Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Neslihan Abacı"'
Autor:
Sema Sırma Ekmekci, Zeliha Emrence, Neslihan Abacı, Melda Sarıman, Burcu Salman, Cumhur Gökhan Ekmekci, Çağrı Güleç
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 4, Pp 226-233 (2020)
Objective: T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive disease resulting from the accumulation of genetic changes that affect the development of T-cells. The precise role of lymphoid enhancerbinding factor 1 (LEF1) in T-ALL has been
Externí odkaz:
https://doaj.org/article/ab5f21f53d8345288e0d07ab581f2dbc
Autor:
Melda Sarıman, Neslihan Abacı, Sema Sırma Ekmekçi, Aris Çakiris, Ferda Perçin Paçal, Duran Üstek, Mesut Ayer, Mustafa Nuri Yenerel, Sevgi Beşışık, Kıvanç Çefle, Şükrü Palandüz, Şükrü Öztürk
Publikováno v:
Balkan Medical Journal, Vol 36, Iss 1, Pp 23-31 (2019)
Background: Multiple myeloma is a plasma cell dyscrasia characterized by transformation of B cells into malignant cells. Although there are data regarding the molecular pathology of multiple myeloma, the molecular mechanisms of the disease have not b
Externí odkaz:
https://doaj.org/article/6e465c95b66b417ab3cfbcd8bf7ca046
Association between endothelial nitric oxide synthase intron 4a/b polymorphism and aortic dissection
Autor:
Ahmet Ekmekçi, Mahmut Uluganyan, Barış Güngör, Neslihan Abacı, Kazım Serhan Özcan, Gokhan Ertaş, Aycan Zencirci, Ahmet Yavuz Balcı, Sema Sırma Ekmekçi, Nurten Sayar, Duran Ustek, Mehmet Eren
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 1, Pp 55-60 (2014)
Objectives: The genetic risk factors that contribute to the risk of developing aortic dissection (AD) have been studied. We assessed the association of endothelial nitric oxide synthase (eNOS) gene polymorphism with AD. Study design: Patients who und
Externí odkaz:
https://doaj.org/article/2f8ffa623aac46558c8d3d7e6f14351b
Autor:
Sümbül Gezer, Zeliha Emrence, Tuğrul Elverdi, Muhlis Cem Ar, Burcu Salman Yaylaz, Ferda Paçal, Ayşegül Ünüvar, Melda Sarıman, Ahmet Emre Eşkazan, Serap Karaman, Ayşe Salihoğlu, Zeynep Karakaş, Neslihan Abacı, Sema Sırma-Ekmekci
Publikováno v:
Advances in Laboratory Medicine / Avances en Medicina de Laboratorio. 4:92-97
Objectives Acute myeloid leukemia (AML) is a highly heterogeneous disease. Although patients can be classified into risk groups based on their genetic changes, the prognosis of disease within these categories varies widely. This situation raises the
Autor:
Sümbül Gezer, Zeliha Emrence, Tuğrul Elverdi, Muhlis Cem Ar, Burcu Salman Yaylaz, Ferda Paçal, Ayşegül Ünüvar, Melda Sarıman, Ahmet Emre Eşkazan, Serap Karaman, Ayşe Salihoğlu, Zeynep Karakaş, Neslihan Abacı, Sema Sırma-Ekmekci
Publikováno v:
Advances in Laboratory Medicine / Avances en Medicina de Laboratorio. 4:98-104
Resumen Objectivos La leucemia mieloide aguda (AML, por sus siglas en inglés) es una enfermedad muy heterogénea. Aunque se puede clasificar a los pacientes en grupos de riesgo según sus mutaciones genéticas, el pronóstico dentro de cada categor
Autor:
Burcu Salman Yaylaz, Melda Seriman, Ahmet Ekmekçi, Emel Ergül, Mahmut Uluganyan, Fulya Coşan, Özgün Melike Gedar Totuk, Neslihan Abacı
Publikováno v:
Volume: 11, Issue: 1 12-20
Experimed
Experimed
Amaç: Kardiyovasküler hastalıklar ve kanser metastazında sıklıkla araştı-rılan matriks metalloproteinazlar (MMPs) ekstraselüler matriks düzenle-yicileridir. Çalışmamız, aort diseksiyonu olan hastalarda MMP9 genindeki spesifik polimorfi
Autor:
Ilhan Tahrali, Nilgun Akdeniz, Vuslat Yilmaz, Umut C. Kucuksezer, Fatma B. Oktelik, Ozkan Ozdemir, Esin Cetin-Aktas, Yelda Ogutmen, Arzu Ergen, Neslihan Abaci, Erdem Tuzun, Oral Oncul, Gunnur Deniz
Publikováno v:
Emerging Microbes and Infections, Vol 11, Iss 1, Pp 2698-2710 (2022)
The modulatory effect of C-Vx, a novel therapeutic agent, on the immune system of COVID-19 patients was investigated. The functions of T and NK cells of COVID-19 patients with different disease severity were evaluated by flow cytometry in response to
Externí odkaz:
https://doaj.org/article/a3f280e2158e4a97a3fb68af30eb1231
Publikováno v:
Journal of Research in Medical Sciences, Vol 24, Iss 1, Pp 56-56 (2019)
Background: Type 2 diabetes (T2DM) is characterized by hyperglycemia and insulin deficiency. Sirtuin 1 (SIRT1), serving as a deacetylase, is critical in the regulation of glucose and lipid metabolism. Recently, a number of studies have been conducted
Externí odkaz:
https://doaj.org/article/460600dadb154345824534ac1017a30c