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Clinical Chemistry and Laboratory Medicine|May 19, 2005
Autoantibodies against intrinsic factor (IF) measured with an ELISA using recombinant human IF as both catching and detecting reagentEbba Nexo, Ben Nooroya, Anne-Mette Hvas, et al.Nutrients|August 17, 2018
Dietary Intake of Vitamin B12 is Better for Restoring a Low B12 Status Than a Daily High-Dose Vitamin Pill: An Experimental Study in RatsEva Greibe, Ole Nymark, Sergey N Fedosov, et al.European Journal of Clinical Investigation|June 10, 2011
Trefoil factor family peptides in the human foetus and at birthMie H Samson, Steen S Poulsen, Rima Obeid, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|August 30, 2014
Organometallic B12-DNA conjugate: synthesis, structure analysis, and studies of binding to human B12-transporter proteinsMiriam Hunger, Elena Mutti, Alexander Rieder, et al.Clinical Biochemistry|March 11, 2010
Metformin induces reductions in plasma cobalamin and haptocorrin bound cobalamin levels in elderly diabetic patientsSharon Leung, Andre Mattman, Floyd Snyder, et al.Nutrients|October 17, 2018
Differences in Tissue Distribution of Cyano⁻B12 and Hydroxo⁻B12 One Week after Oral Intake: An Experimental Study in Male Wistar RatsEva Greibe, Ole Nymark, Sergey N Fedosov, et al.Nutrients|July 17, 2013
Metformin lowers serum cobalamin without changing other markers of cobalamin status: a study on women with polycystic ovary syndromeEva Greibe, Birgitta Trolle, Mustafa V Bor, et al.The Journal of Biological Chemistry|January 15, 2002
Comparative analysis of cobalamin binding kinetics and ligand protection for intrinsic factor, transcobalamin, and haptocorrinSergey N Fedosov, Lars Berglund, Natalya U Fedosova, et al.European Journal of Nutrition|October 18, 2017
Increase in circulating holotranscobalamin after oral administration of cyanocobalamin or hydroxocobalamin in healthy adults with low and normal cobalamin statusEva Greibe, Namita Mahalle, Vijayshri Bhide, et al.Journal of Inherited Metabolic Disease|July 8, 2010
Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in the TCN2 gene: a study of two affected siblings, their brother, and their parentsPeter H Nissen, Maria Nordwall, Elke Hoffmann-Lücke, et al.Pageof 15