Canlyniadau Chwilio - Alexandre Montpetit
- Dangos 1 - 20 canlyniadau o 39
- Ewch i'r Dudalen Nesaf
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Genetic Analysis of 103 Candidate Genes for Coronary Artery Disease and Associated Phenotypes in a Founder Population Reveals a New Association between Endothelin-1 and High-Densit... gan Guillaume Paré, David Serre, Diane Brisson, Sonia S. Anand, Alexandre Montpetit, G Tremblay, James C. Engert, Thomas J. Hudson, Daniel Gaudet
Cyhoeddwyd 2007Artigo -
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Buccals are likely to be a more informative surrogate tissue than blood for epigenome-wide association studies gan Robert Lowe, Carolina Gemma, Huriya Beyan, Mohammed I. Hawa, Alexandra Bazeos, Richard David Leslie, Alexandre Montpetit, Vardhman K. Rakyan, Sreeram V. Ramagopalan
Cyhoeddwyd 2013Artigo -
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Disruption of AP1S1, Causing a Novel Neurocutaneous Syndrome, Perturbs Development of the Skin and Spinal Cord gan Alexandre Montpetit, Stéphanie Côté, Edna Brustein, Christian A. Drouin, Line Lapointe, Michèle Boudreau, Caroline Meloche, Régen Drouin, Thomas J. Hudson, Pierre Drapeau, Patrick Cossette
Cyhoeddwyd 2008Artigo -
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CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup gan Simon C. Warby, Alexandre Montpetit, Anna Hayden, Jeffrey B. Carroll, Stefanie Butland, Henk Visscher, Jennifer A. Collins, Alicia Semaka, Thomas J. Hudson, Michael R. Hayden
Cyhoeddwyd 2009Artigo -
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Transcriptomic profiling of severe and critical COVID-19 patients reveals alterations in expression, splicing and polyadenylation gan Marjorie Labrecque, Elsa Brunet‐Ratnasingham, Laura K. Hamilton, Daniel Auld, Alexandre Montpetit, J. Brent Richards, Madéleine Durand, Simon Rousseau, Andrés Finzi, Daniel E. Kaufmann, Martine Tétreault
Cyhoeddwyd 2025Artigo -
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NALP1 Influences Susceptibility to Human Congenital Toxoplasmosis, Proinflammatory Cytokine Response, and Fate of <i>Toxoplasma gondii</i> -Infected Monocytic Cells gan William H. Witola, Ernest Mui, Aubrey Hargrave, Susan Liu, Magali Hypolite, Alexandre Montpetit, Pierre Cavaillès, Cordelia Bisanz, Marie‐France Cesbron‐Delauw, Gilbert J. Fournié, Rima McLeod
Cyhoeddwyd 2010Artigo -
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HLA class I alleles tag <i>HLA-DRB1</i> * <i>1501</i> haplotypes for differential risk in multiple sclerosis susceptibility gan Michael J. Chao, Martin Barnardo, Matthew R. Lincoln, Sreeram V. Ramagopalan, Blanca Herrera, David A. Dyment, Alexandre Montpetit, A. Dessa Sadovnick, Julian C. Knight, George C. Ebers
Cyhoeddwyd 2008Artigo -
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Identification of T. gondii epitopes, adjuvants, and host genetic factors that influence protection of mice and humans gan Tze Guan Tan, Ernest Mui, Hua Cong, William H. Witola, Alexandre Montpetit, Stephen P. Muench, John Sidney, Jeff Alexander, Alessandro Sette, Michael E. Grigg, Ajesh Maewal, Rima McLeod
Cyhoeddwyd 2010Artigo -
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Impaired Innate Immunity in Mice Deficient in Interleukin-1 Receptor-Associated Kinase 4 Leads to Defective Type 1 T Cell Responses, B Cell Expansion, and Enhanced Susceptibility t... gan Samantha Ribeiro Béla, Míriam Santos Dutra, Ernest Mui, Alexandre Montpetit, Sérgio C. Oliveira, Sérgio C. Oliveira, Rosa Maria Esteves Arantes, Lis Ribeiro do Valle Antonelli, Rima McLeod, Ricardo T. Gazzinelli
