Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gulcin Gunden"'
Autor:
Beyhan Durak Aras, Sevgi Isik, Hava Uskudar Teke, Abdulvahap Aslan, Filiz Yavasoglu, Zafer Gulbas, Fatih Demirkan, Hulya Ozen, Oguz Cilingir, Nur Sena Inci, Gulcin Gunden, Tuba Bulduk, Ebru Erzurumluoglu Gokalp, Sinem Kocagil, Sevilhan Artan, Olga Meltem Akay
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Abstract Background Deletion of 13q14 [del(13q)] is the most common cytogenetic change (50%) in chronic lymphoblastic leukemia (CLL), and it is a good prognostic factor if it is detected as a sole aberration by FISH. However, it is observed the clini
Externí odkaz:
https://doaj.org/article/ce7069f8615f4634a0687320dd93d0ec
Autor:
Sevgi Isik, Gulcin Gunden, Eren Gunduz, Olga Meltem Akay, Abdulvahap Aslan, Hulya Ozen, Oguz Cilingir, Ebru Erzurumluoglu Gokalp, Sinem Kocagil, Sevilhan Artan, Zafer Gulbas, Beyhan Durak Aras
Publikováno v:
Cytogenetic and genome research. 161(10-11)
Deletion 13q [del(13q)] is a favorable prognostic marker if it is detected as a sole abnormality in chronic lymphocytic leukemia (CLL). However the clinical courses of cases with isolated del(13q) are quite heterogeneous. In our study, we investigate
Autor:
Sevgi Isik, Sinem Kocagil, Sevilhan Artan, Gulcin Gunden, Beyhan Durak Aras, Hava Üsküdar Teke, Ebru Erzurumluoğlu, Nur Oguz Davutoglu, Oguz Cilingir
Publikováno v:
Volume: 43, Issue: 5 480-484
Osmangazi Tıp Dergisi
Osmangazi Tıp Dergisi
Chronic lymphocytic leukemia (CLL) is known as type of leukemia originating from clonal mature B lymphocytes and has genetic heterogeneity. Many studies have been done to clarify the genome of CLL. In these studies, del(13q) is reported as the most c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3e04d877a760acc339c9b0deede9f03
https://dergipark.org.tr/tr/pub/otd/issue/64629/916009
https://dergipark.org.tr/tr/pub/otd/issue/64629/916009
Autor:
Hulya Ozen, Sevgi Isik, Beyhan Durak Aras, Filiz Yavasoglu, Oguz Cilingir, Ebru Erzurumluoglu Gokalp, Abdulvahap Aslan, Fatih Demirkan, Nur Sena Inci, Sevilhan Artan, Hava Üsküdar Teke, Olga Meltem Akay, Sinem Kocagil, Tuba Bulduk, Zafer Gulbas, Gulcin Gunden
Publikováno v:
Molecular Cytogenetics
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-7 (2021)
Background: deletion of 13q14 [del(13q)] is the most common cytogenetic change (50%) in chronic lymphoblastic leukemia (CLL), and it is a good prognostic factor if it is detected as a sole aberration by FISH. However, it is observed the clinical cour
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90a90b4571096163dfc0db70fb9bfc76
http://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9314
http://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9314
Autor:
Gulcin Gunden, Hava Üsküdar Teke, Beyhan Durak Aras, Ebru Erzurumluoglu Gokalp, Sevgi Isik, Sevilhan Artan, Oguz Cilingir
Publikováno v:
Cancer genetics.
In acute myeloid leukemia, t(8;21) detected with a frequency of 10% is associated with good prognosis. However, variant t(8;21) is observed in 4% of these cases, and although the prognostic effects of these variant translocations have not been clearl
Autor:
Sevgi Işık, Gülçin Günden, Hava Üsküdar Teke, Olga Meltem Akay, Nur Oğuz Davutoğlu, Vahap Aslan, Mustafa Karagülle, Hülya Özen, Oğuz Çilingir, Sevilhan Artan, Beyhan Durak Aras
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 4, Pp 237-244 (2022)
Objective: Objective: Chronic myeloid leukemia (CML) is a clonal hematologic disorder characterized by t(9;22) translocation, in which cytogenetic aberrations can occur in Ph(+) and (-) clones. These aberrations develop due to clonal evolution as wel
Externí odkaz:
https://doaj.org/article/a95fde8945ec4d30beebeb0b5d0db1a9