Balint Nagy

Budapest, BU, Hungary

Last Updated: 09/26/2026

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Found 14 publications

Mitochondrial Alpha-Keto Acid Dehydrogenase Complexes: Recent Developments on Structure and Function in Health and Disease.

Mitochondrial Alpha-Keto Acid Dehydrogenase Complexes: Recent Developments on Structure and Function in Health and Disease.

Journal: Sub-cellular biochemistry

Published: July 04, 2024

Structural and Biochemical Investigation of Selected Pathogenic Mutants of the Human Dihydrolipoamide Dehydrogenase.

Structural and Biochemical Investigation of Selected Pathogenic Mutants of the Human Dihydrolipoamide Dehydrogenase.

Journal: International journal of molecular sciences

Published: May 30, 2023

Functional Versatility of the Human 2-Oxoadipate Dehydrogenase in the L-Lysine Degradation Pathway toward Its Non-Cognate Substrate 2-Oxopimelic Acid.

Functional Versatility of the Human 2-Oxoadipate Dehydrogenase in the L-Lysine Degradation Pathway toward Its Non-Cognate Substrate 2-Oxopimelic Acid.

Journal: International journal of molecular sciences

Published: June 23, 2022

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.

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.

Journal: Biochimica et biophysica acta. General subjects

Published: November 17, 2020

Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism.

Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism.

Journal: The Journal of biological chemistry

Published: January 22, 2020

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

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

Journal: Human molecular genetics

Published: May 28, 2019

Relationship between cardiovascular diseases and circulating cell-free nucleic acids in human plasma.

Relationship between cardiovascular diseases and circulating cell-free nucleic acids in human plasma.

Journal: Biomarkers in medicine

Published: July 21, 2018

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.

Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.

Journal: European journal of human genetics : EJHG

Published: November 27, 2015

Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance.

Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance.

Journal: PloS one

Published: June 30, 2015

Expression of VEGF in neonatal urinary obstruction: does expression of VEGF predict hydronephrosis?

Expression of VEGF in neonatal urinary obstruction: does expression of VEGF predict hydronephrosis?

Journal: Medical science monitor : international medical journal of experimental and clinical research

Published: May 09, 2015

Detection of sex chromosome aneuploidies using quantitative fluorescent PCR in the Hungarian population.

Detection of sex chromosome aneuploidies using quantitative fluorescent PCR in the Hungarian population.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: October 02, 2014

Genetic aspects of preeclampsia and the HELLP syndrome.

Genetic aspects of preeclampsia and the HELLP syndrome.

Journal: Journal of pregnancy

Published: November 30, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026