Cyhoeddwyd 2012Artigo -
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A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis gan Matthew R. Lincoln, Alexandre Montpetit, M. Zameel Cader, Janna Saarela, David A. Dyment, Milvi Tiislar, Vincent Ferretti, Pentti J. Tienari, A. Dessa Sadovnick, Leena Peltonen, George C. Ebers, Thomas J. Hudson
Cyhoeddwyd 2005Artigo -
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MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy gan Diego Martinelli, Lorena Travaglini, Christian A. Drouin, Irène Ceballos-Picot, Teresa Rizza, Enrico Bertini, Rosalba Carrozzo, Stefania Petrini, Pascale de Lonlay, Maya El Hachem, Laurence Hubert, Alexandre Montpetit, Giuliano Torre, Carlo Dionisi‐Vici
Cyhoeddwyd 2013Artigo -
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An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the <i>HLA-DRB1</i> locus gan Gabriele C. DeLuca, S. V. Ramagopalan, Blanca Herrera, David A. Dyment, Matthew R. Lincoln, Alexandre Montpetit, Maura Pugliatti, Martin Barnardo, Neil Risch, A. Dessa Sadovnick, Melody Chao, Stefano Sotgiu, Thomas J. Hudson, George C. Ebers
Cyhoeddwyd 2007Artigo -
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Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the <i>TYK2</i> gene gan David A. Dyment, M. Zameel Cader, Michael J. Chao, Matthew R. Lincoln, Katie Morrison, Giulio Disanto, Julia M. Morahan, Gabriele C. DeLuca, A. Dessa Sadovnick, Pierre Lepage, Alexandre Montpetit, George C. Ebers, Sreeram V. Ramagopalan
Cyhoeddwyd 2012Artigo -
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Duplication of 7q34 is specific to juvenile pilocytic astrocytomas and a hallmark of cerebellar and optic pathway tumours gan Karine Jacob, Steffen Albrecht, Caroline Sollier, Damien Faury, E Sader, Alexandre Montpetit, David Serre, Péter Hauser, Miklós Garami, László Bognár, Z. Hanzély, J. Montes, Jeffrey Atkinson, J-P. Farmer, Éric Bouffet, Cynthia Hawkins, Uri Tabori, Nada Jabado
Cyhoeddwyd 2009Artigo -
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Integrative genomic analysis of matched primary and metastatic pediatric osteosarcoma gan Gian Luca Negri, Bruno M. Grande, Alberto Delaidelli, Amal M. El-Naggar, Dawn R. Cochrane, Ching C. Lau, Timothy J. Triche, Richard A. Moore, Steven J.M. Jones, Alexandre Montpetit, Marco A. Marra, David Malkin, Ryan D. Morin, Poul H. Sorensen
Cyhoeddwyd 2019Artigo -
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Genome-wide profiling using single-nucleotide polymorphism arrays identifies novel chromosomal imbalances in pediatric glioblastomas gan Hui‐Qi Qu, Karine Jacob, Sarah Fatet, Bing Ge, David W. Barnett, Olivier Delattre, Damien Faury, Alexandre Montpetit, Lauren A. Solomon, Péter Hauser, Miklós Garami, László Bognár, Zoltan Hansely, Robert Mio, Jean‐Pierre Farmer, Steffen Albrecht, Constantin Polychronakos, Cynthia Hawkins, Nada Jabado
Cyhoeddwyd 2010Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Allele
Computational biology
Genetic association
Cancer research
Disease
Haplotype
Bioinformatics
Genome
Immunology
Genome-wide association study
Locus (genetics)
Mutation
Population
SNP
Genotyping
Antibody
Antigen
Cancer
Environmental health
Evolutionary biology
Exome
Exome sequencing
Gene expression