Søgeresultater - Mark Samuels
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Propranolol reduces IFN-γ driven PD-L1 immunosuppression and improves anti-tumour immunity in ovarian cancer af Marta Falcinelli, Gheed Alhity, S. Baron, Myrthe Mampay, Marcus Allen, Mark Samuels, Wendell Jones, Chiara Cilibrasi, Renée L. Flaherty, Georgios Giamas, Premal H. Thaker, Melanie S. Flint
Udgivet 2023Artigo -
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Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred af Steven C. Hunt, Paul N. Hopkins, Katrina Bulka, Michael T. McDermott, Thomas L. Thorne, B B Wardell, Benjamin R. Bowen, Dennis G. Ballinger, Mark H. Skolnick, Mark Samuels
Udgivet 2000Artigo -
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Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II af Masoud Shekarabi, Nathalie Girard, Jean‐Baptiste Rivière, Patrick A. Dion, Martin Houle, André Toulouse, Ronald G. Lafrenière, F. Vercauteren, Pascale Hince, Janet Laganière, Daniel Rochefort, Laurence Faivre, Mark Samuels, Guy A. Rouleau
Udgivet 2008Artigo -
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Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome af José‐Mario Capo‐Chichi, Sanjay Kumar Bharti, Joshua A. Sommers, Tony Yammine, Éliane Chouery, Lysanne Patry, Guy A. Rouleau, Mark Samuels, Fadi F. Hamdan, Jacques L. Michaud, Robert Brosh, André Mégarbané, Zoha Kibar
Udgivet 2012Artigo -
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Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis af George Papanikolaou, Mark Samuels, E H Ludwig, Marcia L.E. MacDonald, Patrick L. Franchini, Marie‐Pierre Dubé, Lisa Andres, Julie MacFarlane, Nikos Sakellaropoulos, Marianna Politou, Elizabeta Nemeth, Jay Thompson, Jenni Risler, Catherine Zaborowska, Ryan Babakaiff, Christopher C Radomski, Terry D. Pape, Owen Davidas, John Christakis, Pierre Brissot, Gillian Lockitch, Tomas Ganz, Michael R. Hayden, Y. Paul Goldberg
Udgivet 2003Artigo -
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Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates af Ronald G. Lafrenière, Marcia L.E. MacDonald, Marie‐Pierre Dubé, Julie MacFarlane, Mary O’Driscoll, Bernard Brais, Sébastien Meilleur, Ryan R. Brinkman, Owen Dadivas, Terry D. Pape, Christèle Platon, Chris Radomski, Jenni Risler, Jay Thompson, Ana-Maria Guerra-Escobio, Gudarz Davar, Xandra O. Breakefield, Simon N. Pimstone, Roger Green, William Pryse‐Phillips, Y. Paul Goldberg, H. Banfield Younghusband, Michael R. Hayden, Robin Sherrington, Guy A. Rouleau, Mark Samuels
Udgivet 2004Artigo -
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De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia af Julie Gauthier, Nathalie Champagne, Ronald G. Lafrenière, Lan Xiong, Dan Spiegelman, Edna Brustein, Mathieu Lapointe, Huashan Peng, Mélanie Côté, Anne Noreau, Fadi F. Hamdan, Anjené Addington, Judith L. Rapoport, Lynn E. DeLisi, Marie‐Odile Krebs, Ridha Joober, Ferid Fathalli, Fayçal Mouaffak, A. Pejmun Haghighi, Christian Néri, Marie‐Pierre Dubé, Mark Samuels, Claude Marineau, Eric A. Stone, Philip Awadalla, Philip Barker, Salvatore Carbonetto, Pierre Drapeau, Guy A. Rouleau, Kathleen Daignault, Ousmane Diallo, Joannie Duguay, Marina Drits, Édouard Henrion, Philippe Jolivet, Frédéric Kuku, Karine Lachapelle, Guy Laliberté, Sandra B. Laurent, Meijiang Liao, Carlos Marino, Amélie Piton, A Raymond, Annie Reynolds, Daniel Rochefort, Judith St‐Onge, Pascale Thibodeau, Kazuya Tsurudome, Yanlian Yang, Sophie Leroy, Katia Ossian, Mélanie Chayet, David Gourion
Udgivet 2010Artigo
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