Viktor Stranecky

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 99 publications

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

Recurrent Single-Nucleotide Insertions in the Mitochondrial Second Light-Strand Promoter Cause Tubulointerstitial Kidney Disease.

Journal: medRxiv : the preprint server for health sciences
Published: August 20, 2026

SGLT2 inhibitor therapy is associated with IL-10/TGF-α/sVEGFR3 signalling and adipose tissue remodelling in advanced heart failure.

SGLT2 inhibitor therapy is associated with IL-10/TGF-α/sVEGFR3 signalling and adipose tissue remodelling in advanced heart failure.

Journal: Journal of molecular and cellular cardiology plus
Published: April 23, 2026

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression.

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression.

Journal: bioRxiv : the preprint server for biology
Published: September 26, 2025

De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity.

De novo EHMT2 variants cause an autosomal dominant EHMT2-related Kleefstra syndrome via loss of G9a methyltransferase activity.

Journal: Nature communications
Published: September 23, 2025

Single-Molecule Real-Time Sequencing for MUC1 VNTR Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Single-Molecule Real-Time Sequencing for MUC1 VNTR Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN
Published: August 27, 2025

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Single-Molecule Real-Time Sequencing for MUC1 Variable Number of Tandem Repeat Variation to Improve Autosomal Dominant Tubulointerstitial Kidney Disease Diagnosis.

Journal: Journal of the American Society of Nephrology : JASN
Published: August 27, 2025

Analyses of ATP7B mRNA in Nasopharyngeal Swab Samples Increase Yields of Wilson Disease Molecular Genetic Diagnostics.

Analyses of ATP7B mRNA in Nasopharyngeal Swab Samples Increase Yields of Wilson Disease Molecular Genetic Diagnostics.

Journal: Human mutation
Published: August 05, 2025

A missense mutation in the SAA1 protein causing hereditary amyloid A amyloidosis.

A missense mutation in the SAA1 protein causing hereditary amyloid A amyloidosis.

Journal: Kidney international
Published: July 24, 2025

Differential regulation of gene co-expression modules in muscles and liver of preterm newborns.

Differential regulation of gene co-expression modules in muscles and liver of preterm newborns.

Journal: Frontiers in cell and developmental biology
Published: June 14, 2025

Faster postnatal decline in hepatic erythropoiesis than granulopoiesis in human newborns.

Faster postnatal decline in hepatic erythropoiesis than granulopoiesis in human newborns.

Journal: Frontiers in pediatrics
Published: February 07, 2025

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.

Journal: PloS one
Published: January 30, 2025

Genetic Landscape of Amyotrophic Lateral Sclerosis in Czech Patients.

Genetic Landscape of Amyotrophic Lateral Sclerosis in Czech Patients.

Journal: Journal of neuromuscular diseases
Published: July 26, 2024
Showing 1-12 of 99

Last Updated: 09/26/2026