Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Umit Ure"'
Autor:
Muge Sayitoglu, M. Cem Ar, Ozden Hatirnaz, Seniz Ongoren, Umit Ure, Zafer Baslar, Sema Sirma, Yildiz Aydin, Ugur Ozbek, Burhan Ferhanoglu
Publikováno v:
Turkish Journal of Hematology, Vol 25, Iss 03, Pp 124-132 (2008)
Objective: Monitoring minimal residual disease has become increasingly important in clinical practice of ALL management. Break-point fusion regions of leukaemia related chromosomal aberrations and rearranged immunoglobulin (Ig) and T cell-receptor (T
Externí odkaz:
https://doaj.org/article/45eca62205b643b1a59d83d6d08cef21
Publikováno v:
Bagcilar Medical Bulletin, Vol 7, Iss 3, Pp 279-287 (2022)
Objective:Cytopenias are common complications in HIV-positive individuals, generally correlated with the stage of the disease. Prevalence of cytopenias depends on the stage of HIV infection, gender, race, geographic location, and nutritional status.
Externí odkaz:
https://doaj.org/article/17e65b1afc5547bf93d80ec685a7d4d4
Autor:
Yucel, Erbilgin, Muge, Sayitoglu, Ozden, Hatirnaz, Omer, Dogru, Arzu, Akcay, Gulen, Tuysuz, Tiraje, Celkan, Gonul, Aydogan, Zafer, Salcioglu, Cetin, Timur, Lebriz, Yuksel-Soycan, Umit, Ure, Sema, Anak, Leyla, Agaoglu, Omer, Devecioglu, Inci, Yildiz, Ugur, Ozbek
Publikováno v:
Disease Markers, Vol 28, Iss 6, Pp 353-360 (2010)
Disease markers
Disease markers
The NOTCH signaling pathway plays important role in the development of multicellular organisms, as it regulates cell proliferation, survival, and differentiation. In adults, it is essential for the T- or B-lymphocyte lineage commitment. NOTCH1 and FB
Autor:
Ozden Hatirnaz, Leyla Agaoglu, Umit Ure, Muge Sayitoglu, Ugur Ozbek, Yucel Erbilgin, Arzu Akcay, Omer Dogru, Gonul Aydogan, Gülen Tüysüz, Cetin Timur, Omer Devecioglu, Lebriz Yuksel-Soycan, Zafer Salcioglu, Tiraje Celkan, Sema Anak, Inci Yildiz
Publikováno v:
Disease Markers. 28:353-360
The NOTCH signaling pathway plays important role in the development of multicellular organisms, as it regulates cell proliferation, survival, and differentiation. In adults, it is essential for the T- or B-lymphocyte lineage commitment.NOTCH1and FBXW
Autor:
Yildiz Aydin, Şükriye Yilmaz, Zafer Baslar, Seniha Hacıhanefioğlu, Teoman Soysal, Burhan Ferhanoglu, Birsen Ülkü, S. Purisa, Ayhan Deviren, Yelda Tarkan-Argüden, Ayşe Çırakoğlu, Umit Ure, Gülgün S. Güven, Dilhan Kuru, Şeniz Öngören, Ahmet Emre Eskazan, Gürsel Çetin, Nukhet Tuzuner, M. Cem Ar
Publikováno v:
Biotechnology & Biotechnological Equipment. 23:1515-1520
Chronic myeloid leukaemia (CML) is a clonal haematological disease characterised by t(9;22)(q34;q11) which is called Philadelphia (Ph) chromosome. Highly improved haematological and cytogenetic results were obtained in chronic phase CML with the intr
Autor:
Ugur Ozbek, Teoman Soysal, Burhan Ferhanoglu, Ozden Hatirnaz, Tayfun Ozcelik, Cemaliye B Akyerli, Cem Ar, Umit Ure
Publikováno v:
American Journal of Hematology
SOCS-1, an important protein in the JAK/STAT pathway, has a role in the down stream of BCR-ABL protein kinase. We investigated 56 CML patients and 16 controls for the methylation status of SOCS-1 gene promoter and Exon 2 regions. Exon 2 was found to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4ceccd6cb079861e3ca88a2437c77d5
https://hdl.handle.net/11693/23413
https://hdl.handle.net/11693/23413
Autor:
Mehmet Kendir, Dogan Selcuk, Onur Kirkizlar, Zeynep Karaali, Umit Ure, Rumeyza Kazancioglu, Gulsen Ozbay
Publikováno v:
International urology and nephrology. 39(2)
Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal disorder of bone marrow. It is characterized by blood cells lacking membrane proteins that are normally attached by the glycosylphosphatidylinositol (GPI) anchor. The cellular defect arises in a h
Autor:
Müge Sayitoğlu, Yücel Erbilgin, Özden Hatırnaz, İnci Yıldız, Tiraje Celkan, Sema Anak, Ömer Devecioğlu, Gönül Aydoğan, Serap Karaman, Nazan Sarper, Çetin Timur, Ümit Üre, Uğur Özbek
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 4, Pp 325-333 (2012)
OBJECTIVE: T-cell acute lymphoblastic leukemia (T-ALL) is associated with recurrent chromosomal aberrations and abnormal ectopic gene expression during T-cell development. In order to gain insight into the pathogenesis of T-ALL this study aimed to me
Externí odkaz:
https://doaj.org/article/b81ce4f098fd45aea7c8caae301e35cf