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List of works by Beata Burzyńska

A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

scientific article

A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report

scientific article published on 28 October 2020

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

scientific article published in January 2004

A1166C polymorphism of the angiotensin AT1 receptor (AT1R) gene alters endothelial response to statin treatment

scientific article published on 01 January 2007

Altered gene expression pattern in peripheral blood mononuclear cells in patients with acute myocardial infarction

scientific article

Asthma and hyperbilirubinemia: a new aspect to analyze?

scientific article published on 01 October 2019

Changes in MicroRNA Expression during Rabbit Hemorrhagic Disease Virus (RHDV) Infection

scientific article published on 31 August 2020

Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I.

scientific article published on 13 April 2013

Circulating miR-30a-5p as a prognostic biomarker of left ventricular dysfunction after acute myocardial infarction. ⬇️

scientific article published on 29 June 2018

Coexistence of Gilbert syndrome with hereditary haemolytic anaemias

scientific article published on 03 May 2012

Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia.

scientific article

Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics

scientific article published on 16 February 2017

Different statins produce highly divergent changes in gene expression profiles of human hepatoma cells: a pilot study.

scientific article

Diversity of thalassemia variants in Poland - screening by real-time PCR.

scientific article

Feto-maternal haemorrhage assessment in a woman with a large population of red blood cells containing fetal haemoglobin

scientific article published in August 2014

Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure

scientific article

Genetic engineering and molecular characterization of yeast strain expressing hybrid human-yeast squalene synthase as a tool for anti-cholesterol drug assessment

scientific article published on 12 January 2016

Graphene oxide down-regulates genes of the oxidative phosphorylation complexes in a glioblastoma

article

Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation

scientific article published on 22 October 2019

Interindividual variability of atorvastatin treatment influence on the MPO gene expression in patients after acute myocardial infarction

scientific article published on 23 December 2015

Investigating the effects of statins on cellular lipid metabolism using a yeast expression system

scientific article

Molecular analysis of three novel G6PD variants: G6PD Pedoplis-Ckaro, G6PD Piotrkow and G6PD Krakow

scientific article published on 8 December 2007

Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency

scientific article published on 01 January 2006

Molecular evidence that exercise training has beneficial effects on cardiac performance

scientific article published on June 2016

Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA.

scientific article published on 15 June 2009

Serum microRNA in patients undergoing atrial fibrillation ablation

scientific article published on 10 March 2020

Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism

scientific article published on 01 January 1999

The effects of statins on the mevalonic acid pathway in recombinant yeast strains expressing human HMG-CoA reductase.

scientific article

The first reported case of G6PD deficiency due to Seoul mutation in Poland

scientific article published on May 2014

The rs12526453 Polymorphism in an Intron of the PHACTR1 Gene and Its Association with 5-Year Mortality of Patients with Myocardial Infarction

scientific article published on 18 June 2015

The use of real-time PCR technique in the detection of novel protein 4.2 gene mutations that coexist with thalassaemia alpha in a single patient.

scientific article published on 08 June 2009

Theoretical model of reticulocyte to erythrocyte shape transformation

scientific article published on 20 June 2006

Theoretical model of thalassemic erythrocyte shape transformation

scientific article published on 03 July 2008

Transcriptional profiling of left ventricle and peripheral blood mononuclear cells in a rat model of postinfarction heart failure.

scientific article

Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay

scientific article

Will global transcriptome analysis allow the detection of novel prognostic markers in coronary artery disease and heart failure?

scientific article published on September 2013

[The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]

scientific article published on 01 April 2009

miR-22-5p revealed as a potential biomarker involved in the acute phase of myocardial infarction via profiling of circulating microRNAs.

scientific article published on 27 July 2016

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