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

Extracellular vesicle profiling reveals novel autism signatures in patient-derived forebrain organoids.

细胞外囊泡分析揭示了患者来源的前脑类器官中新的自闭症特征。

Stankovic Isidora, Smit Phillip, Cross Jonathan, Rai Alin, Wolujewicz Paul, Greening David, Colak Dilek

A Report of a Child with SEC31A-Related Neurodevelopmental Disorder

一份关于患有 SEC31A 相关神经发育障碍儿童的报告

AlTassan, Ruqaiah; AlQudairy, Hanan; Saydo, Biam; Alammari, Aseel; Londoño, Kelly J Cardona; Ramzan, Khushnooda; Colak, Dilek; Arold, Stefan T; Kaya, Namik

Performance of a novel DiaRD-HCV RNA RTqPCR kit for quantification of HCV RNA in clinical samples

一种新型 DiaRD-HCV RNA RT-qPCR 试剂盒在临床样本中 HCV RNA 定量分析中的性能

Cuhaci, Ulker; Durmaz, Bengul; Toptan, Hande; Koroglu, Mehmet; Mutlu, Derya; Colak, Dilek; Durmaz, Rıza

Astrocytic RNA degradation suppresses calcium signaling to support synapse function and restrain anxiety

星形胶质细胞RNA降解抑制钙信号传导,从而支持突触功能并抑制焦虑

Lituma, Pablo J; Deveci, Aykut; Barrio-Alonso, Estibaliz; Tan, Kun; Wilkinson, Miles F; Castillo, Pablo E; Colak, Dilek

Extracellular Vesicle Profiling Reveals Novel Autism Signatures in Patient-Derived Forebrain Organoids.

细胞外囊泡分析揭示了患者来源的前脑类器官中新的自闭症特征

Stankovic Isidora, Smit Phillip, Cross Jonathan, Wolujewicz Paul, Greening David, Colak Dilek

Identification of Diagnostic and Prognostic Subnetwork Biomarkers for Women with Breast Cancer Using Integrative Genomic and Network-Based Analysis

利用整合基因组学和网络分析方法鉴定乳腺癌女性患者的诊断和预后子网络生物标志物

Al-Harazi, Olfat; El Allali, Achraf; Kaya, Namik; Colak, Dilek

A novel missense mutation in ISCA2 causes aberrant splicing and leads to multiple mitochondrial dysfunctions syndrome 4

ISCA2基因中的一种新型错义突变导致异常剪接,进而引发多发性线粒体功能障碍综合征4。

Al-Hassnan, Zuhair; AlDosary, Mazhor; AlHargan, Aljouhra; AlQudairy, Hanan; Almass, Rawan; Alahmadi, Khaled Omar; AlShahrani, Saif; AlBakheet, Albandary; Almuhaizea, Mohammad A; Taylor, Robert W; Colak, Dilek; Kaya, Namik

AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model

AMFR功能障碍会导致人类常染色体隐性遗传性痉挛性截瘫,在临床前模型中,他汀类药物治疗有效。

Deng, Ruizhi; Medico-Salsench, Eva; Nikoncuk, Anita; Ramakrishnan, Reshmi; Lanko, Kristina; Kühn, Nikolas A; van der Linde, Herma C; Lor-Zade, Sarah; Albuainain, Fatimah; Shi, Yuwei; Yousefi, Soheil; Capo, Ivan; van den Herik, Evita Medici; van Slegtenhorst, Marjon; van Minkelen, Rick; Geeven, Geert; Mulder, Monique T; Ruijter, George J G; Lütjohann, Dieter; Jacobs, Edwin H; Houlden, Henry; Pagnamenta, Alistair T; Metcalfe, Kay; Jackson, Adam; Banka, Siddharth; De Simone, Lenika; Schwaede, Abigail; Kuntz, Nancy; Palculict, Timothy Blake; Abbas, Safdar; Umair, Muhammad; AlMuhaizea, Mohammed; Colak, Dilek; AlQudairy, Hanan; Alsagob, Maysoon; Pereira, Catarina; Trunzo, Roberta; Karageorgou, Vasiliki; Bertoli-Avella, Aida M; Bauer, Peter; Bouman, Arjan; Hoefsloot, Lies H; van Ham, Tjakko J; Issa, Mahmoud; Zaki, Maha S; Gleeson, Joseph G; Willemsen, Rob; Kaya, Namik; Arold, Stefan T; Maroofian, Reza; Sanderson, Leslie E; Barakat, Tahsin Stefan

Exposure to Cadmium Telluride Quantum Dots and Gene Expression Profile of Huh-7 Hepatocellular Carcinoma Cell Line

碲化镉量子点暴露对Huh-7肝癌细胞系基因表达谱的影响

Alothaid, Hani; Al-Anazi, Mashael R; Al-Qahtani, Arwa A; Colak, Dilek; Yusuf, Azeez; Aldughaim, Mohammed S; Mahzari, Ali M; Habibullah, Mahmoud M; Alarifi, Saud; Alkahtani, Saad; Al-Qahtani, Ahmed A

Astrocytes derived from ASD individuals alter behavior and destabilize neuronal activity through aberrant Ca(2+) signaling

来自自闭症谱系障碍患者的星形胶质细胞通过异常的Ca(2+)信号传导改变行为并破坏神经元活动。

Allen, Megan; Huang, Ben S; Notaras, Michael J; Lodhi, Aiman; Barrio-Alonso, Estibaliz; Lituma, Pablo J; Wolujewicz, Paul; Witztum, Jonathan; Longo, Francesco; Chen, Maoshan; Greening, David W; Klann, Eric; Ross, M Elizabeth; Liston, Conor; Colak, Dilek