Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Maria Zanti"'
Autor:
Maria Zanti, Maria A. Loizidou, Denise G. O’Mahony, Leila Dorling, Joe Dennis, Peter Devilee, Douglas F. Easton, Mihalis I. Panayiotidis, Andreas Hadjisavvas, Kyriaki Michailidou
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: It is estimated that around 5% of breast cancer cases carry pathogenic variants in established breast cancer susceptibility genes. However, the underlying prevalence and gene-specific population risk estimates in Cyprus are currently un
Externí odkaz:
https://doaj.org/article/1ed6479f76b24713ac02555701450926
Autor:
Maria Zanti, Kyriaki Michailidou, Maria A. Loizidou, Christina Machattou, Panagiota Pirpa, Kyproula Christodoulou, George M. Spyrou, Kyriacos Kyriacou, Andreas Hadjisavvas
Publikováno v:
BMC Bioinformatics, Vol 22, Iss 1, Pp 1-21 (2021)
Abstract Background Next-generation sequencing (NGS) represents a significant advancement in clinical genetics. However, its use creates several technical, data interpretation and management challenges. It is essential to follow a consistent data ana
Externí odkaz:
https://doaj.org/article/2504d4d34e724e00946dd853e8e06165
Autor:
Anastasis Oulas, Maria Zanti, Marios Tomazou, Margarita Zachariou, George Minadakis, Marilena M Bourdakou, Pavlos Pavlidis, George M Spyrou
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0238665 (2021)
This study aims to highlight SARS-COV-2 mutations which are associated with increased or decreased viral virulence. We utilize genetic data from all strains available from GISAID and countries' regional information, such as deaths and cases per milli
Externí odkaz:
https://doaj.org/article/a6c2749562614ee591ac95a61aaabdf4
Autor:
Kyproula Christodoulou, Andreas Hadjisavvas, Maria A. Loizidou, Maria Zanti, Kyriacos Kyriacou, Kyriaki Michailidou, Christina Machattou, Panagiota Pirpa, George M. Spyrou
Publikováno v:
BMC Bioinformatics, Vol 22, Iss 1, Pp 1-21 (2021)
BMC Bioinformatics
BMC Bioinformatics
Background Next-generation sequencing (NGS) represents a significant advancement in clinical genetics. However, its use creates several technical, data interpretation and management challenges. It is essential to follow a consistent data analysis pip
Autor:
Kyriacos Kyriacou, Andreas Kousios, Kyriakos Ioannou, Louiza Potamiti, Theo M. Luider, Orthodoxia Nicolaou, Christoph Stingl, Revekka Papacharalampous, Andreas Hadjisavvas, George Neophytou, Lola Koniali, Kleitos Sokratous, Maria Zanti
Publikováno v:
Nephrology (Carlton, Vic.)
Nephrology, 25(12), 937-949. Wiley-Blackwell Publishing Ltd
Nephrology, 25(12), 937-949. Wiley-Blackwell Publishing Ltd
Aim Alport syndrome (AS) is the second most common hereditary kidney disease caused by mutations in collagen IV genes. Patients present with microhaematuria that progressively leads to proteinuria and end stage renal disease. Currently, no specific t
Autor:
George M. Spyrou, Anastasis Oulas, Jan Richter, Christina Christodoulou, Maria Zanti, Marios Tomazou, Kyproula Christodoulou, Kyriaki Michailidou
Publikováno v:
BMC Genomic Data
Background This study aims to characterize SARS-CoV-2 mutations which are primarily prevalent in the Cypriot population. Moreover, using computational approaches, we assess whether these mutations are associated with changes in viral virulence. Metho
Autor:
Marios Tomazou, Marilena M. Bourdakou, George M. Spyrou, Pavlos Pavlidis, George Minadakis, Anastasis Oulas, Maria Zanti, Margarita Zachariou
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0238665 (2021)
PLoS ONE
PLoS ONE
This study aims to highlight SARS-COV-2 mutations which are associated with increased or decreased viral virulence. We utilize genetic data from all strains available from GISAID and countries’ regional information, such as deaths and cases per mil
Autor:
Elena Spanou, Maria A. Loizidou, George M. Spyrou, Andreas Hadjisavvas, Flora Kyriakou, Kyriaki Michailidou, Eleni Kakouri, Kyriacos Kyriacou, Panagiota Pirpa, Maria Zanti, George A. Tanteles, Yiola Marcou, Christina Machattou
Publikováno v:
Cancers
Volume 12
Issue 11
Cancers, Vol 12, Iss 3140, p 3140 (2020)
Volume 12
Issue 11
Cancers, Vol 12, Iss 3140, p 3140 (2020)
Simple Summary In Cyprus, approximately 9% of triple-negative (negative in common breast cancer receptors—estrogen, progesterone, and human epidermal growth factor receptor 2 (HER2) receptors) breast cancer (TNBC) patients carry inherited mutations
Autor:
Anastasis Oulas, Anna Onisiforou, Maria Zanti, Kyriaki Savva, Evangelos Karatzas, George M. Spyrou, Sotiroula Afxenti, Marilena M. Bourdakou, Eleni M Loizidou, Nikolas Dietis, George Minadakis, Theodoros Kyprianou, Christiana C Christodoulou, Andrea C. Kakouri, George Kolios, Marios Tomazou, Jan Richter, Christina Christodoulou, Margarita Zachariou
Publikováno v:
Briefings in Bioinformatics
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic is undeniably the most severe global health emergency since the 1918 Influenza outbreak. Depending on its evolutionary trajectory, the virus is expected to establish itself as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13e4c6d4dedea340e0f8830f3064c112
https://doi.org/10.21203/rs.3.rs-78933/v1
https://doi.org/10.21203/rs.3.rs-78933/v1
Autor:
Thamar B van Dijk, Sjaak Philipsen, Maria Zanti, Constantinos Christos Loucari, Marina Kleanthous, Carsten W. Lederer, Coralea Stephanou, Ryo Kurita, Panayiota Papasavva, Petros Patsali, Soteroulla Christou, Yukio Nakamura, Maria Sitarou
Publikováno v:
Human gene therapy methods, 29(1), 60-74. Mary Ann Liebert Inc.
Human Gene Therapy Methods
Human Gene Therapy Methods
The β-hemoglobinopathies sickle cell anemia and β-thalassemia are the focus of many gene-therapy studies. A key disease parameter is the abundance of globin chains because it indicates the level of anemia, likely toxicity of excess or aberrant glob