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Nucleic Acids Research|July 24, 2002
Real-time monitoring of rolling-circle amplification using a modified molecular beacon designMats Nilsson, Mats Gullberg, Fredrik Dahl, et al.Nature Methods|March 23, 2005
In situ genotyping individual DNA molecules by target-primed rolling-circle amplification of padlock probesChatarina Larsson, Jørn Koch, Anders Nygren, et al.Analytical Biochemistry|September 10, 2003
Fluorescence properties, thermal duplex stability, and kinetics of formation of cyanin platinum DNAsFrans M van de Rijke, Robert J Heetebrij, Eduard G Talman, et al.Mutation Research|October 6, 2005
Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutationRoshan S Jahangir Tafrechi, Peter J Svensson, George M C Janssen, et al.Cancer Genetics and Cytogenetics|April 24, 2004
A novel t(6;14)(q25-q27;q32) in acute myelocytic leukemia involves the BCL11B geneVladimir Bezrookove, Shama L van Zelderen-Bhola, Antoinette Brink, et al.Endocrinology and Metabolism Clinics of North America|April 25, 2006
New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndromeJohannes A Maassen, Roshan S Jahangir Tafrechi, George M C Janssen, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|August 7, 2002
Localization and regulation of the growth hormone receptor and growth hormone-binding protein in the rat growth plateEvelien F Gevers, Bram C J van der Eerden, Marcel Karperien, et al.Genes & Development|March 17, 2005
Cancer-associated mutations in chromatin remodeler hSNF5 promote chromosomal instability by compromising the mitotic checkpointRobert G J Vries, Vladimir Bezrookove, Lobke M P Zuijderduijn, et al.Human Molecular Genetics|July 28, 2007
The A3243G tRNALeu(UUR) mutation induces mitochondrial dysfunction and variable disease expression without dominant negative acting translational defects in complex IV subunits at UUR codonsGeorge M C Janssen, Paul J Hensbergen, Frans J van Bussel, et al.European Journal of Human Genetics : EJHG|July 11, 2002
Connexin 26 mutations in cases of sensorineural deafness in eastern AustriaKlemens Frei, Károly Szuhai, Trevor Lucas, et al.Pageof 3