Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Cengiz Yakicier"'
Autor:
Fahrettin Uysal, Burcu Turkgenc, Guven Toksoy, Ozlem M. Bostan, Elif Evke, Oya Uyguner, Cengiz Yakicier, Hulya Kayserili, Ergun Cil, Sehime G. Temel
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
Abstract Background Jervell and Lange-Nielsen syndrome (JLNS) isa recessive model of long QT syndrome which might also be related to possible hearing loss. Although the syndrome has been demonstrated to be originated from homozygous or compound heter
Externí odkaz:
https://doaj.org/article/547b936f1a3f48028b40b8469462b7d9
Autor:
Ahmet Dursun, Hatice Gul Durakbasi-Dursun, Ayse Gul Zamani, Zerrin Gülin Gulbahar, Recep Dursun, Cengiz Yakicier
Publikováno v:
Mediators of Inflammation, Vol 2006 (2006)
Objectives. Behçet's disease (BD) is a systemic vasculitis with recurrent oral and genital ulcers and uveitis. MEFV gene, which is the main factor in familial Mediterranean fever (FMF), is also reported to be a susceptibility gene for BD. The pyrin
Externí odkaz:
https://doaj.org/article/1a521141283e46a497f3d74f81612f03
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 39, Iss 1, Pp 63-65
Externí odkaz:
https://doaj.org/article/f688f767512542039f5a13de06076724
Autor:
I. Orcun Olcay, Berkay Akcay, Mustafa Bahceci, Aydin Arici, Kubra Boynukalin, Cengiz Yakicier, Aysel Ozpinar, Murat Basar
Publikováno v:
Gynecological Endocrinology. 38:461-466
Assisted reproduction technology has two significant problems: low success rates and multiple pregnancies. Because of these problems, the priority in IVF clinics is to develop a potential diagnostic test that can be used to select the embryos with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b35e985f4f88300bb486b522f278e0
https://doi.org/10.1080/09513590.2022.2068520
https://doi.org/10.1080/09513590.2022.2068520
Autor:
Esin Ozturk-Isik, M. Necmettin Pamir, Alpay Ozcan, Koray Özduman, Ayça Erşen Danyeli, Sevim Cengiz, Cengiz Yakicier, Alp Dinçer
Publikováno v:
Journal of Magnetic Resonance Imaging. 51:1799-1809
Background There is a growing interest in noninvasively defining molecular subsets of hemispheric diffuse gliomas based on the isocitrate dehydrogenase (IDH) and telomerase reverse transcriptase gene promoter (TERTp) mutation status, which correspond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97bb7fa27426115632fffd7ea9096561
https://doi.org/10.1002/jmri.26964
https://doi.org/10.1002/jmri.26964
Publikováno v:
OMICS: A Journal of Integrative Biology. 23:486-495
Thyroid cancer (TC) is a very common malignancy worldwide. Chief among the innovative molecular drug targets for TC are epigenetic modifications. Increased telomerase activity in cancer ce...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::007afeb2ab8becef56b1a4fd9b96f62f
https://doi.org/10.1089/omi.2019.0050
https://doi.org/10.1089/omi.2019.0050
Publikováno v:
Turkish Journal of Biochemistry. 44:41-46
BackgroundIVSII-74 T > G is one of the most frequently identified polymorphic sites on the β-globin gene. In our report, we present three cases with low mean corpuscular volume (MCV) value in three and high red blood cell (RBC) value in two of the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a5aa3c9912e3abf0be2b947d1303dc5
https://doi.org/10.1515/tjb-2018-0332
https://doi.org/10.1515/tjb-2018-0332
Autor:
Ali Ozen, Onur Erdogan, Can Erzik, Süheyla Uyar Bozkurt, İrem Peker Eyüboğlu, Ozcan Sonmez, Mustafa Cengiz Yakicier, Fatih Bayrakli
Publikováno v:
Turkish neurosurgery. 30(3)
AIM: To identify the copy number variations that are specific to myxopapillary ependymomas (MPEs) of the cauda equina. MATERIAL and METHODS: The patient cohort included five patients who underwent resection of histologically confirmed MPEs. Tumor sam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff623293683f80623b0fc622bda1e498
https://pubmed.ncbi.nlm.nih.gov/32020572
https://pubmed.ncbi.nlm.nih.gov/32020572
Autor:
Mustafa Akkiprik, Cengiz Yakicier, Guven Yenmis, İrem Peker Eyüboğlu, Şirin Yüksel, Gökçe Güllü Amuran, Elif Naz Bingöl, Pemra Ozbek, Fatma Tokat
Telomeres, and telomere length in particular, have broad significance for genome biology and thus are prime research targets for complex diseases such as cancers. In this context, BRCA1 and BRCA2 gene mutations have been implicated in relationship to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c419f04625e38008e45f8120f9e6d14
https://hdl.handle.net/20.500.12445/1337
https://hdl.handle.net/20.500.12445/1337
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S29-(2021)
Objective Pediatric glial tumors comprise wide range pathologies which may mimic histomorphological features of each other's but generally have very diverse disease course. WHO Classification of Tumors of Central Nervous System (2016 and 2021) points
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1d2d4aed808ef5e9b30f14dcb7daaa8
https://doi.org/10.1016/j.htct.2021.10.1002
https://doi.org/10.1016/j.htct.2021.10.1002