Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vasiliki, Chini"'
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e37285- (2024)
Valuable insights for preventing sports injuries in athletes have been achieved through advancements in genetics. This study aimed to determine the allelic frequency of distinct single nucleotide polymorphisms (SNPs) in a group of high-level athletes
Externí odkaz:
https://doaj.org/article/c9789ed132ef4072a8a10bebe3066a49
Autor:
Petros P. Sfikakis, Kleio-Maria Verrou, Giannis Ampatziadis-Michailidis, Ourania Tsitsilonis, Dimitrios Paraskevis, Efstathios Kastritis, Evi Lianidou, Paraskevi Moutsatsou, Evangelos Terpos, Ioannis Trougakos, Vasiliki Chini, Menelaos Manoloukos, Panagiotis Moulos, Georgios A. Pavlopoulos, George Kollias, Pantelis Hatzis, Meletios A. Dimopoulos
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
The reasons behind the clinical variability of SARS-CoV-2 infection, ranging from asymptomatic infection to lethal disease, are still unclear. We performed genome-wide transcriptional whole-blood RNA sequencing, bioinformatics analysis and PCR valida
Externí odkaz:
https://doaj.org/article/5544ae135ad64856b321e886966e1db2
Autor:
Ioannis P. Trougakos, Kleio-Maria Verrou, Ourania E. Tsitsilonis, Pantelis Hatzis, Petros P. Sfikakis, Dimitrios Paraskevis, Giannis Ampatziadis-Michailidis, George Kollias, Vasiliki Chini, Efstathios Kastritis, Evangelos Terpos, Meletios A. Dimopoulos, Panagiotis Moulos, Menelaos Manoloukos, Paraskevi Moutsatsou, Evi Lianidou, Georgios A. Pavlopoulos
Despite tremendous efforts by the international research community to understand the pathophysiology of SARS-CoV-2 infection, the reasons behind the clinical variability, ranging from asymptomatic infection to lethal disease, are still unclear. Exist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cc5cc3f4e11ff3e90f09e11150a553a
https://doi.org/10.1101/2021.04.19.21255748
https://doi.org/10.1101/2021.04.19.21255748
Autor:
Vasiliki, Chini, Danai, Stambouli, Florina Mihaela, Nedelea, George Alexandru, Filipescu, Diana, Mina, Marios, Kambouris, Hatem, El-Shantil
Publikováno v:
Eye science. 29(2)
Prenatal diagnosis was requested for an undiagnosed eye disease showing X-linked inheritance in a family. No medical records existed for the affected family members. Mapping of the X chromosome and candidate gene mutation screening identified a c.C26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b80beaf8c79b7c37a49ec4ee3979af53
https://pubmed.ncbi.nlm.nih.gov/26011961
https://pubmed.ncbi.nlm.nih.gov/26011961