日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Unraveling the Role of RSPRY1 in TGF-β Pathway Dysregulation: Insights into the Pathogenesis of Spondyloepimetaphyseal Dysplasia

揭示RSPRY1在TGF-β通路失调中的作用:对脊椎骨骺干骺端发育不良发病机制的深入理解

Gozde Imren ,Beren Karaosmanoglu ,Bihter Muratoglu ,Cansu Ozdemir ,Gulen Eda Utine ,Pelin Ozlem Simsek-Kiper ,Ekim Z Taskiran

Microfluidic Fabrication of Gelatin-Nano Hydroxyapatite Scaffolds for Enhanced Control of Pore Size Distribution and Osteogenic Differentiation of Dental Pulp Stem Cells

明胶-纳米羟基磷灰石支架的微流体制造,用于增强对牙髓干细胞孔径分布和成骨分化的控制

Cem Bayram, Sukru Ozturk, Beren Karaosmanoglu, Merve Gultekinoglu, Ekim Z Taskiran, Kezban Ulubayram, Hamta Majd, Jubair Ahmed, Mohan Edirisinghe

Small cell lung cancer stem cells display mesenchymal properties and exploit immune checkpoint pathways in activated cytotoxic T lymphocytes

小细胞肺癌干细胞表现出间充质特性,并在活化的细胞毒性 T 淋巴细胞中利用免疫检查点通路

M Alper Kursunel, Ekim Z Taskiran, Ece Tavukcuoglu, Hamdullah Yanik, Funda Demirag, Beren Karaosmanoglu, Feyza Gul Ozbay, Aysegul Uner, Dorina Esendagli, Derya Kizilgoz, Ulku Yilmaz, Gunes Esendagli

CD66b+ monocytes represent a proinflammatory myeloid subpopulation in cancer

CD66b+ 单核细胞代表癌症中的促炎性髓系亚群

Utku Horzum, Digdem Yoyen-Ermis, Ekim Z Taskiran, Kerim Bora Yilmaz, Erhan Hamaloglu, Derya Karakoc, Gunes Esendagli

Proerythroblast Cells of Diamond-Blackfan Anemia Patients With RPS19 and CECR1 Mutations Have Similar Transcriptomic Signature

患有 RPS19 和 CECR1 突变的 Diamond-Blackfan 贫血患者的幼红细胞具有相似的转录组特征

Beren Karaosmanoglu, M Alper Kursunel, Duygu Uckan Cetinkaya, Fatma Gumruk, Gunes Esendagli, Sule Unal, Ekim Z Taskiran

FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs!

由细胞浆苯丙氨酰-tRNA合成酶基因双等位基因突变引起的FARS1相关疾病:不仅仅是肺部!

Luise A Schuch, Maria Forstner, Christina K Rapp, Yang Li, Desiree E C Smith, Marisa I Mendes, Florent Delhommel, Michael Sattler, Nagehan Emiralioğlu, Ekim Z Taskiran, Diclehan Orhan, Nural Kiper, Meino Rohlfs, Tim Jeske, Maximilian Hastreiter, Michael Gerstlauer, Alba Torrent-Vernetta, Antonio Mor

Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD

ANKS6 突变导致 ESRD 出现肾痨样表型

Ekim Z Taskiran, Emine Korkmaz, Safak Gucer, Can Kosukcu, Figen Kaymaz, Cansu Koyunlar, Elizabeth C Bryda, Moumita Chaki, Dongmei Lu, Komal Vadnagara, Cengiz Candan, Rezan Topaloglu, Franz Schaefer, Massimo Attanasio, Carsten Bergmann, Fatih Ozaltin

DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN

DGKE 变异型可导致类似于膜增生性肾小球肾炎的肾小球微血管病

Fatih Ozaltin, Binghua Li, Alysha Rauhauser, Sung-Wan An, Oguz Soylemezoglu, Ipek Isik Gonul, Ekim Z Taskiran, Tulin Ibsirlioglu, Emine Korkmaz, Yelda Bilginer, Ali Duzova, Seza Ozen, Rezan Topaloglu, Nesrin Besbas, Shazia Ashraf, Yong Du, Chaoying Liang, Phylip Chen, Dongmei Lu, Komal Vadnagara, Su