Zobrazeno 1 - 10
of 699
pro vyhledávání: '"Péter Antal"'
Autor:
Linda Lóczi, Réka P. Szabó, Rita Orbán-Kálmándi, Rebeka Hodossy-Takács, Anikó Szilvási, Zoltán Szalai, Gábor Nagy, Péter Antal-Szalmás, Balázs Nemes, Zsuzsa Bagoly
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionThe development of de novo anti-HLA donor specific antibodies (DSAs) is associated with poor outcomes in kidney transplant recipients. It is surmised that an interaction between DSAs and the graft endothelium cause tissue injury, however,
Externí odkaz:
https://doaj.org/article/980b1d6c772a4aa8947cc7d4641752f8
Publikováno v:
Diagnostics, Vol 14, Iss 14, p 1494 (2024)
Aim of the study was to investigate the demographic data and disease course characteristics of patients with Sjögren’s syndrome (SS) and inflammatory joint pain of various origins and to search for factors that might help with the distinction of p
Externí odkaz:
https://doaj.org/article/1747fd924a9f46e6a96afe5710cbce6d
Autor:
Domonkos Pogány, Péter Antal
Publikováno v:
PLoS ONE, Vol 19, Iss 3, p e0300906 (2024)
Given the prolonged timelines and high costs associated with traditional approaches, accelerating drug development is crucial. Computational methods, particularly drug-target interaction prediction, have emerged as efficient tools, yet the explainabi
Externí odkaz:
https://doaj.org/article/3b24ef5bb80d44e2aedb174bf8443d35
Autor:
Andrea Sümegi, Zoltán Hendrik, Tamás Gáll, Enikő Felszeghy, Katalin Szakszon, Péter Antal-Szalmás, Lívia Beke, Ágnes Papp, Gábor Méhes, József Balla, György Balla
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Wolcott-Rallison Syndrome (WRS) is a rare autosomal recessive disease that is the most common cause of neonatal diabetes in consanguineous families. WRS is caused by various genetic alterations of the Eukaryotic Translation Initia
Externí odkaz:
https://doaj.org/article/b8de95c394044360a0eca743029979ac
Autor:
Péter P. Ujma, Nóra Eszlári, András Millinghoffer, Bence Bruncsics, Dóra Török, Péter Petschner, Péter Antal, Bill Deakin, Gerome Breen, György Bagdy, Gabriella Juhász
Publikováno v:
Brain and Behavior, Vol 12, Iss 1, Pp n/a-n/a (2022)
Abstract Introduction Educational attainment is a substantially heritable trait, and it has recently been linked to specific genetic variants by genome‐wide association studies (GWASs). However, the effects of such genetic variants are expected to
Externí odkaz:
https://doaj.org/article/361c85f92e23431795abd9f73d6f0849
Autor:
Bence Bolgár, Péter Antal
Publikováno v:
BMC Bioinformatics, Vol 18, Iss 1, Pp 1-18 (2017)
Abstract Background Computational fusion approaches to drug-target interaction (DTI) prediction, capable of utilizing multiple sources of background knowledge, were reported to achieve superior predictive performance in multiple studies. Other studie
Externí odkaz:
https://doaj.org/article/39fd95a8498a48beb050a0ec1e005405
Autor:
Eszter Szánthó, Harjit Pal Bhattoa, Mária Csobán, Péter Antal-Szalmás, Anikó Újfalusi, János Kappelmayer, Zsuzsanna Hevessy
Publikováno v:
PLoS ONE, Vol 9, Iss 3, p e91647 (2014)
BACKGROUND: To date no age-related reference ranges are available for serum thymidine kinase (TK1) activity. Being a proliferation marker, it may be used as a prognostic marker in malignant diseases, including chronic lymphocytic leukemia (CLL). Our
Externí odkaz:
https://doaj.org/article/a10e3b4925f246769d9ece8a23b2dc7e
Autor:
Orsolya Lautner-Csorba, András Gézsi, Dániel J Erdélyi, Gábor Hullám, Péter Antal, Ágnes F Semsei, Nóra Kutszegi, Gábor Kovács, András Falus, Csaba Szalai
Publikováno v:
PLoS ONE, Vol 8, Iss 8, p e69843 (2013)
In this study we investigated whether polymorphisms in the folate pathway influenced the risk of childhood acute lymphoblastic leukemia (ALL) or the survival rate of the patients. For this we selected and genotyped 67 SNPs in 15 genes in the folate p
Externí odkaz:
https://doaj.org/article/3239944fe57942fc9032608dee870256
Autor:
Ildikó Ungvári, Gábor Hullám, Péter Antal, Petra Sz Kiszel, András Gézsi, Éva Hadadi, Viktor Virág, Gergely Hajós, András Millinghoffer, Adrienne Nagy, András Kiss, Ágnes F Semsei, Gergely Temesi, Béla Melegh, Péter Kisfali, Márta Széll, András Bikov, Gabriella Gálffy, Lilla Tamási, András Falus, Csaba Szalai
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33573 (2012)
Genetic studies indicate high number of potential factors related to asthma. Based on earlier linkage analyses we selected the 11q13 and 14q22 asthma susceptibility regions, for which we designed a partial genome screening study using 145 SNPs in 120
Externí odkaz:
https://doaj.org/article/72061c370a5d4d07b9445acdba41760b
Publikováno v:
In Journal of Chromatography A 22 February 2024 1717