Forestier L - Search Results

1

Deep intronic mutation and pseudo exon activation as a novel muscular hypertrophy modifier in cattle.

Bouyer C, Forestier L, Renand G, Oulmouden A. Bouyer C, et al. Among authors: forestier l. PLoS One. 2014 May 14;9(5):e97399. doi: 10.1371/journal.pone.0097399. eCollection 2014. PLoS One. 2014. PMID: 24827585 Free PMC article.

2

The Blonde d'Aquitaine T3811>G3811 mutation in the myostatin gene: association with growth, carcass, and muscle phenotypes in veal calves.

Vinet A, Bouyer C, Forestier L, Oulmouden A, Blanquet V, Picard B, Cassar-Malek I, Bonnet M, Rocha D, Renand G. Vinet A, et al. Among authors: forestier l. J Anim Sci. 2021 Feb 1;99(2):skab039. doi: 10.1093/jas/skab039. J Anim Sci. 2021. PMID: 33624102 Free PMC article.

3

A composite six bp in-frame deletion in the melanocortin 1 receptor (MC1R) gene is associated with the Japanese brindling coat colour in rabbits (Oryctolagus cuniculus).

Fontanesi L, Scotti E, Colombo M, Beretti F, Forestier L, Dall'Olio S, Deretz S, Russo V, Allain D, Oulmouden A. Fontanesi L, et al. Among authors: forestier l. BMC Genet. 2010 Jul 1;11:59. doi: 10.1186/1471-2156-11-59. BMC Genet. 2010. PMID: 20594318 Free PMC article.

4

Characterization of the rabbit agouti signaling protein (ASIP) gene: transcripts and phylogenetic analyses and identification of the causative mutation of the nonagouti black coat colour.

Fontanesi L, Forestier L, Allain D, Scotti E, Beretti F, Deretz-Picoulet S, Pecchioli E, Vernesi C, Robinson TJ, Malaney JL, Russo V, Oulmouden A. Fontanesi L, et al. Among authors: forestier l. Genomics. 2010 Mar;95(3):166-75. doi: 10.1016/j.ygeno.2009.11.003. Epub 2009 Dec 11. Genomics. 2010. PMID: 20004240 Free article.

5

Characterization of the bovine PRKAG3 gene: structure, polymorphism, and alternative transcripts.

Roux M, Nizou A, Forestier L, Ouali A, Levéziel H, Amarger V. Roux M, et al. Among authors: forestier l. Mamm Genome. 2006 Jan;17(1):83-92. doi: 10.1007/s00335-005-0093-0. Epub 2006 Jan 13. Mamm Genome. 2006. PMID: 16416094

6

PHEX^L222P Mutation Increases Phex Expression in a New ENU Mouse Model for XLH Disease.

El Hakam C, Parenté A, Baraige F, Magnol L, Forestier L, Di Meo F, Blanquet V. El Hakam C, et al. Among authors: forestier l. Genes (Basel). 2022 Jul 28;13(8):1356. doi: 10.3390/genes13081356. Genes (Basel). 2022. PMID: 36011266 Free PMC article.

7

Glycosylation-related gene expression profiling in the brain and spleen of scrapie-affected mouse.

Guillerme-Bosselut F, Forestier L, Jayat-Vignoles C, Vilotte JL, Popa I, Portoukalian J, Le Dur A, Laude H, Julien R, Gallet PF. Guillerme-Bosselut F, et al. Among authors: forestier l. Glycobiology. 2009 Aug;19(8):879-89. doi: 10.1093/glycob/cwp062. Epub 2009 Apr 22. Glycobiology. 2009. PMID: 19386898

8

Identification and characterisation of the murine homologue of the gene responsible for cystinosis, Ctns.

Cherqui S, Kalatzis V, Forestier L, Poras I, Antignac C. Cherqui S, et al. Among authors: forestier l. BMC Genomics. 2000;1:2. doi: 10.1186/1471-2164-1-2. Epub 2000 Dec 6. BMC Genomics. 2000. PMID: 11121245 Free PMC article.

9

Glycosylation-related gene expression in prion diseases: PrPSc accumulation in scrapie infected GT1 cells depends on beta-1,4-linked GalNAc-4-SO4 hyposulfation.

Barret A, Forestier L, Deslys JP, Julien R, Gallet PF. Barret A, et al. Among authors: forestier l. J Biol Chem. 2005 Mar 18;280(11):10516-23. doi: 10.1074/jbc.M412635200. Epub 2005 Jan 4. J Biol Chem. 2005. PMID: 15632154 Free article.

10

Butyrate regulation of glycosylation-related gene expression: evidence for galectin-1 upregulation in human intestinal epithelial goblet cells.

Gaudier E, Forestier L, Gouyer V, Huet G, Julien R, Hoebler C. Gaudier E, et al. Among authors: forestier l. Biochem Biophys Res Commun. 2004 Dec 17;325(3):1044-51. doi: 10.1016/j.bbrc.2004.10.141. Biochem Biophys Res Commun. 2004. PMID: 15541394

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