Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Yelda Tarkan-Argüden"'
Autor:
Bengisu GÖKKAYA, Sezen ATASOY, Ayşe ÇIRAKOĞLU, Yelda TARKAN ARGÜDEN, R. Dilhan KURU, Şükriye YILMAZ, Şeniz ÖNGÖREN, Ayhan DEVİREN
Publikováno v:
Bezmiâlem Science, Vol 10, Iss 3, Pp 370-375 (2022)
Objective:Acute lymphoblastic leukemia (ALL) is a disease related to the overproduction of immature lymphocytes. For diagnosis and classification of ALL, recognizing chromosome aberrations using conventional cytogenetic analysis (CCA) is essential. H
Externí odkaz:
https://doaj.org/article/3e1a7cfe9287447e97b7e4d56f89284a
Autor:
Yelda Tarkan Argüden, Sezen Atasoy, Ayhan Deviren, Ayşe Çirakoğlu, R. Dilhan Kuru, Şeniz Öngören, Şükriye Yilmaz, Bengisu Gökkaya
Publikováno v:
Bezmialem Science. 10:370-375
Objective: Acute lymphoblastic leukemia (ALL) is a disease related to the overproduction of immature lymphocytes. For diagnosis and classification of ALL, recognizing chromosome aberrations using conventional cytogenetic analysis (CCA) is essential.
Autor:
Seda Ekizoglu, Ayhan Deviren, R. Dilhan Kuru, Şeniz Öngören, Yelda Tarkan Argüden, Şükriye Yilmaz, Ayşe Çırakoğlu
Publikováno v:
Pamukkale Medical Journal. :585-590
Autor:
Ayşe Çırakoğlu, Raif Çakmur, Ugur Ozbek, Zeliha Gormez, Sibel Aylin Ugur Iseri, Nihan Hande Akçakaya, Barış Salman, Yelda Tarkan Argüden, Berril Dönmez Çolakoğlu, Zuhal Yapici, Seniha Hacıhanefioğlu
Publikováno v:
NeuroMolecular Medicine. 21:54-59
Arguden, Yelda Tarkan/0000-0002-5405-3365; Ozbek, Ugur/0000-0001-5319-0547; Akcakaya, Nihan Hande/0000-0001-8414-4017 Beta-propeller protein-associated neurodegeneration (BPAN) is an X-linked rare dominant disorder of autophagy. The role of WDR45 has
Autor:
Şükriye Yilmaz, Yelda Tarkan Argüden, Rahiye Kuru, Ayhan Deviren, Teoman Soysal, M. Cem Ar, Ayşe Çirakoğlu
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 39:409-413
Autor:
Selin Coşkun, Şükriye Yilmaz, Şeniz Öngören, Seniha Hacihanefioğlu, Yelda Tarkan Argüden, Ayşe Çirakoğlu, R. Dilhan Kuru
Publikováno v:
Volume: 3, Issue: 3 122-129
Sağlık Bilimlerinde İleri Araştırmalar Dergisi
Sağlık Bilimlerinde İleri Araştırmalar Dergisi
Amaç: Miyelodiplastik sendrom (MDS) olgularının %30-50’sinde kromozom anomalileri gözlenmektedir. En sık gözlenen anomaliler trizomi 8, monozomi 7/7q-, monozomi 5/5qve 20q- olarak belirlenmiştir. Bu anomalilerin saptanmasında konvansiyonel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72b5ce4838e3df6938e43f93576508a1
https://dergipark.org.tr/tr/pub/sabiad/issue/57700/793043
https://dergipark.org.tr/tr/pub/sabiad/issue/57700/793043
Autor:
Gülgün S, Güven, Yelda, Tarkan Argüden, Şeniz, Öngören, Ayhan, Deviren, Yıldız, Aydın, Seniha, Hacıhanefioglu
Publikováno v:
Turkish journal of haematology : official journal of Turkish Society of Haematology. 23(2)
t(1;3)(p36;p21) is a recurrent reciprocal translocation found in a subset of myelodysplastic syndrome (MDS)/acute myelogenous leukemia (AML) characterized by trilineage dysplasia, especially dysmegakaryopoiesis and poor prognosis. In the literature,
Autor:
Çirakoǧlu, A., Yelda Tarkan Argüden, Devireń, A., Kuru, D., Yilmaz, Ş, Berrak, S. G., Canpolat, C., Hacihanefioǧlu, S.
Publikováno v:
Turkish Journal of Hematology, Vol 25, Iss 03, Pp 152-154 (2008)
Scopus-Elsevier
Scopus-Elsevier
It is known that clonal chromosomal changes in childhood ALL are nonrandom and important markers for diagnosis, prognosis and relaps. In this report we present 4 year-old boy with ALL-L1 who has complex chromosomal rearrangements. Chromosome analysis
Autor:
Seniha Hacihanefioğlu, Şükriye Yilmaz, İpek Mine Gürsel, Dilhan Kuru, Yelda Tarkan Argüden, Ayhan Deviren, Ayşe Çirakoğlu
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 32:15-23
Objective: Myelodysplastic syndromes (MDS) are a heterogeneous group of malignant clonal hematopoietic stem cell disorders characterized by bone marrow failure, ineffective hematopoiesis, peripheral blood cytopenias, atypic cytological profile, incre
Autor:
Teoman Soysal, Ahmet Emre Eskazan, Ayşe Çırakoğlu, Seniha Hacıhanefioğlu, Yelda Tarkan Argüden, Şeniz Öngören, Ayhan Deviren, Birsen Ülkü, Muhlis Cem Ar, Şükriye Yilmaz, Dilhan Kuru
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 03, Pp 186-192 (2011)
The Philadelphia (Ph) chromosome, consisting of the t(9;22)(q34;q11) translocation, is observed in ~90% of patients with chronic myeloid leukemia (CML). Variant Ph translocations are observed in 5%-10% of CML patients. In variant translocations 3 and