Search Results - "Greif, Hagar"
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Trehalose alleviates the phenotype of Machado-Joseph disease mouse models
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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Frataxin‐deficient neurons and mice models of Friedreich ataxia are improved by TAT‐MTScs‐FXN treatment
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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Heterologous mitochondrial targeting sequences can deliver functional proteins into mitochondria
Published in The international journal of biochemistry & cell biology (01-12-2016)“…Mitochondrial Targeting Sequences (MTSs) are responsible for trafficking nuclear-encoded proteins into mitochondria. Once entering the mitochondria, the MTS is…”
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Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy
Published in Acta neuropathologica (01-12-2022)“…Oculopharyngeal muscular dystrophy (OPMD) is a rare muscle disease characterized by an onset of weakness in the pharyngeal and eyelid muscles. The disease is…”
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Frataxin‐deficient neurons and mice models of Friedreich ataxia are improved by TAT ‐ MTS cs‐ FXN treatment
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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TAT‐MTS‐MCM fusion proteins reduce MMA levels and improve mitochondrial activity and liver function in MCM‐deficient cells
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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A flow cytometry-based reporter assay identifies macrolide antibiotics as nonsense mutation read-through agents
Published in Journal of molecular medicine (Berlin, Germany) (01-04-2016)“…A large number of human diseases are caused by nonsense mutations. These mutations result in premature protein termination and the expression of truncated,…”
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The protein kinase C-related PKC-L(eta) gene product is localized in the cell nucleus
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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Mutations at vicinity of catalytic sites of hepatitis C virus NS3 serine protease gene isolated from hepatocellular carcinoma tissue
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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The Protein Kinase C-Related PKC-L(η) Gene Product Is Localized in the Cell Nucleus
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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