Labelle Y - Search Results

1

Characterization of the human fumarylacetoacetate hydrolase gene and identification of a missense mutation abolishing enzymatic activity.

Labelle Y, Phaneuf D, Leclerc B, Tanguay RM. Labelle Y, et al. Hum Mol Genet. 1993 Jul;2(7):941-6. doi: 10.1093/hmg/2.7.941. Hum Mol Genet. 1993. PMID: 8364576

2

Cloning and expression analysis of a cDNA encoding fumarylacetoacetate hydrolase: post-transcriptional modulation in rat liver and kidney.

Labelle Y, Phaneuf D, Tanguay RM. Labelle Y, et al. Gene. 1991 Aug 15;104(2):197-202. doi: 10.1016/0378-1119(91)90250-f. Gene. 1991. PMID: 1916290

3

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15.

Phaneuf D, Labelle Y, Bérubé D, Arden K, Cavenee W, Gagné R, Tanguay RM. Phaneuf D, et al. Among authors: labelle y. Am J Hum Genet. 1991 Mar;48(3):525-35. Am J Hum Genet. 1991. PMID: 1998338 Free PMC article.

4

Localization of cells in the rat brain expressing fumarylacetoacetate hydrolase, the deficient enzyme in hereditary tyrosinemia type 1.

Labelle Y, Puymirat J, Tanguay RM. Labelle Y, et al. Biochim Biophys Acta. 1993 Jan 22;1180(3):250-6. doi: 10.1016/0925-4439(93)90046-4. Biochim Biophys Acta. 1993. PMID: 8422430

5

Assessment of the prevalence of the 985A>G MCAD mutation in the French-Canadian population using allele-specific PCR.

Giroux S, Dubé-Linteau A, Cardinal G, Labelle Y, Laflamme N, Giguère Y, Rousseau F. Giroux S, et al. Among authors: labelle y. Clin Genet. 2007 Jun;71(6):569-75. doi: 10.1111/j.1399-0004.2007.00809.x. Clin Genet. 2007. PMID: 17539907

6

Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression.

Mazroui R, Huot ME, Tremblay S, Filion C, Labelle Y, Khandjian EW. Mazroui R, et al. Among authors: labelle y. Hum Mol Genet. 2002 Nov 15;11(24):3007-17. doi: 10.1093/hmg/11.24.3007. Hum Mol Genet. 2002. PMID: 12417522

7

Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.

Mazroui R, Huot ME, Tremblay S, Boilard N, Labelle Y, Khandjian EW. Mazroui R, et al. Among authors: labelle y. Hum Mol Genet. 2003 Dec 1;12(23):3087-96. doi: 10.1093/hmg/ddg335. Epub 2003 Oct 7. Hum Mol Genet. 2003. PMID: 14532325

8

Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation.

Labelle Y, Zucman J, Stenman G, Kindblom LG, Knight J, Turc-Carel C, Dockhorn-Dworniczak B, Mandahl N, Desmaze C, Peter M, et al. Labelle Y, et al. Hum Mol Genet. 1995 Dec;4(12):2219-26. doi: 10.1093/hmg/4.12.2219. Hum Mol Genet. 1995. PMID: 8634690

9

Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.

Laflamme C, Filion C, Labelle Y. Laflamme C, et al. Among authors: labelle y. Hum Mutat. 2004 Dec;24(6):502-8. doi: 10.1002/humu.20102. Hum Mutat. 2004. PMID: 15523651

10

The PLAGL1 gene is down-regulated in human extraskeletal myxoid chondrosarcoma tumors.

Poulin H, Labelle Y. Poulin H, et al. Among authors: labelle y. Cancer Lett. 2005 Sep 28;227(2):185-91. doi: 10.1016/j.canlet.2004.12.007. Epub 2005 Jan 8. Cancer Lett. 2005. PMID: 16112421

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