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

Surface-Capped Protein Nanoparticles for Nonviral Gene Delivery

用于非病毒基因递送的表面包覆蛋白纳米颗粒

Xhyliu, Fjorela; Yao, Yao; Ko, Yeongun; Grasman, Grant; Raymond, Jeffery E; Chang, Albert; Deng, Yuxuan; Dominic, Grant; Triebwasser, Michael; Lahann, Joerg

Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia

了解先兆子痫中补体系统末端途径内的罕见基因变异

Lokki, A Inkeri; Triebwasser, Michael; Daly, Emma; Kurki, Mitja I; Perola, Markus; Auro, Kirsi; Salmon, Jane E; Anuja, Java; Daly, Mark; Atkinson, John P; Laivuori, Hannele; Meri, Seppo

Diagnostic evaluation to identify infection-attributable stillbirth

诊断评估以识别感染引起的死胎

Coggins, Sarah A; Triebwasser, Jourdan E; Puopolo, Karen M

Genetic association of preeclampsia to von Willebrand factor and its size-regulator ADAMTS13

先兆子痫与血管性血友病因子及其大小调节因子ADAMTS13的遗传关联

Lokki, A Inkeri; Triebwasser, Michael; Daly, Emma; Kurki, Mitja I; Perola, Markus; Auro, Kirsi; Java, Anuja; Salmon, Jane E; Heinonen, Seppo; Kajantie, Eero; Kere, Juha; Lassila, Riitta; Daly, Mark; Atkinson, John P; Laivuori, Hannele; Meri, Seppo

Coronary Venous Air Embolism in Placenta Accreta Spectrum Cesarean Hysterectomy

冠状静脉空气栓塞合并胎盘植入谱系剖宫产子宫切除术

Opipari, AnneMarie; Spizman, Jocelyn; Triebwasser, Jourdan; Uppal, Shitanshu; Russell, Mark; Pancaro, Carlo

Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy

利用靶向造血干细胞的脂质纳米颗粒构建致死性α-地中海贫血小鼠模型,并通过慢病毒基因治疗进行治疗。

Chappell, Maxwell E; Breda, Laura; Tricoli, Lucas; Guerra, Amaliris; Jarocha, Danuta; Castruccio Castracani, Carlo; Papp, Tyler E; Tanaka, Naoto; Hamilton, Nolan; Triebwasser, Michael P; Ghiaccio, Valentina; Fedorky, Megan T; Gollomp, Kandace L; Bochenek, Veronica; Roche, Aoife M; Everett, John K; Cook, Emma J; Bushman, Frederic D; Teawtrakul, Nattiya; Glentis, Stavros; Kattamis, Antonis; Mui, Barbara L; Tam, Ying K; Weissman, Drew; Abdulmalik, Osheiza; Parhiz, Hamideh; Rivella, Stefano

Rare variants in genes coding for components of the terminal pathway of the complement system in preeclampsia

先兆子痫中编码补体系统末端途径成分的基因罕见变异

Lokki, A; Triebwasser, Michael; Daly, Emma; Cohort, Finnpec; Kurki, Mrtja; Perola, Markus; Auro, Kirsi; Salmon, Jane; Java, Anuja; Daly, Mark; Atkinson, John; Laivuori, Hannele; Meri, Seppo

In vivo hematopoietic stem cell modification by mRNA delivery

通过mRNA递送对体内造血干细胞进行修饰

Breda, Laura; Papp, Tyler E; Triebwasser, Michael P; Yadegari, Amir; Fedorky, Megan T; Tanaka, Naoto; Abdulmalik, Osheiza; Pavani, Giulia; Wang, Yongping; Grupp, Stephan A; Chou, Stella T; Ni, Houping; Mui, Barbara L; Tam, Ying K; Weissman, Drew; Rivella, Stefano; Parhiz, Hamideh

Electronic Reminder to Transition Care After Hypertensive Disorders of Pregnancy: A Randomized Controlled Trial

电子提醒在妊娠期高血压疾病患者过渡到护理阶段的作用:一项随机对照试验

Triebwasser, Jourdan E; Lewey, Jennifer; Walheim, Lauren; Sehdev, Harish M; Srinivas, Sindhu K

Identification of complement factor H variants that predispose to pre-eclampsia: A genetic and functional study

鉴定易患先兆子痫的补体因子H变异体:一项遗传和功能研究

Lokki, A Inkeri; Ren, Zhen; Triebwasser, Michael; Daly, Emma; Perola, Markus; Auro, Kirsi; Burwick, Richard; Salmon, Jane E; Daly, Mark; Laivuori, Hannele; Atkinson, John P; Java, Anuja; Meri, Seppo