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Clinical Pharmacology and Therapeutics|December 29, 2006
CYP3A5 genotype markedly influences the pharmacokinetics of tacrolimus and sirolimus in kidney transplant recipientsL Renders, M Frisman, M Ufer, et al.
Archives of Gynecology and Obstetrics|February 8, 2013
Aurora kinase inhibitor AZD1152 has an additional effect of platinum on a sequential application at the human ovarian cancer cell line SKOV3Yaxi Ma, Jörg Weimer, Regina Fredrik, et al.
Journal of Medical Genetics|August 21, 2020
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in <i>protein kinase D1</i>Svenja Alter, Andreas David Zimmer, Misun Park, et al.
Physical Review Letters|February 1, 2008
Polarization studies of resonant forbidden reflections in liquid crystalsP Fernandes, P Barois, S T Wang, et al.
European Journal of Medical Genetics|May 25, 2015
Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotypeJulia Kolarova, Imke Tangen, Susanne Bens, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delayJörg Weimer, Simone Metzke-Heidemann, Hansjörg Plendl, et al.
European Journal of Medical Genetics|July 9, 2011
A 2 Mb deletion in 14q13 associated with severe developmental delay and hemophagocytic lymphohistiocytosisAlmuth Caliebe, Jose I Martin Subero, Hiltrud Muhle, et al.
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