Works by KOLLIA, PANAGOULA

Results: 34

Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and δβ-thalassemia.

Published in:

American Journal of Hematology, 2008, v. 83, n. 9, p. 760, doi. 10.1002/ajh.21243

By:

Kalamaras, Angelos;
Chassanidis, Christos;
Samara, Maria;
Papadakis, Manoussos N.;
Vagena, Andromachi;
Aleporou-Marinou, Vassiliki;
Patrinos, George P.;
Kollia, Panagoula

Publication type:

Article

Increased γ-globin gene expression in β-thalassemia intermedia patients correlates with a mutation in 3′HS1.

Published in:

American Journal of Hematology, 2007, v. 82, n. 11, p. 1005, doi. 10.1002/ajh.20979

By:

Papachatzopoulou, Adamantia;
Kaimakis, Polynikis;
Pourfarzad, Farzin;
Menounos, Panagiotis G.;
Evangelakou, Panagiota;
Kollia, Panagoula;
Grosveld, Frank G.;
Patrinos, George P.

Publication type:

Article

Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in Central Greece compared to the rest of the country.

Published in:

American Journal of Hematology, 2007, v. 82, n. 7, p. 634, doi. 10.1002/ajh.20889

By:

Samara, Maria;
Chiotoglou, Ioanna;
Kalamaras, Angelos;
Likousi, Sophia;
Chassanidis, Christos;
Vagena, Andromahi;
Vagenas, Christos;
Eftichiadis, Eftichios;
Vamvakopoulos, Nikolaos;
Patrinos, George P.;
Kollia, Panagoula

Publication type:

Article

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the βS/Benin haplotype.

Published in:

American Journal of Hematology, 2005, v. 80, n. 1, p. 79, doi. 10.1002/ajh.20400

By:

George P. Patrinos;
Piera Samperi;
Luca lo Nigro;
Panagoula Kollia;
Gino Schiliro;
Manoussos N. Papadakis

Publication type:

Article

Impact of ACE and ApoE polymorphisms on myocardial perfusion: correlation with myocardial single photon emission computed tomographic imaging.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 10, p. 595, doi. 10.1038/jhg.2009.83

By:

Georgoulias, Panagiotis;
Wozniak, Greta;
Samara, Maria;
Chiotoglou, Ioanna;
Kontos, Angelos;
Tzavara, Chara;
Valotassiou, Varvara;
Georgitsi, Marianthi;
Aleporou-Marinou, Vassiliki;
Patrinos, George P;
Kollia, Panagoula

Publication type:

Article

PB1992: PROTEOMIC ANALYSIS REVEALS AUTOPHAGY INHIBITION IN MYELODYSPLASTIC SYNDROMES.

Published in:

HemaSphere, 2023, v. 7, p. 1, doi. 10.1097/01.HS9.0000974784.63963.90

By:

Tsekoura, Georgia;
Agathangelidis, Andreas;
Kontandreopoulou, Xristina‐Nefeli;
Taliouraki, Aggeliki;
Diamantopoulos, Panagiotis;
Viniou, Nora;
Aleporou, Vassiliki;
Papassideri, Issidora;
Kollia, Panagoula

Publication type:

Article

Association of GSTP1 inactivating polymorphism with acute myeloid leukemia and its specific chromosomal abnormalities.

Published in:

2017

By:

Daraki, Aggeliki;
Zachaki, Sophia;
Rosmaraki, Faidra;
Kalomoiraki, Marina;
Aleporou-Marinou, Vassiliki;
Sambani, Constantina;
Kollia, Panagoula;
Manola, Kalliopi N.

Publication type:

Letter to the Editor

Evidence for regulation of oxidative stress by latent membrane protein 1 oncoprotein in patients with low-grade leukemic B cell lymphoma with latent Epstein-Barr virus infection.

Published in:

Leukemia & Lymphoma, 2014, v. 55, n. 8, p. 1904, doi. 10.3109/10428194.2013.867487

By:

Papadopoulou, Vasiliki;
Diamantopoulos, Panagiotis T.;
Kontandreopoulou, Elina;
Polonyfi, Katerina;
Variami, Eleni;
Kouzis, Panagiotis;
Galanopoulos, Athanasios;
Spanakis, Nikolaos;
Zervakis, Konstantinos;
Iliakis, Theodoros;
Perrea, Despoina;
Kollia, Panagoula;
Vassilakopoulos, Theodoros P.;
Pangalis, Gerassimos A.;
Kyrtsonis, Christine;
Vaiopoulos, George;
Viniou, Nora-Athina

Publication type:

Article

Correlation of Fc-γ RIIA polymorphisms with latent Epstein-Barr virus infection and latent membrane protein 1 expression in patients with low grade B-cell lymphomas.

