Zobrazeno 1 - 10
of 12
pro vyhledávání: '"G. Ozan Çetin"'
Publikováno v:
Volume: 14, Issue: 1 215-221
Pamukkale Tıp Dergisi
Pamukkale Tıp Dergisi
Amaç: Kadın Hastalıkları ve Doğum kliniğimizde çeşitli endikasyonlarla gerçekleştirilen genetik amniyosentez olgularından elde edilen sonuçları değerlendirmeyi amaçlamaktayız.Gereç ve Yöntem: Çalışmamızda Kasım 2018- Ağustos 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0385ab05750ea3dca1ee1b42bf440666
https://doi.org/10.31362/patd.795264
https://doi.org/10.31362/patd.795264
Autor:
Levent Elmas, Vildan Caner, G. Ozan Çetin, Gulseren Bagci, Nur Büyükpınarbaşılı, Emre Tepeli, Füsun Düzcan
Publikováno v:
Molecular Biology Reports. 39:335-341
Excision Repair Cross-Complementing Group 1 (ERCC1) is an important DNA repair gene, playing critical role in nucleotide excision repair pathway and having a significant influence on genomic instability. Some studies support that ERCC1 might be a pot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::639d35a6c14e981375eb7bff9e7cd057
https://doi.org/10.1007/s11033-011-0743-0
https://doi.org/10.1007/s11033-011-0743-0
Autor:
Vildan Caner, Nilay Şen Türk, Gulseren Bagci, G. Ozan Çetin, Nur Büyükpınarbaşılı, Emre Tepeli, Esin Koç
Publikováno v:
Molecular Biology Reports. 39:375-380
DNA repair plays a key role in prevention of carcinogenesis and one of the most important DNA repair mechanisms is nucleotide excision repair (NER) pathway. This pathway includes a number of genes such as excision repair cross-complementing group 1 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bd2b60803c1c41a4b00ee09f4b03f54
https://doi.org/10.1007/s11033-011-0748-8
https://doi.org/10.1007/s11033-011-0748-8
Autor:
Huseyin Bagci, G. Ozan Çetin, Fatma Özdemir, Türker Şahiner, Peter Heutink, Füsun Düzcan, Vincenzo Bonifati, Mehmet Zencir
Publikováno v:
Movement Disorders, 18(7), 799-830. John Wiley & Sons Inc.
This population-based study on parkinsonism in a genetically isolated community from a rural area of Turkey aimed to provide a selective evaluation of environmental and heritable risk factors. An increased prevalence of parkinsonism (4.1%) was detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417b076f85453e6365abc19a67e41f60
https://doi.org/10.1002/mds.10440
https://doi.org/10.1002/mds.10440
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 82:53-56
Acta Obstet Gynecol Scand 2003; 82: 53-56. © Acta Obstet Gynecol Scand 2003 Background. Cytogenetic studies in patients with reproductive failure Aim. To investigate the contribution of chromosomal abnormalities in sub fertility and in couples with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5008463ceed455a33847db1eeec6651
https://doi.org/10.1034/j.1600-0412.2003.820109.x
https://doi.org/10.1034/j.1600-0412.2003.820109.x
Autor:
Lale Şatiroğlu Tufan, C. Nur Semerci, Tarkan Kalkan, Gülseren Bağci, Metin Eser, Özkan Öztürk, G. Ozan Çetin
A 30-year-old male patient referred to our clinic for unraveling the underlying etiology of the azoospermia. He had no unusual medical history. At physical examination, obesity, short neck and gynecomastia were noted. All hormone levels were normal e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3be8da31bd14f4c6733f5c9b47fe9db3
https://doi.org/10.5336/medsci.2011-23453
https://doi.org/10.5336/medsci.2011-23453
Background. Cytogenetic studies in patients with reproductive failure Aim. To investigate the contribution of chromosomal abnormalities in sub fertility and in couples with repeated abortions. Methods. Hundred and 13 couples who had at least two or m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f133de72406b3a0ac7476468df082be
https://hdl.handle.net/11499/5307
https://hdl.handle.net/11499/5307
Autor:
Bernd Wollnik, Memnune Yuksel-Apak, Füsun Düzcan, Türker Şahiner, Ismet Bayramoglu, Serap Özden, G. Ozan Çetin, Huseyin Bagci
Publikováno v:
Ophthalmic genetics. 23(1)
To describe the clinical features, mode of inheritance, and linkage analysis of ten affected members of a three-generation family with progressive optic atrophy and progressive hearing loss.The proband, a 10-year-old boy, presented with progressive v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d012e228c9c6211b7e271363f8a6db42
https://pubmed.ncbi.nlm.nih.gov/11910556
https://pubmed.ncbi.nlm.nih.gov/11910556
Autor:
SEMERCİ, C. Nur, ESER, Metin, TUFAN, Lale ŞATIROĞLU, KALKAN, Tarkan, ÖZTÜRK, G. Ozan ÇETİN Özkan, BAĞCI, Gülseren
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences; Dec2012, Vol. 32 Issue 6, p1732-1736, 5p, 4 Black and White Photographs, 3 Diagrams
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