Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Aysegul Bayrak"'
Autor:
Ali Ucur, Kivanc Cefle, Meliha Nalcaci, Sukru Palanduz, Gulcin Bagatır, Aysegul Bayrak, Aynur Daglar Aday, Akif Selim Yavuz, Sukru Ozturk, Veysel Sabri Hancer, Simge Erdem
Publikováno v:
Journal of Hematopathology. 14:151-156
Myeloid/lymphoid neoplasm is a rare malignancy with an aggressive course and rapid transformation to acute myeloid leukemia (AML), or less frequently to acute lymphoblastic leukemia (ALL). Cases with t(8;22)(p11;q11) BCR-FGFR1 fusion gene may be misd
Autor:
E Nikerel, Kivanc Cefle, Sukru Ozturk, Melih Aktan, Aysegul Bayrak, Gulcin Bagatır, Halim Issever, Sukru Palanduz, Ali Ucur, Gözde Öztan
Publikováno v:
Balkan Journal of Medical Genetics, Vol 23, Iss 1, Pp 15-24 (2020)
Balkan Journal of Medical Genetics : BJMG
Balkan Journal of Medical Genetics : BJMG
Chronic lymphocytic leukemia (CLL) is a neoplasm characterized by excessive accumulation of B lymphocytes in the peripheral blood, bone marrow and lymph nodes. We assessed the expressions of 22 genes in the p53 pathway in 30 CLL patients and 15 healt
Publikováno v:
International Journal of Contemporary Educational Research, Vol 11, Iss 3 (2024)
The study examined how prospective teachers defined effective teaching; the methods and techniques used by pre-service teachers during their teaching practicum and their reasons to use; and how these instructional techniques fit specific teaching pri
Externí odkaz:
https://doaj.org/article/b63b469509a74965bf81e19a0acc3f5a
Autor:
Kivanc Cefle, Akif Selim Yavuz, Sukru Ozturk, Aynur Daglar Aday, Sukru Palanduz, M. Ozbalak, Aysegul Bayrak, Meliha Nalcaci
Publikováno v:
Leukemia Research. 111:106725
Variant Philadelphia (Ph) translocations involving chromosome 7 are rarely seen in Chronic Myeloid Leukemia (CML) patients. It is aimed to contribute new cases to the literature by reviewing the cases in our archive and shed light into the understand
Autor:
Sukru Ozturk, Ali Ucur, M. Karabagli, İbrahim Firat, B. Karan, Aysegul Bayrak, Alper Baran, Funda Yildirim, Z. Mutlu, Umit Ugurlu
Publikováno v:
Veterinární medicína. 62:226-230
Autor:
Aysegul, Bayrak, Sukru, Palanduz, Ender, Coskunpinar, Oner, Sanli, Abdullah, Armagan, Serkan, Karakus, Ramazan, Topaktas, Kivanc, Cefle, Sukru, Ozturk, Ali, Ucur
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Background: The process of development of bladder cancer features alteration of normal biological conditions caused by changes in molecular pathways. Removing control over regulation of these pathways could lead to changes in signal transduction and
Autor:
İbrahim Firat, Sukru Ozturk, Z. Mutlu, M. Karabagli, Aysegul Bayrak, Alper Baran, Funda Yildirim, Umit Ugurlu, Ali Ucur, B. Karan
Publikováno v:
Veterinární medicína. 64:49-49
Autor:
Seher YALÇIN, Ayşegül BAYRAKTAR
Publikováno v:
International Journal of Contemporary Educational Research, Vol 8, Iss 4, Pp 158-169 (2022)
The aim of this study was to compare reading strategies and habits in terms of reading achievement of select age-group participants from the Programme for International Student Assessment (PISA) 2009 and the International Assessment of Adult Competen
Externí odkaz:
https://doaj.org/article/bad53d8578684d0ea9002ceac2481a4b
Autor:
Aysegul Bayrak, Sukru Ozturk, Nebil Ark, Sukru Palanduz, Kıvanç Bektaş Kayhan, Esra Gunduz, Davut Pehlivan, Mehmet Gunduz, Kivanc Cefle, Shinichi Abe
Publikováno v:
Journal of Hard Tissue Biology. 18:131-134
Hereditary Gingival Fibromatosis (HGF) is a rare, benign disorder characterized by slowly progressive fibrous overgrowth of the gingiva. HGF occurs in several forms as a Mendelian trait (usually as an autosomal dominant condition), in malformation sy
Publikováno v:
Balkan Medical Journal, Vol 30, Iss 2, Pp 250-252 (2013)
Volume: 2013, Issue: 2 250-252
Balkan Medical Journal
Volume: 2013, Issue: 2 250-252
Balkan Medical Journal
Background: Carriers of structural chromosomal rearrangements such as Robertsonian or reciprocal translocations have an increased risk of spontaneous abortion and producing offspring with genetic abnormalities. Case Report: We report a man with balan