Search Results - "Greif, Hagar"

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  1. 1

    Trehalose alleviates the phenotype of Machado-Joseph disease mouse models by Santana, Magda M, Paixão, Susana, Cunha-Santos, Janete, Silva, Teresa Pereira, Trevino-Garcia, Allyson, Gaspar, Laetitia S, Nóbrega, Clévio, Nobre, Rui Jorge, Cavadas, Cláudia, Greif, Hagar, Pereira de Almeida, Luís

    Published in Journal of translational medicine (09-04-2020)
    “…Machado-Joseph disease (MJD), also known as spinocerebellar ataxia type 3, is the most common of the dominantly inherited ataxias worldwide and is…”
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    Journal Article
  2. 2

    Frataxin‐deficient neurons and mice models of Friedreich ataxia are improved by TAT‐MTScs‐FXN treatment by Britti, Elena, Delaspre, Fabien, Feldman, Anat, Osborne, Melissa, Greif, Hagar, Tamarit, Jordi, Ros, Joaquim

    Published in Journal of cellular and molecular medicine (01-02-2018)
    “…Friedreich ataxia (FA) is a rare disease caused by deficiency of frataxin, a mitochondrial protein. As there is no cure available for this disease, many…”
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    Journal Article
  3. 3

    Heterologous mitochondrial targeting sequences can deliver functional proteins into mitochondria by Marcus, Dana, Lichtenstein, Michal, Cohen, Natali, Hadad, Rita, Erlich-Hadad, Tal, Greif, Hagar, Lorberboum-Galski, Haya

    “…Mitochondrial Targeting Sequences (MTSs) are responsible for trafficking nuclear-encoded proteins into mitochondria. Once entering the mitochondria, the MTS is…”
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    Frataxin‐deficient neurons and mice models of Friedreich ataxia are improved by TAT ‐ MTS cs‐ FXN treatment by Britti, Elena, Delaspre, Fabien, Feldman, Anat, Osborne, Melissa, Greif, Hagar, Tamarit, Jordi, Ros, Joaquim

    Published in Journal of cellular and molecular medicine (01-02-2018)
    “…Friedreich ataxia (FA) is a rare disease caused by deficiency of frataxin, a mitochondrial protein. As there is no cure available for this disease, many…”
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    Journal Article
  6. 6

    TAT‐MTS‐MCM fusion proteins reduce MMA levels and improve mitochondrial activity and liver function in MCM‐deficient cells by Erlich‐Hadad, Tal, Hadad, Rita, Feldman, Anat, Greif, Hagar, Lictenstein, Michal, Lorberboum‐Galski, Haya

    Published in Journal of cellular and molecular medicine (01-03-2018)
    “…Methylmalonic aciduria (MMA) is a disorder of organic acid metabolism resulting from a functional defect of the mitochondrial enzyme, methylmalonyl‐CoA mutase…”
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    The protein kinase C-related PKC-L(eta) gene product is localized in the cell nucleus by GREIF, H, BEN-CHAIM, J, SHIMON, T, BECHOR, E, ELDAR, H, LIVNEH, E

    Published in Molecular and Cellular Biology (01-03-1992)
    “…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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  10. 10

    Mutations at vicinity of catalytic sites of hepatitis C virus NS3 serine protease gene isolated from hepatocellular carcinoma tissue by ZEMEL, Romy, KAZATSKER, Ana, GREIF, Franklin, BEN-ARI, Ziv, GREIF, Hagar, ALMOG, Orna, TUR-KASPA, Ran

    Published in Digestive diseases and sciences (01-11-2000)
    “…The mechanism of hepatitis C virus (HCV) -induced hepatotocellular carcinoma (HCC) is still unknown, but in vitro studies clearly suggest that HCV proteins…”
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    Journal Article
  11. 11

    The Protein Kinase C-Related PKC-L(η) Gene Product Is Localized in the Cell Nucleus by Greif, Hagar, Ben-Chaim, Jacob, Shimon, Tova, Bechor, Edna, Eldar, Hagit, Livneh, Etta

    Published in Molecular and cellular biology (01-03-1992)
    “…The tumor promoters phorbol esters are thought to induce changes in cell growth and gene expression by direct activation of protein kinase C (PKC). However,…”
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    Journal Article