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Results: 80,353
Number of items: 80,353
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Harwit, M., Houde, M., Sonnentrucker, P., Boogert, A. C. A., Cernicharo, J., De Beck, E., Decin, L., Henkel, C., Higgins, R. D., Jellema, W., Kraus, A., McCoey, C., Melnick, G. J., Menten, K. M., Risacher, C., Teyssier, D., Vaillancourt, J. E., Alcolea, J., Bujarrabal, V., ... Waters, L. B. F. M. (2010). Polarisation observations of VY Canis Majoris H2O 5(32)-4(41) 620.701 GHz maser emission with HIFI. Astronomy & Astrophysics, 521, L51. https://doi.org/10.1051/0004-6361/201015042 -
Meuwese, M. C., Broekhuizen, L. N., Kuikhoven, M., Heeneman, S., Lutgens, E., Gijbels, M. J. J., Nieuwdorp, M., Peutz, C. J., Stroes, E. S. G., Vink, H., & van den Berg, B. M. (2010). Endothelial surface layer degradation by chronic hyaluronidase infusion induces proteinuria in apolipoprotein e-deficient mice. PLoS ONE, 5(12), e14262. https://doi.org/10.1371/journal.pone.0014262 -
Vega, H., Trainer, A. H., Gordillo, M., Crosier, M., Kayserili, H., Skovby, F., Uzielli, M. L. G., Schnur, R. E., Manouvrier, S., Blair, E., Hurst, J. A., Forzano, F., Meins, M., Simola, K. O. J., Raas-Rothschild, A., Hennekam, R. C. M., & Jabs, E. W. (2010). Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome. Journal of Medical Genetics, 47(1), 30-37. https://doi.org/10.1136/jmg.2009.068395 -
Noordik, E., van der Klink, J. J. L., Klingen, E. F., Nieuwenhuijsen, K., & van Dijk, F. J. H. (2010). Exposure-in-vivo containing interventions to improve work functioning of workers with anxiety disorder: a systematic review. BMC Public Health, 10(1), 598. https://doi.org/10.1186/1471-2458-10-598 -
Kalenscher, T., Tobler, P. N., Huijbers, W., Daselaar, S. M., & Pennartz, C. M. A. (2010). Neural signatures of intransitive preferences. Frontiers in Human Neuroscience, 4, 49. https://doi.org/10.3389/fnhum.2010.00049
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