Kết quả tìm kiếm - Mark Samuels
- Đang hiển thị 1 - 15 kết quả của 15
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Purification and characterization of a specific RNA polymerase II transcription factor. Bằng Mark Samuels, Phillip A. Sharp
Được phát hành 1986Artigo -
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Separation and characterization of factors mediating accurate transcription by RNA polymerase II. Bằng Mark Samuels, Andrew Fire, Phillip A. Sharp
Được phát hành 1982Artigo -
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Interactions between RNA polymerase II, factors, and template leading to accurate transcription. Bằng Andrew Fire, Mark Samuels, Phillip A. Sharp
Được phát hành 1984Artigo -
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RNA binding by Sxl proteins in vitro and in vivo. Bằng Mark Samuels, Daniel Bopp, Richard A. Colvin, Robert F. Roscigno, Mariano A. Garcia‐Blanco, Paul Schedl
Được phát hành 1994Artigo -
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Propranolol reduces IFN-γ driven PD-L1 immunosuppression and improves anti-tumour immunity in ovarian cancer Bằng 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
Được phát hành 2023Artigo -
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Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred Bằng 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
Được phát hành 2000Artigo -
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Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II Bằng 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
Được phát hành 2008Artigo -
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Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome Bằng 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
Được phát hành 2012Artigo -
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Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis Bằng 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
Được phát hành 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 Bằng 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
Được phát hành 2004Artigo -
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De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia Bằng 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
Được phát hành 2010Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Gene
Genetics
RNA
Biochemistry
Molecular biology
Gene expression
Chemistry
Computational biology
DNA
Linguistics
Medicine
Neuroscience
Philosophy
Promoter
RNA polymerase
RNA polymerase II
Transcription (linguistics)
Identification (biology)
Internal medicine
Mutation
Polymerase
RNA polymerase I
RNA splicing
RNA-dependent RNA polymerase
Transcription factor II D
Botany
Cancer research
Cell
Cell biology