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Items: 20

1.

Straightjacket/α2δ3 deregulation is associated with cardiac conduction defects in myotonic dystrophy type 1.

Auxerre-Plantié E, Nakamori M, Renaud Y, Huguet A, Choquet C, Dondi C, Miquerol L, Takahashi MP, Gourdon G, Junion G, Jagla T, Zmojdzian M, Jagla K.

Elife. 2019 Dec 12;8. pii: e51114. doi: 10.7554/eLife.51114.

2.

Bruno-3 regulates sarcomere component expression and contributes to muscle phenotypes of myotonic dystrophy type 1.

Picchio L, Legagneux V, Deschamps S, Renaud Y, Chauveau S, Paillard L, Jagla K.

Dis Model Mech. 2018 May 21;11(5). pii: dmm031849. doi: 10.1242/dmm.031849.

3.

TRAP-rc, Translating Ribosome Affinity Purification from Rare Cell Populations of Drosophila Embryos.

Bertin B, Renaud Y, Aradhya R, Jagla K, Junion G.

J Vis Exp. 2015 Sep 10;(103). doi: 10.3791/52985.

4.

Drosophila small heat shock protein CryAB ensures structural integrity of developing muscles, and proper muscle and heart performance.

Wójtowicz I, Jabłońska J, Zmojdzian M, Taghli-Lamallem O, Renaud Y, Junion G, Daczewska M, Huelsmann S, Jagla K, Jagla T.

Development. 2015 Mar 1;142(5):994-1005. doi: 10.1242/dev.115352.

5.

Development of a broad-based ADME panel for use in pharmacogenomic studies.

Brown AM, Renaud Y, Ross C, Hansen M, Mongrain I, Valois D, Carleton BC, Hayden MR, Dubé MP, Tardif JC, Phillips MS.

Pharmacogenomics. 2014 Jun;15(9):1185-95. doi: 10.2217/pgs.14.81.

PMID:
25141894
6.

Transcriptional properties and splicing of the flamenco piRNA cluster.

Goriaux C, Desset S, Renaud Y, Vaury C, Brasset E.

EMBO Rep. 2014 Apr;15(4):411-8. doi: 10.1002/embr.201337898. Epub 2014 Feb 20.

7.

Novel Drosophila model of myotonic dystrophy type 1: phenotypic characterization and genome-wide view of altered gene expression.

Picchio L, Plantie E, Renaud Y, Poovthumkadavil P, Jagla K.

Hum Mol Genet. 2013 Jul 15;22(14):2795-810. doi: 10.1093/hmg/ddt127. Epub 2013 Mar 21.

PMID:
23525904
8.

DroPNet: a web portal for integrated analysis of Drosophila protein-protein interaction networks.

Renaud Y, Baillif A, Perez JB, Agier M, Mephu Nguifo E, Mirouse V.

Nucleic Acids Res. 2012 Jul;40(Web Server issue):W134-9. doi: 10.1093/nar/gks434. Epub 2012 May 27.

9.

Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis.

Villani AC, Lemire M, Louis E, Silverberg MS, Collette C, Fortin G, Nimmo ER, Renaud Y, Brunet S, Libioulle C, Belaiche J, Bitton A, Gaudet D, Cohen A, Langelier D, Rioux JD, Arnott ID, Wild GE, Rutgeerts P, Satsangi J, Vermeire S, Hudson TJ, Franchimont D.

PLoS One. 2009 Sep 28;4(9):e7154. doi: 10.1371/journal.pone.0007154.

10.

Performance of commercial platforms for rapid genotyping of polymorphisms affecting warfarin dose.

King CR, Porche-Sorbet RM, Gage BF, Ridker PM, Renaud Y, Phillips MS, Eby C.

Am J Clin Pathol. 2008 Jun;129(6):876-83. doi: 10.1309/1E34UAPR06PJ6HML.

PMID:
18480003
11.

Combination of phenotype assessments and CYP2C9-VKORC1 polymorphisms in the determination of warfarin dose requirements in heavily medicated patients.

Michaud V, Vanier MC, Brouillette D, Roy D, Verret L, Noel N, Taillon I, O'Hara G, Gossard D, Champagne M, Goodman K, Renaud Y, Brown A, Phillips M, Ajami AM, Turgeon J.

Clin Pharmacol Ther. 2008 May;83(5):740-8. Epub 2007 Nov 14.

PMID:
18030307
12.

Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.

Engert JC, Lemire M, Faith J, Brisson D, Fujiwara TM, Roslin NM, Brewer CG, Montpetit A, Darmond-Zwaig C, Renaud Y, Doré C, Bailey SD, Verner A, Tremblay G, St-Pierre J, Bétard C, Platko J, Rioux JD, Morgan K, Hudson TJ, Gaudet D.

Eur J Hum Genet. 2008 Jan;16(1):105-14. Epub 2007 Sep 5.

13.

The need for recurring funding of SUS nursing schools: a FLU student's perspective.

Renaud Y.

Fla Nurse. 2006 Sep;54(3):11-2. No abstract available.

PMID:
17112098
14.

Association study between the CX3CR1 gene and asthma.

Tremblay K, Lemire M, Provost V, Pastinen T, Renaud Y, Sandford AJ, Laviolette M, Hudson TJ, Laprise C.

Genes Immun. 2006 Dec;7(8):632-9. Epub 2006 Nov 2.

PMID:
17082760
15.

The molecular basis of glutamate formiminotransferase deficiency.

Hilton JF, Christensen KE, Watkins D, Raby BA, Renaud Y, de la Luna S, Estivill X, MacKenzie RE, Hudson TJ, Rosenblatt DS.

Hum Mutat. 2003 Jul;22(1):67-73. Erratum in: Hum Mutat. 2003 Nov;22(5):416.

PMID:
12815595
16.

Polymorphisms in toll-like receptor 4 are not associated with asthma or atopy-related phenotypes.

Raby BA, Klimecki WT, Laprise C, Renaud Y, Faith J, Lemire M, Greenwood C, Weiland KM, Lange C, Palmer LJ, Lazarus R, Vercelli D, Kwiatkowski DJ, Silverman EK, Martinez FD, Hudson TJ, Weiss ST.

Am J Respir Crit Care Med. 2002 Dec 1;166(11):1449-56. Epub 2002 Sep 25.

PMID:
12406828
17.

5' flanking variants of resistin are associated with obesity.

Engert JC, Vohl MC, Williams SM, Lepage P, Loredo-Osti JC, Faith J, Doré C, Renaud Y, Burtt NP, Villeneuve A, Hirschhorn JN, Altshuler D, Groop LC, Després JP, Gaudet D, Hudson TJ.

Diabetes. 2002 May;51(5):1629-34.

18.

[Facial vascular pain and sympathalgia. Therapeutic trial].

Renaud Y, Herbouiller M, Lajat Y.

Rev Stomatol Chir Maxillofac. 1984;85(3):189-92. French.

PMID:
6588457
19.

[Cylindroma of the oral cavity (11 cases)].

Renaud Y, Delaire J, Gaillard A, Billet J, Leroux MJ.

Rev Stomatol Chir Maxillofac. 1973 Jan;74(1):1-19. French. No abstract available.

PMID:
4351708
20.

[Synopsis of a case of sub-mandibular thyroid goiter].

Delaire J, Billet J, Renaud Y.

Rev Stomatol Chir Maxillofac. 1967 Dec;68(8):646-50. French. No abstract available.

PMID:
5242965

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