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Stéphane Dubois

Showing results (1-10 of 15) with videos related to

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Molecular Vision|August 19, 2011
Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma modelTim Footz, Stéphane Dubois, Mansoor Sarfarazi, et al.
Investigative Ophthalmology & Visual Science|May 27, 2003
Gene expression profile of the human trabecular meshwork: NEIBank sequence tag analysisStanislav I Tomarev, Graeme Wistow, Vincent Raymond, et al.
Studies in Health Technology and Informatics|November 17, 2006
Design of a decision support system for chronic diseases coupling generic therapeutic algorithms with guideline-based specific rulesVahid Ebrahiminia, Christine Riou, Brigitte Seroussi, et al.
Molecular Vision|September 29, 2009
The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-EastInbal Avisar, Moshe Lusky, Anat Robinson, et al.
Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
BMC Medical Informatics and Decision Making|June 1, 2010
How to translate therapeutic recommendations in clinical practice guidelines into rules for critiquing physician prescriptions? Methods and application to five guidelinesJean-Baptiste Lamy, Vahid Ebrahiminia, Christine Riou, et al.
Human Molecular Genetics|August 22, 2002
Founder TIGR/myocilin mutations for glaucoma in the Québec populationMathieu Faucher, Jean-Louis Anctil, Marc-André Rodrigue, et al.
Genes|March 3, 2019
Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle ControlYosr Hamdi, Martin Leclerc, Martine Dumont, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Molecular Vision|August 19, 2011
Co-variation of STI1 and WDR36/UTP21 alters cell proliferation in a glaucoma modelTim Footz, Stéphane Dubois, Mansoor Sarfarazi, et al.
Investigative Ophthalmology & Visual Science|May 27, 2003
Gene expression profile of the human trabecular meshwork: NEIBank sequence tag analysisStanislav I Tomarev, Graeme Wistow, Vincent Raymond, et al.
Studies in Health Technology and Informatics|November 17, 2006
Design of a decision support system for chronic diseases coupling generic therapeutic algorithms with guideline-based specific rulesVahid Ebrahiminia, Christine Riou, Brigitte Seroussi, et al.
Molecular Vision|September 29, 2009
The novel Y371D myocilin mutation causes an aggressive form of juvenile open-angle glaucoma in a Caucasian family from the Middle-EastInbal Avisar, Moshe Lusky, Anat Robinson, et al.
Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 13, 2004
Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation familyBruno Mortemousque, Patrizia Amati-Bonneau, François Couture, et al.
BMC Medical Informatics and Decision Making|June 1, 2010
How to translate therapeutic recommendations in clinical practice guidelines into rules for critiquing physician prescriptions? Methods and application to five guidelinesJean-Baptiste Lamy, Vahid Ebrahiminia, Christine Riou, et al.
Human Molecular Genetics|August 22, 2002
Founder TIGR/myocilin mutations for glaucoma in the Québec populationMathieu Faucher, Jean-Louis Anctil, Marc-André Rodrigue, et al.
Genes|March 3, 2019
Functional Analysis of Promoter Variants in Genes Involved in Sex Steroid Action, DNA Repair and Cell Cycle ControlYosr Hamdi, Martin Leclerc, Martine Dumont, et al.
Journal of Medical Genetics|February 21, 2013
Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresiaMark E Samuels, Jacek Majewski, Najmeh Alirezaie, et al.
Pageof 2