Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Beata Burzyńska"'
Autor:
Beata Hukowska-Szematowicz, Agata Maciejak-Jastrzębska, Małgorzata Blatkiewicz, Karolina Maciak, Monika Góra, Joanna Janiszewska, Beata Burzyńska
Publikováno v:
Viruses, Vol 12, Iss 9, p 965 (2020)
Current knowledge on the role of microRNAs (miRNAs) in rabbit hemorrhagic disease virus (RHDV) infection and the pathogenesis of rabbit hemorrhagic disease (RHD) is still limited. RHDV replicates in the liver, causing hepatic necrosis and liver failu
Externí odkaz:
https://doaj.org/article/2e225377dcd14ae3a291e5d99343e92c
Autor:
Augustin Toma, Claudia dos Santos, Beata Burzyńska, Monika Góra, Marek Kiliszek, Natalie Stickle, Holger Kirsten, Leah B. Kosyakovsky, Bo Wang, Sean van Diepen, Slava Epelman, Yishay Szekely, John C. Marshall, Filio Billia, Patrick R. Lawler
Publikováno v:
Circulation research. 131(1)
Autor:
Anna Teresa Kobrzycka, Adrian Mateusz Stankiewicz, Joanna Goscik, Monika Gora, Beata Burzynska, Roksana Iwanicka-Nowicka, Krystyna Pierzchala-Koziec, Marek Wieczorek
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 16 (2022)
BackgroundVagus nerve is one of the crucial routes in communication between the immune and central nervous systems. The impaired vagal nerve function may intensify peripheral inflammatory processes. This effect subsides along with prolonged recovery
Externí odkaz:
https://doaj.org/article/2f799512b51f46ea97bb377562abadc3
Publikováno v:
Medycyna wieku rozwojowego. 13(2)
THE AIM of the study is a genetic analysis of hereditary chronic nonspherocytic anaemia in a case, caused by mutation in the glucose-6-phosphate dehydrogenase gene.The activity of G6PD enzyme was established. PCR method and DNA sequencing were implem
Autor:
Karolina Maciak, Anna Adamowicz-Salach, Jaroslaw Poznanski, Monika Gora, Jan Fronk, Beata Burzynska
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
BackgroundRed cell pyruvate kinase deficiency (PKD) is a defect of glycolysis causing congenital non-spherocytic hemolytic anemia. PKD is transmitted as an autosomal recessive trait. The clinical features of PKD are highly variable, from mild to life
Externí odkaz:
https://doaj.org/article/95fc731f9f88471d858bbb6ecfb86135
Autor:
Katarzyna Rawa, Roman J. Szczesny, Ewelina P. Owczarek, Anna Adamowicz-Salach, Anna Klukowska, Urszula Demkow, Danuta Plochocka, Pawel Szczesny, Monika Gora, Andrzej Dziembowski, Beata Burzynska
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background The thalassemia syndromes are classified according to the globin chain or chains whose production is affected. β-thalassemias are caused by point mutations or, more rarely, deletions or insertions of a few nucleotides in the β-g
Externí odkaz:
https://doaj.org/article/fc2fa0a2aaf14b5aa45fdaf66d2a68f1
Autor:
Clint Mizzi, Eleni Dalabira, Judit Kumuthini, Nduna Dzimiri, Istvan Balogh, Nazli Başak, Ruwen Böhm, Joseph Borg, Paola Borgiani, Nada Bozina, Henrike Bruckmueller, Beata Burzynska, Angel Carracedo, Ingolf Cascorbi, Constantinos Deltas, Vita Dolzan, Anthony Fenech, Godfrey Grech, Vytautas Kasiulevicius, Ľudevít Kádaši, Vaidutis Kučinskas, Elza Khusnutdinova, Yiannis L Loukas, Milan Macek, Halyna Makukh, Ron Mathijssen, Konstantinos Mitropoulos, Christina Mitropoulou, Giuseppe Novelli, Ioanna Papantoni, Sonja Pavlovic, Giuseppe Saglio, Jadranka Sertić, Maja Stojiljkovic, Andrew P Stubbs, Alessio Squassina, Maria Torres, Marek Turnovec, Ron H van Schaik, Konstantinos Voskarides, Salma M Wakil, Anneke Werk, Maria Del Zompo, Branka Zukic, Theodora Katsila, Ming Ta Michael Lee, Alison Motsinger-Rief, Howard L Mc Leod, Peter J van der Spek, George P Patrinos
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172595 (2017)
[This corrects the article DOI: 10.1371/journal.pone.0162866.].
Externí odkaz:
https://doaj.org/article/bfb926067d6344b3b90c530f5e7e1bb4
Autor:
Clint Mizzi, Eleni Dalabira, Judit Kumuthini, Nduna Dzimiri, Istvan Balogh, Nazli Başak, Ruwen Böhm, Joseph Borg, Paola Borgiani, Nada Bozina, Henrike Bruckmueller, Beata Burzynska, Angel Carracedo, Ingolf Cascorbi, Constantinos Deltas, Vita Dolzan, Anthony Fenech, Godfrey Grech, Vytautas Kasiulevicius, Ľudevít Kádaši, Vaidutis Kučinskas, Elza Khusnutdinova, Yiannis L Loukas, Milan Macek, Halyna Makukh, Ron Mathijssen, Konstantinos Mitropoulos, Christina Mitropoulou, Giuseppe Novelli, Ioanna Papantoni, Sonja Pavlovic, Giuseppe Saglio, Jadranka Setric, Maja Stojiljkovic, Andrew P Stubbs, Alessio Squassina, Maria Torres, Marek Turnovec, Ron H van Schaik, Konstantinos Voskarides, Salma M Wakil, Anneke Werk, Maria Del Zompo, Branka Zukic, Theodora Katsila, Ming Ta Michael Lee, Alison Motsinger-Rief, Howard L Mc Leod, Peter J van der Spek, George P Patrinos
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162866 (2016)
Pharmacogenomics aims to correlate inter-individual differences of drug efficacy and/or toxicity with the underlying genetic composition, particularly in genes encoding for protein factors and enzymes involved in drug metabolism and transport. In sev
Externí odkaz:
https://doaj.org/article/65d317caa72545be89067d0f39dc3afe
Autor:
Anna Szpakowicz, Marek Kiliszek, Witold Pepinski, Ewa Waszkiewicz, Maria Franaszczyk, Malgorzata Skawronska, Rafal Ploski, Anna Niemcunowicz-Janica, Beata Burzynska, Dorota Tulacz, Agata Maciejak, Marcin Jakub Kaminski, Grzegorz Opolski, Wlodzimierz Jerzy Musial, Karol Adam Kaminski
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0129820 (2015)
The rs12526453 (C/G) is a single nucleotide polymorphism in an intron of the PHACTR1 gene (phosphatase and actin regulator 1). The C allele is associated with increased risk of coronary artery disease in an unknown mechanism. We investigated its asso
Externí odkaz:
https://doaj.org/article/617119898743425a8fa3d177f2bd5ade
Autor:
Marek Kiliszek, Beata Burzynska, Marcin Michalak, Monika Gora, Aleksandra Winkler, Agata Maciejak, Agata Leszczynska, Ewa Gajda, Janusz Kochanowski, Grzegorz Opolski
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e50054 (2012)
Despite a substantial progress in diagnosis and therapy, acute myocardial infarction (MI) is a major cause of mortality in the general population. A novel insight into the pathophysiology of myocardial infarction obtained by studying gene expression
Externí odkaz:
https://doaj.org/article/2442d27dce0d4aa3b832c63a8e1278c2