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

Bi-allelic variants in OLA1 cause a neurodevelopmental disorder with joint hypermobility

OLA1基因的双等位基因变异会导致一种伴有关节过度活动的神经发育障碍。

AlAbdi, Lama; Sezer, Abdullah; Alzahrani, Fatema; Cevik, Sebiha; Demir, Zanyar; Abdullah, Nor Linda; Durukan, Özlem; Dallı, Efe; Hashem, Mais O; Abuyousef, Omar; Aljamal, Bayan; Helaby, Rana; Radwan, Mona; Jaafar, Amal; Alshidi, Tarfa; Salem, Israa; Hamid, Halima; Alhaddad, Bader; Bakur, Khadijah; Taşdelen, Elifcan; Kılıç, Mustafa; Al-Owain, Mohammed; Alhashem, Amal; Bratland, Eirik; Paulsen, Julie; Houge Douzgos, Gunnar; Politi, Anya Revah; Uguen, Kevin; Masson, Emmanuelle; Audebert, Severine; AlAnzi, Talal; Arold, Stefan T; Ergin, Bora; Ibrahim, Leena A; Kaplan, Oktay I; Alkuraya, Fowzan S

Abnormal Amplitude-Integrated Electroencephalography and Acidosis as Key Criteria Initiating Therapeutic Hypothermia in Asphyxiated Newborns - Data From the German Hypothermia Registry

异常振幅整合脑电图和酸中毒是启动窒息新生儿治疗性低温疗法的关键标准——来自德国低温登记处的数据

Demir, Sebiha; Groteklaes, Anne; Dresbach, Till; Müller, Andreas; Sabir, Hemmen

ARL13B regulates juxtaposed cilia-cilia elongation in BBSome dependent manner in Caenorhabditis elegans

ARL13B 以 BBSome 依赖的方式调节秀丽隐杆线虫中并列纤毛-纤毛伸长

Merve Gül Turan, Hanife Kantarci, Sebiha Cevik, Oktay I Kaplan

A homozygous frameshift variant in the CILK1 gene causes cranioectodermal dysplasia

CILK1基因的纯合移码变异会导致颅外胚层发育不良

Sezer, Abdullah; Oner, Sukru S; Saat, Hanife; Turan, Merve G; Gungor, Tulin; Cevik, Sebiha; Erol, Asli; Yenisert, Ferhan; Catalbas, Kerem; Ozbakir, Derya Hazal; Kocagil, Sinem; Cilingir, Oğuz; Ergun, Mehmet Ali; Kaplan, Oktay I

Dual-Function Bis-Tetraphenylethenes for Selective Metal Ion and Glutathione Detection and Current Transformer Application

用于选择性金属离子和谷胱甘肽检测及电流互感器应用的双功能双四苯乙烯

Bayindir, Sinan; Akar, Sebiha; Hussein, Abdullah S; Lafzi, Ferruh; Orak, İkram

Correlation of low birth pH with cognitive and language outcomes at two years

低出生体液pH值与两岁时的认知和语言发育结果的相关性

Abdelrahman, Khaled; Groteklaes, Anne; Demir, Sebiha; Jiménez Cruz, Jorge; Dresbach, Till; Mueller, Andreas; Sabir, Hemmen

CilioGenics: an integrated method and database for predicting novel ciliary genes

CilioGenics:一种预测新型纤毛基因的综合方法和数据库

Mustafa S Pir, Efe Begar, Ferhan Yenisert, Hasan C Demirci, Mustafa E Korkmaz, Asli Karaman, Sofia Tsiropoulou, Elif Nur Firat-Karalar, Oliver E Blacque, Sukru S Oner, Osman Doluca, Sebiha Cevik, Oktay I Kaplan

Synthesis of Phenol-Hydrazide-Appended Tetraphenylethenes as Novel On-Off-On Cascade Sensors of Copper and Glutathione

合成酚-酰肼修饰的四苯乙烯作为新型铜和谷胱甘肽的开关级联传感器

Bayindir, Sinan; Akar, Sebiha

CiliaMiner: an integrated database for ciliopathy genes and ciliopathies

CiliaMiner:纤毛病基因和纤毛病的综合数据库

Turan, Merve Gül; Orhan, Mehmet Emin; Cevik, Sebiha; Kaplan, Oktay I

WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium

WDR31 与 GTP 酶激活蛋白 (GAP) ELMOD 和 RP2 在调节 IFT 复合物和将 BBSome 募集到纤毛方面表现出功能冗余性。

Cevik, Sebiha; Peng, Xiaoyu; Beyer, Tina; Pir, Mustafa S; Yenisert, Ferhan; Woerz, Franziska; Hoffmann, Felix; Altunkaynak, Betul; Pir, Betul; Boldt, Karsten; Karaman, Asli; Cakiroglu, Miray; Oner, S Sadik; Cao, Ying; Ueffing, Marius; Kaplan, Oktay I