Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Victor, Murcia Pienkowski"'
Autor:
Victor Murcia Pienkowski, Piotr Skoczylas, Agata Zaremba, Stanisław Kłęk, Martyna Balawejder, Paweł Biernat, Weronika Czarnocka, Oskar Gniewek, Łukasz Grochowalski, Małgorzata Kamuda, Bartłomiej Król-Józaga, Joanna Marczyńska-Grzelak, Giovanni Mazzocco, Rafał Szatanek, Jakub Widawski, Joanna Welanyk, Zofia Orzeszko, Mirosław Szura, Grzegorz Torbicz, Maciej Borys, Łukasz Wohadlo, Michał Wysocki, Marek Karczewski, Beata Markowska, Tomasz Kucharczyk, Marek J. Piatek, Maciej Jasiński, Michał Warchoł, Jan Kaczmarczyk, Agnieszka Blum, Anna Sanecka-Duin
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
PurposeDeveloping innovative precision and personalized cancer therapeutics is essential to enhance cancer survivability, particularly for prevalent cancer types such as colorectal cancer. This study aims to demonstrate various approaches for discove
Externí odkaz:
https://doaj.org/article/6fcb309f7f8d4220b4c4013fc5af9be6
Autor:
Renata Woroniecka, Grzegorz Rymkiewicz, Lukasz M. Szafron, Katarzyna Blachnio, Laura A. Szafron, Zbigniew Bystydzienski, Barbara Pienkowska-Grela, Klaudia Borkowska, Jolanta Rygier, Aleksandra Kotyl, Natalia Malawska, Katarzyna Wojtkowska, Joanna Parada, Anita Borysiuk, Victor Murcia Pienkowski, Malgorzata Rydzanicz, Beata Grygalewicz
Publikováno v:
PLoS ONE, Vol 17, Iss 2 (2022)
The occurrence of MYC-negative Burkitt lymphoma (BL) has been discussed for many years. The real frequency of the MYC insertion in MYC-negative BL is still unknown. Fine-needle aspiration biopsies of 108 consecutive patients with clinicopathologicall
Externí odkaz:
https://doaj.org/article/899befa948ae4f5796b8b73e02bd4489
Autor:
Victor Murcia Pienkowski, Tamara Boschert, Piotr Skoczylas, Anna Sanecka-Duin, Maciej Jasiński, Bartłomiej Król-Józaga, Giovanni Mazzocco, Sławomir Stachura, Lukas Bunse, Jan Kaczmarczyk, Edward W Green, Agnieszka Blum
Cellular immunotherapies, such as those utilizing T lymphocytes expressing native or engineered T cell receptors (TCRs), have already demonstrated therapeutic efficacy. However, some high-affinity TCRs have also proved to be fatal due to off-target i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcc91836419b590cecb1cf602c32ffae
https://doi.org/10.1101/2023.04.11.536336
https://doi.org/10.1101/2023.04.11.536336
Autor:
Victor Murcia Pienkowski, Saima Riazuddin, Matthew J. Schultz, S. Amer Riazuddin, Foong-Yen Lim, Nicola Perrotti, Claudia Gonzaga-Jauregui, Muhammad A. Usmani, Zubair M. Ahmed, Hane Lee, Erik G. Puffenberger, Anneke J.A. Kievit, Tommaso Pippucci, Pamela Magini, Emma Colao, M. Mahdi Motazacker, Rebecca Hernan, Mureed Hussain, Karlla W. Brigatti, Wendy K. Chung, Matias Wagner, Marco Seri, Mohsin Shahzad, Brendan C. Lanpher, Zhiyv Niu, Karolina Matuszewska, Hans van Bokhoven, Faiza Rasheed, J. S. Klein Wassink-Ruiter, Kristen J. Rasmussen, Verena Kraus, Jessica Kianmahd, Julian A. Martinez-Agosto, Flavia Palombo, Rafał Płoski, Sheikh Riazuddin
Publikováno v:
American Journal of Human Genetics, 108, 1330-1341
American journal of human genetics, 108(7), 1330-1341. Cell Press
Am J Hum Genet
American Journal of Human Genetics, 108, 7, pp. 1330-1341
American Journal of Human Genetics, 108(7), 1330-1341. CELL PRESS
American Journal of Human Genetics, 108(7), 1330-1341. Cell Press
Am. J. Hum. Genet. 108, 1330-1341 (2021)
American journal of human genetics, 108(7), 1330-1341. Cell Press
Am J Hum Genet
American Journal of Human Genetics, 108, 7, pp. 1330-1341
American Journal of Human Genetics, 108(7), 1330-1341. CELL PRESS
American Journal of Human Genetics, 108(7), 1330-1341. Cell Press
Am. J. Hum. Genet. 108, 1330-1341 (2021)
Adaptor protein (AP) complexes mediate selective intracellular vesicular trafficking and polarized localization of somatodendritic proteins in neurons. Disease-causing alleles of various subunits of AP complexes have been implicated in several herita
Autor:
Renata Woroniecka, Grzegorz Rymkiewicz, Lukasz M. Szafron, Katarzyna Blachnio, Laura A. Szafron, Zbigniew Bystydzienski, Barbara Pienkowska-Grela, Klaudia Borkowska, Jolanta Rygier, Aleksandra Kotyl, Natalia Malawska, Katarzyna Wojtkowska, Joanna Parada, Anita Borysiuk, Victor Murcia Pienkowski, Malgorzata Rydzanicz, Beata Grygalewicz
