Toulouse A - Search Results

1

Lack of association between the hSKCa3 channel gene CAG polymorphism and schizophrenia.

Joober R, Benkelfat C, Brisebois K, Toulouse A, Lafrenière RG, Turecki G, Lal S, Bloom D, Labelle A, Lalonde P, Fortin D, Alda M, Palmour R, Rouleau GA. Joober R, et al. Among authors: toulouse a. Am J Med Genet. 1999 Apr 16;88(2):154-7. Am J Med Genet. 1999. PMID: 10206235

2

T102C polymorphism in the 5HT2A gene and schizophrenia: relation to phenotype and drug response variability.

Joober R, Benkelfat C, Brisebois K, Toulouse A, Turecki G, Lal S, Bloom D, Labelle A, Lalonde P, Fortin D, Alda M, Palmour R, Rouleau GA. Joober R, et al. Among authors: toulouse a. J Psychiatry Neurosci. 1999 Mar;24(2):141-6. J Psychiatry Neurosci. 1999. PMID: 10212557 Free PMC article.

3

Analysis of 14 CAG repeat-containing genes in schizophrenia.

Joober R, Benkelfat C, Toulouse A, Lafrenière RG, Lal S, Ajroud S, Turecki G, Bloom D, Labelle A, Lalonde P, Alda M, Morgan K, Palmour R, Rouleau GA. Joober R, et al. Among authors: toulouse a. Am J Med Genet. 1999 Dec 15;88(6):694-9. Am J Med Genet. 1999. PMID: 10581491

4

DRD3 and DAT1 genes in schizophrenia: an association study.

Joober R, Toulouse A, Benkelfat C, Lal S, Bloom D, Labelle A, Lalonde P, Turecki G, Rouleau GA. Joober R, et al. Among authors: toulouse a. J Psychiatr Res. 2000 Jul-Oct;34(4-5):285-91. doi: 10.1016/s0022-3956(00)00018-2. J Psychiatr Res. 2000. PMID: 11104840

5

Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.

Toulouse A, Rochefort D, Roussel J, Joober R, Rouleau GA. Toulouse A, et al. Genomics. 2003 Aug;82(2):162-71. doi: 10.1016/s0888-7543(03)00101-0. Genomics. 2003. PMID: 12837267

6

Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.

Toulouse A, Au-Yeung F, Gaspar C, Roussel J, Dion P, Rouleau GA. Toulouse A, et al. Hum Mol Genet. 2005 Sep 15;14(18):2649-60. doi: 10.1093/hmg/ddi299. Epub 2005 Aug 8. Hum Mol Genet. 2005. PMID: 16087686

7

Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II.

Shekarabi M, Girard N, Rivière JB, Dion P, Houle M, Toulouse A, Lafrenière RG, Vercauteren F, Hince P, Laganiere J, Rochefort D, Faivre L, Samuels M, Rouleau GA. Shekarabi M, et al. Among authors: toulouse a. J Clin Invest. 2008 Jul;118(7):2496-505. doi: 10.1172/JCI34088. J Clin Invest. 2008. PMID: 18521183 Free PMC article.

8

Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice.

Dion P, Shanmugam V, Gaspar C, Messaed C, Meijer I, Toulouse A, Laganiere J, Roussel J, Rochefort D, Laganiere S, Allen C, Karpati G, Bouchard JP, Brais B, Rouleau GA. Dion P, et al. Among authors: toulouse a. Neurobiol Dis. 2005 Apr;18(3):528-36. doi: 10.1016/j.nbd.2004.09.021. Neurobiol Dis. 2005. PMID: 15755680

9

Allelic methylation bias of the RARB2 tumor suppressor gene promoter in cancer.

Pappas JJ, Toulouse A, Hébert J, Fetni R, Bradley WE. Pappas JJ, et al. Among authors: toulouse a. Genes Chromosomes Cancer. 2008 Nov;47(11):978-93. doi: 10.1002/gcc.20603. Genes Chromosomes Cancer. 2008. PMID: 18663751

10

RARbeta2 specificity in mediating RA inhibition of growth of lung cancer-derived cells.

Toulouse A, Morin J, Dion PA, Houle B, Bradley WE. Toulouse A, et al. Lung Cancer. 2000 May;28(2):127-37. doi: 10.1016/s0169-5002(99)00122-1. Lung Cancer. 2000. PMID: 10717330

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