Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Gülgün S, Güven"'
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:
Ilknur Suer, Betul Yuceturk, Omer Faruk Karatas, Mehmet Yilmaz, Gülgün S. Güven, Mustafa Ozen, Harun Cansiz, Buge Oz
Publikováno v:
ResearcherID
Larynx cancer (LCa) is an aggressive malignancy, which is the second most common malignant neoplasm of head and neck squamous cell carcinoma. Its incidences have been reported to increase and therapeutic options mostly fail to give positive clinical
Autor:
Asuman Koparir, Mustafa Ozen, Omer Faruk Karatas, Heyko Skladny, Hatip Aydin, Erkan Koparir, Elif Fenercioglu, Gülgün S. Güven, Alper Gezdirici, Mehmet Seven, Hakan Ulucan
Publikováno v:
Clinical Dysmorphology. 23:1-7
Dyggve-Melchior-Clausen syndrome (DMC) (MIM #223800) is a rare autosomal-recessive type of skeletal dysplasia accompanied by variable degrees of intellectual disability (ID). It is characterized by progressive spondyloepimetaphyseal dysplasia leading
Autor:
Mustafa Ozen, Buge Oz, Chad J. Creighton, Omer Faruk Karatas, Michael Ittmann, Mehmet Yilmaz, Gülgün S. Güven, Betul Yuceturk, Harun Cansiz, Ilknur Suer
Publikováno v:
BMC Cancer
Background Emerging evidences proposed that microRNAs are associated with regulation of distinct physio-pathological processes including development of normal stem cells and carcinogenesis. In this study we aimed to investigate microRNA profile of ca
Autor:
Ayse Serap Yalin, Mehmet Riza Altiparmak, Aydın Tunçkale, Bahadir Batar, Mehmet Güven, Sinan Trabulus, Gülgün S. Güven
Publikováno v:
Genetic Testing and Molecular Biomarkers. 17:202-206
Patients with end-stage renal disease display enhanced genomic damage. We investigated the presence of genomic damage in the peripheral lymphocytes by using the micronucleus (MN) test and the factors associated with the MN frequency in hemodialysis (
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:
Beril Kucumen, Melda Yenerel, Bahadir Batar, Mehmet Güven, Adnan Yuksel, Mustafa Unal, Ebru Gorgun, Gülgün S. Güven, Umut Asli Dinc, Tümer Ulus
Publikováno v:
Ophthalmic Research. 46:31-37
Purpose: To determine the possible effects of glutathione S-transferase (GST) M1, GSTT1 and GSTP1 genetic polymorphisms on the risk of developing age-related macular degeneration (AMD). Patients and Methods: This case-control study included a total o
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
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
Publikováno v:
Gene. 582(1)
DNA repair plays a critical role in response to ionizing radiation (IR) and developing of radiotherapy induced normal tissue reactions. In our study, we investigated the association of radiotherapy related acute side effects, with X-ray repair cross