Search Results - Efrat Lev-Lehman

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  1. 1
    Genetics of Angelman Syndrome

    Genetics of Angelman Syndrome by Yong-hui Jiang, Efrat Lev-Lehman, Jan Bressler, Ting‐Fen Tsai, Arthur L. Beaudet

    Published 1999
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  2. 2
    Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in mice

    Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in mice by Rachel Beeri, Christian Andrés, Efrat Lev-Lehman, Rina Timberg, Tamir Huberman, Moshe Shani, Hermona Soreq

    Published 1995
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  3. 3
    The Angelman Syndrome-Associated Protein, E6-AP, Is a Coactivator for the Nuclear Hormone Receptor Superfamily

    The Angelman Syndrome-Associated Protein, E6-AP, Is a Coactivator for the Nuclear Hormone Receptor Superfamily by Zafar Nawaz, David M. Lonard, Carolyn L. Smith, Efrat Lev-Lehman, Sophia Y. Tsai, Ming‐Jer Tsai, Bert W. O’Malley

    Published 1999
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  4. 4
    Molecular cloning and construction of the coding region for human acetylcholinesterase reveals a G + C-rich attenuating structure.

    Molecular cloning and construction of the coding region for human acetylcholinesterase reveals a G + C-rich attenuating structure. by Hermona Soreq, Revital Ben-Aziz, Catherine A. Prody, Shlomo Seidman, Averell Gnatt, L Neville, J. Lieman-Hurwitz, Efrat Lev-Lehman, Dalia Ginzberg, Y Lipidot-Lifson

    Published 1990
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  5. 5
    A Highly Significant Association between a COMT Haplotype and Schizophrenia

    A Highly Significant Association between a COMT Haplotype and Schizophrenia by Sagiv Shifman, Michal Bronstein, Meira Sternfeld, Anne Pisanté-Shalom, Efrat Lev-Lehman, Abraham Weizman, Ilya Reznik, Baruch Spivak, Nimrod Grisaru, Leon Karp, Richard Schiffer, Moshe Kotler, Rael D. Strous, Marnina Swartz‐Vanetik, Haim Y. Knobler, Eilat Shinar, J. Beckmann, Benjamin Yakir, Neil Risch, Naomi B. Zak, Ariel Darvasi

    Published 2002
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  6. 6
    Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome

    Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome by Michael F. Wangler, Claudia Gonzaga‐Jauregui, Tomasz Gambin, Samantha Penney, Timothy J. M. Moss, Atul R. Chopra, Frank J. Probst, Fan Xia, Yaping Yang, Steven L. Werlin, Ieva Eglite, Liene Korņejeva, Carlos A. Bacino, Dustin Baldridge, Jeffrey L. Neul, Efrat Lev Lehman, Austin Larson, Joke Beuten, Donna M. Muzny, Shalini N. Jhangiani, Richard A. Gibbs, James R. Lupski, Arthur L. Beaudet

    Published 2014
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