Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Georgios, Nasioulas"'
Autor:
Eirini Papadopoulou, Georgia Pepe, Spiridon Konitsiotis, Maria Chondrogiorgi, Nikolaos Grigoriadis, Vasilios K. Kimiskidis, Georgios Tsivgoulis, Dimos D. Mitsikostas, Elisabeth Chroni, Eleni Domouzoglou, Georgios Tsaousis, Georgios Nasioulas
Publikováno v:
Journal of the Neurological Sciences. 447:120609
Autor:
Angela Apessos, Georgios Nasioulas
Publikováno v:
Breast Cancer Essentials ISBN: 9783030731465
Breast cancer is the most commonly diagnosed cancer worldwide and the leading cause of cancer-related death in women. Approximately 10% of cases are hereditary, caused by mutations in genes responsible for cell growth and survival and DNA maintenance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d9d9d3f571e8c1b67965b39c8bb6556
https://doi.org/10.1007/978-3-030-73147-2_3
https://doi.org/10.1007/978-3-030-73147-2_3
Autor:
Petros N, Karamanakos, Dimitrios T, Trafalis, Dionysios J, Papachristou, Eleftheria S, Panteli, Maria, Papavasilopoulou, Andreas, Karatzas, Dimitrios, Kardamakis, Georgios, Nasioulas, Marios, Marselos
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 22(5)
Glioblastoma multiforme (GBM) is the most common and aggressive malignancy of the central nervous system. Treatment usually involves a combination of surgical resection, chemotherapy, and radiotherapy, but ultimately this condition is incurable. Besi
Autor:
N. Diamantopoulos, Georgios Nasioulas, Nikolaos Tsoulos, Theofanis Floros, Dana Lucia Stanculeanu, Christos Markopoulos, Eirini Papadopoulou, Konstantinos Agiannitopoulos, Konstantinos Papazisis, Georgia Pepe, V. Venizelos, A Ungureanu, Sualp Tansan, E Banu, Dan Tudor Eniu, S Songül Yalçin, Mehmet Tekinel, Georgios N. Tsaousis, Rodoniki Iosifidou, Grigorios Xepapadakis
Publikováno v:
Annals of Oncology. 30:v36
Background The application of the Next Generation Sequencing (NGS) technology has facilitated multigene panel testing for hereditary breast cancer (BC) in clinical practice. We performed a retrospective analysis of individuals referred for testing in
Autor:
Vahit Ozmen, Konstantinos Papazisis, Ourania Katopodi, Dan Tudor Eniu, Christos Markopoulos, Rodoniki Iosifidou, A Ungureanu, Mehmet Tekinel, Sualp Tansan, Nikolaos Tsoulos, Georgia Pepe, Dana Lucia Stanculeanu, S Kambouri, Angela Apessos, Konstantinos Agiannitopoulos, Grigorios Xepapadakis, V. Venizelos, Anna Koumarianou, Georgios Nasioulas, Ioannis Xanthakis, S Songül Yalçin, N. Diamantopoulos, Theofanis Floros, Serban Negru, E Banu, Georgios N. Tsaousis, Eirini Papadopoulou
Publikováno v:
Cancer Research. 79:P4-03
BACKGOUND: Hereditary cancer predisposition syndromes are believed to be responsible for approximately 5-10% of all diagnosed cancer cases. In the past, single genes analysis of certain high risk genes was used for the determination of the genetic ca
Autor:
Konstantinos Agiannitopoulos, Ioannis Natsiopoulos, Nikolaos Touroutoglou, Vassiliki Metaxa-Mariatou, Konstantinos Papazisis, V. Venizelos, Antonios Keramopoulos, Aristeidis Tsiftsoglou, Maria Vasilaki-Antonatou, Angela Apessos, Christos Markopoulos, Georgios Nasioulas, Eirini Papadopoulou, Stylianos Kakolyris, Georgios Kesisis, Nikolaos Bredakis, Grigorios Xepapadakis
Publikováno v:
Cancer Research. 75:P1-03
AIM: The aim of this study was to further delineate the extent and nature of mutations in the BRCA1 and BRCA2 genes, responsible for hereditary breast and ovarian cancer in Greek families. MATERAILS & METHODS: Genomic DNA was isolated from whole peri
Autor:
Alexandru Blidaru, Dana Lucia Stanculeanu, S Kambouri, Georgia Pepe, Angela Apessos, Dan Tudor Eniu, A Ungureanu, Nikolaos Tsoulos, Konstantinos Agiannitopoulos, Angelica Chiorean, Georgios Nasioulas, L Ciule, Georgios N. Tsaousis, E Banu, D Mateescu
Publikováno v:
Cancer Research. 78:P3-03
INTRODUCTION Hereditary breast cancer is estimated to account for approximately 10% of all breast cancer cases. In addition, an estimated 15-20% of those affected by breast cancer have a positive family history. Despite the fact that BRCA1 and BRCA2
Autor:
Pierangela Grignani, M Mihalatos, Tiziana Venesio, Silvia Bione, Angela Apessos, Francesca Cattaneo, Georgios Nasioulas, Sara Molatore, Guglielmina Nadia Ranzani
Publikováno v:
Genetics in Medicine. 9:836-841
Purpose: Familial adenomatous polyposis is a phenotypically heterogeneous disease predisposing to colorectal cancer. It is dominantly transmitted, when associated with the APC gene, and recessively inherited, when associated with MUTYH gene. We searc
Autor:
Anna Samanidou-Voyadjoglou, Eleni Patsoula, Georgios Nasioulas, Gregory Spanakos, Jenny Kremastinou, N. C. Vakalis
Publikováno v:
Medical and Veterinary Entomology. 21:36-43
Specimens belonging to the Anopheles maculipennis complex were collected as larvae or resting adults from May 2003 to November 2004 in the area of the Athens 2004 Olympic Rowing Centre in Schinias, Attiki, Greece, and identified by morphological and
Autor:
Elias Davilas, Eleftherios Georgakopoulos, Georgios Nasioulas, Konstantinos Dardoufas, Niki Agnanti, Filipos Aggelakis, Vasilios Sotiriou, Irini Karydas, Eirini Papadopoulou, Stavroula Georgakopoulou, Alexander Koliopanos
Publikováno v:
Annals of the New York Academy of Sciences. 1075:235-243
In this study, we examined several molecular markers in prostate and breast cancer patients and in normal individuals. The markers tested were: variations in the quantity of plasma DNA, glutathione-S-transferase P1 gene (GSTP1), Ras association domai