078124. eCollection 2022. Health Serv Insights. 2022. PMID: 35360089 Free PMC article.

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