Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Constantina A. Sarri"'
Autor:
Constantina A Sarri, Georgios E Papadopoulos, Anna Papa, Athanasios Tsakris, Danai Pervanidou, Agoritsa Baka, Constantina Politis, Charalambos Billinis, Christos Hadjichristodoulou, Zissis Mamuris, MALWEST project
Publikováno v:
PLoS ONE, Vol 13, Iss 10, p e0205557 (2018)
The MHC class II region in humans is highly polymorphic. Each MHC molecule is formed by an α and a β chain, produced by different genes, creating an antigen-binding groove. In the groove there are several pockets into which antigens anchor and fit.
Externí odkaz:
https://doaj.org/article/1562f7f04ccf43ab8b22973a7a077ab6
Publikováno v:
Immunology Letters. 238:75-95
Background: HLA-class II proteins hold important roles in key physiological processes. The purpose of this study was to compile all class II alleles reported in human population and investigate patterns in pocket variants and their combinations, focu
Publikováno v:
Microbiology and immunology.
The human leukocyte antigen (HLA) system plays a significant role via the regulation of the immune system and contributes to the progression and protection of many diseases. In our previous study, several HLA-DRB1 alleles were found to have a suscept
Autor:
Constantina A Sarri, Maria Markantoni, Costas Stamatis, Anna Papa, Athanasios Tsakris, Danai Pervanidou, Agoritsa Baka, Constantina Politis, Charalambos Billinis, Christos Hadjichristodoulou, Zissis Mamuris, MALWEST project
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0165952 (2016)
WNV is a zoonotic neurotropic flavivirus that has recently emerged globally as a significant cause of viral encephalitis. The last five years, 624 incidents of WNV infection have been reported in Greece. The risk for severe WNV disease increases amon
Externí odkaz:
https://doaj.org/article/2bb27b40cfa445e1b86fac29108c39d5
Autor:
Constantina A. Sarri, Bernard Dutrillaux, Anne-Marie Dutrillaux, Zissis Mamuris, Themis Giannoulis
Publikováno v:
Bulletin of Entomological Research
Bulletin of Entomological Research, Cambridge University Press (CUP), 2020, 110 (3), pp.321-327. ⟨10.1017/S0007485319000737⟩
Bulletin of Entomological Research, Cambridge University Press (CUP), 2020, 110 (3), pp.321-327. ⟨10.1017/S0007485319000737⟩
A dual molecular and cytogenetic study was performed with the aim to improve the controversial systematic classification of some species of Lamiinae (Coleoptera: Cerambycidae). The karyotypes of species belonging to genera Morimus, Herophila, Dorcadi
Autor:
Theologia Sarafidou, Aikaterini Patsatsi, Angeliki Roussaki-Schulze, Costas Stamatis, Polyxeni Gidarokosta, Dimitrios Sotiriadis, Yiannis Vasilopoulos, Zissis Mamuris, Efterpi Zafiriou, Constantina A. Sarri
Publikováno v:
Molecular Diagnosis & Therapy. 21:137-152
Netherton syndrome (OMIM #256500) is a rare but severe autosomal recessive form of ichthyosis that affects the skin, hair, and immune system. The identification of SPINK5, which encodes for the serine protease inhibitor LEKTI, as the gene responsible
Autor:
Constantina Liakou, Costas Stamatis, Ioanna Galara, Katerina A. Moutou, Nikos Argyrakoulis, Vassilis Godosopoulos, Constantina A. Sarri, Mathaios Kolovos, Zissis Mamuris, Vasiliki Stasinou
Publikováno v:
Food Research International. 69:151-155
In this study, analysis of 348 food products was performed based on a universal 16S rDNA marker. The purpose was to check whether the content of the product in particular species listed on the label corresponded with the actual composition of the pro
Autor:
Christos Tsakalidis, Aikaterini Patsatsi, Asimina Galli-Tsinopoulou, Evgenia Babatseva, Constantina A. Sarri, Nikolaos Nikolaidis, George Mitsiakos, Paraskevi Karagianni, Zissis Mamuris, Ilias Chatziioannidis, Maria Lithoxopoulou
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2015 (2015)
Case Reports in Pediatrics, Vol 2015 (2015)
Netherton syndrome, a rare autosomal recessive genetic disorder, is classified as an ichthyosiform syndrome. In this report we present the case of a neonate with erythroderma shortly after birth, accompanied by severe hypernatremia, recurrent infecti
Autor:
L Aggelou, Theologia Sarafidou, Constantina A. Sarri, Yiannis Vasilopoulos, Dimitrios Sotiriadis, Efterpi Zafiriou, A V Roussaki-Schulze, Aikaterini Patsatsi, Aikaterini Kyriakou, D Papadopoulou, E Mendrinou, Zissis Mamuris
Publikováno v:
The pharmacogenomics journal. 17(3)
Psoriasis is a multifactorial skin disease affecting ~2% of world's population, causing a dramatic decrease in patients' quality of life and a significant increase in health-care expenses. Biological agents such as the anti-TNFα ones had an enormous
Publikováno v:
HLA. 88:60-61
The new allele DRB1*11:192 exon 2 differs from the DRB1*11:01:01:01 by three substitutions.