Publikováno v:
PLoS ONE, Vol 17, Iss 2 (2022)
The occurrence of MYC-negative Burkitt lymphoma (BL) has been discussed for many years. The real frequency of the MYC insertion in MYC-negative BL is still unknown. Fine-needle aspiration biopsies of 108 consecutive patients with clinicopathologicall
Autor:
Katarzyna Zielniok, Małgorzata Rydzanicz, Anna Burdzinska, Leszek Paczek, Victor Murcia Pienkowski, Agnieszka Koppolu, Radoslaw Zagozdzon
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8160, p 8160 (2021)
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8160, p 8160 (2021)
Mesenchymal stromal cell (MSC) therapy is making its way into clinical practice, accompanied by research into strategies improving their therapeutic potential. Preconditioning MSCs with hypoxia-inducible factors-α (HIFα) stabilizers is an alternati
Autor:
Victor Murcia Pienkowski, Thomas Meitinger, Sylvia Stockler, Maja Tarailo-Graovac, Astrid Blaschek, Tobias B. Haack, Bader Alhaddad, Burkhard Adis-Dutschmann, Korbinian M. Riedhammer, Katharina Vill, Robin van der Lee, Robert Kopajtich, Ingeborg Krägeloh-Mann, Jessica J. Y. Lee, Uwe Ahting, Maren Wenzel, Rafał Płoski, Clara D.M. van Karnebeek, Krystyna Szymańska, Agnieszka Pollak
Publikováno v:
Brain 144, 411-419 (2021)
Brain, 144(2), 411-419. Oxford University Press
Brain, 144, pp. 411-419
Brain
Brain, 144, 411-419
Brain, 144(2), 411-419. Oxford University Press
Brain, 144, pp. 411-419
Brain
Brain, 144, 411-419
Claudin-11, a tight junction protein, is indispensable in the formation of the radial component of myelin. Here, we report de novo stop-loss variants in the gene encoding claudin-11, CLDN11, in three unrelated individuals presenting with an early-ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab9a2cccb33e925ff5f310305c81f0b
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60758
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=60758
Autor:
Miroslaw Bik-Multanowski, Agnieszka Pollak, Ewa Sledziewska-Gojska, Aneta Kaniak-Golik, Jolanta Fijak-Moskal, Jarosław Poznański, Rafał Płoski, Victor Murcia Pienkowski, Renata Kuberska, Małgorzata Rydzanicz, Agnieszka Halas
REV3L encodes a catalytic subunit of DNA polymerase zeta (Pol zeta) which is essential for the tolerance of DNA damage by inducing translesion synthesis (TLS). So far, the only Mendelian disease associated with REV3L was Moebius syndrome (3 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b09a60cb62833baa58a52d5bb4aa7f2
https://ruj.uj.edu.pl/xmlui/handle/item/270271
https://ruj.uj.edu.pl/xmlui/handle/item/270271
Autor:
Agnieszka Stembalska, Małgorzata Rydzanicz, Wojciech Walas, Piotr Gasperowicz, Agnieszka Pollak, Victor Murcia Pienkowski, Mateusz Biela, Magdalena Klaniewska, Zuzanna Gamrot, Ewa Gronska, Rafal Ploski, Robert Smigiel
Publikováno v:
Genes
Genes, 2022, 13 (5), pp.725. ⟨10.3390/genes13050725⟩
Genes, 2022, 13 (5), pp.725. ⟨10.3390/genes13050725⟩
International audience; LAS1L encodes a nucleolar ribosomal biogenesis protein and is also a component of the Five Friends of Methylated CHTOP (5FMC) complex. Mutations in the LAS1L gene can be associated with Wilson–Turner syndrome (WTS) and, much
Autor:
Małgorzata Rydzanicz, Marlena Młynek, Agnieszka Pollak, Dorota Wicher, Agnieszka Stembalska, Anna Gambin, Katarzyna Wojciechowska, Piotr Stawiński, Krystyna H. Chrzanowska, Monika Lejman, Barbara Poszewiecka, Rafał Płoski, Katarzyna Pachota, Karolina Matuszewska, Marzena Kucharczyk, Małgorzata Krajewska-Walasek, Anna Materna-Kiryluk, Victor Murcia Pienkowski, Agata Cieślikowska, Joanna Kosińska
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 1245, p 1245 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 9; Issue 5; Pages: 1245
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 9; Issue 5; Pages: 1245
De novo balanced chromosomal aberrations (BCAs), such as reciprocal translocations and inversions, are genomic aberrations that, in approximately 25% of cases, affect the human phenotype. Delineation of the exact structure of BCAs may provide a preci