S. Tremblay

发表

É. Khandjian, E. Bechara, L. Davidovic, 2006, Nucleic acids research.

HCaRG increases renal cell migration by a TGF-α autocrine loop mechanism

S. Tremblay, C. Hader, N. Solban, 2005 .

HCaRG increases renal cell migration by a TGF-alpha autocrine loop mechanism.

S. Tremblay, N. Solban, D. Gingras, 2005, American journal of physiology. Renal physiology.

Progesterone receptors regulate gallbladder motility.

G. Fried, S. Tremblay, F. Hould, 1988, The Journal of surgical research.

RNA Granules: Functions within Presynaptic Terminals and Postsynaptic Spines

É. Khandjian, L. Davidovic, S. Tremblay, 2009 .

Nuclear Fragile X Mental Retardation Protein Is localized to Cajal Bodies

P. De Koninck, É. Khandjian, J. Côté, 2013, PLoS genetics.

Genetic testing for amyotrophic lateral sclerosis in Canada – an assessment of current practices

A. Izenberg, S. Tremblay, C. O'Connell, 2021, Amyotrophic lateral sclerosis & frontotemporal degeneration.

A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture.

J. Mandel, S. Tremblay, E. W. Khandjian, 1995, Human molecular genetics.

Fibronectin gene expression in proliferating, quiescent, and SV40-infected mouse kidney cells.

S. Tremblay, E. W. Khandjian, H. Türler, 1992, Experimental cell research.

The fragile X mental retardation protein has nucleic acid chaperone properties.

É. Khandjian, S. Tremblay, C. Gabus, 2004, Nucleic acids research.

HCaRG increases renal cell migration by a TGF- (cid:1) autocrine loop mechanism

S. Tremblay, C. Hader, N. Solban, 2005 .

Successful use of long-term frozen lymphocytes for the establishment of lymphoblastoid cell lines.

S. Tremblay, E. W. Khandjian, É. W. Khandjian, 1998, Clinical biochemistry.

The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.

É. Khandjian, L. Davidovic, S. Tremblay, 2007, Human molecular genetics.

Fragile X mental retardation protein : To be or not to be a translational repressor

É. Khandjian, S. Tremblay, P. Koninck, 2005 .

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

É. Khandjian, S. Tremblay, Y. Labelle, 2002, Human molecular genetics.

HCaRG is a novel regulator of renal epithelial cell growth and differentiation causing G2M arrest.

W. Schürch, S. Tremblay, N. Solban, 2003, American journal of physiology. Renal physiology.

Dicer-Derived MicroRNAs Are Utilized by the Fragile X Mental Retardation Protein for Assembly on Target RNAs

É. Khandjian, L. Davidovic, S. Tremblay, 2006, Journal of biomedicine & biotechnology.

Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules

P. De Koninck, É. Khandjian, L. Davidovic, 2016, PLoS genetics.

10th International Symposium on SHR and Molecular Medicine¶May 2 – 4, 2001, Berlin-Buch

K. Fuxe, Z. Díaz-Cabiale, E. Lakatta, 2001, Journal of Molecular Medicine.

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

É. Khandjian, S. Tremblay, Y. Labelle, 2003, Human molecular genetics.

Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles.

É. Khandjian, L. Davidovic, S. Tremblay, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Mapping of quantitative trait loci (QTL) of differential stress gene expression in rat recombinant inbred strains

Z. Pausova, S. Tremblay, P. Hamet, 2000, Journal of hypertension.

Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome

I. Krantz, Soma Das, S. Tremblay, 2017, Journal of Human Genetics.

Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome

I. Krantz, Soma Das, S. Tremblay, 2018, Journal of Human Genetics.

Hormonal Regulation of Estradiol 17β‐Hydroxysteroid Dehydrogenase Activity in the ZR‐75‐1 Human Breast Cancer Cell Line

S. Tremblay, D. Poirier, F. Labrie, 1990 .

É. Khandjian, D. Radzioch, S. Tremblay, 2011, PloS one.

Correction: Fragile Mental Retardation Protein Interacts with the RNA-Binding Protein Caprin1 in Neuronal RiboNucleoProtein Complexes

P. De Koninck, É. Khandjian, S. Tremblay, 2012, PLoS ONE.

Fragile Mental Retardation Protein Interacts with the RNA-Binding Protein Caprin1 in Neuronal RiboNucleoProtein Complexes

P. De Koninck, É. Khandjian, S. Tremblay, 2012, PloS one.

Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.

É. Khandjian, J. Mandel, S. Tremblay, 1998, Human molecular genetics.

HCaRG, a Novel Calcium-regulated Gene Coding for a Nuclear Protein, Is Potentially Involved in the Regulation of Cell Proliferation*

S. Tremblay, N. Solban, P. Hamet, 2000, The Journal of Biological Chemistry.

[The fragile X syndrome: one protein missing and 1001 disoriented mRNAs].

P. De Koninck, L. Davidovic, S. Tremblay, 2006, Medecine sciences : M/S.

The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.

L. Davidovic, S. Tremblay, B. Bardoni, 2006, Human molecular genetics.