Zobrazeno 1 - 10
of 202
pro vyhledávání: '"S. Anak"'
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss , Pp 69- (2020)
Externí odkaz:
https://doaj.org/article/071a4e997f224133aa08af2bfee5025d
Publikováno v:
Asia Petroleum Geoscience Conference and Exhibition (APGCE).
Autor:
Ayşegül Ünüvar, Deniz Tugcu, Mustafa Bilici, Zeynep Karakas, S. Anak, Rumeysa Tuna, Şifa Şahin, Serap Karaman
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss, Pp 69-(2020)
Akademický článek
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Akademický článek
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Autor:
Ü, Özgen, S, Anak, U, Özbek, N, Sarper, E, Eryılmaz, L, Ağaoğlu, Ö, Devecioğlu, N, Yalman, G, Gedikoğlu
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 17(4)
Wilms tumor 1 (WT1) gene is a tumor supressor gene, expressed in malignant and normal hematopoietic progenitor cells. Prognostic significance of this gene in childhood acute lymphoid leukemia (ALL) is not clear. We evaluated the presence of WT1 expre
Autor:
N, Sarper, U, Özbek, L, Ağaoğlu, Ü, Özgen, A, Kandilci, S, Sırma, S, Anak, N, Yalman, E, Eryılmaz, Ö, Devecioğlu, G, Gedikoğlu
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 17(4)
BCR/ABL expression, which is the molecular equivalent of the Philadelphia chromosome, is an independent poor risk factor in acute lymphoblastic leukemia (ALL). We used a two-step (nested) reverse transcriptase polimerase chain reaction (RT-PCR) assay
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 17(3)
A four year-old-girl with Diamond-Blackfan anemia (DBA) that was resistant to corticosteroid treatment and transfusion dependent underwent (bone marrow transplantation) BMT from HLA identical sibling. The patient was conditioned with busulfan and cyc
Autor:
Ure U, Hatırnaz Ng O, S. Anak, Omer Devecioglu, Cetin Timur, Ugur Ozbek, Nazan Sarper, Yucel Erbilgin, Inci Yildiz, Gonul Aydogan, Tiraje Celkan, Muge Sayitoglu, Serap Karaman
Publikováno v:
Turkish Journal of Haematology
Turkish Journal of Hematology, Vol 29, Iss 4, Pp 325-333 (2012)
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 andabnormal ectopic gene expression during T-cell development. In order to gain insight into the pathogenesis of T-ALLthis study aimed to meas
Publikováno v:
Pediatric Hematology and Oncology. 21:267-272
Since the first description of infection-associated hemophagocytosis (IAHS), the list of precipitating infectious agents causing hemophagocytic syndrome has grown. A lymphohistiocytic proliferation with hemophagocytosis may develop as a result of mac