Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Seniha Hacihanefioğlu"'
Autor:
Yelda Tarkan Argüden, Dilhan Kuru, Ayşe Çırakoğlu, Şükriye Yılmaz, Şeniz Öngören Aydın, Cem Muhlis Ar, Ayhan Deviren, Teoman Soysal, Seniha Hacıhanefioglu
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 1, Pp 82-84 (2015)
Externí odkaz:
https://doaj.org/article/2a756deca15c4b0882447edb6e5be75f
Autor:
Dilhan Kuru, Yelda Tarkan Argüden, Muhlis Cem Ar, Ayşe Çırakoğlu, Şeniz Öngören, Şükriye Yılmaz, Ahmet Emre Eşkazan, Ayhan Deviren, Teoman Soysal, Seniha Hacıhanefioğlu, Birsen Ülkü
Publikováno v:
Turkish Journal of Hematology, Vol 28, Iss 03, Pp 186-192 (2011)
Objective: 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 transloca
Externí odkaz:
https://doaj.org/article/2ecd7491b74f46fe8ad1a70931bb2d19
Publikováno v:
Genetics and Molecular Biology, Vol 29, Iss 1, Pp 142-147 (2006)
Sister chromatid exchange (SCE) and chromosome aberrations (CA) in peripheral lymphocytes has been widely used in assessing exposure to mutagens and carcinogens. One of the extensively studied genotoxins is benzo[alpha]pyrene (BaP). We studied the ab
Externí odkaz:
https://doaj.org/article/7d1fa9547e254663987d165aadbac89c
Autor:
Ayse Cirakoglu, Ayhan Deviren, Yelda Tarkan-Arguden, Seniha Hacihanefioglu, Cengiz Canpolat, Su Gulsun Berrak, Sukriye Yilmaz, Dilhan Kuru
Publikováno v:
Turkish Journal of Hematology, Vol 25, Iss 03, Pp 152-154 (2008)
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
Externí odkaz:
https://doaj.org/article/19f791270cf1472bbe63ddbf5e57f4f6
Publikováno v:
Sakarya Tıp Dergisi, Vol 6, Iss 3, Pp 0-0 (2016)
Amaç: Kronik Lenfositik Lösemi (KLL), lenfoproliferatif bir hastalık olup, ortalama görülme yaşının 65 olduğu heterojen bir klinik gösterir. En yaygın kromozomal değişim 13q14 ve 17p13 delesyonlarıdır. Her iki bölgenin kaybı da köt
Externí odkaz:
https://doaj.org/article/15b9d0a0eb1948d8ae7464e87cd5df68
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:
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:
Ayhan Deviren, Şükriye Yilmaz, Ayşe Çirakoğlu, Seniha Hacihanefioğlu, Dilhan Kuru, Seyfettin Uludağ, Gülgün S. Güven, Yelda Tarkan-Argüden
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 30:1185-1188
ABS TRACT Objective: Recurrent pregnancy loss is an important problem affecting couples trying to conceive. Genetic factors, particularly chromosomal abnormalities appear to be highly associated with reproductive loss. The frequency of presence of at