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Clinical Chemistry|February 5, 2013
Importance of the efficiency of double-stranded DNA formation in cDNA synthesis for the imprecision of microarray expression analysisHans G Thormar, Bjarki Gudmundsson, Freyja Eiriksdottir, et al.European Journal of Human Genetics : EJHG|June 12, 2020
Web-based return of BRCA2 research results: one-year genetic counselling experience in IcelandVigdis Stefansdottir, Eirny Thorolfsdottir, Hakon B Hognason, et al.Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|December 7, 2017
Late detection of a shigellosis outbreak in a school in MadridJ Jonsson, M C Del Álvarez-Castillo, J C Sanz, et al.Nutrition and Cancer|October 12, 2007
Positive association between DNA strand breaks in peripheral blood mononuclear cells and polyunsaturated fatty acids in red blood cells from womenAudur Y Thorlaksdottir, Jon J Jonsson, Laufey Tryggvadottir, et al.Immunology and Cell Biology|March 8, 2006
IL10 and IL12B polymorphisms each influence IL-12p70 secretion by dendritic cells in response to LPSJudy C Peng, Sazaly Abu Bakar, Michelle M Richardson, et al.Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|November 12, 2005
Late detection of a shigellosis outbreak in a school in MadridJ Jonsson, M del Carmen Alvarez-Castillo, J C Sanz, et al.Genomics|April 16, 1998
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardationM Piccini, F Vitelli, M Bruttini, et al.Lipids|August 21, 2007
Positive association between plasma antioxidant capacity and n-3 PUFA in red blood cells from womenA Y Thorlaksdottir, G V Skuladottir, A L Petursdottir, et al.Nucleic Acids Research|July 28, 2018
Northern lights assay: a versatile method for comprehensive detection of DNA damageBjarki Gudmundsson, Hans G Thormar, Albert Sigurdsson, et al.Journal of Medical Genetics|May 23, 1998
Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?J J Jonsson, A Renieri, P G Gallagher, et al.Pageof 14