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Items: 9

1.

Transcriptional regulation of mouse hypoglossal motor neuron somatotopic map formation.

Chen X, Wang JW, Salin-Cantegrel A, Dali R, Stifani S.

Brain Struct Funct. 2016 Nov;221(8):4187-4202. Epub 2015 Dec 19.

PMID:
26687503
2.

Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics.

Salin-Cantegrel A, Shekarabi M, Rasheed S, Charron FM, Laganière J, Gaudet R, Dion PA, Lapointe JY, Rouleau GA.

PLoS One. 2013 May 28;8(5):e65294. doi: 10.1371/journal.pone.0065294. Print 2013.

3.

Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum.

Shekarabi M, Moldrich RX, Rasheed S, Salin-Cantegrel A, Laganière J, Rochefort D, Hince P, Huot K, Gaudet R, Kurniawan N, Sotocinal SG, Ritchie J, Dion PA, Mogil JS, Richards LJ, Rouleau GA.

J Neurosci. 2012 Mar 14;32(11):3865-76. doi: 10.1523/JNEUROSCI.3679-11.2012.

4.

Establishment of motor neuron-V3 interneuron progenitor domain boundary in ventral spinal cord requires Groucho-mediated transcriptional corepression.

Todd KJ, Lan-Chow-Wing N, Salin-Cantegrel A, Cotter A, Zagami CJ, Lo R, Stifani S.

PLoS One. 2012;7(2):e31176. doi: 10.1371/journal.pone.0031176. Epub 2012 Feb 17.

5.

Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum.

Salin-Cantegrel A, Rivière JB, Shekarabi M, Rasheed S, Dacal S, Laganière J, Gaudet R, Rochefort D, Lesca G, Gaspar C, Dion PA, Lapointe JY, Rouleau GA.

J Biol Chem. 2011 Aug 12;286(32):28456-65. doi: 10.1074/jbc.M111.226894. Epub 2011 May 31.

6.

Cellular expression of the K+-Cl- cotransporter KCC3 in the central nervous system of mouse.

Shekarabi M, Salin-Cantegrel A, Laganière J, Gaudet R, Dion P, Rouleau GA.

Brain Res. 2011 Feb 16;1374:15-26. doi: 10.1016/j.brainres.2010.12.010. Epub 2010 Dec 11.

PMID:
21147077
7.

HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3.

Salin-Cantegrel A, Shekarabi M, Holbert S, Dion P, Rochefort D, Laganière J, Dacal S, Hince P, Karemera L, Gaspar C, Lapointe JY, Rouleau GA.

Hum Mol Genet. 2008 Sep 1;17(17):2703-11. doi: 10.1093/hmg/ddn172. Epub 2008 Jun 19.

PMID:
18566107
8.

Distal truncation of KCC3 in non-French Canadian HMSN/ACC families.

Salin-Cantegrel A, Rivière JB, Dupré N, Charron FM, Shekarabi M, Karéméra L, Gaspar C, Horst J, Tekin M, Deda G, Krause A, Lippert MM, Willemsen MA, Jarrar R, Lapointe JY, Rouleau GA.

Neurology. 2007 Sep 25;69(13):1350-5.

PMID:
17893295
9.

FoxO1a-cyclic GMP-dependent kinase I interactions orchestrate myoblast fusion.

Bois PR, Brochard VF, Salin-Cantegrel AV, Cleveland JL, Grosveld GC.

Mol Cell Biol. 2005 Sep;25(17):7645-56.

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