Sehime G Temel
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Explore the profile of Sehime G Temel including associated specialties, affiliations and a list of published articles.
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27
Citations
269
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Recent Articles
1.
Dilektasli A, Durak V, Armagan E, Korkmaz E, Kiras G, Sen A, et al.
Risk Manag Healthc Policy
. 2025 Feb;
18:579-592.
PMID: 40008028
Purpose: Pandemics put healthcare workers (HCWs) at risk of infections, making emergency department (ED) triage critical. This study aims to compare smart innovative self-kiosk triage (SKT) with routine triage (RT)....
2.
Abuelrub A, Erol I, Nalbant Bingol N, Sag S, Temel S, Durdagi S
ACS Chem Neurosci
. 2025 Jan;
PMID: 39791913
is implicated in a range of conditions, including autism spectrum disorder, intellectual disability, seizures, autosomal recessive nonsyndromic intellectual disability, heterotaxy, and ciliary dysfunction. In order to understand the molecular mechanisms...
3.
Kim A, Sakin I, Viviano S, Tuncel G, Aguilera S, Goles G, et al.
Life Sci Alliance
. 2024 Aug;
7(10).
PMID: 39168639
Intellectual and developmental disabilities result from abnormal nervous system development. Over a 1,000 genes have been associated with intellectual and developmental disabilities, driving continued efforts toward dissecting variant functionality to...
4.
Ozcelik F, Dundar M, Yildirim A, Henehan G, Vicente O, Sanchez-Alcazar J, et al.
Funct Integr Genomics
. 2024 Aug;
24(4):138.
PMID: 39147901
Artificial intelligence (AI) platforms have emerged as pivotal tools in genetics and molecular medicine, as in many other fields. The growth in patient data, identification of new diseases and phenotypes,...
5.
Aliyeva L, Ongen Y, Eren E, Sarisozen M, Alemdar A, Temel S, et al.
J Mol Diagn
. 2024 Jul;
26(9):754-769.
PMID: 39025364
Osteogenesis imperfecta (OI) is the most common inherited connective tissue disease of the bone, characterized by recurrent fractures and deformities. In patients displaying the OI phenotype, genotype-phenotype correlation is used...
6.
Ma M, Ganapathi M, Zheng Y, Tan K, Kanca O, Bove K, et al.
Genet Med
. 2024 Mar;
26(7):101125.
PMID: 38522068
Purpose: YKT6 plays important roles in multiple intracellular vesicle trafficking events but has not been associated with Mendelian diseases. Methods: We report 3 unrelated individuals with rare homozygous missense variants...
7.
Turkgenc B, Baydar C, Deniz I, Akcay A, Ergoren M, Sag S, et al.
Appl Immunohistochem Mol Morphol
. 2023 Oct;
31(10):690-696.
PMID: 37796154
Sudden cardiac death is a sudden, unexpected death developed by one of the many different causes of cardiac arrest that occur within 1 hour of the onset of new symptoms....
8.
Bisgin A, Sag S, Dogan M, Yildirim M, Gumus A, Akkus N, et al.
Breast
. 2022 Jun;
65:15-22.
PMID: 35753294
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...
9.
Cekic S, Huriyet H, Hortoglu M, Kasap N, Ozen A, Karakoc-Aydiner E, et al.
Clin Exp Immunol
. 2022 May;
209(1):83-89.
PMID: 35511492
STAT3 plays an important role in various complex and sometimes contradictory pathways such as proliferation, differentiation, migration, inflammation, and apoptosis. The transcriptional activity of the STAT3 gene is controlled by...
10.
Sabanci A, Erkan Alkan P, Mujde C, Polat H, Erguzeloglu C, Bisgin A, et al.
Int J Nanomedicine
. 2022 Feb;
17:351-379.
PMID: 35115773
Purpose: SARS-CoV-2-infected individuals may be asymptomatic, and therefore, the virus is highly contagious. We aimed to develop an agent to control viral replication in the upper respiratory tract and to...