Publications | Centre de recherche CERVO

Export 12 results:

Filtres: Keyword is Ribonucleoproteins [Enlever les filtres]

2015

Yue Y, Castrichini M, Srivastava U, Fabris F, Shah K, Li Z, Qu Y, El-Sherif N, Zhou Z, January C, M Hussain M, Jiang X-, Sobie EA, Wahren-Herlenius M, Chahine M, Capecchi P-, Laghi-Pasini F, Lazzerini P-, Boutjdir M. Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome. Circulation. 2015;132(4):230-40.

2013

Dury AY, Fatimy RE, Tremblay S, Rose TM, Côté J, De Koninck P, Khandjian EW. Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies. PLoS Genet. 2013;9(10):e1003890.

Sanchez G, Dury AY, Murray LM, Biondi O, Tadesse H, Fatimy RE, Kothary R, Charbonnier F, Khandjian EW, Côté J. A novel function for the survival motoneuron protein as a translational regulator. Hum Mol Genet. 2013;22(4):668-84.

2012

Sephton CF, Cenik B, Cenik BK, Herz J, Yu G. TDP-43 in central nervous system development and function: clues to TDP-43-associated neurodegeneration. Biol Chem. 2012;393(7):589-94.

Fatimy RE, Tremblay S, Dury AY, Solomon S, De Koninck P, Schrader JW, Khandjian EW. Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. PLoS ONE. 2012;7(6):e39338.

2006

Davidovic L, Bechara E, Gravel M, Jaglin XH, Tremblay S, Sík A, Bardoni B, Khandjian EW. The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons. Hum Mol Genet. 2006;15(9):1525-38.

2005

Davidovic L, Huot M-, Khandjian EW. Lost once, the Fragile X Mental Retardation protein is now back onto brain polyribosomes. RNA Biol. 2005;2(1):1-3.

2004

Khandjian EW, Huot M-, Tremblay S, Davidovic L, Mazroui R, Bardoni B. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles. Proc Natl Acad Sci USA. 2004;101(36):13357-62.

2003

Mazroui R, Huot M-, Tremblay S, Boilard N, Labelle Y, Khandjian EW. Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs. Hum Mol Genet. 2003;12(23):3087-96.

1998

Khandjian EW, Bardoni B, Corbin F, Sittler A, Giroux S, Heitz D, Tremblay S, Pinset C, Montarras D, Rousseau F, Mandel J. Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis. Hum Mol Genet. 1998;7(13):2121-8.

1997

Drouin R, Angers M, Dallaire N, Rose TM, Khandjian EW, Rousseau F. Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region. Hum Mol Genet. 1997;6(12):2051-60.

1976

Khandjian EW, Turian G. Release of RNA--DNA-protein complex during differentiation of the water mould Allomyces arbuscula. Cell Differ. 1976;5(3):171-88.

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