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Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Nagy N, Pal M, Kun J, Galik B, Urban P, Medvecz M, Fabos B, Neller A, Abdolreza A, Danis J, Szabo V, Yang Z, Fenske S, Biel M, Gyenesei A, Adam E, Szell M. Nagy N, et al. Among authors: szabo v. Int J Mol Sci. 2024 Jan 20;25(2):1271. doi: 10.3390/ijms25021271. Int J Mol Sci. 2024. PMID: 38279271 Free PMC article.
Impaired regulation of PMCA activity by defective CFTR expression promotes epithelial cell damage in alcoholic pancreatitis and hepatitis.
Madácsy T, Varga Á, Papp N, Tél B, Pallagi P, Szabó V, Kiss A, Fanczal J, Rakonczay Z Jr, Tiszlavicz L, Rázga Z, Hohwieler M, Kleger A, Gray M, Hegyi P, Maléth J. Madácsy T, et al. Among authors: szabo v. Cell Mol Life Sci. 2022 Apr 28;79(5):265. doi: 10.1007/s00018-022-04287-1. Cell Mol Life Sci. 2022. PMID: 35484438 Free PMC article.
Human pancreatic ductal organoids with controlled polarity provide a novel ex vivo tool to study epithelial cell physiology.
Varga Á, Madácsy T, Görög M, Kiss A, Susánszki P, Szabó V, Jójárt B, Dudás K, Farkas G Jr, Szederkényi E, Lázár G, Farkas A, Ayaydin F, Pallagi P, Maléth J. Varga Á, et al. Among authors: szabo v. Cell Mol Life Sci. 2023 Jun 28;80(7):192. doi: 10.1007/s00018-023-04836-2. Cell Mol Life Sci. 2023. PMID: 37380797 Free PMC article.
Lack of Rybp in Mouse Embryonic Stem Cells Impairs Cardiac Differentiation.
Ujhelly O, Szabo V, Kovacs G, Vajda F, Mallok S, Prorok J, Acsai K, Hegedus Z, Krebs S, Dinnyes A, Pirity MK. Ujhelly O, et al. Among authors: szabo v. Stem Cells Dev. 2015 Sep 15;24(18):2193-205. doi: 10.1089/scd.2014.0569. Epub 2015 Jun 25. Stem Cells Dev. 2015. PMID: 26110923
Orai1 calcium channel inhibition prevents progression of chronic pancreatitis.
Szabó V, Csákány-Papp N, Görög M, Madácsy T, Varga Á, Kiss A, Tél B, Jójárt B, Crul T, Dudás K, Bagyánszki M, Bódi N, Ayaydin F, Jee S, Tiszlavicz L, Stauderman KA, Hebbar S, Pallagi P, Maléth J. Szabó V, et al. JCI Insight. 2023 Jul 10;8(13):e167645. doi: 10.1172/jci.insight.167645. JCI Insight. 2023. PMID: 37227782 Free PMC article.
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration.
Han JH, Rodenburg K, Hayman T, Calzetti G, Kaminska K, Quinodoz M, Marra M, Wallerich S, Allon G, Nagy ZZ, Knézy K, Li Y, Chen R, Barboni MTS, Yang P, Pennesi ME, van den Born LI, Varsányi B, Szabó V, Sharon D, Banin E, Ben-Yosef T, Roosing S, Koenekoop RK, Rivolta C. Han JH, et al. Among authors: szabo v. Genet Med. 2024 Feb 28:101106. doi: 10.1016/j.gim.2024.101106. Online ahead of print. Genet Med. 2024. PMID: 38420906 Free article.
125 results