Published in:

Leukemia & Lymphoma, 2013, v. 54, n. 9, p. 2030, doi. 10.3109/10428194.2012.762512

By:

Diamantopoulos, Panagiotis T.;
Kalotychou, Vassiliki;
Polonyfi, Katerina;
Sofotasiou, Maria;
Anastasopoulou, Amalia;
Galanopoulos, Athanassios;
Spanakis, Nikolaos;
Vassilakopoulos, Theodoros;
Angelopoulou, Maria;
Siakantaris, Maria;
Variami, Eleni;
Poziopoulos, Christos;
Terpos, Evangelos;
Kollia, Panagoula;
Viniou, Nora-Athina

Publication type:

Article

Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greecea.

Published in:

Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 226, doi. 10.1111/j.1749-6632.1990.tb24310.x

By:

LOUKOPOULOS, DIMITRIS;
HADJI, ANNA;
PAPADAKIS, MANOS;
KARABABA, PHOTINI;
SINOPOULOU, KLIO;
BOUSSIOU, MARINA;
KOLLIA, PANAGOULA;
XENAKIS, MATHILDE;
ANTSAKLIS, ARIS;
MESOGHITIS, SPYRIDON;
LOUTRADI, APHRODITE;
FESSAS, PHAEDON

Publication type:

Article

Sickle Cell Thalassemia in Greece.

Published in:

Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 508, doi. 10.1111/j.1749-6632.1990.tb24346.x

By:

VOSKARIDOU, ERSI;
KOLLIA, PANAGOULA;
LOUKOPOULOS, DIMITRIS

Publication type:

Article

Prenatal Diagnosis of Thalassemia Intermedia: Is It Justified?

Published in:

Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 521, doi. 10.1111/j.1749-6632.1990.tb24351.x

By:

KOLLIA, PANAGOULA;
VOSKARIDOU, ERSI;
ROMBOS, JOHN;
LOUTRADI, APHRODITE;
MARINAKIS, THEODOROS;
FESSAS, PHAEDON;
LOUKOPOULOS, DIMITRIS

Publication type:

Article

Induction of MMP‐3 and MMP‐9 expression during Helicobacter pylori infection via MAPK signaling pathways.

Published in:

Helicobacter, 2023, v. 28, n. 4, p. 1, doi. 10.1111/hel.12987

By:

Karayiannis, Ioannis;
Martinez‐Gonzalez, Beatriz;
Kontizas, Eleftherios;
Kokkota, Androniki Voulgari;
Petraki, Kalliopi;
Mentis, Andreas;
Kollia, Panagoula;
Sgouras, Dionyssios Nicholas

Publication type:

Article

Analysis of the κ light chain variable region in multiple myeloma.

Published in:

British Journal of Haematology, 1996, v. 94, n. 2, p. 306, doi. 10.1046/j.1365-2141.1996.d01-1815.x

By:

Kosmas, Christos;
Viniou, Nora-Athina;
Stamato poulos, Kostas;
Courtenay-Luck, Nigel S.;
Papadaki, Theodora;
Kollia, Panagoula;
Paterakis, George;
Anagnostou, Dimitra;
Yataganas, Xenophon;
Loukopoulos, Dimitris

Publication type:

Article

Darwinian molecular imaging in nuclear cardiology.

Published in:

2010

By:

Georgoulias, Panagiotis;
Tsougos, Ioannis;
Valotassiou, Varvara;
Samara, Maria;
Kollia, Panagoula

Publication type:

Letter

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Published in:

Human Mutation, 2007, v. 28, n. 2, p. 206, doi. 10.1002/humu.9479

By:

Giardine, Belinda;
van Baal, Sjozef;
Kaimakis, Polynikis;
Riemer, Cathy;
Miller, Webb;
Samara, Maria;
Kollia, Panagoula;
Anagnou, Nicholas P.;
Chui, David H.K.;
Wajcman, Henri;
Hardison, Ross C.;
Patrinos, George P.

