Resultados da busca - Georges Nemer

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  1. 1
    Familial Hypercholesterolemia: The Lipids or the Genes?

    Familial Hypercholesterolemia: The Lipids or the Genes? por Akl C. Fahed, Georges Nemer

    Publicado em 2011
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  2. 2
    Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing?

    Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing? por Athar Khalil, Amina Kamar, Georges Nemer

    Publicado em 2020
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  3. 3
    Diet, Genetics, and Disease: A Focus on the Middle East and North Africa Region

    Diet, Genetics, and Disease: A Focus on the Middle East and North Africa Region por Akl C. Fahed, Karim Sleiman, Theresa Farhat, Georges Nemer

    Publicado em 2012
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  4. 4
    Cooperative Interaction between GATA-4 and GATA-6 Regulates Myocardial Gene Expression

    Cooperative Interaction between GATA-4 and GATA-6 Regulates Myocardial Gene Expression por Frédéric Charron, Pierre Paradis, Odile Bronchain, Georges Nemer, Mona Nemer

    Publicado em 1999
    Obter o texto integral
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  5. 5
    Turicibacter and Catenibacterium as potential biomarkers in autism spectrum disorders

    Turicibacter and Catenibacterium as potential biomarkers in autism spectrum disorders por Perla Gerges, Dhinoth Bangarusamy, Tania Bitar, Abbas Alameddine, Georges Nemer, Walid Hleihel

    Publicado em 2024
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  6. 6
    A novel mutation in theGATA4 gene in patients with Tetralogy of Fallot

    A novel mutation in theGATA4 gene in patients with Tetralogy of Fallot por Georges Nemer, Fatimah Fadlalah, Julnar Usta, Mona Nemer, Ghassan Dbaibo, Mounir Obeid, Fadi Bitar

    Publicado em 2006
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  7. 7
    The Kruppel-like transcription factor KLF13 is a novel regulator of heart development

    The Kruppel-like transcription factor KLF13 is a novel regulator of heart development por Geneviève Lavallée, Gregor Andelfinger, Mathieu Nadeau, Chantal Lefèbvre, Georges Nemer, Marko E. Horb, Mona Nemer

    Publicado em 2006
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  8. 8
    NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

    NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity por Ossama Abou Hassan, Akl C. Fahed, Manal Batrawi, Mariam Arabi, Marwan M. Refaat, Steven R. DePalma, Jonathan G. Seidman, Christine E. Seidman, Fadi Bitar, Georges Nemer

    Publicado em 2015
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  9. 9
    A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease

    A Murine Model of Holt-Oram Syndrome Defines Roles of the T-Box Transcription Factor Tbx5 in Cardiogenesis and Disease por Benoit G. Bruneau, Georges Nemer, Joachim P. Schmitt, Frédéric Charron, Lynda Robitaille, Sophie Jeanne Cécile Caron, David A. Conner, Manfred Gessler, Mona Nemer, Christine E. Seidman, Jonathan G. Seidman

    Publicado em 2001
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  10. 10
    Mutations in<i>SDR9C7</i>gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis

    Mutations in<i>SDR9C7</i>gene encoding an enzyme for vitamin A metabolism underlie autosomal recessive congenital ichthyosis por Yohya Shigehara, Shujiro Okuda, Georges Nemer, Adele Chedraoui, Ryota Hayashi, Fadi Bitar, Hiroyuki Nakai, Ossama Abbas, Laetitia Daou, Riichiro Abe, Maria Bou Sleiman, Abdul Ghani Kibbi, Mazen Kurban, Yutaka Shimomura

    Publicado em 2016
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  11. 11
    A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

    A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects por Maximilian Posch, Michael Gramlich, Margaret Sunde, Katharina Schmitt, S. H. Y. Lee, Silke Richter, A.H. Kersten, Andreas Perrot, A. Panek, Iman Al Khatib, Georges Nemer, André Mégarbané, Rainer Dietz, Brigitte Stiller, Felix Berger, Richard P. Harvey, C. Özcelik

    Publicado em 2009
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  12. 12
    <i>BRCA1</i> and <i>BRCA2</i> Mutations in Ethnic Lebanese Arab Women With High Hereditary Risk Breast Cancer

    <i>BRCA1</i> and <i>BRCA2</i> Mutations in Ethnic Lebanese Arab Women With High Hereditary Risk Breast Cancer por Nagi S. El Saghir, Nathalie K. Zgheib, Hussein Assi, Katia Khoury, Yannick Bidet, Sara Jaber, Raghid Charara, Rania Farhat, Firas Kreidieh, Stephanie Decousus, P. Romero, Georges Nemer, Ziad Salem, Ali Shamseddine, Arafat Tfayli, Jaber Abbas, Faek R. Jamali, Muhieddine Seoud, Deborah K. Armstrong, Yves–Jean Bignon, Nancy Uhrhammer

    Publicado em 2015
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