Zobrazeno 1 - 7
of 7
pro vyhledávání: '"GEORGE LYPAS"'
Autor:
Mustafa Özdoğan, Eirini Papadopoulou, Nikolaos Tsoulos, Aikaterini Tsantikidi, Vasiliki-Metaxa Mariatou, Georgios Tsaousis, Evgenia Kapeni, Evgenia Bourkoula, Dimitrios Fotiou, Georgios Kapetsis, Ioannis Boukovinas, Nikolaos Touroutoglou, Athanasios Fassas, Achilleas Adamidis, Paraskevas Kosmidis, Dimitrios Trafalis, Eleni Galani, George Lypas, Bülent Orhan, Sualp Tansan, Tahsin Özatlı, Onder Kırca, Okan Çakır, George Nasioulas
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-21 (2021)
Abstract Background Tumor molecular profile analysis by Next Generation Sequencing technology is currently widely applied in clinical practice and has enabled the detection of predictive biomarkers of response to targeted treatment. In parallel with
Externí odkaz:
https://doaj.org/article/4d6aebbe3cc044afac237bd8eaa91cee
Autor:
Konstantinos Agiannitopoulos, Eirini Papadopoulou, Georgios N. Tsaousis, Georgia Pepe, Stavroula Kampouri, Eleni Patsea, George Lypas, George Nasioulas
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Carriers with pathogenic variants in MSH2 have increased risk to develop colorectal, endometrium, ovarian, and other types of cancer. The PALB2 is associated with breast, ovarian, pancreatic, and prostate cancer. We describe the c
Externí odkaz:
https://doaj.org/article/2f71d7a46691488889c81edc5d993354
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
Autor:
Nikolaos Tsoulos, Sualp Tansan, Georgios N. Tsaousis, Aikaterini Tsantikidi, Dimitrios Fotiou, Bülent Orhan, Achilleas Adamidis, Eleni Galani, George Lypas, Vasiliki-Metaxa Mariatou, Evgenia Bourkoula, George Nasioulas, Ioannis Boukovinas, Okan Çakır, Dimitrios T. Trafalis, Evgenia Kapeni, Paraskevas Kosmidis, Mustafa Ozdogan, Eirini Papadopoulou, Onder Kirca, Tahsin Özatlı, Athanasios Fassas, Georgios Kapetsis, Nikolaos Touroutoglou
Publikováno v:
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-21 (2021)
BMC Medical Genomics
BMC Medical Genomics
Background Tumor molecular profile analysis by Next Generation Sequencing technology is currently widely applied in clinical practice and has enabled the detection of predictive biomarkers of response to targeted treatment. In parallel with targeted
Autor:
Aikaterini Tsantikidi, Nikolaos Tsoulos, Georgios Kapetsis, Nikolaos Touroutoglou, Evgenia Kapeni, Eirini Papadopoulou, George Lypas, Vasiliki Metaxa-Mariatou, Dimitrios Fotiou, George Tsaousis, Evgenia Bourkoula, Onder Kirca, George Nasioulas, Athanasios Fassas, Okan Çakır, Tahsin Özatlı, Tansan Sualp, Bülent Orhan, Eleni Galani, Dimitrios T. Trafalis, Mustafa Ozdogan, Achilleas Adamidis, Ioannis Boukovinas, Paraskevas Kosmidis
Background: Tumor molecular profile is of great importance for the detection of biomarkers of response to targeted treatment due to the increased availability, with concomitant reduction of cost, of Next Generation Sequencing technology (NGS). In par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac406df53df68253d90159c5f777c5a
https://doi.org/10.21203/rs.3.rs-96233/v1
https://doi.org/10.21203/rs.3.rs-96233/v1
Autor:
George Nasioulas, Konstantinos Agiannitopoulos, Georgia Pepe, Stavroula Kampouri, Eleni Patsea, George Lypas, Eirini Papadopoulou, Georgios N. Tsaousis
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Carriers with pathogenic variants in MSH2 have increased risk to develop colorectal, endometrium, ovarian, and other types of cancer. The PALB2 is associated with breast, ovarian, pancreatic, and prostate cancer. We describe the case of a
Autor:
Vasiliki Mollaki, Despoina Kalfakakou, George Lypas, Drakoulis Yannoukakos, Efstratios Christianakis, George Alexandrakis, Florentia Fostira, Eirini Zacharopoulou, Maria Tzouvala, Irene Konstantopoulou
Publikováno v:
Cancer genetics. 220
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder caused by germline mutations in the STK11 tumor suppressor gene. PJS patients face a cumulative cancer risk as high as 93% for all sites combined. The present study reports the spectr