Zobrazeno 1 - 10
of 93
pro vyhledávání: '"István Balogh"'
Autor:
Orsolya Feró, Dóra Varga, Éva Nagy, Zsolt Karányi, Éva Sipos, József Engelhardt, Nóra Török, István Balogh, Borbála Vető, István Likó, Ábel Fóthi, Zoltán Szabó, Gábor Halmos, László Vécsei, Tamás Arányi, Lóránt Székvölgyi
Publikováno v:
Scientific Data, Vol 11, Iss 1, Pp 1-12 (2024)
Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the death of motor neurons, the aetiology of which is essentially unknown. Here, we present an integrative epigenomic study in blood samples from seve
Externí odkaz:
https://doaj.org/article/f835840c5d2e4e40af2979ffd5e752d1
Autor:
László Madar, Viktória Majoros, Zsuzsanna Szűcs, Orsolya Nagy, Tamás Babicz, Henriett Butz, Attila Patócs, István Balogh, Katalin Koczok
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 20, p 15334 (2023)
Hereditary breast cancer is most commonly attributed to germline BRCA1 and BRCA2 gene variants. The vast majority of BRCA1 and BRCA2 mutation carriers are single heterozygotes, and double heterozygosity (DH) is a very rare finding. Here, we describe
Externí odkaz:
https://doaj.org/article/d4a41755114a412b8e008900c748dc41
Autor:
Lívia Sira, Noémi Zsíros, László Bidiga, Sándor Barna, Zsolt Kanyári, Edit B. Nagy, Nicolas Guillaume, Damian Wild, Katalin Rázsó, Szilvia Andó, István Balogh, Endre V. Nagy, Zoltán Balogh
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundSplanchnic vein thrombosis due to co-existing metastatic pancreatic neuroendocrine tumour (pNET) and JAK2V617F mutation is a rare condition.Case reportHere we present a case of a young woman with complete remission of a non-functioning grad
Externí odkaz:
https://doaj.org/article/a6f835a82bff439b8f9a502667300fca
Autor:
Andrea Xue, István Lénárt, Judit Kincs, Hajnalka Szabó, Andrea Párniczky, István Balogh, Anna Deák, Péter Béla Monostori, Krisztina Hegedűs, Attila J. Szabó, Ildikó Szatmári
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 3, p 47 (2023)
The aim of this study is to evaluate the strategy of the cystic fibrosis newborn screening (CFNBS) programme in Hungary based on the results of the first year of screening. A combined immunoreactive trypsinogen (IRT) and pancreatitis-associated prote
Externí odkaz:
https://doaj.org/article/33e10d86ad0c4f319a9b3710cff1f77c
Autor:
Gréta Gombos, Nikolett Németh, Ondrej Pös, Jakub Styk, Gergely Buglyó, Tomas Szemes, Ludovit Danihel, Bálint Nagy, István Balogh, Beáta Soltész
Publikováno v:
Pharmaceutics, Vol 15, Iss 7, p 1904 (2023)
Exosomes have the potential to be the future of personalized diagnostics and therapy. They are nano-sized particles between 30 and 100 nm flowing in the extracellular milieu, where they mediate cell–cell communication and participate in immune syst
Externí odkaz:
https://doaj.org/article/fd226508b2e740a190aff05fb58d4739
Autor:
Ádám Csók, Tamás Micsik, Zsófia Magyar, Tamás Tornóczky, Levente Kuthi, Yumika Nishi, Krisztina Szirák, Monika Csóka, Gábor Ottóffy, Beáta Soltész, István Balogh, Gergely Buglyó
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 10, p 8793 (2023)
Wilms’ tumor (WT) is the most common renal malignancy in children. In diffuse hyperplastic perilobar nephroblastomatosis (DHPLN), nephrogenic rests result in a bulky enlargement of the kidney, a condition considered as a premalignant state before W
Externí odkaz:
https://doaj.org/article/b8c5ae2b8cfb4223853507c574444cde
Autor:
Éva Márton, Alexandra Varga, András Penyige, Zsuzsanna Birkó, István Balogh, Bálint Nagy, Melinda Szilágyi
Publikováno v:
Toxins, Vol 15, Iss 2, p 140 (2023)
Xenoestrogens are natural or synthetic compounds that mimic the effect of endogenous estrogens and might cause cancer. We aimed to compare the global transcriptomic response to zearalenone (ZEA; mycotoxin) and bisphenol A (BPA; plastic additive) with
Externí odkaz:
https://doaj.org/article/62da4fe4e5f043278734469ad4e3cad1
Autor:
Tímea Margit Szabó, István Balogh, Anikó Ujfalusi, Zsuzsanna Szűcs, László Madar, Katalin Koczok, Beáta Bessenyei, Ildikó Csürke, Katalin Szakszon
Publikováno v:
Genes, Vol 13, Iss 12, p 2367 (2022)
The ADNP-gene-related neurodevelopmental disorder Helsmoortel–Van der Aa syndrome is a rare syndromic-intellectual disability—an autism spectrum disorder first described by Helsmoortel and Van der Aa in 2014. Recently, a large cohort including 78
Externí odkaz:
https://doaj.org/article/8a0081ef823f4721af3143e0557bbb12
Publikováno v:
Genes, Vol 13, Iss 11, p 2086 (2022)
Chromosome abnormalities play a crucial role in reproductive failure. The presence of numerical or structural aberrations may induce recurrent pregnancy loss or primary infertility. The main purpose of our study was to determine the types and frequen
Externí odkaz:
https://doaj.org/article/fd70daa9294745349c665218786a07c5
Autor:
Zsuzsanna Szűcs, Éva Pinti, Irén Haltrich, Orsolya Pálné Szén, Tibor Nagy, Endre Barta, Gábor Méhes, László Bidiga, Olga Török, Anikó Ujfalusi, Katalin Koczok, István Balogh
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 21, p 13076 (2022)
Duchenne muscular dystrophy (DMD) is the most common inherited muscle dystrophy. Patients are characterized by muscle weakness, gross motor delay, and elevated serum creatinine kinase (CK) levels. The disease is caused by mutations in the DMD gene lo
Externí odkaz:
https://doaj.org/article/c8965ed35a0843a38f54342d72ffd1b7