Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Angela, Apessos"'
Autor:
Georgios N. Tsaousis, Eirini Papadopoulou, Angela Apessos, Konstantinos Agiannitopoulos, Georgia Pepe, Stavroula Kampouri, Nikolaos Diamantopoulos, Theofanis Floros, Rodoniki Iosifidou, Ourania Katopodi, Anna Koumarianou, Christos Markopoulos, Konstantinos Papazisis, Vasileios Venizelos, Ioannis Xanthakis, Grigorios Xepapadakis, Eugeniu Banu, Dan Tudor Eniu, Serban Negru, Dana Lucia Stanculeanu, Andrei Ungureanu, Vahit Ozmen, Sualp Tansan, Mehmet Tekinel, Suayib Yalcin, George Nasioulas
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-19 (2019)
Abstract Background Hereditary cancer predisposition syndromes are responsible for approximately 5–10% of all diagnosed cancer cases. In the past, single-gene analysis of specific high risk genes was used for the determination of the genetic cause
Externí odkaz:
https://doaj.org/article/dc43f140d22c4f09805d95f871555460
Autor:
ANGELA APESSOS, KONSTANTINOS AGIANNITOPOULOS, GEORGIA PEPE, GEORGIOS N. TSAOUSIS, PANAGIOTA PITTA, CHRYSANTHI BILI, LINA FLORENTIN, EMMANOUEL SALOUSTROS, ELEFTHERIOS KAMPLETSAS, DIMITRIOS TRYFONOPOULOS, NIKOLAOS TSOUKALAS, EVANGELOS BOURNAKIS, FLORA ZAGOURI, ATHANASSIOS KOTSAKIS, ANNA KOUMARIANOU, IPPOKRATIS KORANTZIS, IOANNIS BOUKOVINAS, GEORGE LYPAS, GEORGIOS FOUNTZILAS, VASILIKI MICHALAKI, SPYRIDON XYNOGALOS, HELENA LINARDOU, EIRINI PAPADOPOULOU, GEORGE NASIOULAS, VASSILIS GEORGOULIAS
Publikováno v:
Anticancer research. 42(12)
Male breast cancer (MBC) is a very rare disorder affecting approximately 1 in 833 men. Genetic predisposition is one of the most important risk factors of MBC with BRCA2 being the most commonly mutated gene in males diagnosed with breast cancer. Howe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a852445b90d523e02fa54397b3d744e8
https://pubmed.ncbi.nlm.nih.gov/36456130
https://pubmed.ncbi.nlm.nih.gov/36456130
Autor:
Ourania Katopodi, George Nasioulas, Stavroula Kampouri, Georgia Pepe, Rodoniki Iosifidou, Dan Tudor Eniu, Eirini Papadopoulou, Anna Koumarianou, Christos Markopoulos, Mehmet Tekinel, Serban Negru, Ioannis Xanthakis, V. Venizelos, Grigorios Xepapadakis, Sualp Tansan, Vahit Ozmen, Konstantinos Papazisis, Suayib Yalcin, Georgios N. Tsaousis, Nikolaos Diamantopoulos, E Banu, Theofanis Floros, Dana Lucia Stanculeanu, Konstantinos Agiannitopoulos, A Ungureanu, Angela Apessos
Publikováno v:
BMC Cancer, Vol 19, Iss 1, Pp 1-19 (2019)
BMC Cancer
BMC Cancer
Background Hereditary cancer predisposition syndromes are responsible for approximately 5–10% of all diagnosed cancer cases. In the past, single-gene analysis of specific high risk genes was used for the determination of the genetic cause of cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff3831322b30ce306016cfb29342a6e6
http://link.springer.com/article/10.1186/s12885-019-5756-4
http://link.springer.com/article/10.1186/s12885-019-5756-4
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:
George Nasioulas, Angeliki Tsirigoti, Nikolaos Tsoulos, Eugenia Bourkoula, Angela Apessos, Georgia Pepe, Eirini Papadopoulou, Konstantinos Agiannitopoulos, Georgios N. Tsaousis, Chrisoula Efstathiadou, Vasiliki Metaxa-Mariatou
Publikováno v:
World Journal of Gastrointestinal Oncology
Gastrointestinal malignancies are among the leading causes of cancer-related deaths worldwide. Like all human malignancies they are characterized by accumulation of mutations which lead to inactivation of tumor suppressor genes or activation of oncog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b5a97d289c19e41705cf958b701b0e4
http://europepmc.org/articles/PMC5108979
http://europepmc.org/articles/PMC5108979
Autor:
Vasiliki Metaxa-Mariatou, Jubrail Dahabreh, Angela Apessos, Aggeliki Rapti, Vasileios Karavasilis, N Papageorgiou, Charalampos Zoublios, Mina Gaga, P. Zarogoulidis, Dimitrios Veldekis, George Nasioulas, Gerasimos Aravantinos, Stylianos Kakolyris, Konstantinos Zarogoulidis, Dimitrios Kasarakis, Napoleon Karagiannidis, Fotis Vlastos, Angeliki Tsirigoti, Eirini Papadopoulou, Konstantinos Agiannitopoulos, Nikolaos Tsoulos
Publikováno v:
Oncology Letters. 10:2176-2184
It has been reported that certain patients with non-small-cell lung cancer (NSCLC) that harbor activating somatic mutations within the tyrosine kinase domain of the epidermal growth factor receptor (EGFR) gene may be effectively treated using targete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b986f1f27c3c729a9a76c822e13137f
https://doi.org/10.3892/ol.2015.3600
https://doi.org/10.3892/ol.2015.3600
Autor:
Grigorios Xepapadakis, V. Venizelos, Georgios N. Tsaousis, George Nasioulas, Eirini Papadopoulou, Christos Markopoulos, Chrysoula Efstathiadou, Angela Apessos, Vasiliki Metaxa-Mariatou, Aris P. Tsiftsoglou, Konstantinos Agiannitopoulos, Georgia Pepe, Angeliki Tsirigoti, Ioannis Natsiopoulos
Publikováno v:
Cancer genetics. 220
Germline mutations in the BRCA1 and BRCA2 genes are associated with hereditary predisposition to breast and ovarian cancer. Sensitive and accurate detection of BRCA1 and BRCA2 mutations is crucial for personalized clinical management of individuals a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2c48780dba309186d11ecf172201b0e
https://pubmed.ncbi.nlm.nih.gov/29310832
https://pubmed.ncbi.nlm.nih.gov/29310832
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f3f3c1339ea75eb99ce557f2d873da9
https://doi.org/10.1158/1538-7445.sabcs18-p4-03-07
https://doi.org/10.1158/1538-7445.sabcs18-p4-03-07
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c36ab9916f69a86b199106faf58cfc3
https://doi.org/10.1158/1538-7445.sabcs14-p1-03-08
https://doi.org/10.1158/1538-7445.sabcs14-p1-03-08
Autor:
Maroun Elkhoury, Angela Apessos, Falah Khatib, Shaheenah Dawood, Annette Hamadi, Faraz Khan, Milicent Bello
Publikováno v:
Journal of Clinical Oncology. 36:e13509-e13509
e13509Background: Hereditary cancer accounts for approximately 10% of all cancers. An estimated 15-20% of all cancer patients have positive family history. However, until recently mutations in high...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3d3abd03547d9a0f46562a6c6772982
https://doi.org/10.1200/jco.2018.36.15_suppl.e13509
https://doi.org/10.1200/jco.2018.36.15_suppl.e13509