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

Human iPSC-Derived MSCs Induce Neurotrophic Effects and Improve Metabolic Activity in Acute Neuronal Injury Models

人类 iPSC 衍生的 MSC 可在急性神经元损伤模型中诱导神经营养作用并改善代谢活性

Keiji Kawatani, Genesis Omana Suarez, Ralph B Perkerson 3rd, Ephraim E Parent, Toshihiko Nambara, Joshua A Knight, Tammee M Parsons, Kshama Gupta, Francis Shue, Alla Alnobani, Prasanna Vibhute, Hancheng Cai, Hugo Guerrero-Cázares, John A Copland 3rd, Alfredo Quiñones-Hinojosa, Takahisa Kanekiyo

ABCA7 deficiency causes neuronal dysregulation by altering mitochondrial lipid metabolism

ABCA7 缺乏通过改变线粒体脂质代谢导致神经元失调

Keiji Kawatani #, Marie-Louise Holm #, Skylar C Starling, Yuka A Martens, Jing Zhao, Wenyan Lu, Yingxue Ren, Zonghua Li, Peizhou Jiang, Yangying Jiang, Samantha K Baker, Ni Wang, Bhaskar Roy, Tammee M Parsons, Ralph B Perkerson 3rd, Hanmei Bao, Xianlin Han, Guojun Bu, Takahisa Kanekiyo

Secretome from iPSC-derived MSCs exerts proangiogenic and immunosuppressive effects to alleviate radiation-induced vascular endothelial cell damage

来自 iPSC 衍生 MSC 的分泌蛋白组发挥促血管生成和免疫抑制作用,以减轻辐射引起的血管内皮细胞损伤

Kshama Gupta, Ralph B Perkerson 3rd, Tammee M Parsons, Ramacharan Angom, Danilyn Amerna, Jeremy D Burgess, Yingxue Ren, Pamela J McLean, Debabrata Mukhopadhyay, Prasanna Vibhute, Zbigniew K Wszolek, Abba C Zubair, Alfredo Quiñones-Hinojosa, Takahisa Kanekiyo

A mutant methionyl-tRNA synthetase-based toolkit to assess induced-mesenchymal stromal cell secretome in mixed-culture disease models

一种基于突变型甲硫氨酰-tRNA合成酶的工具包,用于评估混合培养疾病模型中诱导间充质基质细胞的分泌组

Jeremy D Burgess ,Danilyn Amerna ,Emily S Norton ,Tammee M Parsons ,Ralph B Perkerson 3rd ,Ayman H Faroqi ,Zbigniew K Wszolek ,Hugo Guerrero Cazares ,Takahisa Kanekiyo ,Marion Delenclos ,Pamela J McLean

A Mutant Methionyl-tRNA Synthetase-Based toolkit to assess induced-Mesenchymal Stromal Cell secretome in mixed-culture disease models

基于突变型甲硫氨酰-tRNA 合成酶的工具包,用于评估混合培养疾病模型中的诱导间充质基质细胞分泌组

Jeremy D Burgess, Danilyn Amerna, Emily S Norton, Tammee M Parsons, Ralph B Perkerson 3rd, Ayman H Faroqi, Zbigniew K Wszolek, Hugo Guerrero Cazares, Takahisa Kanekiyo, Marion Delenclos, Pamela J McLean

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

作为国际 FTLD-TDP 全基因组测序联盟的一部分,全基因组分析揭示了新的疾病风险因素,并增加了对 FTLD 免疫功能障碍的支持

Cyril Pottier, Yingxue Ren, Ralph B Perkerson 3rd, Matt Baker, Gregory D Jenkins, Marka van Blitterswijk, Mariely DeJesus-Hernandez, Jeroen G J van Rooij, Melissa E Murray, Elizabeth Christopher, Shannon K McDonnell, Zachary Fogarty, Anthony Batzler, Shulan Tian, Cristina T Vicente, Billie Matchett,