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

Whole-genome sequencing uncovers two loci for coronary artery calcification and identifies ARSE as a regulator of vascular calcification

全基因组测序揭示冠状动脉钙化的两个位点,并确定 ARSE 是血管钙化的调节剂

Paul S de Vries, Matthew P Conomos, Kuldeep Singh, Christopher J Nicholson, Deepti Jain, Natalie R Hasbani, Wanlin Jiang, Sujin Lee, Christian L Lino Cardenas, Sharon M Lutz, Doris Wong, Xiuqing Guo, Jie Yao, Erica P Young, Catherine Tcheandjieu, Austin T Hilliard, Joshua C Bis, Lawrence F Bielak, M

Matrix Gla Protein Levels Are Associated With Arterial Stiffness and Incident Heart Failure With Preserved Ejection Fraction

基质 Gla 蛋白水平与动脉僵硬和射血分数保留的心力衰竭发生率相关

Rajeev Malhotra #, Christopher J Nicholson #, Dongyu Wang, Vijeta Bhambhani, Samantha Paniagua, Charles Slocum, Haakon H Sigurslid, Christian L Lino Cardenas, Rebecca Li, Sophie L Boerboom, Yin-Ching Chen, Shih-Jen Hwang, Chen Yao, Fumito Ichinose, Donald B Bloch, Mark E Lindsay, Gregory D Lewis, Ja

Ageing causes an aortic contractile dysfunction phenotype by targeting the expression of members of the extracellular signal-regulated kinase pathway

衰老通过靶向细胞外信号调节激酶通路成员的表达导致主动脉收缩功能障碍表型

Christopher J Nicholson, Yi Xing, Sophie Lee, Stephanie Liang, Shivani Mohan, Caitlin O'Rourke, Joshua Kang, Kathleen G Morgan

HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

HDAC9 与动脉粥样硬化主动脉钙化有关,并影响血管平滑肌细胞表型

Rajeev Malhotra, Andreas C Mauer, Christian L Lino Cardenas, Xiuqing Guo, Jie Yao, Xiaoling Zhang, Florian Wunderer, Albert V Smith, Quenna Wong, Sonali Pechlivanis, Shih-Jen Hwang, Judy Wang, Lingyi Lu, Christopher J Nicholson, Georgia Shelton, Mary D Buswell, Hanna J Barnes, Haakon H Sigurslid, Ch

Reversal of Aging-Induced Increases in Aortic Stiffness by Targeting Cytoskeletal Protein-Protein Interfaces

通过靶向细胞骨架蛋白-蛋白质界面逆转衰老引起的主动脉僵硬性增加

Christopher J Nicholson, Kuldeep Singh, Robert J Saphirstein, Yuan Z Gao, Qian Li, Joanna G Chiu, Paul Leavis, Germaine C Verwoert, G F Mitchell; AortaGen Consortium; Tyrone Porter, Kathleen G Morgan

MicroRNA-203 mimics age-related aortic smooth muscle dysfunction of cytoskeletal pathways

MicroRNA-203 模拟与年龄相关的主动脉平滑肌细胞骨架通路功能障碍

Christopher J Nicholson, Francesca Seta, Sophie Lee, Kathleen G Morgan

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss.

DNMT1基因突变会导致遗传性感觉神经病,并伴有痴呆和听力丧失

Klein Christopher J, Botuyan Maria-Victoria, Wu Yanhong, Ward Christopher J, Nicholson Garth A, Hammans Simon, Hojo Kaori, Yamanishi Hiromitch, Karpf Adam R, Wallace Douglas C, Simon Mariella, Lander Cecilie, Boardman Lisa A, Cunningham Julie M, Smith Glenn E, Litchy William J, Boes Benjamin, Atkinson Elizabeth J, Middha Sumit, B Dyck P James, Parisi Joseph E, Mer Georges, Smith David I, Dyck Peter J