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

Increased Bone Morphogenetic Protein-Responsive Transcription Factors in Distinct Endothelial and Mesenchymal Cells in Pulmonary Artery Hypertension

肺动脉高压中不同内皮细胞和间充质细胞中骨形态发生蛋白反应性转录因子增加

Andruska, Adam Michael; Cantu Valadez, Rodrigo; Ichimura, Kenzo; Chu, Pauline; Zhang, Tianyi; Schimmel, Katharina; Wang, Lingli; Cao, Aiqin; Aldred, Micheala A; Spiekerkoetter, Edda

When "loss-of-function" means proteostasis burden: Thinking again about coding DNA variants

当“功能丧失”意味着蛋白质稳态负担时:重新思考编码DNA变异

Shovlin, Claire L; Aldred, Micheala A

Acute endothelial stresses identify microRNA let-7b-5p and non-coding SLC11A2 (NRAMP2/DMT1) exon as biomarkers that overlap with those detected in malignant and non-malignant diseases

急性内皮应激可将microRNA let-7b-5p和非编码SLC11A2(NRAMP2/DMT1)外显子鉴定为生物标志物,这些标志物与在恶性和非恶性疾病中检测到的标志物存在重叠。

Bielowka, Adrianna M; Patel, Dilip; Li, Dongyang; Bernabeu-Herrero, Maria E; Game, Laurence; Aldred, Micheala A; Mollet, Inês G; Shovlin, Claire L

Alterations in Mitochondrial Function in Pulmonary Vascular Diseases.

肺血管疾病中线粒体功能的改变

Farha Samar, Asosingh Kewal, Hassoun Paul M, Barnard John, Comhair Suzy, Reichard Andrew, Wanner Nicholas, Radeva Milena, Aldred Micheala A, Beck Gerald J, Berman-Rosenzweig Erika, Borlaug Barry A, Finet J Emanuel, Frantz Robert P, Grunig Gabriele, Hemnes Anna R, Hill Nicholas, Horn Evelyn M, Jellis Christine, Leopold Jane A, Mehra Reena, Park Margaret M, Rischard Franz P, Tang W H Wilson, Erzurum Serpil C

Lung Single-Cell Transcriptomics Reveal Diverging Pathobiology and Opportunities for Precision Targeting in Scleroderma-Associated Versus Idiopathic Pulmonary Arterial Hypertension

肺单细胞转录组学揭示硬皮病相关性肺动脉高压与特发性肺动脉高压不同的病理生物学机制及精准治疗机会

Tuhy, Tijana; Coursen, Julie C; Graves, Tammy; Patatanian, Michael; Cherry, Christopher; Niedermeyer, Shannon E; Khan, Sarah L; Rosen, Darin T; Croglio, Michael P; Elnashar, Mohab; Kolb, Todd M; Mathai, Stephen C; Damico, Rachel L; Hassoun, Paul M; Shimoda, Larissa A; Suresh, Karthik; Aldred, Micheala A; Simpson, Catherine E

Loss of Tbx4 Affects Postnatal Lung Development and Predisposes to Pulmonary Hypertension

Tbx4基因缺失会影响出生后肺部发育并易导致肺动脉高压

Maldonado-Velez, Gabriel; Mickler, Elizabeth A; Cook, Todd G; Aldred, Micheala A

Adaptation of ACMG/AMP Guidelines for Clinical Classification of BMPR2 Variants in Pulmonary Arterial Hypertension Resolves Variants of Unclear Pathogenicity in ClinVar

ACMG/AMP指南在肺动脉高压BMPR2变异体临床分类中的应用解决了ClinVar数据库中致病性不明的变异体问题。

Eichstaedt, Christina A; Maldonado-Velez, Gabriel; Machado, Rajiv D; Gräf, Stefan; Dooijes, Dennis; Balachandar, Srimmitha; Coulet, Florence; Day, Kristina; Eyries, Melanie; Macaya, Daniela; Shaukat, Memoona; Southgate, Laura; Tenorio-Castano, Jair; Chung, Wendy K; Welch, Carrie L; Aldred, Micheala A

The mitochondrial unfolded protein response and metabolic reprogramming promote PASMC proliferation in response to sphingosine kinase-1/sphingosine-1-phosphate signaling.

线粒体未折叠蛋白反应和代谢重编程促进 PASMC 增殖,以响应鞘氨醇激酶-1/鞘氨醇-1-磷酸信号传导

Lockett Angelia D, Snow Aaron, Adogamhe Pontian, Sysol Justin, Yadav Manas, Mubuuke Tendo, Gomes Marta T, Cook Todd, Fisher Amanda, Aldred Micheala A, Machado Roberto F

Integrative Multiomics in the Lung Reveals a Protective Role of Asporin in Pulmonary Arterial Hypertension

肺部整合多组学研究揭示了天冬氨酸蛋白在肺动脉高压中的保护作用

Hong, Jason; Medzikovic, Lejla; Sun, Wasila; Wong, Brenda; Ruffenach, Grégoire; Rhodes, Christopher J; Brownstein, Adam; Liang, Lloyd L; Aryan, Laila; Li, Min; Vadgama, Arjun; Kurt, Zeyneb; Schwantes-An, Tae-Hwi; Mickler, Elizabeth A; Gräf, Stefan; Eyries, Mélanie; Lutz, Katie A; Pauciulo, Michael W; Trembath, Richard C; Perros, Frédéric; Montani, David; Morrell, Nicholas W; Soubrier, Florent; Wilkins, Martin R; Nichols, William C; Aldred, Micheala A; Desai, Ankit A; Trégouët, David-Alexandre; Umar, Soban; Saggar, Rajan; Channick, Richard; Tuder, Rubin M; Geraci, Mark W; Stearman, Robert S; Yang, Xia; Eghbali, Mansoureh

Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT

导致提前终止密码子的突变会造成遗传性出血性毛细血管扩张症(HHT)的细胞和临床变异。

Bernabéu-Herrero, Maria E; Patel, Dilipkumar; Bielowka, Adrianna; Zhu, JiaYi; Jain, Kinshuk; Mackay, Ian S; Chaves Guerrero, Patricia; Emanuelli, Giulia; Jovine, Luca; Noseda, Michela; Marciniak, Stefan J; Aldred, Micheala A; Shovlin, Claire L