Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sibel Oğuzkan-Balcı"'
Autor:
Fahriye Ekşi, Sacide Pehlivan, Mustafa Bilge Erdoğan, Ayşen Bayram, Sibel Oğuzkan-Balcı, Birol Yamak, Mustafa Pehlivan
Publikováno v:
Biotechnology & Biotechnological Equipment, Vol 31, Iss 6, Pp 1173-1177 (2017)
The basic underlying factor for cardiovascular diseases is atherosclerosis, which is a multifactorial disease driven by environmental and genetic factors. We aimed to study the genetic polymorphism in mannose binding lectin-2 (MBL2) and macrophage mi
Externí odkaz:
https://doaj.org/article/1a2be9dc92374262a959cdf30caa7ab6
Autor:
Ersin Akarsu, Zeynel Abidin Sayiner, Sibel Oğuzkan Balcı, Can Demirel, Zehra Bozdag, Murat Korkmaz, Ibrahim Yılmaz
Publikováno v:
Revista da Associação Médica Brasileira, Volume: 69, Issue: 1, Pages: 112-118, Published: 09 JAN 2023
SUMMARY OBJECTIVE: Pathological destruction of insulin signaling molecules such as insulin receptor substrate, especially due to the increase in suppressors of cytokine signaling molecules, has been demonstrated in experimental diabetes. The contribu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daabc8c38f09eca4226ef4d66ec74436
https://doi.org/10.1590/1806-9282.20220856
https://doi.org/10.1590/1806-9282.20220856
Autor:
Şenay Görücü Yılmaz, Salam Almasri, Yasemin Yuyucu Karabulut, Murat Korkmaz, Öznur Bucak, Sibel Oğuzkan Balcı
Publikováno v:
Omics : a journal of integrative biology.
Alzheimer's disease (AD) is a neurodegenerative disease characterized by progressive memory loss and cognitive decline, with hallmark pathologies related to amyloid beta (Aβ) and TAU. Natural phytochemicals show promise for drug discovery to fill th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cee9357f6b5dc485d43f8112a763cd2c
https://pubmed.ncbi.nlm.nih.gov/36594931
https://pubmed.ncbi.nlm.nih.gov/36594931
Publikováno v:
Molecular Pain. 19:174480692311521
Migraine is a neurological disease characterized by severe headache attacks. Combinations of different genetic variations such as copy number variation (CNV) in a gene and microRNA (miRNA) expression can provide a holistic approach to the disease as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::518f53566ea4feee6fd2dcf34e9bace0
https://doi.org/10.1177/17448069231152104
https://doi.org/10.1177/17448069231152104