Zobrazeno 1 - 10
of 243
pro vyhledávání: '"Ewa, Bartnik"'
Autor:
Paulina Chmiel, Maria Krotewicz, Anna Szumera-Ciećkiewicz, Ewa Bartnik, Anna M. Czarnecka, Piotr Rutkowski
Publikováno v:
Current Oncology, Vol 31, Iss 1, Pp 307-323 (2024)
Soft tissue sarcomas (STS) originating from connective tissue rarely affect the lymph nodes. However, involvement of lymph nodes in STS is an important aspect of prognosis and treatment. Currently, there is no consensus on the diagnosis and managemen
Externí odkaz:
https://doaj.org/article/31600efdc8274a86803e7cc96918616e
Autor:
Paweł Sobczuk, Anna Brodziak, Mohammed Imran Khan, Stuti Chhabra, Michał Fiedorowicz, Marlena Wełniak-Kamińska, Kamil Synoradzki, Ewa Bartnik, Agnieszka Cudnoch-Jędrzejewska, Anna M. Czarnecka
Publikováno v:
Translational Oncology, Vol 13, Iss 3, Pp - (2020)
The increase in the life expectancy of patients with renal cell carcinoma (RCC) in the last decade is due to changes that have occurred in the area of preclinical studies. Understanding cancer pathophysiology and the emergence of new therapeutic opti
Externí odkaz:
https://doaj.org/article/7f27cf15af5d4629acb2e02a1955a988
Autor:
Kamil Jozef Synoradzki, Ewa Bartnik, Anna M. Czarnecka, Michał Fiedorowicz, Wiktoria Firlej, Anna Brodziak, Agnieszka Stasinska, Piotr Rutkowski, Paweł Grieb
Publikováno v:
Cancers, Vol 13, Iss 17, p 4284 (2021)
The TP53 gene is mutated in 50% of human tumors. Oncogenic functions of mutant TP53 maintain tumor cell proliferation and tumor growth also in osteosarcomas. We collected data on TP53 mutations in patients to indicate which are more common and descri
Externí odkaz:
https://doaj.org/article/b182db150ce64fb9b253783b302d8b65
Autor:
Karolina Stachyra, Monika Dudzisz-Śledź, Elżbieta Bylina, Anna Szumera-Ciećkiewicz, Mateusz J. Spałek, Ewa Bartnik, Piotr Rutkowski, Anna M. Czarnecka
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 12, p 6305 (2021)
Merkel cell carcinoma (MCC) is an uncommon and highly aggressive skin cancer. It develops mostly within chronically sun-exposed areas of the skin. MCPyV is detected in 60–80% of MCC cases as integrated within the genome and is considered a major ri
Externí odkaz:
https://doaj.org/article/c07d7a889fec4cd2a8779f157a6b8aac
Autor:
Agnieszka Piotrowska-Nowak, Joanna L. Elson, Agnieszka Sobczyk-Kopciol, Aleksandra Piwonska, Aleksandra Puch-Walczak, Wojciech Drygas, Rafal Ploski, Ewa Bartnik, Katarzyna Tonska
Publikováno v:
Frontiers in Genetics, Vol 9 (2019)
The etiology of common complex diseases is multifactorial, involving both genetic, and environmental factors. A role for mitochondrial dysfunction and mitochondrial DNA (mtDNA) variation has been suggested in the pathogenesis of common complex traits
Externí odkaz:
https://doaj.org/article/dc54714436ae4e63b4f9d4e6d7d90914
Autor:
Biruta Kierdaszuk, Magdalena Kaliszewska, Joanna Rusecka, Joanna Kosińska, Ewa Bartnik, Katarzyna Tońska, Anna M. Kamińska, Anna Kostera-Pruszczyk
Publikováno v:
Genes, Vol 12, Iss 1, p 54 (2020)
Mitochondrial encephalomyopathies comprise a group of heterogeneous disorders resulting from impaired oxidative phosphorylation (OxPhos). Among a variety of symptoms progressive external ophthalmoplegia (PEO) seems to be the most common. The aim of t
Externí odkaz:
https://doaj.org/article/c07ae59449ed42d19d0bcf8a6beff3da
Autor:
Katarzyna Kozak, Paweł Teterycz, Tomasz Świtaj, Hanna Koseła-Paterczyk, Sławomir Falkowski, Tadeusz Morysiński, Ewa Bartnik, Anna M. Czarnecka, Michał Wągrodzki, Iwona Ługowska, Piotr Rutkowski
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 10, p 3129 (2020)
Introduction: Synovial sarcoma (SaSy) is a high-grade, malignant soft tissue sarcoma (STS) accounting for 5–9% of STS. The aim of this study was to analyse outcomes of patients with localised SaSy treated in a single institution with a uniform neo-
Externí odkaz:
https://doaj.org/article/f9bf0e86083049fb98b43a26cfa6116c
Autor:
Anna M. Czarnecka, Kamil Synoradzki, Wiktoria Firlej, Ewa Bartnik, Pawel Sobczuk, Michal Fiedorowicz, Pawel Grieb, Piotr Rutkowski
Publikováno v:
Cancers, Vol 12, Iss 8, p 2130 (2020)
Osteosarcoma (OS) is the most frequent primary bone cancer in children and adolescents and the third most frequent in adults. Many inherited germline mutations are responsible for syndromes that predispose to osteosarcomas including Li Fraumeni syndr
Externí odkaz:
https://doaj.org/article/13253bfa5284484a87056115a9da837f
Autor:
Mateusz Jacek Spałek, Katarzyna Kozak, Anna Małgorzata Czarnecka, Ewa Bartnik, Aneta Borkowska, Piotr Rutkowski
Publikováno v:
Cancers, Vol 12, Iss 8, p 2061 (2020)
Due to the heterogeneity of soft tissue sarcomas (STS), the choice of the proper perioperative treatment regimen is challenging. Neoadjuvant therapy has attracted increasing attention due to several advantages, particularly in patients with locally a
Externí odkaz:
https://doaj.org/article/ea78c6b2a28346f293b68e817e6a5a3a
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 13, p 4576 (2020)
The common mutation BRAFV600 in primary melanomas activates the mitogen-activated protein kinase/extracellular-signal-regulated kinase (MAPK/ERK) pathway and the introduction of proto-oncogene B-Raf (BRAF) and mitogen-activated protein kinase kinase
Externí odkaz:
https://doaj.org/article/ac1656fd4c684f0fb6325b334a37f4b6