Pages that link to "Q59554094"
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The following pages link to Beata Burzyńska (Q59554094):
Displayed 41 items.
- Maria Joanna Radomska (Q8864510) (← links)
- Gene expression profiling reveals potential prognostic biomarkers associated with the progression of heart failure (Q28262080) (← links)
- A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics (Q28554199) (← links)
- Compound heterozygosity of two missense mutations in the NADH-cytochrome b5 reductase gene of a Polish patient with type I recessive congenital methaemoglobinaemia. (Q30332864) (← links)
- Investigating the effects of statins on cellular lipid metabolism using a yeast expression system (Q33521217) (← links)
- Transcriptional profiling of left ventricle and peripheral blood mononuclear cells in a rat model of postinfarction heart failure. (Q34481362) (← links)
- Altered gene expression pattern in peripheral blood mononuclear cells in patients with acute myocardial infarction (Q34490950) (← links)
- The effects of statins on the mevalonic acid pathway in recombinant yeast strains expressing human HMG-CoA reductase. (Q35017735) (← links)
- The rs12526453 Polymorphism in an Intron of the PHACTR1 Gene and Its Association with 5-Year Mortality of Patients with Myocardial Infarction (Q35667272) (← links)
- Two novel C-terminal frameshift mutations in the β-globin gene lead to rapid mRNA decay (Q36396254) (← links)
- Molecular evidence that exercise training has beneficial effects on cardiac performance (Q37027249) (← links)
- Will global transcriptome analysis allow the detection of novel prognostic markers in coronary artery disease and heart failure? (Q37389353) (← links)
- 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. (Q37420161) (← links)
- Different statins produce highly divergent changes in gene expression profiles of human hepatoma cells: a pilot study. (Q38499630) (← links)
- Theoretical model of reticulocyte to erythrocyte shape transformation (Q40302540) (← links)
- Correction: A European Spectrum of Pharmacogenomic Biomarkers: Implications for Clinical Pharmacogenomics (Q42320992) (← links)
- The first reported case of G6PD deficiency due to Seoul mutation in Poland (Q42375139) (← links)
- 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 (Q44752260) (← links)
- Characterization of a novel mutation in the NADH-cytochrome b5 reductase gene responsible for rare hereditary methaemoglobinaemia type I. (Q44829660) (← links)
- miR-22-5p revealed as a potential biomarker involved in the acute phase of myocardial infarction via profiling of circulating microRNAs. (Q46507195) (← links)
- Molecular analysis of three novel G6PD variants: G6PD Pedoplis-Ckaro, G6PD Piotrkow and G6PD Krakow (Q46861084) (← links)
- Feto-maternal haemorrhage assessment in a woman with a large population of red blood cells containing fetal haemoglobin. (Q50460367) (← links)
- Novel beta-spectrin mutations in hereditary spherocytosis associated with decreased levels of mRNA. (Q50605425) (← links)
- Genetic engineering and molecular characterization of yeast strain expressing hybrid human-yeast squalene synthase as a tool for anti-cholesterol drug assessment. (Q51565685) (← links)
- Diversity of thalassemia variants in Poland - screening by real-time PCR. (Q54505505) (← links)
- Circulating miR-30a-5p as a prognostic biomarker of left ventricular dysfunction after acute myocardial infarction. (Q55501361) (← links)
- Agata Maciejak (Q59683404) (← links)
- Graphene oxide down-regulates genes of the oxidative phosphorylation complexes in a glioblastoma (Q60921316) (← links)
- 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 (Q73205340) (← links)
- Molecular and haematological studies of four families with hereditary spherocytosis resulting from band 3 deficiency (Q80129953) (← links)
- A1166C polymorphism of the angiotensin AT1 receptor (AT1R) gene alters endothelial response to statin treatment (Q80580628) (← links)
- Theoretical model of thalassemic erythrocyte shape transformation (Q81695121) (← links)
- Coexistence of Gilbert syndrome with hereditary haemolytic anaemias (Q84066552) (← links)
- [The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia] (Q84742412) (← links)
- Interindividual variability of atorvastatin treatment influence on the MPO gene expression in patients after acute myocardial infarction (Q86961817) (← links)
- Serum microRNA in patients undergoing atrial fibrillation ablation (Q90208368) (← links)
- Hereditary xerocytosis - spectrum and clinical manifestations of variants in the PIEZO1 gene, including co-occurrence with a novel β-globin mutation (Q91030421) (← links)
- Asthma and hyperbilirubinemia: a new aspect to analyze? (Q91993207) (← links)
- Changes in MicroRNA Expression during Rabbit Hemorrhagic Disease Virus (RHDV) Infection (Q98904574) (← links)
- A Family Affected by a Life-Threatening Erythrocyte Defect Caused by Pyruvate Kinase Deficiency With Normal Iron Status: A Case Report (Q102066818) (← links)
- Agata Leszczynska (Q122105117) (← links)