E-LIB Suche - Ergebnisse für: Belzil, Anne

1

New proteins in the rat CYP2B subfamily: Presence in liver ..:

Desrochers, Marc ; Christou, Maro ; Jefcoate, Colin..
Biochemical Pharmacology. 52 (1996) 8 - p. 1311-1319 , 1996

Link: https://doi.org/10.1016/..

2

Localization of a phenobarbital-responsive element (PBRE) i..:

Trottier, Eric ; Belzil, Anne ; Stoltz, Catherine.
Gene. 158 (1995) 2 - p. 263-268 , 1995

Link: https://doi.org/10.1016/..

3

Potential of Skin Fibroblasts for Application to Anterior C..:

Tremblay, Pierrot ; Cloutier, Réjean ; Lamontagne, Jean...
Cell Transplantation. 20 (2011) 4 - p. 535-542 , 2011

Link: https://doi.org/10.3727/..

4

Torn ACL: a new bioengineered substitute brought from the l..:

Goulet, Francine ; Rancourt, Denis ; Cloutier, Réjean...
Applied Bionics and Biomechanics. 1 (2004) 2 - p. 115-121 , 2004

Link: https://doi.org/10.1533/..

5

Torn ACL: A New Bioengineered Substitute Brought from the L..:

Goulet, Francine ; Rancourt, Denis ; Cloutier, Réjean...
Applied Bionics and Biomechanics. 1 (2004) 2 - p. 115-121 , 2004

Link: https://doi.org/10.1155/..

6

Potential of Skin Fibroblasts for Application to Anterior C..:

Pierrot Tremblay ; Réjean Cloutier ; Jean Lamontagne...
https://doi.org/10.3727/096368910X536482. , 2011

Link: https://doi.org/10.3727/..

7

Torn ACL: A New Bioengineered Substitute Brought from the L..:

Francine Goulet ; Denis Rancourt ; Réjean Cloutier...
http://dx.doi.org/10.3233/ABB-2004-9693535. , 2004

Link: https://doi.org/10.3233/..

8

Exome Sequencing IdentifiesFUSMutations as a Cause of Essen..:

Dupre, Nicolas ; Merner, Nancy ; Girard, Simon...
Neurology. 80 (2013) 7_supplement - p. , 2013

Link: https://doi.org/10.1212/..

9

Exome sequencing reveals SPG11 mutations causing juvenile A..:

Daoud, Hussein ; Zhou, Sirui ; Noreau, Anne...
Neurobiology of Aging. 33 (2012) 4 - p. 839.e5-839.e9 , 2012

Link: https://doi.org/10.1016/..

10

Deleterious mutations in the essential mRNA metabolism fact..:

Kaneb, Hannah M. ; Folkmann, Andrew W. ; Belzil, Véronique V....
Human Molecular Genetics. 24 (2014) 5 - p. 1363-1373 , 2014

Link: https://doi.org/10.1093/..

11

Analysis of OPTN as a causative gene for amyotrophic latera..:

Belzil, Véronique V. ; Daoud, Hussein ; Desjarlais, Anne...
Neurobiology of Aging. 32 (2011) 3 - p. 555.e13-555.e14 , 2011

Link: https://doi.org/10.1016/..

12

Identification of a FUS splicing mutation in a large family..:

Belzil, Véronique V ; St-Onge, Judith ; Daoud, Hussein...
Journal of Human Genetics. 56 (2010) 3 - p. 247-249 , 2010

Link: https://doi.org/10.1038/..

13

Deleterious mutations in the essential mRNA metabolism fact..:

Kaneb, Hannah M ; Folkmann, Andrew W ; Belzil, Véronique V...
qt7289p1vq. , 2015

Link: https://escholarship.org..

14

Exome Sequencing Identifies FUS Mutations as a Cause of Ess..:

Merner, Nancy D ; Girard, Simon L ; Catoire, Hélène...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415547. , 2012

Link: http://www.ncbi.nlm.nih...