Eszter E. Balogh
Budapest, BU 1083, Hungary
Last Updated: 09/26/2026
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Found 8 publications
Podocin oligomers regulate the ordering of nephrin chains, providing the molecular basis of NPHS2 interallelic interactions.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 14, 2026
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 20, 2020
Effect of single-nucleotide polymorphisms on specific reproduction parameters in Hungarian Large White sows.
Journal: Acta veterinaria Hungarica
Published: June 27, 2019
Identification, Structural and Functional Characterization of Dormancy Regulator Genes in Apricot (Prunus armeniaca L.).
Journal: Frontiers in plant science
Published: December 20, 2018
Zebrafish Models of Rare Hereditary Pediatric Diseases.
Journal: Diseases (Basel, Switzerland)
Published: April 27, 2018
Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies.
Journal: Pediatric nephrology (Berlin, Germany)
Published: January 09, 2018
C-terminal oligomerization of podocin mediates interallelic interactions.
Journal: Biochimica et biophysica acta. Molecular basis of disease
Published: December 23, 2017
QMPSF is sensitive and specific in the detection of NPHP1 heterozygous deletions.
Journal: Clinical chemistry and laboratory medicine
Published: September 12, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026