खोज परिणाम - Vincent Raymond

  • प्रदर्शित 1 - 9 परिणाम 9
परिणाम को परिष्कृत करें
  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 द्वारा Nancy Laurin, Jacques P. Brown, Jean Morissette, Vincent Raymond

    प्रकाशित 2002
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा Vincent Raymond, Peter C. K. Leung, Raymonde Veilleux, Fernand Labrie

    प्रकाशित 1985
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  3. 3
    Detection of fos protein during osteogenesis by monoclonal antibodies.

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

    प्रकाशित 1988
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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. द्वारा Marc G. Caron, Jean‐Martin Beaulieu, Vincent Raymond, Bernard Gagné, Jacques Drouin, Robert J. Lefkowitz, Fernand Labrie

    प्रकाशित 1978
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा Nancy Laurin, Jacques P. Brown, Arnaud Lemainque, Annie Duchesne, Denys Huot, Yves Lacourcière, Gervais Drapeau, Jean Verreault, Vincent Raymond, Jean Morissette

    प्रकाशित 2001
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा Fred B. Berry, Jonathan M. Skarie, Farideh Mirzayans, Yannick Fortin, Thomas J. Hudson, Vincent Raymond, Brian A. Link, Michael A. Walter

    प्रकाशित 2007
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा 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

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    मूलपाठ
    सूची में सहेजें
    में बचाया:
  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 द्वारा 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

    प्रकाशित 2013
    पूर्ण पाठ प्राप्त करें पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:
  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 द्वारा 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

    प्रकाशित 1998
    पूर्ण पाठ प्राप्त करें
    Artigo
    सूची में सहेजें
    में बचाया:

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