Taras Valovka
Innsbruck, Austria
Last Updated: 09/26/2026
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Found 20 publications
Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family.
Journal: Clinical genetics
Published: December 12, 2024
Anti-inflammatory and cytoprotective polypharmacology of Canephron N reveals targeting of the IKK-NF-κB and p38-MK2-RIPK1 axes.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: October 08, 2024
Altered chaperone-nonmuscle myosin II interactions drive pathogenicity of the UNC45A c.710T>C variant in osteo-oto-hepato-enteric syndrome.
Journal: JCI insight
Published: July 31, 2024
The negative adipogenesis regulator Dlk1 is transcriptionally regulated by Ifrd1 (TIS7) and translationally by its orthologue Ifrd2 (SKMc15).
Journal: eLife
Published: April 20, 2023
SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption.
Journal: Genes
Published: January 08, 2023
UNC45A deficiency causes microvillus inclusion disease-like phenotype by impairing myosin VB-dependent apical trafficking.
Journal: The Journal of clinical investigation
Published: September 15, 2021
Characteristic facial features and cortical blindness distinguish the DOCK7-related epileptic encephalopathy.
Journal: Molecular genetics & genomic medicine
Published: November 23, 2020
Fluorescent thermal shift-based method for detection of NF-κB binding to double-stranded DNA.
Journal: Scientific reports
Published: June 03, 2020
Novel PCNT variants in MOPDII with attenuated growth restriction and pachygyria.
Journal: Clinical genetics
Published: May 18, 2020
CR4 Signaling Contributes to a DC-Driven Enhanced Immune Response Against Complement-Opsonized HIV-1.
Journal: Frontiers in immunology
Published: May 15, 2020
Further delineation of putative ACTB loss-of-function variants: A 4-patient series.
Journal: Human mutation
Published: August 02, 2019
Last Updated: 09/26/2026