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Alexandre Montpetit

Showing results (61-70 of 92) with videos related to

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Human Genetics|February 28, 2009
Analyses of associations with asthma in four asthma population samples from Canada and AustraliaDenise Daley, Mathieu Lemire, Loubna Akhabir, et al.
Nature|January 23, 2004
Susceptibility to leprosy is associated with PARK2 and PACRGMarcelo T Mira, Alexandre Alcaïs, Van Thuc Nguyen, et al.
Acta Neuropathologica|June 5, 2012
K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomasDong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, et al.
Plos One|May 19, 2021
The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectoriesKarine Tremblay, Simon Rousseau, Ma'n H Zawati, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomasAdam M Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, et al.
Nature Genetics|October 20, 2009
Global patterns of cis variation in human cells revealed by high-density allelic expression analysisBing Ge, Dmitry K Pokholok, Tony Kwan, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Mutation Research|September 1, 2012
Harnessing genomics to identify environmental determinants of heritable diseaseCarole Lyn Yauk, J Lucas Argueso, Scott S Auerbach, et al.
Pageof 10

Showing results (61-70 of 92) with videos related to

Sort By:
Pageof 10
Human Genetics|February 28, 2009
Analyses of associations with asthma in four asthma population samples from Canada and AustraliaDenise Daley, Mathieu Lemire, Loubna Akhabir, et al.
Nature|January 23, 2004
Susceptibility to leprosy is associated with PARK2 and PACRGMarcelo T Mira, Alexandre Alcaïs, Van Thuc Nguyen, et al.
Acta Neuropathologica|June 5, 2012
K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomasDong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, et al.
Plos One|May 19, 2021
The Biobanque québécoise de la COVID-19 (BQC19)-A cohort to prospectively study the clinical and biological determinants of COVID-19 clinical trajectoriesKarine Tremblay, Simon Rousseau, Ma'n H Zawati, et al.
Acta Neuropathologica|February 19, 2013
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomasAdam M Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, et al.
Nature Genetics|October 20, 2009
Global patterns of cis variation in human cells revealed by high-density allelic expression analysisBing Ge, Dmitry K Pokholok, Tony Kwan, et al.
Plos Genetics|September 13, 2012
Rare copy number variants contribute to congenital left-sided heart diseaseMarc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, et al.
Nature Communications|February 4, 2018
Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Nature Communications|January 6, 2018
APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patientsJean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, et al.
Mutation Research|September 1, 2012
Harnessing genomics to identify environmental determinants of heritable diseaseCarole Lyn Yauk, J Lucas Argueso, Scott S Auerbach, et al.
Pageof 10