Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Bence Agg"'
Autor:
Yvan Devaux, Lu Zhang, Andrew I. Lumley, Kanita Karaduzovic-Hadziabdic, Vincent Mooser, Simon Rousseau, Muhammad Shoaib, Venkata Satagopam, Muhamed Adilovic, Prashant Kumar Srivastava, Costanza Emanueli, Fabio Martelli, Simona Greco, Lina Badimon, Teresa Padro, Mitja Lustrek, Markus Scholz, Maciej Rosolowski, Marko Jordan, Timo Brandenburger, Bettina Benczik, Bence Agg, Peter Ferdinandy, Jörg Janne Vehreschild, Bettina Lorenz-Depiereux, Marcus Dörr, Oliver Witzke, Gabriel Sanchez, Seval Kul, Andy H. Baker, Guy Fagherazzi, Markus Ollert, Ryan Wereski, Nicholas L. Mills, Hüseyin Firat
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract Tools for predicting COVID-19 outcomes enable personalized healthcare, potentially easing the disease burden. This collaborative study by 15 institutions across Europe aimed to develop a machine learning model for predicting the risk of in-h
Externí odkaz:
https://doaj.org/article/54234423656547d89b595a58c9921da7
Autor:
Kanita Karaduzovic‐Hadziabdic, Muhamed Adilovic, Lu Zhang, Andrew I Lumley, Pranay Shah, Muhammad Shoaib, Venkata Satagopam, Prashant Kumar Srivastava, Costanza Emanueli, Simona Greco, Alisia Madè, Teresa Padro, Pedro Domingo, Mitja Lustrek, Markus Scholz, Maciej Rosolowski, Marko Jordan, Bettina Benczik, Bence Ágg, Péter Ferdinandy, Andrew H Baker, Guy Fagherazzi, Markus Ollert, Joanna Michel, Gabriel Sanchez, Hüseyin Firat, Timo Brandenburger, Fabio Martelli, Lina Badimon, Yvan Devaux, COVIRNA consortium (www.covirna.eu)
Publikováno v:
Clinical and Translational Medicine, Vol 14, Iss 10, Pp n/a-n/a (2024)
Externí odkaz:
https://doaj.org/article/71b93a594f694b9f8d534470df0bb9ff
Autor:
Mihály Ruppert, Sevil Korkmaz-Icöz, Bettina Benczik, Bence Ágg, Dávid Nagy, Tímea Bálint, Alex Ali Sayour, Attila Oláh, Bálint András Barta, Kálmán Benke, Péter Ferdinandy, Matthias Karck, Béla Merkely, Tamás Radovits, Gábor Szabó
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Although systolic function characteristically shows gradual impairment in pressure overload (PO)-evoked left ventricular (LV) hypertrophy (LVH), rapid progression to congestive heart failure (HF) occurs in distinct cases. The molecular mecha
Externí odkaz:
https://doaj.org/article/f74fc15bde5a449683825f0f7c0166f2
Autor:
Xu-Wen Wang, Lorenzo Madeddu, Kerstin Spirohn, Leonardo Martini, Adriano Fazzone, Luca Becchetti, Thomas P. Wytock, István A. Kovács, Olivér M. Balogh, Bettina Benczik, Mátyás Pétervári, Bence Ágg, Péter Ferdinandy, Loan Vulliard, Jörg Menche, Stefania Colonnese, Manuela Petti, Gaetano Scarano, Francesca Cuomo, Tong Hao, Florent Laval, Luc Willems, Jean-Claude Twizere, Marc Vidal, Michael A. Calderwood, Enrico Petrillo, Albert-László Barabási, Edwin K. Silverman, Joseph Loscalzo, Paola Velardi, Yang-Yu Liu
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Comprehensive understanding of the human protein-protein interaction network, aka the human interactome, can provide important insights into the molecular mechanisms of complex biological processes and diseases. Here the authors summarize the communi
Externí odkaz:
https://doaj.org/article/0aec14fc0b0a4a9f86440753275acd42
Autor:
Tamara Szabados, Arnold Molnár, Éva Kenyeres, Kamilla Gömöri, Judit Pipis, Bence Pósa, András Makkos, Bence Ágg, Zoltán Giricz, Péter Ferdinandy, Anikó Görbe, Péter Bencsik
