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

Identification of a rare variant in TNNT3 responsible for familial dilated cardiomyopathy through whole-exome sequencing and in silico analysis

通过全外显子组测序和生物信息学分析,鉴定出TNNT3基因中导致家族性扩张型心肌病的罕见变异。

Jadidi, Motahareh; Babaali, Vida; InanlooRahatloo, Kolsoum; Salehi, Najmeh; Mollazadeh, Reza

Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery

由POLR3B基因突变和剪接体机制缺陷引起的颅面畸形导致的智力障碍

Saghi, Mostafa; InanlooRahatloo, Kolsoum; Alavi, Afagh; Kahrizi, Kimia; Najmabadi, Hossein

Evolution of SARS-CoV-2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations

2019年12月至2020年3月下旬SARS-CoV-2基因组的演变:新出现的单倍型和信息丰富的标签核苷酸变异

Safari, Iman; InanlooRahatloo, Kolsoum; Elahi, Elahe

Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains

伊朗SARS-CoV-2毒株研究揭示了不同毒株间的混合感染和重组可能对新毒株的出现做出贡献。

Taghizadeh, Peyman; Salehi, Sadegh; Heshmati, Ali; Houshmand, Seyed Massoud; InanlooRahatloo, Kolsoum; Mahjoubi, Forouzandeh; Sanati, Mohammad Hossein; Yari, Hadi; Alavi, Afagh; Jamehdar, Saeid Amel; Dabiri, Soroosh; Galehdari, Hamid; Haghshenas, Mohammad Reza; Hashemian, Amir Masoud; Heidarzadeh, Abtin; Jahanzad, Issa; Kheyrani, Elham; Piroozmand, Ahmad; Mojtahedi, Ali; Nikoo, Hadi Razavi; Rahimi Bidgoli, Mohammad Masoud; Rezvani, Nayebali; Sepehrnejad, Mehdi; Shakibzadeh, Arash; Shariati, Gholamreza; Seyyedi, Noorossadat; MohammadSaleh Zahraei, Seyed; Safari, Iman; Elahi, Elahe

Sex-based differences in myocardial gene expression in recently deceased organ donors with no prior cardiovascular disease

近期死亡且无既往心血管疾病的器官捐献者心肌基因表达的性别差异

InanlooRahatloo, Kolsoum; Liang, Grace; Vo, Davis; Ebert, Antje; Nguyen, Ivy; Nguyen, Patricia K

iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy

iPSC 衍生的心肌细胞显示左心室致密化不全性心肌病中 TGF-β 信号异常

Kazuki Kodo, Sang-Ging Ong, Fereshteh Jahanbani, Vittavat Termglinchan, Keiichi Hirono, Kolsoum InanlooRahatloo, Antje D Ebert, Praveen Shukla, Oscar J Abilez, Jared M Churko, Ioannis Karakikes, Gwanghyun Jung, Fukiko Ichida, Sean M Wu, Michael P Snyder, Daniel Bernstein, Joseph C Wu

A Rapid, High-Quality, Cost-Effective, Comprehensive and Expandable Targeted Next-Generation Sequencing Assay for Inherited Heart Diseases

一种快速、高质量、经济高效、全面且可扩展的针对遗传性心脏病的靶向下一代测序检测方法

Wilson, Kitchener D; Shen, Peidong; Fung, Eula; Karakikes, Ioannis; Zhang, Angela; InanlooRahatloo, Kolsoum; Odegaard, Justin; Sallam, Karim; Davis, Ronald W; Lui, George K; Ashley, Euan A; Scharfe, Curt; Wu, Joseph C

Mutation in ST6GALNAC5 identified in family with coronary artery disease

冠状动脉疾病家族中发现 ST6GALNAC5 基因突变

Kolsoum InanlooRahatloo, Amir Farhang Zand Parsa, Klaus Huse, Paniz Rasooli, Saeid Davaran, Matthias Platzer, Marcel Kramer, Jian-Bing Fan, Casey Turk, Sasan Amini, Frank Steemers, Kevin Gunderson, Mostafa Ronaghi, Elahe Elahi