Argyro Sgourou

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Transcriptional repression of lncRNA and miRNA subsets mediated by LRF during erythropoiesis

A. Sgourou, Y. Vasilopoulos, G. Georgakilas, 2023, Journal of Molecular Medicine.

LRF Promotes Indirectly Advantageous Chromatin Conformation via BGLT3-lncRNA Expression and Switch from Fetal to Adult Hemoglobin

C. Stathopoulos, A. Sgourou, Vasiliki Chondrou, 2022, International journal of molecular sciences.

Impact of ZBTB7A hypomethylation and expression patterns on treatment response to hydroxyurea

G. Patrinos, A. Symeonidis, A. Sgourou, 2018, Human Genomics.

Individualizing fetal hemoglobin augmenting therapy for β-type hemoglobinopathies patients.

G. Patrinos, T. Katsila, A. Sgourou, 2014, Pharmacogenomics.

Kallmann's Syndrome and Schizophrenia

C. Papageorgiou, N. Georgopoulos, T. Hyphantis, 2004, International journal of psychiatry in medicine.

Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients

Alexia Pavlidaki, P. Kolovos, G. Patrinos, 2017, Human Genomics.

Selective transduction of astrocytic and neuronal CNS subpopulations by lentiviral vectors pseudotyped with Chikungunya virus envelope.

N. Mazarakis, A. Sgourou, I. Eleftheriadou, 2017, Biomaterials.

The β‐globin C→G mutation at 6 bp 3′ to the termination codon causes β‐thalassaemia by decreasing the mRNA level

R. Gibbs, A. Sgourou, M. Antoniou, 2002 .

Functional significance of the thyrotropin receptor germline polymorphism D727E.

R. Paschke, A. Papavassiliou, K. Markou, 2003, Biochemical and biophysical research communications.

Enhanced Central Nervous System Transduction with Lentiviral Vectors Pseudotyped with RVG/HIV-1gp41 Chimeric Envelope Glycoproteins

N. Mazarakis, A. Sgourou, Heyne Lee, 2013, Journal of Virology.

Enhanced CNS transduction with lentiviral vectors 1 pseudotyped with RVG / HIV-1 gp 41 chimeric envelope 2 glycoproteins 3 4

N. Mazarakis, A. Sgourou, Heyne Lee, 2013 .

Thalassaemia mutations within the 5′UTR of the human β‐globin gene disrupt transcription

A. Sgourou, S. Routledge, M. Antoniou, 2004, British journal of haematology.

The multi-faceted functioning portrait of LRF/ZBTB7A

G. Patrinos, A. Sgourou, C. Constantinou, 2019, Human Genomics.

Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study

G. Patrinos, T. Katsila, A. Symeonidis, 2019, Hemoglobin.

Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients.

G. Patrinos, T. Katsila, A. Sgourou, 2016, Pharmacogenomics.

"LRF/ZBTB7A conservation accentuates its potential as a therapeutic target for the hematopoietic disorders".

G. Patrinos, A. Symeonidis, G. Markopoulos, 2020, Gene.

Contingent Synergistic Interactions between Non-Coding RNAs and DNA-Modifying Enzymes in Myelodysplastic Syndromes

A. Symeonidis, A. Sgourou, Vasiliki Chondrou, 2022, International journal of molecular sciences.

Physiological levels of HBB transgene expression from S/MAR element-based replicating episomal vectors.

A. Sgourou, S. Routledge, M. Antoniou, 2009, Journal of biotechnology.

Arsenic exposure promotes the emergence of cardiovascular diseases

S. Kakkos, I. Kalavrouziotis, A. Sgourou, 2021, Reviews on environmental health.

Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacy.

G. Patrinos, T. Katsila, A. Sgourou, 2016, Pharmacogenomics.

Key Pharmacogenomic Considerations for Sickle Cell Disease Patients.

G. Patrinos, T. Katsila, A. Sgourou, 2017, Omics : a journal of integrative biology.

Autonomously functioning thyroid nodules in a former iodine-deficient area commonly harbor gain-of-function mutations in the thyrotropin signaling pathway.

A. Papavassiliou, K. Markou, N. Georgopoulos, 2003, European journal of endocrinology.

A somatic mutation in the thyrotropin receptor gene in a patient with an autonomous nodule within a multinodular goiter.

A. Papavassiliou, K. Markou, N. Georgopoulos, 2002, Hormones.

Simple in vitro generation of human leukocyte antigen-G-expressing T-regulatory cells through pharmacological hypomethylation for adoptive cellular immunotherapy against graft-versus-host disease.

A. Sgourou, D. Marioli, S. Taraviras, 2017, Cytotherapy.

Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients.

G. Patrinos, T. Katsila, A. Symeonidis, 2019, Pharmacogenomics.

Association of genome variations in the renin-angiotensin system with physical performance

G. Patrinos, A. Sgourou, V. Fotopoulos, 2012, Human Genomics.

Implementation and Evaluation of a Three‐Dimensional Virtual Reality Biology Lab versus Conventional Didactic Practices in Lab Experimenting with the Photonic Microscope

Dimitrios Kalles, Anthi Karatrantou, Argyro Sgourou, 2019, Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology.

Developmental Dyslexia: Insights from EEG-Based Findings and Molecular Signatures—A Pilot Study

Katerina D. Tzimourta, V. Zakopoulou, P. Christodoulides, 2024, Brain sciences.

Mechanical stress affects methylation pattern of GNAS isoforms and osteogenic differentiation of hAT-MSCs.

G. Nakos, T. Fotsis, A. Sgourou, 2017, Biochimica et biophysica acta. Molecular cell research.

Adventure-Style Serious Game for a Science Lab

Dimitrios Kalles, Achilleas Kameas, Vasilis Zafeiropoulos, 2014, EC-TEL.

“Crosstalk between non-coding RNAs and transcription factor LRF in non-small cell lung cancer”

G. Ntaliarda, Georgios Psarias, K. Athanasopoulou, 2024, Non-coding RNA research.

Low- and Medium-Throughput Variant Detection Methods: A Historical Perspective

George P. Patrinos, Argyro Sgourou, Adamantia Papachatzopoulou, 2017 .