Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fatma Belgin, Ataç"'
Autor:
Neslihan Bascil Tutuncu, Hpb Cebi, Fatma Belgin Ataç, T Tutuncu, Nazli Gulsoy Kirnap, Hasibe Verdi, Yaprak Yılmaz Yalçın, Asli Nar
Publikováno v:
Balkan Journal of Medical Genetics, Vol 24, Iss 1, Pp 73-80 (2021)
Differentiated thyroid carcinomas (DTC) are the most common form of endocrine malignancies. The role of genetic variations in the development of papillary thyroid carcinoma (PTC) is approximately 60.0-70.0%. The X-ray repair cross-complementing group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e28fdf2035b2291ccf28c5fe915a3a3
https://doaj.org/article/60621fb3bc724622ae39040f590f9d2e
https://doaj.org/article/60621fb3bc724622ae39040f590f9d2e
Autor:
Neslihan, Başçıl Tütüncü, Hasibe, Verdi, Yaprak, Yalçın, Pınar, Baysan Çebi, Sibel, Kınık, Tanju, Tütüncü, Fatma Belgin, Ataç
Publikováno v:
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation. 20(6)
Lipotoxicity and glucolipotoxicity are among the mostimportanttriggers of beta-cell failure in patients with type 2 and posttransplant diabetes. Because the Golgi apparatus is a vital organelle in secretory cells like beta cells, its behavior under s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::550d0edebd67b32061eba001431e64c4
https://pubmed.ncbi.nlm.nih.gov/35791832
https://pubmed.ncbi.nlm.nih.gov/35791832
Autor:
Hasibe Verdi, Aylin Tarcan, Namik Ozbek, Ayşe Ecevit, N Mutlu Karakaş, Yaprak Yılmaz Yalçın, Ali Haberal, M Ağah Tekindal, Fatma Belgin Ataç, Beril Özdemir
OBJECTIVE The aim of this study was to analyze maternal and neonatal interleukin 6 (IL-6) (-174 G/C) polymorphism and to determine effect on preterm birth and neonatal morbidity. STUDY DESIGN One hundred and sixty-four mothers (100 term births, 64 pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9ceb82e455074a5a492dc8434eeb5c5
https://avesis.gazi.edu.tr/publication/details/9997ed84-a9ee-491d-b419-a2f3a4855eaf/oai
https://avesis.gazi.edu.tr/publication/details/9997ed84-a9ee-491d-b419-a2f3a4855eaf/oai
Publikováno v:
Hemodialysis International. 8:81-82
Vascular access thrombosis is a frequent complication in hemodialysis (HD) patients. Genetic mutations, inflammation, and changes in the vascular wall are some factors that are thought to increase thrombosis risk. In this study, we tested for possibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b461e4669f0d67b59b809a5bb5b08c36
https://doi.org/10.1111/j.1492-7535.2004.0085k.x
https://doi.org/10.1111/j.1492-7535.2004.0085k.x
Autor:
F.N. Ozdemir, Hasibe Verdi, Turan Colak, Ali Akcay, Siren Sezer, Zubeyde Arat, Fatma Belgin Ataç, Mehmet Haberal, M Terzioğlu
Publikováno v:
Tissue Antigens. 60:554-554
Chronic allograft dysfunction (CAD) is a complex phenomenon caused by underlying kidney disease and superimposed environmental and genetic factors. We investigated the relationship between polymorphism in the gene encoding for angiotensin-converting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9dad189e92c600d764ce510f7545c96
https://doi.org/10.1034/j.1399-0039.2002.00013.x
https://doi.org/10.1034/j.1399-0039.2002.00013.x