Szabo E - Search Results

1

Underlying molecular alterations in human dihydrolipoamide dehydrogenase deficiency revealed by structural analyses of disease-causing enzyme variants.

Szabo E, Wilk P, Nagy B, Zambo Z, Bui D, Weichsel A, Arjunan P, Torocsik B, Hubert A, Furey W, Montfort WR, Jordan F, Weiss MS, Adam-Vizi V, Ambrus A. Szabo E, et al. Hum Mol Genet. 2019 Oct 15;28(20):3339-3354. doi: 10.1093/hmg/ddz177. Hum Mol Genet. 2019. PMID: 31334547 Free PMC article.

2

Crystal structures of the disease-causing D444V mutant and the relevant wild type human dihydrolipoamide dehydrogenase.

Szabo E, Mizsei R, Wilk P, Zambo Z, Torocsik B, Weiss MS, Adam-Vizi V, Ambrus A. Szabo E, et al. Free Radic Biol Med. 2018 Aug 20;124:214-220. doi: 10.1016/j.freeradbiomed.2018.06.008. Epub 2018 Jun 20. Free Radic Biol Med. 2018. PMID: 29908278

3

Structure of the dihydrolipoamide succinyltransferase (E2) component of the human alpha-ketoglutarate dehydrogenase complex (hKGDHc) revealed by cryo-EM and cross-linking mass spectrometry: Implications for the overall hKGDHc structure.

Nagy B, Polak M, Ozohanics O, Zambo Z, Szabo E, Hubert A, Jordan F, Novaček J, Adam-Vizi V, Ambrus A. Nagy B, et al. Among authors: szabo e. Biochim Biophys Acta Gen Subj. 2021 Jun;1865(6):129889. doi: 10.1016/j.bbagen.2021.129889. Epub 2021 Mar 5. Biochim Biophys Acta Gen Subj. 2021. PMID: 33684457 Free article.

4

Current Approaches in Molecular Enzymology.

Szabo E, Ambrus A. Szabo E, et al. Life (Basel). 2022 Feb 24;12(3):336. doi: 10.3390/life12030336. Life (Basel). 2022. PMID: 35330087 Free PMC article.

5

[Diagnostics of inborn errors of metabolism: laboratory approaches].

Szabó E, Balogh L, Szabó A, Szatmári I. Szabó E, et al. Among authors: szabo a. Orv Hetil. 2017 Dec;158(48):1903-1907. doi: 10.1556/650.2017.30899. Orv Hetil. 2017. PMID: 29172660 Review. Hungarian.

6

Discovery and development of extreme selective inhibitors of the ITD and D835Y mutant FLT3 kinases.

Baska F, Sipos A, Őrfi Z, Nemes Z, Dobos J, Szántai-Kis C, Szabó E, Szénási G, Dézsi L, Hamar P, Cserepes MT, Tóvári J, Garamvölgyi R, Krekó M, Őrfi L. Baska F, et al. Among authors: szabo e. Eur J Med Chem. 2019 Dec 15;184:111710. doi: 10.1016/j.ejmech.2019.111710. Epub 2019 Oct 5. Eur J Med Chem. 2019. PMID: 31614258

7

Endocannabinoid-mediated modulation of Gq/11 protein-coupled receptor signaling-induced vasoconstriction and hypertension.

Szekeres M, Nádasy GL, Turu G, Soltész-Katona E, Benyó Z, Offermanns S, Ruisanchez É, Szabó E, Takáts Z, Bátkai S, Tóth ZE, Hunyady L. Szekeres M, et al. Among authors: szabo e. Mol Cell Endocrinol. 2015 Mar 5;403:46-56. doi: 10.1016/j.mce.2015.01.012. Epub 2015 Jan 13. Mol Cell Endocrinol. 2015. PMID: 25595485

8

Functional Comparison of Blood-Derived Human Neural Progenitor Cells.

Szabó E, Juhász F, Hathy E, Reé D, Homolya L, Erdei Z, Réthelyi JM, Apáti Á. Szabó E, et al. Int J Mol Sci. 2020 Nov 30;21(23):9118. doi: 10.3390/ijms21239118. Int J Mol Sci. 2020. PMID: 33266139 Free PMC article.

9

Chiral analysis of amino acid neurotransmitters and neuromodulators in mouse brain by CE-LIF.

Jakó T, Szabó E, Tábi T, Zachar G, Csillag A, Szökő E. Jakó T, et al. Among authors: szabo e. Electrophoresis. 2014 Oct;35(19):2870-6. doi: 10.1002/elps.201400224. Epub 2014 Jul 28. Electrophoresis. 2014. PMID: 24931272

10

Investigation of de novo mutations in a schizophrenia case-parent trio by induced pluripotent stem cell-based in vitro disease modeling: convergence of schizophrenia- and autism-related cellular phenotypes.

Hathy E, Szabó E, Varga N, Erdei Z, Tordai C, Czehlár B, Baradits M, Jezsó B, Koller J, Nagy L, Molnár MJ, Homolya L, Nemoda Z, Apáti Á, Réthelyi JM. Hathy E, et al. Among authors: szabo e. Stem Cell Res Ther. 2020 Nov 27;11(1):504. doi: 10.1186/s13287-020-01980-5. Stem Cell Res Ther. 2020. PMID: 33246498 Free PMC article.

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