Výsledky vyhledávání - Vered Raz
- Zobrazuji výsledky 1 - 10 z 10
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The nuclear lamina promotes telomere aggregation and centromere peripheral localization during senescence of human mesenchymal stem cells Autor Vered Raz, Bart J. Vermolen, Yuval Garini, J. J. M. Onderwater, Mieke Mommaas-Kienhuis, Abraham J. Koster, Ian Young, Hans J. Tanke, Roeland W. Dirks
Vydáno 2008Artigo -
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Poly(A) binding protein nuclear 1 levels affect alternative polyadenylation Autor Eleonora de Klerk, Andrea Venema, Seyed Yahya Anvar, Jelle J. Goeman, OuHua Hu, Capucine Trollet, George Dickson, Johan T. den Dunnen, Silvère M. van der Maarel, Vered Raz, Peter A.C. ‘t Hoen
Vydáno 2012Artigo -
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A decline in PABPN1 induces progressive muscle weakness in Oculopharyngeal muscle dystrophy and in muscle aging Autor Seyed Yahya Anvar, Yotam Raz, Nisha Verwey, Barbara van der Sluijs, Andrea Venema, Jelle J. Goeman, John Vissing, Silvère M. van der Maarel, Peter A.C. ‘t Hoen, Baziel G.M. van Engelen, Vered Raz
Vydáno 2013Artigo -
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Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients Autor Seyed Yahya Anvar, Peter A.C. ‘t Hoen, Andrea Venema, Barbara van der Sluijs, Baziel G.M. van Engelen, M.M.J. Snoeck, John Vissing, Capucine Trollet, George Dickson, Aymeric Chartier, Martine Simonelig, Gert‐Jan B. van Ommen, Silvère M. van der Maarel, Vered Raz
Vydáno 2011Artigo -
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Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres Autor Capucine Trollet, Seyed Yahya Anvar, Andrea Venema, Iain P. Hargreaves, Keith Foster, Alban Vignaud, Arnaud Ferry, Elisa Négroni, Christophe Hourdé, Martín A. Baraibar, Peter A.C. ‘t Hoen, J. Eric Davies, David C. Rubinsztein, Simon Heales, Vincent Mouly, Silvère M. van der Maarel, Gillian Butler‐Browne, Vered Raz, George Dickson
Vydáno 2010Artigo -
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Diffusion‐tensor magnetic resonance imaging captures increased skeletal muscle fibre diameters in Becker muscular dystrophy Autor Donnie Cameron, Tooba Abbassi‐Daloii, Laura G.M. Heezen, Nienke M. van de Velde, Zaïda Koeks, Thom T. J. Veeger, Melissa T. Hooijmans, Salma el Abdellaoui, Sjoerd G. van Duinen, Jan J.G.M. Verschuuren, Maaike van Putten, Annemieke Aartsma‐Rus, Vered Raz, Pietro Spitali, Erik H. Niks, Hermien E. Kan
Vydáno 2023Artigo -
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Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy Autor Marlinde L. van den Boogaard, Richard J.L.F. Lemmers, Judit Balog, Mariëlle Wohlgemuth, Mari Auranen, Satomi Mitsuhashi, Patrick J. van der Vliet, Kirsten R. Straasheijm, Rob F. P. van den Akker, Marjolein Kriek, Marlies E.Y. Laurense-Bik, Vered Raz, Monique M. van Ostaijen-ten Dam, Kerstin Hansson, E.L. van der Kooi, Sari Kiuru‐Enari, B. Udd, Maarten J. D. van Tol, Ichizo Nishino, Rabi Tawil, Stephen J. Tapscott, Baziel G.M. van Engelen, Silvère M. van der Maarel
Vydáno 2016Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Muscular dystrophy
Anatomy
Medicine
Oculopharyngeal muscular dystrophy
Pathology
Atrophy
Cell biology
Computational biology
Endocrinology
Gene expression
Internal medicine
Phenotype
Animal model
Basal lamina
Bioinformatics
Cadaveric spasm
Cell
Cleavage and polyadenylation specificity factor
Computer science
DNA
DNMT3B
Degeneration (medical)
Diffusion MRI
Epigenetics
Facioscapulohumeral muscular dystrophy
Fibrosis
Gene knockdown