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The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study

Scientific reports, 2016-05, Vol.6 (1), p.26371-26371, Article 26371

2016

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Short-hairpin RNA against aberrant HBB IVSI-110(G>A) mRNA restores β-globin levels in a novel cell model and acts as mono- and combination therapy for β-thalassemia in primary hematopoietic stem cells

Haematologica (Roma), 2018-09, Vol.103 (9), p.e419-e423

2018

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A Novel BaEVRless-Pseudotyped γ-Globin Lentiviral Vector Drives High and Stable Fetal Hemoglobin Expression and Improves Thalassemic Erythropoiesis In Vitro

Human gene therapy, 2019-05, Vol.30 (5), p.601-617

2019

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Recent trends in the gene therapy of β-thalassemia

Journal of Blood Medicine, 2015-01, Vol.6 (default), p.69-85

2015

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nucleotide-binding proteins Nubp1 and Nubp2 are negative regulators of ciliogenesis

Cellular and molecular life sciences : CMLS, 2014-02, Vol.71 (3), p.517-538

2014

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Progress and harmonization of gene editing to treat human diseases: Proceeding of COST Action CA21113 GenE-HumDi

Molecular therapy. Nucleic acids, 2023-12, Vol.34, p.102066-102066, Article 102066

2023

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Suitability of small diagnostic peripheral-blood samples for cell-therapy studies

Cytotherapy (Oxford, England), 2017-02, Vol.19 (2), p.311-326

2017

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Rapid and Sensitive Assessment of Globin Chains for Gene and Cell Therapy of Hemoglobinopathies

Human gene therapy. Part B. Methods, 2018-02, Vol.29 (1), p.60-74

2018

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A Tribute to George Stamatoyannopoulos

Human gene therapy, 2016-04, Vol.27 (4), p.280-286

2016

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Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries

Journal of personalized medicine, 2022-03, Vol.12 (4), p.552

2022

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The nuclear ATPase/adenylate kinase hCINAP is recruited to perinucleolar caps generated upon RNA pol.II inhibition

FEBS letters, 2010-11, Vol.584 (22), p.4559-4564

2010

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Hb A2 Episkopi - a novel δ-globin chain variant [HBD:c.428C>T] in a family of mixed Cypriot-Lebanese descent

Hematology (Luxembourg), 2017-05, Vol.22 (5), p.304-309

2017

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A Minimal Set of SNPs for the Noninvasive Prenatal Diagnosis of β‐Thalassaemia

Annals of human genetics, 2013-03, Vol.77 (2), p.115-124

2013

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hCINAP is an atypical mammalian nuclear adenylate kinase with an ATPase motif: Structural and functional studies

Proteins, structure, function, and bioinformatics, 2012-01, Vol.80 (1), p.206-220

2012

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Hb A 2 Episkopi - a novel δ-globin chain variant [HBD:c.428C>T] in a family of mixed Cypriot-Lebanese descent

Hematology (Luxembourg), 2017-06, Vol.22 (5), p.304-309

2017

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Hb Famagusta—analysis of a novel δ-globin chain variant [HBD:c.60C>A] in four families with diverse globin genotypes

Annals of hematology, 2014-09, Vol.93 (9), p.1625-1627

2014

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Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication

Journal of cell science, 2006-05, Vol.119 (10), p.2035-2047

2006

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Neural stem cells: Mechanisms of fate specification and nuclear reprogramming in regenerative medicine

Biotechnology journal, 2008-12, Vol.3 (12), p.1521-1538

2008

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Amyotrophic lateral sclerosis - The tools of the trait

Biotechnology journal, 2007-05, Vol.2 (5), p.608-621

2007

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Compounds of the anthracycline family of antibiotics elevate human γ-globin expression both in erythroid cultures and in a transgenic mouse model

Blood cells, molecules, & diseases, 2010-03, Vol.44 (2), p.100-106

2010

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Characterization of Iron Complexes in the Red Blood Cells of β-thalassaemia patients using 57Fe Mössbauer Spectroscopy

Journal of molecular structure, 2021-04, Vol.1229, p.129732, Article 129732

2021

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Study of iron complexes in visceral organs and brain from a 57Fe enriched β-thalassaemia mouse model via Mössbauer spectroscopy

Journal of molecular structure, 2020-09, Vol.1215, p.128251, Article 128251

2020

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Variant Curation: Overview and Challenges

Hemoglobin, 2019-11, Vol.43 (6), p.325-325

2019

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The molecular spectrum and distribution of haemoglobinopathies in Cyprus: a 20-year retrospective study

Short-hairpin RNA against aberrant HBB IVSI-110(G>A) mRNA restores β-globin levels in a novel cell model and acts as mono- and combination therapy for β-thalassemia in primary hematopoietic stem cells

A Novel BaEVRless-Pseudotyped γ-Globin Lentiviral Vector Drives High and Stable Fetal Hemoglobin Expression and Improves Thalassemic Erythropoiesis In Vitro

Recent trends in the gene therapy of β-thalassemia

nucleotide-binding proteins Nubp1 and Nubp2 are negative regulators of ciliogenesis

Progress and harmonization of gene editing to treat human diseases: Proceeding of COST Action CA21113 GenE-HumDi

Suitability of small diagnostic peripheral-blood samples for cell-therapy studies

Rapid and Sensitive Assessment of Globin Chains for Gene and Cell Therapy of Hemoglobinopathies

A Tribute to George Stamatoyannopoulos

Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries

The nuclear ATPase/adenylate kinase hCINAP is recruited to perinucleolar caps generated upon RNA pol.II inhibition

Hb A2 Episkopi - a novel δ-globin chain variant [HBD:c.428C>T] in a family of mixed Cypriot-Lebanese descent

A Minimal Set of SNPs for the Noninvasive Prenatal Diagnosis of β‐Thalassaemia

hCINAP is an atypical mammalian nuclear adenylate kinase with an ATPase motif: Structural and functional studies

Hb A 2 Episkopi - a novel δ-globin chain variant [HBD:c.428C>T] in a family of mixed Cypriot-Lebanese descent

Hb Famagusta—analysis of a novel δ-globin chain variant [HBD:c.60C>A] in four families with diverse globin genotypes

Motor protein KIFC5A interacts with Nubp1 and Nubp2, and is implicated in the regulation of centrosome duplication

Neural stem cells: Mechanisms of fate specification and nuclear reprogramming in regenerative medicine

P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL

Amyotrophic lateral sclerosis - The tools of the trait

Compounds of the anthracycline family of antibiotics elevate human γ-globin expression both in erythroid cultures and in a transgenic mouse model

Characterization of Iron Complexes in the Red Blood Cells of β-thalassaemia patients using 57Fe Mössbauer Spectroscopy

Study of iron complexes in visceral organs and brain from a 57Fe enriched β-thalassaemia mouse model via Mössbauer spectroscopy

Variant Curation: Overview and Challenges

An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project

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