Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Urszula Ławrynowicz"'
Autor:
Magdalena Koczkowska, Marcin Jąkalski, Dorota Birkholz-Walerzak, Anna Kostecka, Mariola Iliszko, Magdalena Wójcik, Krzysztof Lewandowski, Katarzyna Milska-Musa, Patrick G. Buckley, Kinga Drężek, Ulana Juhas, Ewa Kuziemska, Agnieszka Maciejewska, Ryszard Pawłowski, Bartosz Wasąg, Natalia Filipowicz, Katarzyna Chojnowska, Urszula Ławrynowicz, Jan P. Dumanski, Beata S. Lipska-Ziętkiewicz, Jakub Mieczkowski, Arkadiusz Piotrowski
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract Numeric sex chromosome abnormalities are commonly associated with an increased cancer risk. Here, we report a 14-year-old boy with a rare mosaic 45, X/48, XYYY karyotype presenting with subtle dysmorphic features and relative height deficien
Externí odkaz:
https://doaj.org/article/eba34127d74f41ed9f5eae096cdf2fbe
Akademický článek
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Autor:
Natalia Filipowicz, Kinga Drężek, Monika Horbacz, Agata Wojdak, Jakub Szymanowski, Edyta Rychlicka-Buniowska, Ulana Juhas, Katarzyna Duzowska, Tomasz Nowikiewicz, Wiktoria Stańkowska, Katarzyna Chojnowska, Maria Andreou, Urszula Ławrynowicz, Magdalena Wójcik, Hanna Davies, Ewa Śrutek, Michał Bieńkowski, Katarzyna Milian-Ciesielska, Marek Zdrenka, Aleksandra Ambicka, Marcin Przewoźnik, Agnieszka Harazin-Lechowska, Agnieszka Adamczyk, Jacek Kowalski, Dariusz Bała, Dorian Wiśniewski, Karol Tkaczyński, Krzysztof Kamecki, Marta Drzewiecka, Paweł Wroński, Jerzy Siekiera, Izabela Ratnicka, Jerzy Jankau, Karol Wierzba, Jarosław Skokowski, Karol Połom, Mikołaj Przydacz, Łukasz Bełch, Piotr Chłosta, Marcin Matuszewski, Krzysztof Okoń, Olga Rostkowska, Andrzej Hellmann, Karol Sasim, Piotr Remiszewski, Marek Sierżęga, Stanisław Hać, Jarosław Kobiela, Łukasz Kaska, Michał Jankowski, Diana Hodorowicz-Zaniewska, Janusz Jaszczyński, Wojciech Zegarski, Wojciech Makarewicz, Rafał Pęksa, Joanna Szpor, Janusz Ryś, Łukasz Szylberg, Arkadiusz Piotrowski, Jan P Dumanski
Publikováno v:
PLoS ONE, Vol 17, Iss 4, p e0266111 (2022)
The progress in translational cancer research relies on access to well-characterized samples from a representative number of patients and controls. The rationale behind our biobanking are explorations of post-zygotic pathogenic gene variants, especia
Externí odkaz:
https://doaj.org/article/b558d36b91ac463bb740f5c0a9b37da2
Autor:
Kinga Drężek, Łukasz Bełch, Rafał Pęksa, Karol Sasim, Joanna Szpor, Marek Sierzega, Ewa Śrutek, Wojciech Zegarski, Edyta Rychlicka-Buniowska, Marcin Przewoźnik, Monika Horbacz, Łukasz Kaska, Arkadiusz Piotrowski, Dorian Wiśniewski, Krzysztof Okoń, Marek Zdrenka, Karol Tkaczyński, Michał Jankowski, Agnieszka Adamczyk, Dariusz Bała, Katarzyna Chojnowska, Krzysztof Kamecki, Wiktoria Stańkowska, Aleksandra Ambicka, Łukasz Szylberg, Diana Hodorowicz-Zaniewska, Janusz Jaszczyński, Magdalena Wójcik, Urszula Ławrynowicz, Mikolaj Przydacz, Jakub Szymanowski, Jarosław Kobiela, Hanna Davies, Izabela Ratnicka, Karol Wierzba, Janusz Ryś, Stanisław Hać, Jarosław Skokowski, Natalia Filipowicz, Jerzy Jankau, Agata Wojdak, Ulana Juhas, Andrzej Hellmann, Marta Drzewiecka, Wojciech Makarewicz, Piotr Remiszewski, Paweł Wroński, Karol Polom, Michał Bieńkowski, Katarzyna Duzowska, Jerzy Siekiera, Marcin Matuszewski, Jacek Kowalski, Jan P. Dumanski, Katarzyna Milian-Ciesielska, Maria Andreou, Olga Rostkowska, Tomasz Nowikiewicz, Agnieszka Harazin-Lechowska, Piotr Chlosta
The progress in translational cancer research relies on access to well-characterized samples from a representative number of patients and controls. The rationale behind our biobanking are explorations of post-zygotic pathogenic gene variants, especia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ae857a624ee6c48cb2b62fe440167f0
