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

Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies

利用遗传性心肌病中共同的和相反的遗传机制

Kramarenko, Daria R; Haydarlou, Poeya; Powell, George J; Rämö, Joel T; Janan, Riyad; Prince, Claire; Zimmerman, Dominic S; Theotokis, Pantazis; Thami, Prisca K; Haas, Jan; Garnier, Sophie; Rühle, Frank; Poel, Edwin; Schmidt, Amand F; Day, Sharlene; Helms, Adam; Lampert, Rachel; Parikh, Victoria; Ingles, Jodie; Olivotto, Iacopo; Lakdawala, Neal; Owens, Anjali; Saberi, Sara; Stendhal, John; Ashley, Euan; Gray, Belinda; Russell, Mark W; Ryan, Thomas D; Rossano, Joseph W; Abrams, Dominic; Miller, Erin; Lin, Kimberly; Maurizi, Niccolo; Argiro, Alessia; Berry, Colin; Cooper, Rob; Flett, Andrew S; Gardner, Roy S; Greenwood, John P; Halliday, Brian P; Hutchings, David; Mahmod, Masliza; McCann, Gerry P; Page, Stephen P; Peebles, Charles; Raman, Betty; Swoboda, Peter; Varnava, Amanda; Wright, David; Prasad, Sanjay; Cook, Stuart; Tayal, Upsala Paz; Buchan, Rachel; Walsh, Roddy; Wilde, Arthur A M; Meder, Benjamin; Charron, Philippe; Goel, Anuj; Amin, Ahmad S; Ellinor, Patrick T; Aragam, Krishna G; Tadros, Rafik; Pinto, Yigal M; Ho, Carolyn Y; Watkins, Hugh; Ware, James S; Bezzina, Connie R; Jurgens, Sean J

Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results.

对来自奥克尼和设得兰群岛创始人群的 4,198 名苏格兰参与者进行了可操作的基因变异分析,并实施了结果反馈机制

Kerr Shona M, Klaric Lucija, Muckian Marisa D, Johnston Kiera, Drake Camilla, Halachev Mihail, Cowan Emma, Snadden Lesley, Dean John, Zheng Sean L, Thami Prisca K, Ware James S, Tzoneva Gannie, Shuldiner Alan R, Miedzybrodzka Zosia, Wilson James F

Unsupervised feature extraction using deep learning empowers discovery of genetic determinants of the electrocardiogram

利用深度学习进行无监督特征提取,有助于发现心电图的遗传决定因素。

Sieliwonczyk, Ewa; Sau, Arunashis; Patlatzoglou, Konstantinos; McGurk, Kathryn A; Pastika, Libor; Thami, Prisca K; Mangino, Massimo; Zheng, Sean L; Powell, George; Curran, Lara; Buchan, Rachel J; Theotokis, Pantazis; Peters, Nicholas S; Loeys, Bart; Kramer, Daniel B; Waks, Jonathan W; Ng, Fu Siong; Ware, James S

Transcriptomic Signatures of Progression to Tuberculosis Disease Among Close Contacts in Brazil

巴西密切接触者结核病进展的转录组特征

Mendelsohn, Simon C; Andrade, Bruno B; Mbandi, Stanley Kimbung; Andrade, Alice M S; Muwanga, Vanessa M; Figueiredo, Marina C; Erasmus, Mzwandile; Rolla, Valeria C; Thami, Prisca K; Cordeiro-Santos, Marcelo; Penn-Nicholson, Adam; Kritski, Afranio L; Hatherill, Mark; Sterling, Timothy R; Scriba, Thomas J

Defining the Functional Influence of Endothelial Cell-Expressed Oncogenic Activating Mutations on Vascular Morphogenesis and Capillary Assembly.

明确内皮细胞表达的致癌激活突变对血管形态发生和毛细血管组装的功能影响

Lin Prisca K, Sun Zheying, Davis George E

Extracellular Matrix Remodeling in Vascular Disease: Defining Its Regulators and Pathological Influence

血管疾病中的细胞外基质重塑:阐明其调控因子和病理影响

Lin, Prisca K; Davis, George E

Elucidating the Morphogenic and Signaling Roles of Defined Growth Factors Controlling Human Endothelial Cell Lumen Formation Versus Sprouting Behavior

阐明特定生长因子在控制人内皮细胞管腔形成与出芽行为中的形态发生和信号传导作用

Prisca K Lin ,Gretchen M Koller ,George E Davis

Increased Matrix Metalloproteinase-1 Activation Enhances Disruption and Regression of k-RasV12-Expressing Arteriovenous Malformation-Like Vessels

基质金属蛋白酶-1 活性增加会增强 k-RasV12 表达动静脉畸形样血管的破坏和退化

Zheying Sun, Prisca K Lin, Ksenia Yrigoin, Scott S Kemp, George E Davis

Whole genome sequencing reveals population diversity and variation in HIV-1 specific host genes

全基因组测序揭示了HIV-1特异性宿主基因的群体多样性和变异性

Thami, Prisca K; Choga, Wonderful T; Dandara, Collet; O'Brien, Stephen J; Essex, Myron; Gaseitsiwe, Simani; Chimusa, Emile R

Endothelial k-RasV12 Expression Induces Capillary Deficiency Attributable to Marked Tube Network Expansion Coupled to Reduced Pericytes and Basement Membranes

内皮细胞 k-RasV12 表达诱导毛细血管缺陷,其原因是管状网络显著扩张,同时伴有周细胞和基底膜减少。

Sun, Zheying; Kemp, Scott S; Lin, Prisca K; Aguera, Kalia N; Davis, George E