Canlyniadau Chwilio - Vincent Raymond

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Mireinio'r Canlyniadau
  1. 1
    Recurrent Mutation of the Gene Encoding sequestosome 1 (SQSTM1/p62) in Paget Disease of Bone

    Recurrent Mutation of the Gene Encoding sequestosome 1 (SQSTM1/p62) in Paget Disease of Bone gan Nancy Laurin, Jacques P. Brown, Jean Morissette, Vincent Raymond

    Cyhoeddwyd 2002
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    Artigo
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  2. 2
    Vasopressin rapidly stimulates phosphatidic acid‐phosphatidylinositol turnover in rat anterior pituitary cells

    Vasopressin rapidly stimulates phosphatidic acid‐phosphatidylinositol turnover in rat anterior pituitary cells gan Vincent Raymond, Peter C. K. Leung, Raymonde Veilleux, Fernand Labrie

    Cyhoeddwyd 1985
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  3. 3
    Detection of fos protein during osteogenesis by monoclonal antibodies.

    Detection of fos protein during osteogenesis by monoclonal antibodies. gan P. De Togni, Henry Niman, Vincent Raymond, Paul E. Sawchenko, Inder M. Verma

    Cyhoeddwyd 1988
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  4. 4
    Dopaminergic receptors in the anterior pituitary gland. Correlation of [3H]dihydroergocryptine binding with the dopaminergic control of prolactin release.

    Dopaminergic receptors in the anterior pituitary gland. Correlation of [3H]dihydroergocryptine binding with the dopaminergic control of prolactin release. gan Marc G. Caron, Jean‐Martin Beaulieu, Vincent Raymond, Bernard Gagné, Jacques Drouin, Robert J. Lefkowitz, Fernand Labrie

    Cyhoeddwyd 1978
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  5. 5
    Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31

    Paget Disease of Bone: Mapping of Two Loci at 5q35-qter and 5q31 gan Nancy Laurin, Jacques P. Brown, Arnaud Lemainque, Annie Duchesne, Denys Huot, Yves Lacourcière, Gervais Drapeau, Jean Verreault, Vincent Raymond, Jean Morissette

    Cyhoeddwyd 2001
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  6. 6
    FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A

    FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A gan Fred B. Berry, Jonathan M. Skarie, Farideh Mirzayans, Yannick Fortin, Thomas J. Hudson, Vincent Raymond, Brian A. Link, Michael A. Walter

    Cyhoeddwyd 2007
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  7. 7
    Sensitivity Analyses of Exposure Estimates from a Quantitative Job-exposure Matrix (SYN-JEM) for Use in Community-based Studies

    Sensitivity Analyses of Exposure Estimates from a Quantitative Job-exposure Matrix (SYN-JEM) for Use in Community-based Studies gan Peters, Susan, Kromhout, Hans, Portengen, Lützen, Olsson, Ann, Kendzia, Benjamin, Vincent, Raymond, Savary, Barbara, Lavoué, Jérôme, Cavallo, Domenico, Cattaneo, Andrea, Mirabelli, Dario, Plato, Nils, Fevotte, Joelle, Pesch, Beate, Brüning, Thomas, Straif, Kurt, Vermeulen, Roel

    Cyhoeddwyd 2013
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  8. 8
    Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia

    Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia gan Mark E. Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernández, Ferrán Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Élie Haddad, Alan Hodgkinson, Youssef Idaghdour, Valérie Marchand, Jacques L. Michaud, Marc‐André Rodrigue, Sylvie Desjardins, Stéphane Dubois, Françoise Le Deist, Philip Awadalla, Vincent Raymond, Bruno Maranda

    Cyhoeddwyd 2013
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  9. 9
    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly

    Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly gan Alan J. Mears, Tim Jordan, Farideh Mirzayans, Stéphane Dubois, Tsutomu Kume, Michael Parlee, Robert Ritch, Ben F. Koop, Wen-Lin Kuo, Colin C. Collins, Jody Marshall, Douglas B. Gould, W G Pearce, Peter Carlsson, Sven Enerbäck, Jean Morissette, Shomi S. Bhattacharya, Brigid L.M. Hogan, Vincent Raymond, Michael A. Walter

    Cyhoeddwyd 1998
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    Artigo
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