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

Characterization of human induced pluripotent stems cells: Current approaches, challenges, and future solutions

人类诱导性多能干细胞的表征:当前方法、挑战和未来解决方案

Sahana Suresh Babu, Haritha Duvvuru, Jillian Baker, Stephanie Switalski, Mehdi Shafa, Krishna Morgan Panchalingam, Saedeh Dadgar, Justin Beller, Behnam Ahmadian Baghbaderani

Computational fluid dynamics modeling, a novel, and effective approach for developing scalable cell therapy manufacturing processes

计算流体动力学建模是开发可扩展细胞治疗制造工艺的一种新颖、有效的方法

Mehdi Shafa, Krishna M Panchalingam, Tylor Walsh, Thomas Richardson, Behnam Ahmadian Baghbaderani

Long-Term Stability and Differentiation Potential of Cryopreserved cGMP-Compliant Human Induced Pluripotent Stem Cells

冷冻保存的符合cGMP标准的人类诱导多能干细胞的长期稳定性和分化潜能

Mehdi Shafa ,Tylor Walsh ,Krishna Morgan Panchalingam ,Thomas Richardson ,Laura Menendez ,Xinghui Tian ,Sahana Suresh Babu ,Saedeh Dadgar ,Justin Beller ,Fan Yang ,Behnam Ahmadian Baghbaderani

Human-Induced Pluripotent Stem Cells Manufactured Using a Current Good Manufacturing Practice-Compliant Process Differentiate Into Clinically Relevant Cells From Three Germ Layers

采用符合现行良好生产规范的工艺制造的人类诱导性多能干细胞可从三个胚层分化为临床相关细胞

Mehdi Shafa, Fan Yang, Thomas Fellner, Mahendra S Rao, Behnam Ahmadian Baghbaderani

Investigation of tRNA(Leu/Lys) and ATPase 6 genes mutations in Huntington's disease

亨廷顿病中tRNA(Leu/Lys)和ATPase 6基因突变的研究

Kasraie, Sadaf; Houshmand, Massoud; Banoei, Mohammad Mehdi; Ahari, Solmaz Etemad; Panahi, Mehdi Shafa Shariat; Shariati, Parvin; Bahar, Mohammad; Moin, Mostafa

Do haplogroups H and U act to increase the penetrance of Alzheimer's disease?

单倍群H和U是否会增加阿尔茨海默病的患病率?

Fesahat, Farzaneh; Houshmand, Massoud; Panahi, Mehdi Shafa Shariat; Gharagozli, Kurosh; Mirzajani, Farzaneh

Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients

对伊朗多发性硬化症患者线粒体tRNA(Leu/Lys)、NDI和ATPase 6/8的研究

Ahari, Solmaz Etemad; Houshmand, Massoud; Panahi, Mehdi Shafa Shariat; Kasraie, Sadaf; Moin, Mostafa; Bahar, Mohammad Ali

Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!

亨廷顿病与线粒体DNA缺失:突变亨廷顿蛋白和CAG重复序列扩增的事件还是常规机制?!

Banoei, Mohammad Mehdi; Houshmand, Massoud; Panahi, Mehdi Shafa Shariat; Shariati, Parvin; Rostami, Maryam; Manshadi, Masoumeh Dehghan; Majidizadeh, Tayebeh

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

波斯多发性硬化症患者线粒体D-loop区变异:K和A单倍群是风险因素!!

Hassani-Kumleh, Hassan; Houshmand, Massoud; Panahi, Mehdi Shafa Shariat; Riazi, Gholam Hossein; Sanati, Mohammad Hossein; Gharagozli, Kurosh; Ghabaee, Mojdeh