Publication type:

Article

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.

Published in:

Human Mutation, 2005, v. 26, n. 5, p. 399, doi. 10.1002/humu.20225

By:

Patrinos, George P.;
Kollia, Panagoula;
Papadakis, Manoussos N.

Publication type:

Article

Novel Sequence Variations in the CER1 Gene Are Strongly Associated with Low Bone Mineral Density and Risk of Osteoporotic Fracture in Postmenopausal Women.

Published in:

Calcified Tissue International, 2012, v. 91, n. 1, p. 15, doi. 10.1007/s00223-012-9602-9

By:

Koromila, Theodora;
Dailiana, Zoe;
Samara, Stavroula;
Chassanidis, Chris;
Tzavara, Chara;
Patrinos, George;
Aleporou-Marinou, Vassiliki;
Kollia, Panagoula

Publication type:

Article

The 5' Regulatory Region of the Human Fetal Globin Genes is a Gene Conversion Hotspot.

Published in:

Hemoglobin, 2008, v. 32, n. 6, p. 572, doi. 10.1080/03630260802507824

By:

Kalamaras, Angelos;
Chassanidis, Christos;
Samara, Maria;
Chiotoglou, Ioanna;
Vamvakopoulos, Nikolaos K.;
Papadakis, Manoussos N.;
Kollia*, Panagoula;
Patrinos, George P.

Publication type:

Article

Thumb duplication: molecular analysis of different clinical types.

Published in:

European Journal of Orthopaedic Surgery & Traumatology, 2019, v. 29, n. 2, p. 421, doi. 10.1007/s00590-018-2343-3

By:

Kyriazis, Zisis;
Kollia, Panagoula;
Grivea, Ioanna;
Varitimidis, Sokratis E.;
Constantoulakis, Pantelis;
Dailiana, Zoe H.

Publication type:

Article

Bone morphogenetic proteins (BMPs) expression in the femoral heads of patients with avascular necrosis.

Published in:

Molecular Biology Reports, 2013, v. 40, n. 7, p. 4465, doi. 10.1007/s11033-013-2538-y

By:

Samara, Stavroula;
Dailiana, Zoe;
Varitimidis, Sokratis;
Chassanidis, Christos;
Koromila, Theodora;
Malizos, Konstantinos;
Kollia, Panagoula

Publication type:

Article

The G516T CYP2B6 Germline Polymorphism Affects the Risk of Acute Myeloid Leukemia and Is Associated with Specific Chromosomal Abnormalities.

Published in:

PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088879

By:

Daraki, Aggeliki;
Zachaki, Sophia;
Koromila, Theodora;
Diamantopoulou, Paraskevi;
Pantelias, Gabriel E.;
Sambani, Constantina;
Aleporou, Vasiliki;
Kollia, Panagoula;
Manola, Kalliopi N.

Publication type:

Article

Hydroxyurea and Hemin Affect Both the Transcriptional and Post-Transcriptional Mechanisms of Some Globin Genes in Human Adult Erythroid Cellsa.

Published in:

Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 449, doi. 10.1111/j.1749-6632.1998.tb10517.x

By:

KOLLIA, PANAGOULA;
FIBACH, EITAN;
POLITOU, MARIANNA;
NOGUCHI, CONSTANCE T.;
SCHECHTER, ALAN N.;
LOUKOPOULOS, DIMITRIS

Publication type:

Article

Aγ-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5′ regulatory region of the human Aγ-globin gene.

Published in:

American Journal of Hematology, 2001, v. 66, n. 2, p. 99, doi. 10.1002/1096-8652(200102)66:2<99::AID-AJH1024>3.0.CO;2-9

By:

Patrinos, George P.;
Kollia, Panagoula;
Papapanagiotou, Elisavet;
Loutradi-Anagnostou, Aphrodite;
Loukopoulos, Dimitris;
Papadakis, Manoussos N.

Publication type:

Article

Survivin Messenger RNA Levels in Epstein-Barr Viruse Positive Patients With Leukemic Low-Grade B-Cell Lymphomas Expressing the Latent Membrane Protein 1: Evidence of Apoptotic Function?

