Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Konstantinos Xanthopoulos"'
Autor:
Korina Karagianni, Dimitra Dafou, Konstantinos Xanthopoulos, Theodoros Sklaviadis, Eirini Kanata
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-18 (2024)
Abstract Background Amyotrophic Lateral Sclerosis (ALS) is a highly heterogenous neurodegenerative disorder that primarily affects upper and lower motor neurons, affecting additional cell types and brain regions. Underlying molecular mechanisms are s
Externí odkaz:
https://doaj.org/article/228409947e794c3da43b949786e67eb0
Autor:
Nikoletta Christoudia, Nikolaos Bekas, Eirini Kanata, Athanasia Chatziefsthathiou, Spyros Pettas, Korina Karagianni, Susana Margarida Da Silva Correia, Matthias Schmitz, Inga Zerr, Ioannis Tsamesidis, Konstantinos Xanthopoulos, Dimitra Dafou, Theodoros Sklaviadis
Publikováno v:
Redox Biology, Vol 72, Iss , Pp 103133- (2024)
Prion diseases, also known as Transmissible Spongiform Encephalopathies (TSEs), are protein-based neurodegenerative disorders (NDs) affecting humans and animals. They are characterized by the conformational conversion of the normal cellular prion pro
Externí odkaz:
https://doaj.org/article/19173e07dce8450892cda6e75342de7d
Autor:
Athanasia Chatziefstathiou, Sezgi Canaslan, Eirini Kanata, Kostas Vekrellis, Vasilios C. Constantinides, George P. Paraskevas, Elisabeth Kapaki, Matthias Schmitz, Inga Zerr, Konstantinos Xanthopoulos, Theodoros Sklaviadis, Dimitra Dafou
Publikováno v:
Biomedicines, Vol 12, Iss 6, p 1253 (2024)
Background: Accurate diagnosis of Alzheimer’s disease (AD) and frontotemporal dementia (FTD) represents a health issue due to the absence of disease traits. We assessed the performance of a SIMOA panel in cerebrospinal fluid (CSF) from 43 AD and 33
Externí odkaz:
https://doaj.org/article/127f9daea5874ba586a16f6d90faab5a
Autor:
Ioannis Gkekas, Aimilia-Christina Vagiona, Nikolaos Pechlivanis, Georgia Kastrinaki, Katerina Pliatsika, Sebastian Iben, Konstantinos Xanthopoulos, Fotis E. Psomopoulos, Miguel A. Andrade-Navarro, Spyros Petrakis
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disease caused by a trinucleotide (CAG) repeat expansion in the ATXN1 gene. It is characterized by the presence of polyglutamine (polyQ) intranuclear inclusion bodies (II
Externí odkaz:
https://doaj.org/article/2b770eb2ab1042f792ab4728d497f157
Autor:
Ioannis Paspaltsis, Eirini Kanata, Sotirios Sotiriadis, Susana Silva Correia, Matthias Schmitz, Inga Zerr, Dimitra Dafou, Konstantinos Xanthopoulos, Theodoros Sklaviadis
Publikováno v:
Pathogens, Vol 13, Iss 5, p 420 (2024)
Prions are proteinaceous pathogens responsible for a variety of devastating diseases in mammals, including scrapie in sheep and goats, chronic wasting disease in cervids, and Creutzfeldt–Jakob disease (CJD) in humans. They are characterized by thei
Externí odkaz:
https://doaj.org/article/2cb35df261f54477bf86f0bb5542ccd4
Autor:
Kyriaki Founta, Dimitra Dafou, Eirini Kanata, Theodoros Sklaviadis, Theodoros P. Zanos, Anastasios Gounaris, Konstantinos Xanthopoulos
Publikováno v:
Molecular Medicine, Vol 29, Iss 1, Pp 1-13 (2023)
Abstract Background Amyotrophic lateral sclerosis (ALS) is a rare progressive neurodegenerative disease that affects upper and lower motor neurons. As the molecular basis of the disease is still elusive, the development of high-throughput sequencing
Externí odkaz:
https://doaj.org/article/45dc835205954bdfb5a4c43a066c6851
Autor:
Athanasios Pseftogkas, Jessica Bordini, Michela Frenquelli, Ferdinando Bonfiglio, Masanori Daibata, José Ángel Martínez-Climent, George Mosialos, Davide Rossi, Alessandro Campanella, Konstantinos Xanthopoulos, Paolo Ghia
Publikováno v:
HemaSphere, Vol 7, p e1177106 (2023)
Externí odkaz:
https://doaj.org/article/61f1b3190d4444e1947671f7a5c453be
Autor:
Eirini Kanata, Ioannis Paspaltsis, Sotiris Sotiriadis, Chrysanthi Berberidou, Sophia Tsoumachidou, Dimitra Dafou, Konstantinos Xanthopoulos, Minas Arsenakis, Athanasios Arsenakis, Ioannis Poulios, Theodoros Sklaviadis
Publikováno v:
Molecules, Vol 28, Iss 3, p 1199 (2023)
Photocatalytic inactivation of pathogens in aqueous waste is gaining increasing attention. Several homogeneous and heterogeneous photocatalytic protocols exist using the Fenton’s reagent and TiO2, respectively. A comprehensive study of homogeneous
Externí odkaz:
https://doaj.org/article/a2fefc1a61b047229274a0bb3dc5a569
Autor:
Dimitra Dafou, Eirini Kanata, Spyros Pettas, Nikolaos Bekas, Athanasios Dimitriadis, Garyfalia Kempapidou, Roza Lagoudaki, Paschalis Theotokis, Olga Touloumi, Nikoleta Delivanoglou, Evangelia Kesidou, Konstantinos Xanthopoulos, Nikolaos Grigoriadis, Fotini Nina Papavasiliou, Theodoros Sklaviadis
Publikováno v:
Cells, Vol 11, Iss 22, p 3582 (2022)
RNA editing is an epitranscriptomic modification, leading to targeted changes in RNA transcripts. It is mediated by the action of ADAR (adenosine deaminases acting on double-stranded (ds) RNA and APOBEC (apolipoprotein B mRNA editing enzyme catalytic
Externí odkaz:
https://doaj.org/article/25ba25b3c4374106a886ed7343905e38
Autor:
Gianna Triller, Dimitrios A. Garyfallos, F. Nina Papavasiliou, Theodoros Sklaviadis, Pete Stavropoulos, Konstantinos Xanthopoulos
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 18, p 10629 (2022)
Transmissible spongiform encephalopathies are incurable neurodegenerative diseases, associated with the conversion of the physiological prion protein to its disease-associated counterpart. Even though immunization against transmissible spongiform enc
Externí odkaz:
https://doaj.org/article/775796c3cd924acdb83cf49463efcbe9