Publikováno v:
Antioxidants, Vol 13, Iss 6, p 674 (2024)
Introduction: Ischemic conditionings (ICon) were intensively investigated and several protective signaling pathways were identified. Previously, we have shown the role of matrix metalloproteinases (MMP) in myocardial ischemia/reperfusion injury (MIRI
Externí odkaz:
https://doaj.org/article/a998a5afca6e4aed86cfe654244162be
Autor:
Timea Aczél, Bettina Benczik, Bence Ágg, Tamás Körtési, Péter Urbán, Witold Bauer, Attila Gyenesei, Bernadett Tuka, János Tajti, Péter Ferdinandy, László Vécsei, Kata Bölcskei, József Kun, Zsuzsanna Helyes
Publikováno v:
The Journal of Headache and Pain, Vol 23, Iss 1, Pp 1-20 (2022)
Abstract Background Migraine is a primary headache with genetic susceptibility, but the pathophysiological mechanisms are poorly understood, and it remains an unmet medical need. Earlier we demonstrated significant differences in the transcriptome of
Externí odkaz:
https://doaj.org/article/34bf315a48b64fceb68dee3d9bfd2113
Autor:
Annamária, Agota, Bence, Agg, Kálmán, Benke, József Gábor, Joó, Zoltán, Langmár, Krisztina, Marosi, Zsuzsanna, Lelovics, Zsuzsanna, Lelelovics, Kitti, Deé, Péter, Nagy, Bernadett, Köles, Endre, Horváth, Zsuzsanna, Crespo, Zoltán, Szabolcs, Zsolt B, Nagy
Publikováno v:
Orvosi Hetilap. 153:296-302
Marfan syndrome is a genetic disorder of the connective tissue, which affects approximately 2000–3000 individuals in Hungary. Given its multi-systemic manifestations, this disorder is often difficult to diagnose. To date, the National Marfan Regist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ce028c9ab4caa212e59a3bf900c98c6
https://doi.org/10.1556/oh.2012.29295
https://doi.org/10.1556/oh.2012.29295
Autor:
Olivér M. Balogh, Bettina Benczik, András Horváth, Mátyás Pétervári, Péter Csermely, Péter Ferdinandy, Bence Ágg
Publikováno v:
BMC Bioinformatics, Vol 23, Iss 1, Pp 1-19 (2022)
Abstract Background The investigation of possible interactions between two proteins in intracellular signaling is an expensive and laborious procedure in the wet-lab, therefore, several in silico approaches have been implemented to narrow down the ca
Externí odkaz:
https://doaj.org/article/073a4946c6fc4ab9b241d4a342eb150c
Autor:
Roland Stengl, Bence Ágg, Miklós Pólos, Gábor Mátyás, Gábor Szabó, Béla Merkely, Tamás Radovits, Zoltán Szabolcs, Kálmán Benke
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background Marfan syndrome (MFS) is a genetically determined systemic connective tissue disorder, caused by a mutation in the FBN1 gene. In MFS mainly the cardiovascular, musculoskeletal and ocular systems are affected. The most dangerous ma
Externí odkaz:
https://doaj.org/article/d5770b91bcf14a498d790756b0c096e6
Autor:
Roland Stengl, András Bors, Bence Ágg, Miklós Pólos, Gabor Matyas, Mária Judit Molnár, Bálint Fekete, Dóra Csabán, Hajnalka Andrikovics, Béla Merkely, Tamás Radovits, Zoltán Szabolcs, Kálmán Benke
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-13 (2020)
Abstract Background Marfan syndrome (MFS) is a systemic connective tissue disorder with life-threatening manifestations affecting the ascending aorta. MFS is caused by dominant negative (DN) and haploinsufficient (HI) mutations of the FBN1 gene. Our
Externí odkaz:
https://doaj.org/article/8223e04783934362a464360837cf6ff9