Resultats de la cerca - Mark Samuels

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  1. 1
    Purification and characterization of a specific RNA polymerase II transcription factor.

    Purification and characterization of a specific RNA polymerase II transcription factor. per Mark Samuels, Phillip A. Sharp

    Publicat 1986
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  2. 2
    The complex set of late transcripts from the Drosophila sex determination gene sex-lethal encodes multiple related polypeptides.

    The complex set of late transcripts from the Drosophila sex determination gene sex-lethal encodes multiple related polypeptides. per Mark Samuels, Paul Schedl, Thomas W. Cline

    Publicat 1991
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  3. 3
    Separation and characterization of factors mediating accurate transcription by RNA polymerase II.

    Separation and characterization of factors mediating accurate transcription by RNA polymerase II. per Mark Samuels, Andrew Fire, Phillip A. Sharp

    Publicat 1982
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  4. 4
    Interactions between RNA polymerase II, factors, and template leading to accurate transcription.

    Interactions between RNA polymerase II, factors, and template leading to accurate transcription. per Andrew Fire, Mark Samuels, Phillip A. Sharp

    Publicat 1984
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  5. 5
    5,6-Dichloro-1-β-D-ribofuranosylbenzimidazole inhibits transcription elongation by RNA polymerase II in vitro

    5,6-Dichloro-1-β-D-ribofuranosylbenzimidazole inhibits transcription elongation by RNA polymerase II in vitro per Lewis A. Chodosh, Andrew Fire, Mark Samuels, Phillip A. Sharp

    Publicat 1989
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  6. 6
    RNA binding by Sxl proteins in vitro and in vivo.

    RNA binding by Sxl proteins in vitro and in vivo. per Mark Samuels, Daniel Bopp, Richard A. Colvin, Robert F. Roscigno, Mariano A. Garcia‐Blanco, Paul Schedl

    Publicat 1994
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  7. 7
    The Drosophila female-specific sex-determination gene, Sex-lethal, has stage-, tissue-, and sex-specific RNAs suggesting multiple modes of regulation.

    The Drosophila female-specific sex-determination gene, Sex-lethal, has stage-, tissue-, and sex-specific RNAs suggesting multiple modes of regulation. per Helen K. Salz, Eleanor M. Maine, Linda N. Keyes, Mark Samuels, Thomas W. Cline, Paul Schedl

    Publicat 1989
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  8. 8
    Spatial biology – unravelling complexity within the glioblastoma microenvironment

    Spatial biology – unravelling complexity within the glioblastoma microenvironment per Stephen Robinson, Chrysa Filippopoulou, Simoni Besta, Mark Samuels, Andrea Lauer Betrán, Maha Abu Ajamieh, Viviana Vella, William Jones, Georgios Giamas

    Publicat 2025
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  9. 9
    Propranolol reduces IFN-γ driven PD-L1 immunosuppression and improves anti-tumour immunity in ovarian cancer

    Propranolol reduces IFN-γ driven PD-L1 immunosuppression and improves anti-tumour immunity in ovarian cancer per 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

    Publicat 2023
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  10. 10
    Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred

    Genetic Localization to Chromosome 1p32 of the Third Locus for Familial Hypercholesterolemia in a Utah Kindred per 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

    Publicat 2000
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  11. 11
    Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II

    Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II per 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

    Publicat 2008
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  12. 12
    Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome

    Identification and Biochemical Characterization of a Novel Mutation in<i>DDX11</i>Causing Warsaw Breakage Syndrome per 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

    Publicat 2012
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  13. 13
    Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

    Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis per 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

    Publicat 2003
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  14. 14
    Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

    Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates per 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

    Publicat 2004
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  15. 15
    De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia

    De novo mutations in the gene encoding the synaptic scaffolding protein<i>SHANK3</i>in patients ascertained for schizophrenia per 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

    Publicat 2010
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