Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Sukru, Ozturk"'
Autor:
Murat Kaya, Asmaa Abuaisha, Ilknur Suer, Selman Emiroglu, Fahrunnisa Abanoz, Sukru Palanduz, Kivanc Cefle, Sukru Ozturk
Publikováno v:
European Journal of Breast Health, Vol 20, Iss 2, Pp 102-109 (2024)
Objective: Recent research suggests curcumin extracted from the turmeric plant may inhibit the proliferation of cancer cells by controlling the expression of microRNAs (miRNAs). The effect of phenolic curcumin on miR-638-5p and potential target gene
Externí odkaz:
https://doaj.org/article/1056a37fadde4a0193b15386a3b3525e
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0301995 (2024)
Breast cancer (BC) is the most common cancer among women with high morbidity and mortality. Therefore, new research is still needed for biomarker detection. GSE101124 and GSE182471 datasets were obtained from the Gene Expression Omnibus (GEO) databas
Externí odkaz:
https://doaj.org/article/8a79a1d06972434a8e744369256c7794
Autor:
Esra Guzel Tanoglu, Yavuz Arıkan, Yavuz Selim Kabukcuoglu, Fevziye Kabukcuoglu, Alpaslan Tanoglu, Sukru Ozturk
Publikováno v:
Brazilian Archives of Biology and Technology, Vol 64 (2021)
Abstract Deregulation of miRNA expressions was identified as a novel feature of tumor biology in Ewing sarcoma (EWS). The aim was to evaluate the regulatory role of miR-129-2-3p in EWS cell lines and human EWS tissue samples. EWS cell lines TC-71, TC
Externí odkaz:
https://doaj.org/article/e9ab3b7ea7e44cf78c2c57a171e1379f
Autor:
Betul Bozkurt Bulakcı, Aynur Daglar Aday, Basak Gurtekin, Akif Selim Yavuz, Sukru Ozturk, Kivanc Cefle, Ayse Palanduz, Sukru Palanduz
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 38:668-674
The introduction of tyrosine kinase inhibitors (TKI) has resulted in a significant improvement in the treatment of CML patients. However, some CML patients are resistant to imatinib therapy, the initial TKI therapy in the CML. Therefore, it is import
Autor:
Mustafa Kahraman, Irem Yuksel, Elif Beyza Boz, Hasan Ediz Ozbek, Elif Mert, Aybike Reyhanli, Aslihan Sari, Enes Muhammed Canturk, Ebru Can, Ataberk Demirkol, Mustafa Sencer Toraman, Nilufer Yildirim, Meryem Merve Oren, Sila Hidayet Bozdogan Polat, Osman Kan, Cemal Ayazoglu, Fulya Kahraman Aydogan, Sukru Ozturk, Mehmet Akif Karan
Publikováno v:
International Journal of Travel Medicine and Global Health. 9:161-169
Introduction: Even though Istanbul is one of the centers of the world’s fastest-growing tourism and travel sector, there are limited statistics on the knowledge, attitudes, and practices (KAP) of travelers from this region regarding travel-related
Autor:
Melda Sariman, Burcu Salman Yaylaz, Mesut Ayer, Sema Sirma Ekmekci, Ilknur Suer, Kıvanc Cefle, Sukru Palanduz, Sukru Ozturk, Meliha Nalcaci, Neslihan Abaci
Purpose: Plasma Cell Dyscrasias are a heterogeneous group of hematological diseases. The candidate ten genes identified from our transcriptome data are highly valuable and specific. Methods: We investigated the prognostic biomarker status of these ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e156c1c1ad14539dac924f2d08026a83
https://doi.org/10.21203/rs.3.rs-2370302/v1
https://doi.org/10.21203/rs.3.rs-2370302/v1
Publikováno v:
Balkan Medical Journal, Vol 38, Iss 6, Pp 365-373 (2021)
BACKGROUND Neurofibromatosis type 1 (NF1) is a neurocutaneous disorder that results in a predisposition to the growth of multiple tumors in the central nervous system, the peripheral nervous system, and the skin. The clinical manifestations of neurof
Autor:
Ahmet Burak Dirim, Tugba Kalayci, Seda Safak, Nurane Garayeva, Burak Gultekin, Ozge Hurdogan, Seyhun Solakoglu, Halil Yazici, Kivanc Cefle, Sukru Ozturk, Alaattin Yildiz
Publikováno v:
Clinical rheumatology.
Heme oxygenase-1 (HMOX-1) is an enzyme that regulates heme degradation. Antiinflammatory, antioxidant, and cytoprotective effects of HMOX-1 were also described. It is encoded by the HMOX1 gene, and biallelic mutations cause HMOX-1 deficiency, which i
Publikováno v:
Scottish medical journal. 67(4)
Introduction Ring chromosomes arise from breakage and fusion at distal regions of short and long arms of the chromosomes. The effect of the ring chromosome on the phenotype may vary widely depending on the amount of the deletion in the chromosomal ar
Autor:
Hülya Kayserili, Dilek Uludağ Alkaya, Sukru Palanduz, Ercan Mihci, Nilay Güneş, Banu Güzel Nur, Elifcan Taşdelen, Güven Toksoy, Sukru Ozturk, Tugba Kalayci, Zehra Oya Uyguner, Zuhal Bayramoglu, Beyhan Tüysüz, Umut Altunoglu, Leyla Elkanova, Ezgi Gizem Berkay, Volkan Karaman, Kivanc Cefle
Publikováno v:
American Journal of Medical Genetics Part A. 185:2488-2495
Loss or decrease of function in runt-related transcription factor 2 encoded by RUNX2 is known to cause a rare autosomal-dominant skeletal disorder, cleidocranial dysplasia (CCD). Clinical spectrum and genetic findings in 51 CCD patients from 30 unrel