Zoltan F. Doleschall

7-9 Ráth György Str
Budapest, BU 1122, Hungary

Last Updated: 09/26/2026

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Found 14 publications

Nature versus nurture: genetic background and media composition shape endothelial cell transcriptomes in vitro.

Nature versus nurture: genetic background and media composition shape endothelial cell transcriptomes in vitro.

Journal: Scientific reports

Published: November 03, 2025

Human umbilical vein endothelial cell miRNA secretome highlights endothelial origin of serum miRNAs.

Human umbilical vein endothelial cell miRNA secretome highlights endothelial origin of serum miRNAs.

Journal: Scientific reports

Published: January 07, 2025

Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation.

Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation.

Journal: PloS one

Published: March 16, 2022

MASP-1 Increases Endothelial Permeability.

MASP-1 Increases Endothelial Permeability.

Journal: Frontiers in immunology

Published: January 21, 2019

Transgenic short-QT syndrome 1 rabbits mimic the human disease phenotype with QT/action potential duration shortening in the atria and ventricles and increased ventricular tachycardia/ventricular fibrillation inducibility.

Transgenic short-QT syndrome 1 rabbits mimic the human disease phenotype with QT/action potential duration shortening in the atria and ventricles and increased ventricular tachycardia/ventricular fibrillation inducibility.

Journal: European heart journal

Published: December 19, 2017

Transcriptome analysis of inflammation-related gene expression in endothelial cells activated by complement MASP-1.

Transcriptome analysis of inflammation-related gene expression in endothelial cells activated by complement MASP-1.

Journal: Scientific reports

Published: May 17, 2017

A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics.

A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics.

Journal: European journal of human genetics : EJHG

Published: June 10, 2016

Kinase-Associated Phosphoisoform Assay: a novel candidate-based method to detect specific kinase-substrate phosphorylation interactions in vivo.

Kinase-Associated Phosphoisoform Assay: a novel candidate-based method to detect specific kinase-substrate phosphorylation interactions in vivo.

Journal: BMC plant biology

Published: May 12, 2016

Complement MASP-1 enhances adhesion between endothelial cells and neutrophils by up-regulating E-selectin expression.

Complement MASP-1 enhances adhesion between endothelial cells and neutrophils by up-regulating E-selectin expression.

Journal: Molecular immunology

Published: March 16, 2016

A novel transgenic rabbit model with reduced repolarization reserve: long QT syndrome caused by a dominant-negative mutation of the KCNE1 gene.

A novel transgenic rabbit model with reduced repolarization reserve: long QT syndrome caused by a dominant-negative mutation of the KCNE1 gene.

Journal: British journal of pharmacology

Published: September 24, 2015

PI3K/AKT pathway activation and therapeutic consequences in breast cancer

PI3K/AKT pathway activation and therapeutic consequences in breast cancer

Journal: Magyar onkologia

Published: June 17, 2015

NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn.

NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn.

Journal: mAbs

Published: February 05, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026