Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elena Panayi"'
Autor:
William D. Richardson, Elena Panayi, George Lapathitis, Nicoletta Kessaris, Stavros Malas, Cédric Francius, Frédéric Clotman, Elena Panayiotou
Publikováno v:
Gene Expression Patterns
Gene Expression Patterns, Vol. 13, no. 8, p. 328-334 (2013)
Gene Expression Patterns, Vol. 13, no. 8, p. 328-334 (2013)
The embryonic spinal cord in mice is organized into eleven progenitor domains. Cells in each domain first produce neurons and then switch to specifying glia. Five of these domains known as p3, pMN, p2, p1 and p0 are located in the ventral spinal cord
Autor:
Eleni Fella, Revekka Papacharalambous, Demos Kynigopoulos, Maria Ioannou, Rita Derua, Christiana Christodoulou, Myrto Stylianou, Christos Karaiskos, Alexia Kagiava, Gerasimou Petroula, Chryso Pierides, Maria Kyriakou, Laura Koumas, Paul Costeas, Elena Panayiotou
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Alzheimer’s disease (AD) is a progressive neurodegenerative disease of the brain causing either familial or sporadic dementia. We have previously administered the modified C5a receptor agonist (EP67) for a short period to a transgenic mouse model o
Externí odkaz:
https://doaj.org/article/4c05962d56b94ee2831beb46d9c96d5e
Autor:
Kyriaki Savva, Margarita Zachariou, Demos Kynigopoulos, Eleni Fella, Maria-Ioanna Vitali, Xeni Kosofidou, Michail Spyrou, Irene Sargiannidou, Elena Panayiotou, Nikolas Dietis, George M. Spyrou
Publikováno v:
Life, Vol 13, Iss 5, p 1095 (2023)
Alzheimer’s disease (AD) is a progressive neurodegenerative disease and is the most common type of dementia. Although a considerably large amount of money has been invested in drug development for AD, no disease modifying treatment has been detecte
Externí odkaz:
https://doaj.org/article/dcbacf36dc954ed09385abfc3a44fe05
Autor:
Meropi Mpouzika, Maria Karanikola, Elena Panayiotou, Vasilios Raftopoulos, Nicos Middleton, Elizabeth Papathanassoglou
Publikováno v:
Revista da Escola de Enfermagem da USP, Vol 55 (2021)
ABSTRACT Objective: To synthesize current evidence on nurses' attitudes and/or knowledge on the entire spectrum of patient rights. Method: A systematic search of the literature was performed in Web of Science, PubMed, Scopus and CINAHL. Studies were
Externí odkaz:
https://doaj.org/article/7b48be98ae014b048edb6bb1b13a6baa
Autor:
Elena Panayiotou, Eleni Fella, Savanna Andreou, Revekka Papacharalambous, Petroula Gerasimou, Paul Costeas, Stella Angeli, Ioanna Kousiappa, Savvas Papacostas, Theodoros Kyriakides
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0225417 (2019)
According to the amyloid hypothesis of Alzheimer's disease (AD) the deposition of prefibrillar and fibrillar Aβ peptide sets off the pathogenic cascades of neuroinflammation and neurodegeneration that lead to synaptic and neuronal loss resulting in
Externí odkaz:
https://doaj.org/article/83d887e5f100465fb4158a2ae951ef5f
Autor:
Neoklis Makrides, Elena Panayiotou, Pavlos Fanis, Christos Karaiskos, George Lapathitis, Stavros Malas
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Studies proposed a model for embryonic neurogenesis where the expression levels of the SOXB2 and SOXB1 factors regulate the differentiation status of the neural stem cells. However, the precise role of the SOXB2 genes remains controversial. Therefore
Externí odkaz:
https://doaj.org/article/f5b2eed6f91a422d862c871112f7fb23
Autor:
Eleni Fella, Kleitos Sokratous, Revekka Papacharalambous, Kyriacos Kyriacou, Joy Phillips, Sam Sanderson, Elena Panayiotou, Theodoros Kyriakides
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2017)
Hereditary ATTR V30M amyloidosis is a lethal autosomal dominant sensorimotor and autonomic neuropathy caused by deposition of aberrant transthyretin (TTR). Immunohistochemical examination of sural nerve biopsies in patients with amyloidotic neuropath
Externí odkaz:
https://doaj.org/article/9290f31403a94e17b34a03d819cf7703
Autor:
Elena Panayiotou, Eleni Fella, Revekka Papacharalambous, Stavros Malas, Maria Joao Saraiva, Theodoros Kyriakides
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0175767 (2017)
ATTRV30M amyloid neuropathy is a lethal autosomal dominant sensorimotor and autonomic neuropathy, caused by deposition of amyloid fibrils composed of aberrant transthyretin (TTR). Ages of onset and penetrance exhibit great variability and genetic fac
Externí odkaz:
https://doaj.org/article/72eef27ab6a14f6bbe1243c2b17e5ae9