Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sebnem Ozemri Sağ"'
Autor:
Tuğba Ocak, Ahmet Görünen, Belkıs Nihan Coşkun, Burcu Yağız, Sebnem Ozemri Sağ, Gökhan Ocakoğlu, Ediz Dalkılıç, Yavuz Pehlivan
Publikováno v:
Diagnostics, Vol 14, Iss 6, p 634 (2024)
Familial Mediterranean fever (FMF) is characterized by recurrent episodes of fever and serositis. Blood-based biomarkers determined in FMF patients during attack-free periods could be used to predict the risk of amyloidosis and the severity of the di
Externí odkaz:
https://doaj.org/article/8ea93a66038a4150914fbda2e771c1ed
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 285-292 (2023)
INTRODUCTION: 22q11.2 deletion syndrome (22q11.2 DS) is the most common chromosomal microdeletion disorder. Associated problems in 22q11.2 DS may include cardiac abnormalities, immune dysfunction, facial dysmorphism, with endocrine, genitourinary and
Externí odkaz:
https://doaj.org/article/57cf13b9dde74979ac83bf21eb36059d
Autor:
Ibrahim Boga, Sebnem Ozemri Sag, Nilgun Duman, Sevda Yesim Ozdemir, Mahmut Cerkez Ergoren, Kubilay Dalci, Cem Mujde, Cem Kaan Parsak, Cagla Rencuzogullari, Ozge Sonmezler, Orcun Yalav, Adem Alemdar, Lamiya Aliyeva, Ozlem Bozkurt, Sibel Cetintas, Erdem Cubukcu, Adem Deligonul, Berkcan Dogan, Cemre Ornek Erguzeloglu, Turkkan Evrensel, Sehsuvar Gokgoz, Kazim Senol, Sahsine Tolunay, Esra Akyurek, Neslihan Basgoz, Nuriye Gökçe, Bilge Dundar, Figen Ozturk, Duygu Taskin, Mercan Demirtas, Murat Cag, Omer Diker, Polat Olgun, Sevcan Tug Bozdogan, Munis Dundar, Atil Bisgin, Sehime Gulsun Temel
Publikováno v:
European Journal of Breast Health, Vol 19, Iss 3, Pp 235-252 (2023)
Objective:Breast cancer (BC) is the most common cancer type in women and may be inherited, mostly in an autosomal dominant pattern. The clinical diagnosis of BC relies on the published diagnostic criteria, and analysis of two genes, BRCA1 and BRCA2,
Externí odkaz:
https://doaj.org/article/a71c390801df4f9498bd73b6b92a7cb8
Autor:
Aya Badeea Ismail, Mehmet Sait Dundar, Cemre Ornek Erguzeloglu, Mahmut Cerkez Ergoren, Adem Alemdar, Sebnem Ozemri Sag, Sehime Gulsun Temel
Publikováno v:
Biomedicines, Vol 12, Iss 5, p 968 (2024)
Alzheimer’s disease (AD) is a major global health challenge, especially among individuals aged 65 or older. According to population health studies, Turkey has the highest AD prevalence in the Middle East and Europe. To accurately determine the freq
Externí odkaz:
https://doaj.org/article/911415175df84fada0540492352d7bd9
Autor:
Ayhan Kubar, Sehime Gülsüm Temel, Serdar Beken, Gizem Onder, Ozden Hatirnaz, Ayse Korkmaz, Yasemin Alanay, Ugur Ozbek, Sebnem Ozemri Sag, Mahmut Cerkez Ergoren, Elif Kubar, Candan Zeynep Sonmezalp, Ozlem Doğan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 12, Pp n/a-n/a (2023)
Abstract Background Nucleic acid‐based assays provide an opportunity to screen for genetically encoded diseases like spinal muscular atrophy (SMA), before the onset of symptoms. Nowadays, such assays could be easily utilized as high‐throughputs i
Externí odkaz:
https://doaj.org/article/8e9b296ac0c9461bbb8e809e7092feb7
Autor:
Atil Bisgin, Sebnem Ozemri Sag, Muhammet E. Dogan, Mahmut S. Yildirim, Aydeniz Aydin Gumus, Nejmiye Akkus, Ozgur Balasar, Ceren D. Durmaz, Recep Eroz, Sule Altiner, Adem Alemdar, Lamia Aliyeva, Ibrahim Boga, Fethi S. Cam, Berkcan Dogan, Onur Esbah, Abdullah Hanta, Cem Mujde, Cemre Ornek, Sinem Ozer, Cagla Rencuzogullari, Ozge Sonmezler, Sevcan Tug Bozdogan, Munis Dundar, Sehime G. Temel
Publikováno v:
Breast, Vol 65, Iss , Pp 15-22 (2022)
BRCA1/2 mutations play a significant role in cancer pathogenesis and predisposition particularly in breast, ovarian and prostate cancers. Thus, germline analysis of BRCA1 and BRCA2 is essential for clinical management strategies aiming at the identif
Externí odkaz:
https://doaj.org/article/e63eea3f85294bbebe3b5c247e16a423
Autor:
Pinar Tulay, Mahmut Cerkez Ergoren, Ahmet Alkaya, Eyup Yayci, Sebnem Ozemri Sag, Sehime Gulsum Temel
Publikováno v:
Global Medical Genetics, Vol 07, Iss 04, Pp 128-132 (2020)
Purpose Turner syndrome is a sex chromosomal aberration where majority of the patients have 45,X karyotype, while several patients are mosaic involving 45,X/46,XX; 46,X,i(Xq); and other variants. Cytogenetic analysis, karyotyping, is considered to be
Externí odkaz:
https://doaj.org/article/7aa8ab43a85d400bbb18cdb8f0e42318