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Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia.
Grabowska D, Plochocka D, Jablonska-Skwiecinska E, Chelstowska A, Lewandowska I, Staniszewska K, Majewska Z, Witos I, Burzynska B. Grabowska D, et al. Among authors: burzynska b. Eur J Haematol. 2003 Jun;70(6):404-9. doi: 10.1034/j.1600-0609.2003.00070.x. Eur J Haematol. 2003. PMID: 12756024
A novel mutation in the glucose-6-phosphate dehydrogenase gene in a subject with chronic nonspherocytic hemolytic anemia--characterization of enzyme using yeast expression system and molecular modeling.
Grabowska D, Jablonska-Skwiecinska E, Plochocka D, Chelstowska A, Lewandowska I, Witos I, Majewska Z, Rokicka-Milewska R, Burzynska B. Grabowska D, et al. Among authors: burzynska b. Blood Cells Mol Dis. 2004 Jan-Feb;32(1):124-30. doi: 10.1016/j.bcmd.2003.11.001. Blood Cells Mol Dis. 2004. PMID: 14757426
Diversity of thalassemia variants in Poland - screening by real-time PCR.
Maciag M, Płochocka D, Adamowicz-Salach A, Jackowska T, Mendek-Czajkowska E, Pawelczyk A, Zdebska E, Burzynska B. Maciag M, et al. Among authors: burzynska b. Acta Haematol. 2008;120(3):153-7. doi: 10.1159/000178147. Epub 2008 Nov 28. Acta Haematol. 2008. PMID: 19039207 No abstract available.
Functional expression of human HMG-CoA reductase in Saccharomyces cerevisiae: a system to analyse normal and mutated versions of the enzyme in the context of statin treatment.
Wysocka-Kapcinska M, Lutyk-Nadolska J, Kiliszek M, Plochocka D, Maciag M, Leszczynska A, Rytka J, Burzynska B. Wysocka-Kapcinska M, et al. Among authors: burzynska b. J Appl Microbiol. 2009 Mar;106(3):895-902. doi: 10.1111/j.1365-2672.2008.04060.x. Epub 2009 Jan 27. J Appl Microbiol. 2009. PMID: 19187128
47 results