Showing results (1261-1270 of 1,502) with videos related to

Sort By:
Pageof 151
The Journal of Molecular Diagnostics : JMD|December 26, 2016
Accurate Quantification of T Cells by Measuring Loss of Germline T-Cell Receptor Loci with Generic Single Duplex Droplet Digital PCR AssaysWillem H Zoutman, Rogier J Nell, Mieke Versluis, et al.
Environmental Health Perspectives|May 16, 2000
Does the risk of childhood diabetes mellitus require revision of the guideline values for nitrate in drinking water?J M van Maanen, H J Albering, T M de Kok, et al.
Journal of Neurology|October 31, 2012
ATL1 and REEP1 mutations in hereditary and sporadic upper motor neuron syndromesS T de Bot, J H Veldink, S Vermeer, et al.
JCI Insight|May 18, 2018
CSF1R-dependent myeloid cells are required for NK‑mediated control of metastasisMichal Beffinger, Paulino Tallón de Lara, Sònia Tugues, et al.
Oncotarget|May 11, 2017
Genetic rearrangements result in altered gene expression and novel fusion transcripts in Sézary syndromeKatarzyna Iżykowska, Grzegorz K Przybylski, Claudia Gand, et al.
Plos One|February 10, 2018
Correction: Variability and cost implications of three generations of the Roche LightCycler® 480Maria Dullaert-de Boer, Onno W Akkerman, Marloes Vermeer, et al.
Blood|June 24, 2008
European Organization for Research and Treatment of Cancer and International Society for Cutaneous Lymphoma consensus recommendations for the management of cutaneous B-cell lymphomasNancy J Senff, Evert M Noordijk, Youn H Kim, et al.
Helicobacter|June 6, 2002
Helicobacter pylori does not mediate the formation of carcinogenic N-nitrosaminesI T M Vermeer, M M Gerrits, E J C Moonen, et al.
Journal of Medical Genetics|November 25, 2011
Neonatal onset autosomal dominant polycystic kidney disease (ADPKD) in a patient homozygous for a PKD2 missense mutation due to uniparental disomyM Losekoot, C A L Ruivenkamp, A P Tholens, et al.
Thrombosis and Haemostasis|January 12, 2001
Congenital deficiency of vitamin K dependent coagulation factors in two families presents as a genetic defect of the vitamin K-epoxide-reductase-complexJ Oldenburg, B von Brederlow, A Fregin, et al.
Pageof 151