Oliver Vugrek
Zagreb, 10000, Croatia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 30 publications
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility.
Journal: Human molecular genetics
Published: April 22, 2024
FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma.
Journal: Genes
Published: April 22, 2024
Characterization of Human Immunodeficiency Virus-1 Transmission Clusters and Transmitted Drug-Resistant Mutations in Croatia from 2019 to 2022.
Journal: Viruses
Published: November 16, 2023
HSV-1 miRNAs are post-transcriptionally edited in latently infected human ganglia.
Journal: Journal of virology
Published: September 15, 2023
Effects of S-Adenosylhomocysteine Hydrolase Downregulation on Wnt Signaling Pathway in SW480 Cells.
Journal: International journal of molecular sciences
Published: September 13, 2023
Long-Term Culturing of FreeStyle 293-F Cells Affects Immunoglobulin G Glycome Composition.
Journal: Biomolecules
Published: July 14, 2023
The Virus-Induced Upregulation of the miR-183/96/182 Cluster and the FoxO Family Protein Members Are Not Required for Efficient Replication of HSV-1.
Journal: Viruses
Published: May 24, 2022
In Vitro Confirmation of Siramesine as a Novel Antifungal Agent with In Silico Lead Proposals of Structurally Related Antifungals.
Journal: Molecules (Basel, Switzerland)
Published: May 13, 2021
Diverse SARS-CoV-2 variants preceded the initial COVID-19 outbreak in Croatia.
Journal: Archives of virology
Published: October 20, 2020
Successful sequencing of the first SARS-CoV-2 genomes from Croatian patients.
Journal: Croatian medical journal
Published: July 10, 2020
Promoter methylation status of ASC/TMS1/PYCARD is associated with decreased overall survival and TNM status in patients with early stage non-small cell lung cancer (NSCLC).
Journal: Translational lung cancer research
Published: February 04, 2020
Lowe syndrome - Old and new evidence of secondary mitochondrial dysfunction.
Journal: European journal of medical genetics
Published: January 12, 2020
Last Updated: 09/26/2026