https://doi.org/10.1101/2021.09.03.458865
https://doi.org/10.1101/2021.09.03.458865
Autor:
Monika Ryba-Stanisławowska, Justyna Sakowska, Piotr Trzonkowski, Maciej Zieliński, Urszula Ławrynowicz
Publikováno v:
Expert Review of Clinical Immunology. 15:777-789
Introduction: CD4 + T regulatory cells (Tregs) have been described as the most potent immunosuppressive cells in the human body. They have been found to control autoimmunity, and clinical attempts have been made to apply them to treat autoimmune dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1e34ac4fbb67c963bf75d14891330e3
https://doi.org/10.1080/1744666x.2019.1620602
https://doi.org/10.1080/1744666x.2019.1620602
Autor:
Piotr Gutknecht, Monika Ryba-Stanisławowska, Urszula Ławrynowicz, Bartosz Słomiński, Maria Skrzypkowska, Janusz Siebert
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 108:92-97
Background CCR5 is a chemokine receptor expressed by various populations including leukocytes, smooth muscle cells and endothelium. Δ32 polymorphism of CCR5 gene has been connected with, inter alia, cardiovascular disease development. The aim of our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a1723f55a3f48ac57666a8fd50665bf
https://doi.org/10.1016/j.biocel.2019.01.006
https://doi.org/10.1016/j.biocel.2019.01.006
Autor:
Urszula Ławrynowicz, Ulana Juhas, Jolanta Myśliwska, Monika Ryba-Stanisławowska, Małgorzata Myśliwiec
Publikováno v:
Immunologic Research. 67:70-76
The CD83 molecule is a known marker of dendritic cell differentiation process, and its soluble form (sCD83) exerts immunosuppressive functions. In our research, we examined whether the sCD83 plasma concentration is impaired in DM1 children and if the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a693306382339d90477e6f8413ed26b
https://doi.org/10.1007/s12026-019-09074-y
https://doi.org/10.1007/s12026-019-09074-y
Autor:
Urszula Ławrynowicz, Maria Skrzypkowska, Małgorzata Myśliwiec, Bartosz Słomiński, Jolanta Myśliwska, Monika Ryba-Stanisławowska
Publikováno v:
Cytokine. 114:81-85
In the currently available literature there are no works investigating the correlation between CCR5-Δ32 polymorphism and dyslipidemia in children with type 1 diabetes mellitus (T1D). Therefore, we have decided to explore the potential role played by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::555d51e107f2dea6c3080b504ad2eaff
https://doi.org/10.1016/j.cyto.2018.11.005
https://doi.org/10.1016/j.cyto.2018.11.005
Autor:
Bartosz Słomiński, Jolanta Myśliwska, Urszula Ławrynowicz, Agnieszka Brandt, Maria Skrzypkowska, Monika Ryba-Stanisławowska
Publikováno v:
Molecular and Cellular Endocrinology. 439:256-260
Aim The aim of the study was to assess the relationship between the CCR5-Δ32 polymorphism and the risk of diabetic retinopathy (DR) in patients with DM1. Methods We examined 420 patients and 350 healthy controls. The analysis concerned CCR5-Δ32 pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb4882c8ff82cdf1d5d0222cbdf6a717
https://doi.org/10.1016/j.mce.2016.09.009
https://doi.org/10.1016/j.mce.2016.09.009
Autor:
Maria Skrzypkowska, Bartosz Słomiński, Jolanta Myśliwska, Urszula Ławrynowicz, Agnieszka Brandt, Monika Ryba-Stanisławowska, Małgorzata Myśliwiec
Publikováno v:
Journal of diabetes and its complications. 31(3)
The aim of the study was to assess the relationship between CCR5-Δ32 polymorphism and the coincidence of celiac and autoimmune thyroid diseases with type 1 diabetes mellitus (T1D) in children.420 children with T1D aged 15.5±3.0years and 350 healthy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7711c3443f6ffc194100ed7abaa261c1
https://pubmed.ncbi.nlm.nih.gov/27894748
https://pubmed.ncbi.nlm.nih.gov/27894748