Côté J - Search Results

1

IGF-1R Reduction Triggers Neuroprotective Signaling Pathways in Spinal Muscular Atrophy Mice.

Biondi O, Branchu J, Ben Salah A, Houdebine L, Bertin L, Chali F, Desseille C, Weill L, Sanchez G, Lancelin C, Aïd S, Lopes P, Pariset C, Lécolle S, Côté J, Holzenberger M, Chanoine C, Massaad C, Charbonnier F. Biondi O, et al. Among authors: cote j. J Neurosci. 2015 Aug 26;35(34):12063-79. doi: 10.1523/JNEUROSCI.0608-15.2015. J Neurosci. 2015. PMID: 26311784 Free PMC article.

2

KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.

Tadesse H, Deschênes-Furry J, Boisvenue S, Côté J. Tadesse H, et al. Among authors: cote j. Hum Mol Genet. 2008 Feb 15;17(4):506-24. doi: 10.1093/hmg/ddm327. Epub 2007 Nov 12. Hum Mol Genet. 2008. PMID: 17998247

3

In vivo NMDA receptor activation accelerates motor unit maturation, protects spinal motor neurons, and enhances SMN2 gene expression in severe spinal muscular atrophy mice.

Biondi O, Branchu J, Sanchez G, Lancelin C, Deforges S, Lopes P, Pariset C, Lécolle S, Côté J, Chanoine C, Charbonnier F. Biondi O, et al. Among authors: cote j. J Neurosci. 2010 Aug 25;30(34):11288-99. doi: 10.1523/JNEUROSCI.1764-10.2010. J Neurosci. 2010. PMID: 20739549 Free PMC article.

4

HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.

Hubers L, Valderrama-Carvajal H, Laframboise J, Timbers J, Sanchez G, Côté J. Hubers L, et al. Among authors: cote j. Hum Mol Genet. 2011 Feb 1;20(3):553-79. doi: 10.1093/hmg/ddq500. Epub 2010 Nov 18. Hum Mol Genet. 2011. PMID: 21088113

5

A novel function for the survival motoneuron protein as a translational regulator.

Sanchez G, Dury AY, Murray LM, Biondi O, Tadesse H, El Fatimy R, Kothary R, Charbonnier F, Khandjian EW, Côté J. Sanchez G, et al. Among authors: cote j. Hum Mol Genet. 2013 Feb 15;22(4):668-84. doi: 10.1093/hmg/dds474. Epub 2012 Nov 6. Hum Mol Genet. 2013. PMID: 23136128

6

A novel role for CARM1 in promoting nonsense-mediated mRNA decay: potential implications for spinal muscular atrophy.

Sanchez G, Bondy-Chorney E, Laframboise J, Paris G, Didillon A, Jasmin BJ, Côté J. Sanchez G, et al. Among authors: cote j. Nucleic Acids Res. 2016 Apr 7;44(6):2661-76. doi: 10.1093/nar/gkv1334. Epub 2015 Dec 9. Nucleic Acids Res. 2016. PMID: 26656492 Free PMC article.

7

Muscle-specific expression of the RNA-binding protein Staufen1 induces progressive skeletal muscle atrophy via regulation of phosphatase tensin homolog.

Crawford Parks TE, Ravel-Chapuis A, Bondy-Chorney E, Renaud JM, Côté J, Jasmin BJ. Crawford Parks TE, et al. Among authors: cote j. Hum Mol Genet. 2017 May 15;26(10):1821-1838. doi: 10.1093/hmg/ddx085. Hum Mol Genet. 2017. PMID: 28369467

8

A novel CARM1-HuR axis involved in muscle differentiation and plasticity misregulated in spinal muscular atrophy.

Ravel-Chapuis A, Haghandish A, Daneshvar N, Jasmin BJ, Côté J. Ravel-Chapuis A, et al. Among authors: cote j. Hum Mol Genet. 2022 May 4;31(9):1453-1470. doi: 10.1093/hmg/ddab333. Hum Mol Genet. 2022. PMID: 34791230

9

Activation of p38 signaling increases utrophin A expression in skeletal muscle via the RNA-binding protein KSRP and inhibition of AU-rich element-mediated mRNA decay: implications for novel DMD therapeutics.

Amirouche A, Tadesse H, Lunde JA, Bélanger G, Côté J, Jasmin BJ. Amirouche A, et al. Among authors: cote j. Hum Mol Genet. 2013 Aug 1;22(15):3093-111. doi: 10.1093/hmg/ddt165. Epub 2013 Apr 10. Hum Mol Genet. 2013. PMID: 23575223

10

Misregulation of calcium-handling proteins promotes hyperactivation of calcineurin-NFAT signaling in skeletal muscle of DM1 mice.

Ravel-Chapuis A, Bélanger G, Côté J, Michel RN, Jasmin BJ. Ravel-Chapuis A, et al. Among authors: cote j. Hum Mol Genet. 2017 Jun 15;26(12):2192-2206. doi: 10.1093/hmg/ddx109. Hum Mol Genet. 2017. PMID: 28369518

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