Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Electra Stylianopoulou"'
Autor:
Paraskevi Somalou, Eleftheria Ieronymaki, Kyriaki Feidaki, Ioanna Prapa, Electra Stylianopoulou, Katerina Spyridopoulou, George Skavdis, Maria E. Grigoriou, Panayiotis Panas, Anagnostis Argiriou, Christos Tsatsanis, Yiannis Kourkoutas
Publikováno v:
Microorganisms, Vol 12, Iss 2, p 231 (2024)
As the food and pharmaceutical industry is continuously seeking new probiotic strains with unique health properties, the aim of the present study was to determine the impact of short-term dietary intervention with novel wild-type strains, isolated fr
Externí odkaz:
https://doaj.org/article/ee4bc39de2b74c2090e92055d9b83092
Autor:
Electra Stylianopoulou, Anastasia Daviti, Venetia Giourou, Eleni Gerasimidi, Anastasios Nikolaou, Yiannis Kourkoutas, Maria E. Grigoriou, Katerina E. Paleologou, George Skavdis
Publikováno v:
Brain Sciences, Vol 14, Iss 1, p 35 (2023)
Essential oils exhibit numerous medicinal properties, including antimicrobial, anti-inflammatory and antioxidant effects. Recent studies also indicate that certain essential oils demonstrate anti-amyloidogenic activity against β-amyloid, the protein
Externí odkaz:
https://doaj.org/article/27d2df44f97d42b09e7d9c5fd2fa86fd
Autor:
Dimitrios Troumpoukis, Andreas Rafail Vasileiou, Nikistratos Siskos, Electra Stylianopoulou, Petros Ypsilantis, George Skavdis, Maria E. Grigoriou
Publikováno v:
Biomolecules, Vol 13, Iss 9, p 1337 (2023)
Abracl (ABRA C-terminal-like protein) is a small, non-typical winged-helix protein that shares similarity with the C-terminal domain of the protein ABRA (Actin-Binding Rho-Activating protein). The role of Abracl in the cell remains elusive, although
Externí odkaz:
https://doaj.org/article/2c9fb08a9f4b457a9aac337ebd323b64
Publikováno v:
Brain Sciences, Vol 11, Iss 5, p 581 (2021)
MicroCephaly Primary Hereditary (MCPH) is a rare congenital neurodevelopmental disorder characterized by a significant reduction of the occipitofrontal head circumference and mild to moderate mental disability. Patients have small brains, though with
Externí odkaz:
https://doaj.org/article/ddbad112c33949d2a381521a87f133a3
Autor:
Electra Stylianopoulou, Dimitrios Lykidis, Petros Ypsilantis, Constantinos Simopoulos, George Skavdis, Maria Grigoriou
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33898 (2012)
BackgroundNon Radioactive colorimetric In Situ Hybridization (NoRISH) with hapten labeled probes has been widely used for the study of gene expression in development, homeostasis and disease. However, improvement in the sensitivity of the method is s
Externí odkaz:
https://doaj.org/article/41f60c2d02e34facba99362bc609b18b
Autor:
Lydia Angelopoulou, Electra Stylianopoulou, Konstantinos Tegopoulos, Ioanna Farmakioti, Maria E. Grigoriou, George Skavdis
CRISPR-based technologies have revolutionised genome editing and are widely used for knocking out genes in cell lines and organisms. From a practical perspective, a critical factor that largely influences the successful outcome of CRISPR gene knockou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33c8bfa53f186ac72825f6192e2744ae
https://doi.org/10.1101/2023.04.09.535589
https://doi.org/10.1101/2023.04.09.535589
Publikováno v:
Brain Sciences, Vol 11, Iss 581, p 581 (2021)
Brain Sciences
Brain Sciences
MicroCephaly Primary Hereditary (MCPH) is a rare congenital neurodevelopmental disorder characterized by a significant reduction of the occipitofrontal head circumference and mild to moderate mental disability. Patients have small brains, though with
Autor:
George Skavdis, Margarita Pitsiani, Georgios Kalamakis, Electra Stylianopoulou, Maria Grigoriou, Constantinos Simopoulos, Ioannis Fysekis, Petros Ypsilantis
Publikováno v:
Histochemistry and Cell Biology. 145:175-184
Winged helix proteins have critical roles in a variety of developmental processes. During a screening for genes expressed in the developing forebrain, we identified HSPC280, a non-typical winged helix protein, which shares similarity with a protein-p
Autor:
Peter Nagy, Iordanis Karagiannidis, Christos Androutsos, Luca Farkas, Tomasz Wolańczyk, Zsanett Tarnok, Gerd Lehmkuhl, Vaia Tsironi, Renata Rizzo, Peristera Paschou, S. Klidonas, George Skavdis, Maria Grigoriou, Electra Stylianopoulou, Urszula Szymańska, Markus M. Nöthen, Johannes Hebebrand, Petros Ypsilantis, Constantinos Simopoulos, Csaba Barta, Anastasia Koumoula, Dimitrios Lykidis
Publikováno v:
Genes, Brain and Behavior. 11:444-451
The etiology and pathophysiology of Tourette Syndrome (TS) remain poorly understood. Multiple lines of evidence suggest that a complex genetic background and the cortico-striato-thalamo-cortical circuit are involved. The role of Lhx6 and Lhx8 in the
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1211
Nonradioactive colorimetric in situ hybridization (NoRISH) has been widely applied to analyze gene expression at the single-cell level. Zinc fixation is time efficient and provides excellent tissue morphology. Furthermore, it improves the preservatio