Published in:

Clinical Lymphoma, Myeloma & Leukemia, 2014, v. 14, n. 1, p. 56, doi. 10.1016/j.clml.2013.09.002

By:

Diamantopoulos, Panagiotis T.;
Polonyfi, Katerina;
Sofotasiou, Maria;
Mantzourani, Marina;
Galanopoulos, Athanassios;
Spanakis, Nikolaos;
Papadopoulou, Vasiliki;
Kalala, Fani;
Iliakis, Theodoros;
Zareifi, Danai-Stella;
Kodandreopoulou, Elina;
Vassilakopoulos, Theodoros;
Angelopoulou, Maria;
Siakantaris, Marina;
Terpos, Evangelos;
Variami, Eleni;
Kollia, Panagoula;
Vaiopoulos, George;
Pangalis, Gerassimos;
Viniou, Nora-Athina

Publication type:

Article

Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis.

Published in:

International Journal of Neuroscience, 2015, v. 125, n. 1, p. 32, doi. 10.3109/00207454.2014.899597

By:

Alexoudi, Athanasia;
Zachaki, Sophia;
Stavropoulou, Chrysa;
Chatzi, Ioanna;
Koumbi, Daphne;
Stavropoulou, Kalliopi;
Kollia, Panagoula;
Karageorgiou, Clementine E.;
Sambani, Constantina

Publication type:

Article

Clinical implications for Vascular Endothelial Growth Factor in the lung: friend or foe?

Published in:

Respiratory Research, 2006, v. 7, p. 1, doi. 10.1186/1465-9921-7-128

By:

Papaioannou, Andriana I.;
Kostikas, Konstantinos;
Kollia, Panagoula;
Gourgoulianis, Konstantinos I.

Publication type:

Article

CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal women.

Published in:

Human Genomics, 2013, v. 7, n. 1, p. 1, doi. 10.1186/1479-7364-7-21

By:

Koromila, Theodora;
Georgoulias, Panagiotis;
Dailiana, Zoe;
Ntzani, Evangelia E.;
Samara, Stavroula;
Chassanidis, Chris;
Aleporou-Marinou, Vassiliki;
Kollia, Panagoula

Publication type:

Article

A new COL1A1 mutation in a Greek patient with osteogenesis imperfecta: Response to a low-dose protocol of zoledronic acid and two-year follow-up.

Published in:

2018

By:

Sarantis, Michail;
Kollia, Panagoula;
Samara, Stavroula;
Athanasopoulou, Helen;
Gyftodimou, Yolanda;
Lianou, Dimitra;
Mpourazani, Evdoxia;
Doulgeraki, Artemis

Publication type:

Case Study

Impact of Helicobacter pylori Infection and Its Major Virulence Factor CagA on DNA Damage Repair.

Published in:

Microorganisms, 2020, v. 8, n. 12, p. 2007, doi. 10.3390/microorganisms8122007

By:

Kontizas, Eleftherios;
Tastsoglou, Spyros;
Karamitros, Timokratis;
Karayiannis, Yiannis;
Kollia, Panagoula;
Hatzigeorgiou, Artemis G.;
Sgouras, Dionyssios N.

Publication type:

Article

Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the TWIST1 and EFNB1 Genes.

Published in:

Cleft Palate Craniofacial Journal, 2018, v. 55, n. 8, p. 1092, doi. 10.1177/1055665618760412

By:

Apostolopoulou, Despina;
Kaxira, Olga S.;
Hatzaki, Angeliki;
Panagopoulos, Kanaris P.;
Alexandrou, Konstantinos;
Stratoudakis, Alexander;
Kollia, Panagoula;
Aleporou, Vassiliki

Publication type:

Article

A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl With Craniofrontonasal Syndrome.

Published in:

Cleft Palate Craniofacial Journal, 2012, v. 49, n. 1, p. 109, doi. 10.1597/10-247

By:

Apostolopoulou, Despina;
Stratoudakis, Alexander;
Hatzaki, Angeliki;
Kaxira, Olga S;
Panagopoulos, Kanaris P;
Kollia, Panagoula;
Aleporou, Vassiliki

Publication type:

Article

DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy.

