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Showing results 41 to 60 of 373
Full TextIssue DateTitleAuthor(s)
2004Cerebral creatine kinase deficiency influences metabolite levels and morphology in the mouse brain: a quantitative in vivo 1H and 31P magnetic resonance study.Zandt, H.J.A. in t; Renema, W.K.J.; Streijger, F., et al
2004Characterization of multiple transcripts and isoforms derived from the mouse protein tyrosine phosphatase gene Ptprr.Chirivi, R.G.S.; Dilaver, G.; Vorstenbosch, R.A. van de, et al
2005Charge-state resolved mid-infrared spectroscopy of a gas-phase proteinOomens, J.; Polfer, N.; Moore, D.T., et al
2012The chromatin remodeling complex NuRD establishes the poised state of rRNA genes characterized by bivalent histone modifications and altered nucleosome positionsXie, W.; Ling, T.; Zhou, Y., et al
2010Chromosome missegregation causes colon cancer by APC loss of heterozygosity.Baker, D.J.; Deursen, J.M.A. van
2007Chromosome-wide nucleosome replacement and H3.3 incorporation during mammalian meiotic sex chromosome inactivation.Heijden, G.W. van der; Derijck, A.H.A.; Posfai, E., et al
2011Clearance of p16Ink4a-positive senescent cells delays ageing-associated disordersBaker, D.J.; Wijshake, T.; Tchkonia, T., et al
2010Clinical spectrum of the pseudotumor cerebri complex in children.Tibussek, D.; Schneider, D.T.; Meulebroecke, N. van de, et al
2004A closed binding pocket and global destabilization modify the binding properties of an alternatively spliced form of the second PDZ domain of PTP-BL.Walma, T.; Aelen, J.M.A.; Nabuurs, S.B., et al
2006Coiled-coil interactions modulate multimerization, mitochondrial binding and kinase activity of myotonic dystrophy protein kinase splice isoforms.Herpen, R.E.M.A. van; Tjeertes, J.V.; Mulders, S.A.M., et al
2007Cold collisions catalyse conformational conversionErlekam, U.; Frankowski, M.; Helden, G. von, et al
2009Collagen-based cell migration models in vitro and in vivo.Wolf, K.A.; Alexander, S.; Schacht, V., et al
2009Collective cell migration in morphogenesis, regeneration and cancer.Friedl, P.H.A.; Gilmour, D.
2007Combined loss of Hey1 and HeyL causes congenital heart defects because of impaired epithelial to mesenchymal transition.Fischer, A.; Steidl, C.; Wagner, T.U., et al
2010Complete brain-type creatine kinase deficiency in mice blocks seizure activity and affects intracellular calcium kinetics.Streijger, F.; Scheenen, W.J.J.M.; Luijtelaar, G. van, et al
2010Complex I disorders: causes, mechanisms, and development of treatment strategies at the cellular level.Valsecchi, F.; Koopman, W.J.H.; Manjeri, G.R., et al
2000Compressibility of co intercalated c-60 crystalsSmaalen, S. Van; Dinnebier, R.E.; Milletich, R., et al
2008Conditional deletion of the Itgb4 integrin gene in Schwann cells leads to delayed peripheral nerve regeneration.Zee, C.E.E.M. van der; Kreft, M.; Beckers, G., et al
1997Confining CO molecules in stable orbitsJongma, R.T.; Helden, G. von; Berden, G., et al
2009Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder.Janssen, R.J.R.J.; Distelmaier, F.; Smeets, R.J.P., et al
Showing results 41 to 60 of 373

 

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