Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Andrea Kerti"'
Publikováno v:
Kidney & Blood Pressure Research, Vol 39, Iss 6, Pp 507-515 (2014)
Background/Aims: To assess the relationship between bone and vascular disease and its changes over time after renal transplantation. Metabolic bone disease (MBD) is common in chronic kidney disease (CKD) and is associated with cardiovascular (CV) dis
Externí odkaz:
https://doaj.org/article/71e7c38adcd541a18f0989274c759043
Autor:
Detlef Bockenhauer, François Dragon, Christelle Arrondel, Ákos Szekeres, Kristóf Perczel, Wei-Li Di, Susanne Motameny, Attila Fintha, Maria Kolatsi-Joannou, Eszter Jávorszky, Guillaume Dorval, Salah Marzouk, Kazunori Tomita, Jennifer C. Chandler, Peter Nürnberg, Gusztáv Schay, Veronica A. Kinsler, Ahmed Hossain, Andrea Kerti, András Perczel, Hafsa Hammid, Magdolna Kardos, William Mifsud, Florentina Sava, David Curtis, Corinne Antignac, Felipe D’Arco, Aoife M. Waters, Géraldine Mollet, Mona Tahoun, Gergely Toldi, Tivadar Tulassay, Ana Faro, Anna Szőcs, Jutta Koeglmeier, Kata Kelen, Marwa H. Saied, Holger Thiele, Hywel Williams, Kálmán Tory, Renáta Hamar, Erika Maka, Mario Kaliakatsos, Mariya Moosajee, Gábor Rudas, Máté Varga, Eszter Balogh, Attila Szabo, Dóra K. Menyhárd, Horia Stanescu, Tomas Goncalves, Olivier Gribouval, Regina Légrádi, George S. Reusz, Robert Kleta, Judit Götze, David A. Long
Publikováno v:
Proceedings of the National Academy of Sciences. 117:15137-15147
RNA modifications play a fundamental role in cellular function. Pseudouridylation, the most abundant RNA modification, is catalyzed by the H/ACA small ribonucleoprotein (snoRNP) complex that shares four core proteins, dyskerin (DKC1), NOP10, NHP2, an
Autor:
Eszter, Balogh, Jennifer C, Chandler, Máté, Varga, Mona, Tahoun, Dóra K, Menyhárd, Gusztáv, Schay, Tomas, Goncalves, Renáta, Hamar, Regina, Légrádi, Ákos, Szekeres, Olivier, Gribouval, Robert, Kleta, Horia, Stanescu, Detlef, Bockenhauer, Andrea, Kerti, Hywel, Williams, Veronica, Kinsler, Wei-Li, Di, David, Curtis, Maria, Kolatsi-Joannou, Hafsa, Hammid, Anna, Szőcs, Kristóf, Perczel, Erika, Maka, Gergely, Toldi, Florentina, Sava, Christelle, Arrondel, Magdolna, Kardos, Attila, Fintha, Ahmed, Hossain, Felipe, D'Arco, Mario, Kaliakatsos, Jutta, Koeglmeier, William, Mifsud, Mariya, Moosajee, Ana, Faro, Eszter, Jávorszky, Gábor, Rudas, Marwa H, Saied, Salah, Marzouk, Kata, Kelen, Judit, Götze, George, Reusz, Tivadar, Tulassay, François, Dragon, Géraldine, Mollet, Susanne, Motameny, Holger, Thiele, Guillaume, Dorval, Peter, Nürnberg, András, Perczel, Attila J, Szabó, David A, Long, Kazunori, Tomita, Corinne, Antignac, Aoife M, Waters, Kálmán, Tory
Publikováno v:
Proc Natl Acad Sci U S A
RNA modifications play a fundamental role in cellular function. Pseudouridylation, the most abundant RNA modification, is catalyzed by the H/ACA small ribonucleoprotein (snoRNP) complex that shares four core proteins, dyskerin (DKC1), NOP10, NHP2, an
Publikováno v:
Transplantation Proceedings. 46:2160-2163
Cardiovascular mortality rate in patients with end-stage renal disease is 3 magnitudes higher than in the general population; it remains 10-fold higher after successful renal transplantation (Tx). Among others, obesity and hypertension can exert dele
Autor:
Andrea Kerti, Kálmán Tory, Corinne Antignac, Henriett Pikó, Vincent Morinière, Eszter Jávorszky, Veronika Karcagi, Sophie Saunier, Eszter Balogh
Publikováno v:
Clinical chemistry and laboratory medicine. 55(6)
Background: Nephronophthisis, an autosomal recessive nephropathy, is responsible for 10% of childhood chronic renal failure. The deletion of its major gene, NPHP1, with a minor allele frequency of 0.24% in the general population, is the most common m
Autor:
Andrea Kerti, Orsolya Lakatos, Attila Szabo, Vincent Morinière, Ottó Árkossy, Beata S. Lipska, Kálmán Tory, Franz Schaefer, Peter Sallay, Rózsa Csohány, Gábor Nyírő, George S. Reusz, Tamás Szabó, Corinne Antignac, Virginia Vega-Warner, Tivadar Tulassay
Publikováno v:
Pediatric Nephrology. 28:751-757
The most frequently mutated gene of steroid-resistant nephrotic syndrome (SRNS) is NPHS2. Current guidelines propose the sequencing of all NPHS2 exons only in childhood-onset SRNS.A cohort of 38 Hungarian patients with childhood-onset nephrotic-range
Autor:
Attila Szabo, Orsolya Cseprekál, Kálmán Tory, Arianna Dégi, George S. Reusz, Andrea Kerti, Eva Kis
Publikováno v:
Pediatric Transplantation. 16:564-576
CV diseases are the leading cause of death among patients with ESRD. RTX decreases the CV risk; however, it still remains definitely higher than that of the general population. Large multicenter and longitudinal studies are difficult to perform and h
Autor:
Károly Rácz, Bence Acs, Karolina Feldmann, Peter Gergics, Andrea Kerti, Attila Patócs, Miklós Tóth, Ágnes Szappanos, Rita Bertalan
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 123:79-84
Objective The type 1 and type 2 isoenzymes of the 11β-hydroxysteroid dehydrogenase (HSD11B) play an important role in the prereceptor regulation of glucocorticoid bioavailability and action. The potential importance of gene variants coding HSD11B ha
Autor:
Attila Szabo, György Reusz, Kata Kelen, Andrea Kerti, Orsolya Cseprekál, Antal Szabó, Edina Bíró, Dóra Ferenczi, Eva Kis
Publikováno v:
Pediatric Nephrology. 24:2413-2420
Arterial stiffness (Ast) individually predicts cardiovascular (CV) mortality. Ast increases via vascular calcification and can be characterized by pulse wave velocity (PWV). We assessed the influence of mineral and bone metabolism on Ast in dialyzed
Autor:
Arianna Dégi, Andrea Kerti, Eva Kis, Attila Szabo, Orsolya Cseprekál, Peter Sallay, George S. Reusz
Publikováno v:
Pediatric transplantation. 17(7)
Given the increase in CV morbidity after RTx and the scarcity of CV events in pediatrics, surrogate markers should be assessed to characterize CV damage in this population. AASI is a marker of arterial stiffness in adults, predicting cardio- and cere