Turanli Eda Tahir - Graduate School of Natural and Applied Sciences, Acıbadem University

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论文共 83 篇作者统计合作学者相似作者

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Identification of a splice variant in PSMB10 gene in a multiply affected family with undiagnosed autoinflammatory syndrome

Muhammed Gecgel, Alper Bulbul, Dora Sigli, Inci Onat,Serdal Ugurlu,Eda Tahir Turanli

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 175-175

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Abstract LB021: BAU-243: A novel BCL-2 inhibitor inducing autophagic cell death in glioblastoma, unveiled through multistep virtual screening, comprehensive in vitro and in vivo animal model evaluation

Seyma Calis,Berna Dogan,Asuman Celebi,Ozlem Yapicier,Turker Kilic,Eda Tahir Turanli,Timucin Avsar,Serdar Durdagi

Cancer Researchno. 7_Supplement (2024)

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A rare case of uncharacterized autoinflammatory disease: Patient carrying variations in NLRP3 and TNFRSF1A genes

Ozgur Can Kilinc, Konul Gayibova,Merve Ozkilinc Onen, Umut Inci Onat, Alper Bülbül,Ahmet Can Timucin,Serdal Ugurlu,Eda Tahir Turanli

American journal of medical genetics. Part App.e63715-e63715, (2024)

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Var3PPred: variant prediction based on 3-D structure and sequence analyses of protein-protein interactions on autoinflammatory diseases

Alper Bülbül,Emel Timucin,Ahmet Can Timuçin,Osman Uğur Sezerman,Eda Tahir Turanli

PeerJ (2024): e17297

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HLA-B gene methylation and expression in Behçet's syndrome: a potential role of epigenetics in the pathogenesis

Merve Özkılınç Önen,Elif Everest, Turna Demirci, Pelinsu Köprülü Şen, Esra Kızıltepe Kısakesen,Yeşim Özgüler,Sinem Nihal Esatoğlu,Emire Seyahi,Eda Tahir Turanlı

Clinical and experimental rheumatology (2024)

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Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic cerebrospinal fluid markers

Elif Everest,Ugur Uygunoglu,Melih Tutuncu,Alper Bulbul, Umut Inci Onat, Mehmetcan Unal,Timucin Avsar,Sabahattin Saip,Ugur Bilge,Eda Tahir Turanli,Aksel Siva

PloS oneno. 6 (2023): e0287463-e0287463

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A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants

Kerem Parlar,Eda Tahir Turanli,Eda Nuhoglu Kantarci, Aysa Hacioglu,Asli Kirectepe Aydin,Ali Yagiz Ayla, Umut Voyvoda,Huri Ozdogan,Serdal Ugurlu

Modern rheumatology case reportsno. 1 (2023): 121-124

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Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

Merve Özkılınç Önen, Umut I Onat,Serdal Uğurlu,Ahmet C Timuçin,Devrim Öz Arslan,Elif Everest,Huri Özdoğan,Eda Tahir Turanlı

Rheumatology (Oxford)（2023）

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Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

Merve Özkılınç Önen, Umut I Onat,Serdal Uğurlu,Ahmet Can Timuçin,Devrim Öz Arslan,Elif Everest,Huri Özdoğan,Eda Tahir Turanlı

Rheumatologyno. 9 (2023): 3188-3196

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Prospective outcome analysis of multiple sclerosis cases reveals candidate prognostic markers

E. Everest, U. Uygunoglu, M. Tutuncu, A. Bulbul, U. Onat, M. Unal, T. Avsar, S. Saip, U. Bilge,E. Tahir Turanli, A. Siva

EUROPEAN JOURNAL OF NEUROLOGY (2023): 731-731

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