Published in:

Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0783-1

By:

Tsagiopoulou, Maria;
Papakonstantinou, Nikos;
Moysiadis, Theodoros;
Mansouri, Larry;
Ljungström, Viktor;
Duran-Ferrer, Martí;
Malousi, Andigoni;
Queirós, Ana C.;
Plevova, Karla;
Bhoi, Sujata;
Kollia, Panagoula;
Oscier, David;
Anagnostopoulos, Achilles;
Trentin, Livio;
Ritgen, Matthias;
Pospisilova, Sarka;
Stavroyianni, Niki;
Ghia, Paolo;
Martin-Subero, Jose I.;
Pott, Christiane

Publication type:

Article

The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.

Published in:

2009

By:

Chassanidis, Christos;
Kalamaras, Angelos;
Phylactides, Marios;
Pourfarzad, Farzin;
Likousi, Sophia;
Maroulis, Vassilis;
Papadakis, Manoussos N.;
Vamvakopoulos, Nikolaos K.;
Aleporou-Marinou, Vassiliki;
Patrinos, George P.;
Kollia, Panagoula

Publication type:

journal article

Works by KOLLIA, PANAGOULA

Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and δβ-thalassemia.

Increased γ-globin gene expression in β-thalassemia intermedia patients correlates with a mutation in 3′HS1.

Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in Central Greece compared to the rest of the country.

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the βS/Benin haplotype.

Impact of ACE and ApoE polymorphisms on myocardial perfusion: correlation with myocardial single photon emission computed tomographic imaging.

PB1992: PROTEOMIC ANALYSIS REVEALS AUTOPHAGY INHIBITION IN MYELODYSPLASTIC SYNDROMES.

Association of GSTP1 inactivating polymorphism with acute myeloid leukemia and its specific chromosomal abnormalities.

Evidence for regulation of oxidative stress by latent membrane protein 1 oncoprotein in patients with low-grade leukemic B cell lymphoma with latent Epstein-Barr virus infection.

Correlation of Fc-γ RIIA polymorphisms with latent Epstein-Barr virus infection and latent membrane protein 1 expression in patients with low grade B-cell lymphomas.

Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greece<sup>a</sup>.

Sickle Cell Thalassemia in Greece.

Prenatal Diagnosis of Thalassemia Intermedia: Is It Justified?

Induction of MMP‐3 and MMP‐9 expression during Helicobacter pylori infection via MAPK signaling pathways.

Analysis of the κ light chain variable region in multiple myeloma.

Darwinian molecular imaging in nuclear cardiology.

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.

Novel Sequence Variations in the CER1 Gene Are Strongly Associated with Low Bone Mineral Density and Risk of Osteoporotic Fracture in Postmenopausal Women.

The 5' Regulatory Region of the Human Fetal Globin Genes is a Gene Conversion Hotspot.

Thumb duplication: molecular analysis of different clinical types.

Bone morphogenetic proteins (BMPs) expression in the femoral heads of patients with avascular necrosis.

The G<i><sup>516</sup></i>T <i>CYP2B6</i> Germline Polymorphism Affects the Risk of Acute Myeloid Leukemia and Is Associated with Specific Chromosomal Abnormalities.

Hydroxyurea and Hemin Affect Both the Transcriptional and Post-Transcriptional Mechanisms of Some Globin Genes in Human Adult Erythroid Cells<sup>a</sup>.

Aγ-haplotypes: A new group of genetic markers for thalassemic mutations inside the 5′ regulatory region of the human Aγ-globin gene.

Survivin Messenger RNA Levels in Epstein-Barr Viruse Positive Patients With Leukemic Low-Grade B-Cell Lymphomas Expressing the Latent Membrane Protein 1: Evidence of Apoptotic Function?

Combined GSTP1 and NQO1 germline polymorphisms in the susceptibility to Multiple Sclerosis.

Clinical implications for Vascular Endothelial Growth Factor in the lung: friend or foe?

CER1 gene variations associated with bone mineral density, bone markers, and early menopause in postmenopausal women.

A new COL1A1 mutation in a Greek patient with osteogenesis imperfecta: Response to a low-dose protocol of zoledronic acid and two-year follow-up.

Impact of Helicobacter pylori Infection and Its Major Virulence Factor CagA on DNA Damage Repair.

Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the TWIST1 and EFNB1 Genes.

A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl With Craniofrontonasal Syndrome.

DNA methylation profiles in chronic lymphocytic leukemia patients treated with chemoimmunotherapy.

The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.