Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Vasiliki Chondrou"'
Autor:
Theodora Chatzilygeroudi, Vasiliki Chondrou, Ruben Boers, Stavroula Siamoglou, Katerina Athanasopoulou, Evgenia Verigou, Joost Gribnau, Spyridon Alexis, Vassiliki Labropoulou, Alexandra Kourakli, George P. Patrinos, Argyro Sgourou, Argiris Symeonidis
Publikováno v:
Clinical Epigenetics, Vol 16, Iss 1, Pp 1-17 (2024)
Abstract Background As new treatment options for patients with higher-risk myelodysplastic syndromes are emerging, identification of prognostic markers for hypomethylating agent (HMA) treatment and understanding mechanisms of their delayed and short-
Externí odkaz:
https://doaj.org/article/37ed50421950464dab8771db4a51cff6
Autor:
Magda Spella, Eleftherios Bochalis, Katerina Athanasopoulou, Argyri Chroni, Irene Dereki, Giannoula Ntaliarda, Ifigeneia Makariti, Georgios Psarias, Caterina Constantinou, Vasiliki Chondrou, Argyro Sgourou
Publikováno v:
Non-coding RNA Research, Vol 9, Iss 3, Pp 759-771 (2024)
Epigenetic approaches in direct correlation with assessment of critical genetic mutations in non-small cell lung cancer (NSCLC) are currently very intensive, as the epigenetic components underlying NSCLC development and progression have attained high
Externí odkaz:
https://doaj.org/article/f54a70d529af471c9df8c0c72a7898b2
Autor:
Daniela Theodoridou, Christos-Orestis Tsiantis, Angeliki-Maria Vlaikou, Vasiliki Chondrou, Victoria Zakopoulou, Pavlos Christodoulides, Emmanouil D. Oikonomou, Katerina D. Tzimourta, Charilaos Kostoulas, Alexandros T. Tzallas, Konstantinos I. Tsamis, Dimitrios Peschos, Argyro Sgourou, Michaela D. Filiou, Maria Syrrou
Publikováno v:
Brain Sciences, Vol 14, Iss 2, p 139 (2024)
Developmental dyslexia (DD) is a learning disorder. Although risk genes have been identified, environmental factors, and particularly stress arising from constant difficulties, have been associated with the occurrence of DD by affecting brain plastic
Externí odkaz:
https://doaj.org/article/de9f6162d98349d8acc84a4d370ace74
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 24, p 16069 (2022)
Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal hematopoietic stem cell disorders with maturation and differentiation defects exhibiting morphological dysplasia in one or more hematopoietic cell lineages. They are associated with
Externí odkaz:
https://doaj.org/article/d9dd36e87f3b4b58b7d55acb32113299
Autor:
Caterina Constantinou, Magda Spella, Vasiliki Chondrou, George P. Patrinos, Adamantia Papachatzopoulou, Argyro Sgourou
Publikováno v:
Human Genomics, Vol 13, Iss 1, Pp 1-14 (2019)
Abstract Transcription factors (TFs) consisting of zinc fingers combined with BTB (for broad-complex, tram-track, and bric-a-brac) domain (ZBTB) are a highly conserved protein family that comprises a multifunctional and heterogeneous group of TFs, ma
Externí odkaz:
https://doaj.org/article/535db7814cc149a492ae2364a72bd046
Autor:
Vasiliki Chondrou, Athanasios-Nasir Shaukat, Georgios Psarias, Katerina Athanasopoulou, Evanthia Iliopoulou, Ariadne Damanaki, Constantinos Stathopoulos, Argyro Sgourou
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 13, p 7025 (2022)
The hemoglobin switch from fetal (HbF) to adult (HbA) has been studied intensively as an essential model for gene expression regulation, but also as a beneficial therapeutic approach for β-hemoglobinopathies, towards the objective of reactivating Hb
Externí odkaz:
https://doaj.org/article/aef3718b485344e0a40c1ddffcfba7ec
Autor:
Vasiliki Chondrou, Katerina Trochoutsou, Andreas Panayides, Maria Efthimiou, Georgia Stephanou, Nikos A. Demopoulos
Publikováno v:
Journal of Biological Research - Thessaloniki, Vol 25, Iss 1, Pp 1-13 (2018)
Abstract Background Doxorubicin is a widely used anticancer drug due to its broad spectrum of antitumor activity. Various mechanisms have been proposed for its cytostatic activity, including DNA intercalation, topoisomerase II inhibition, generation
Externí odkaz:
https://doaj.org/article/1855352ac1984477a8683a355cae6bda
Autor:
Vasiliki Chondrou, Eleana F. Stavrou, Georgios Markopoulos, Alexandra Kouraklis-Symeonidis, Vasilios Fotopoulos, Argiris Symeonidis, Efthymia Vlachaki, Panagiota Chalkia, George P. Patrinos, Adamantia Papachatzopoulou, Argyro Sgourou
Publikováno v:
Human Genomics, Vol 12, Iss 1, Pp 1-14 (2018)
Abstract Background We aimed to clarify the emerging epigenetic landscape in a group of genes classified as “modifier genes” of the β-type globin genes (HBB cluster), known to operate in trans to accomplish the two natural developmental switches
Externí odkaz:
https://doaj.org/article/7ba168acd2004aafb36e8c68d294d210
Autor:
Vasiliki Chondrou, Petros Kolovos, Argyro Sgourou, Alexandra Kourakli, Alexia Pavlidaki, Vlasia Kastrinou, Anne John, Argiris Symeonidis, Bassam R. Ali, Adamantia Papachatzopoulou, Theodora Katsila, George P. Patrinos
Publikováno v:
Human Genomics, Vol 11, Iss 1, Pp 1-11 (2017)
Abstract Background Human erythropoiesis is characterized by distinct gene expression profiles at various developmental stages. Previous studies suggest that fetal-to-adult hemoglobin switch is regulated by a complex mechanism, in which many key play
Externí odkaz:
https://doaj.org/article/3090c97367ea435faf044f6e298bd4b4
Autor:
Katerina Athanasopoulou, Vasiliki Chondrou, Panagiotis Xiropotamos, Georgios Psarias, Yiannis Vasilopoulos, Georgios Georgakilas, Argyro Sgourou
Non-coding RNA (ncRNA) species, mainly long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) have been currently imputed for lesser or greater involvement in human erythropoiesis. These RNA subsets operate within a complex circuit with other epigenet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a45abb32cead07b70a14c5cee6e4843d
https://doi.org/10.21203/rs.3.rs-2662510/v1
https://doi.org/10.21203/rs.3.rs-2662510/v1