Resultats de la cerca - Mitrani-Rosenbaum, S

Induction of Epstein-Barr virus nuclear antigen and DNA synthesis in a human epithelial cell line after Epstein-Barr virus infection. per Ben-Bassat, H, Mitrani-Rosenbaum, S, Goldblum, N

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Cycloheximide induces expression of the human interferon beta 1 gene in mouse cells transformed by bovine papillomavirus-interferon beta 1 recombinants. per Maroteaux, L, Chen, L, Mitrani-Rosenbaum, S, Howley, P M, Revel, M

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The Obesogenic and Glycemic Effect of Bariatric Surgery in a Family with a Melanocortin 4 Receptor Loss-of-Function Mutation per Ronit Grinbaum, Nahum Beglaibter, Stella Mitrani-Rosenbaum, Lee M. Kaplan, Danny Ben-Zvi

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In vivo and in vitro genome editing to explore GNE functions per Nili Ilouz, Avi Harazi, Miriam Guttman, Alon Daya, Shmuel Ruppo, Lena Yakovlev, Stella Mitrani-Rosenbaum

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Generation and characterization of a novel gne Knockout Model in Zebrafish per Hagay Livne, Hagay Livne, Tom Avital, Shmuel Ruppo, Avi Harazi, Avi Harazi, Stella Mitrani-Rosenbaum, Alon Daya

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GNE is involved in the early development of skeletal and cardiac muscle. per Irit Milman Krentsis, Ilan Sela, Rachel Eiges, Véronique Blanchard, Markus Berger, Michal Becker Cohen, Stella Mitrani-Rosenbaum

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The proteomic profile of hereditary inclusion body myopathy. per Ilan Sela, Irit Milman Krentsis, Zipora Shlomai, Menachem Sadeh, Ron Dabby, Zohar Argov, Hannah Ben-Bassat, Stella Mitrani-Rosenbaum

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Human primary skeletal muscle cells express glutamate receptor GluR3, are activated by glutamate, and are affected by autoimmune GluR3B antibodies of epilepsy patients per Mia Levite, Mia Levite, Nili Ilouz, Avi Harazi, Hadassa Goldberg-Stern, Hadassa Goldberg-Stern, Eithan Galun, Stella Mitrani-Rosenbaum

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UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle? per Shira Amsili, Hagit Zer, Stephan Hinderlich, Sabine Krause, Michal Becker-Cohen, Daniel G MacArthur, Kathryn N North, Stella Mitrani-Rosenbaum

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Variable myopathic presentation in a single family with novel skeletal RYR1 mutation. per Ruben Attali, Sharon Aharoni, Susan Treves, Ori Rokach, Michal Becker Cohen, Yakov Fellig, Rachel Straussberg, Talya Dor, Muhannad Daana, Stella Mitrani-Rosenbaum, Yoram Nevo

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Uncovering the Role of Hypermethylation by CTG Expansion in Myotonic Dystrophy Type 1 Using Mutant Human Embryonic Stem Cells per Shira Yanovsky-Dagan, Michal Avitzour, Gheona Altarescu, Paul Renbaum, Talia Eldar-Geva, Oshrat Schonberger, Stella Mitrani-Rosenbaum, Ephrat Levy-Lahad, Ramon Y. Birnbaum, Lior Gepstein, Silvina Epsztejn-Litman, Rachel Eiges

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