Beata Burzynska

Beata Burzynska

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Beata Burzynska

Beata Burzynska

Publications by authors named "Beata Burzynska"

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33Publications

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

Blood Cells Mol Dis 2020 02 22;80:102378. Epub 2019 Oct 22.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Poland. Electronic address:

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http://dx.doi.org/10.1016/j.bcmd.2019.102378DOI Listing
February 2020

Asthma and hyperbilirubinemia: a new aspect to analyze?

Postepy Dermatol Alergol 2019 Oct 12;36(5):639-642. Epub 2019 Nov 12.

Department of Allergology, Medical University of Gdańsk, Gdańsk, Poland.

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http://dx.doi.org/10.5114/ada.2019.89511DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906975PMC
October 2019

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

Mol Med Rep 2016 Sep 27;14(3):2867-75. Epub 2016 Jul 27.

Department of Genetics, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, 02‑106 Warsaw, Poland.

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http://dx.doi.org/10.3892/mmr.2016.5566DOI Listing
September 2016

Molecular evidence that exercise training has beneficial effects on cardiac performance.

Ann Transl Med 2016 Jun;4(11):228

1 Department of Cardiology and Internal Diseases, Military Institute of Medicine, Warsaw, Poland ; 2 Department of Clinical Physiology, Medical Centre of Postgraduate Education, Warsaw, Poland ; 3 Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.

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http://dx.doi.org/10.21037/atm.2016.05.53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916357PMC
June 2016

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

BMC Med Genomics 2013 Nov 8;6:49. Epub 2013 Nov 8.

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.

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http://dx.doi.org/10.1186/1755-8794-6-49DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226214PMC
November 2013

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

Acta Haematol 2013 13;130(2):122-5. Epub 2013 Apr 13.

Department of Paediatrics, Haematology and Oncology, Medical University of Warsaw, Warsaw, Poland.

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http://dx.doi.org/10.1159/000347041DOI Listing
October 2013

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

Curr Genomics 2013 Sep;14(6):388-96

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland;

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http://dx.doi.org/10.2174/1389202911314090006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3861890PMC
September 2013

Coexistence of Gilbert syndrome with hereditary haemolytic anaemias.

J Clin Pathol 2012 Jul 3;65(7):663-5. Epub 2012 May 3.

Department of Paediatrics, Haematology and Oncology, Medical University of Warsaw, Warsaw, Poland.

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http://dx.doi.org/10.1136/jclinpath-2011-200580DOI Listing
July 2012

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

Acta Biochim Pol 2011 30;58(4):635-9. Epub 2011 Nov 30.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.

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May 2012

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

Med Wieku Rozwoj 2009 Apr-Jun;13(2):136-9

Zakład Genetyki, Instytut Biochemii i Biofizyki PAN, ul. Pawińskiego 5a, 02-106 Warszawa.

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November 2009

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.

Eur J Haematol 2009 Oct 8;83(4):373-7. Epub 2009 Jun 8.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5A, Warsaw, Poland.

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http://dx.doi.org/10.1111/j.1600-0609.2009.01289.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776934PMC
October 2009

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

Br J Haematol 2009 Aug 15;146(3):326-32. Epub 2009 Jun 15.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Poland.

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http://dx.doi.org/10.1111/j.1365-2141.2009.07759.xDOI Listing
August 2009

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

Acta Haematol 2008 28;120(3):153-7. Epub 2008 Nov 28.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland.

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http://dx.doi.org/10.1159/000178147DOI Listing
February 2009

Theoretical model of thalassemic erythrocyte shape transformation.

J Theor Biol 2008 Oct 3;254(3):575-9. Epub 2008 Jul 3.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.

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http://dx.doi.org/10.1016/j.jtbi.2008.06.029DOI Listing
October 2008

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

Acta Biochim Pol 2007 8;54(4):877-81. Epub 2007 Dec 8.

Institute of Biochemistry and Biophysics, PAS, Warszawa, Poland.

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August 2008

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

Clin Chem Lab Med 2007 ;45(7):839-42

Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.

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http://dx.doi.org/10.1515/CCLM.2007.151DOI Listing
October 2007

Theoretical model of reticulocyte to erythrocyte shape transformation.

J Theor Biol 2006 Nov 20;243(1):24-38. Epub 2006 Jun 20.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.

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http://dx.doi.org/10.1016/j.jtbi.2006.06.011DOI Listing
November 2006