Hagar Greif
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 8 publications
Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy.
Journal: Acta neuropathologica
Published: June 15, 2022
Trehalose alleviates the phenotype of Machado-Joseph disease mouse models.
Journal: Journal of translational medicine
Published: November 09, 2019
TAT-MTS-MCM fusion proteins reduce MMA levels and improve mitochondrial activity and liver function in MCM-deficient cells.
Journal: Journal of cellular and molecular medicine
Published: July 05, 2017
Analysis of Azithromycin Monohydrate as a Single or a Combinatorial Therapy in a Mouse Model of Severe Spinal Muscular Atrophy.
Journal: Journal of neuromuscular diseases
Published: June 10, 2017
Frataxin-deficient neurons and mice models of Friedreich ataxia are improved by TAT-MTScs-FXN treatment.
Journal: Journal of cellular and molecular medicine
Published: April 10, 2017
Heterologous mitochondrial targeting sequences can deliver functional proteins into mitochondria.
Journal: The international journal of biochemistry & cell biology
Published: May 03, 2016
Erratum to: A flow cytometry-based reporter assay identifies macrolide antibiotics as nonsense mutation read-through agents.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: February 22, 2016
A flow cytometry-based reporter assay identifies macrolide antibiotics as nonsense mutation read-through agents.
Journal: Journal of molecular medicine (Berlin, Germany)
Published: July 13, 2015
Showing 1-8 of 8
Last Updated: 09/26/2026