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

Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifs

遗传与心血管代谢风险:人类神经肽Y(2)受体启动子中自然发生的多态性破坏多种转录反应基序

Wei, Zhiyun; Zhang, Kuixing; Wen, Gen; Balasubramanian, Karthika; Shih, Pei-an B; Rao, Fangwen; Friese, Ryan S; Miramontes-Gonzalez, Jose P; Schmid-Schoenbein, Geert W; Kim, Hyung-Suk; Mahata, Sushil K; O'Connor, Daniel T

MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension

遗传性高血压中Chga基因座的microRNA-22和启动子基序多态性:对基因表达和高血压发病机制的功能和治疗意义

Friese, Ryan S; Altshuler, Angelina E; Zhang, Kuixing; Miramontes-Gonzalez, Jose Pablo; Hightower, C Makena; Jirout, Martin L; Salem, Rany M; Gayen, Jiaur R; Mahapatra, Nitish R; Biswas, Nilima; Cale, Mo; Vaingankar, Sucheta M; Kim, Hyung-Suk; Courel, Maïté; Taupenot, Laurent; Ziegler, Michael G; Schork, Nicholas J; Pravenec, Michal; Mahata, Sushil K; Schmid-Schönbein, Geert W; O'Connor, Daniel T

Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressure

基因与环境:人类组织蛋白酶L (CTSL1) 启动子中的新型功能性多态性破坏异生物质反应元件 (XRE),从而改变转录和血压

Mbewe-Campbell, Nzali; Wei, Zhiyun; Zhang, Kuixing; Friese, Ryan S; Mahata, Manjula; Schork, Andrew J; Rao, Fangwen; Chiron, Stephane; Biswas, Nilima; Kim, Hyung-Suk; Mahata, Sushil K; Waalen, Jill; Nievergelt, Caroline M; Hook, Vivian Y; O'Connor, Daniel T

Catecholamine storage vesicles: role of core protein genetic polymorphisms in hypertension

儿茶酚胺储存囊泡:核心蛋白基因多态性在高血压中的作用

Zhang, Kuixing; Chen, Yuqing; Wen, Gen; Mahata, Manjula; Rao, Fangwen; Fung, Maple M; Vaingankar, Sucheta; Biswas, Nilima; Gayen, Jiaur R; Friese, Ryan S; Mahata, Sushil K; Hamilton, Bruce A; O'Connor, Daniel T

Naturally occurring genetic variants in human chromogranin A (CHGA) associated with hypertension as well as hypertensive renal disease

人类嗜铬粒蛋白A (CHGA) 的自然遗传变异与高血压以及高血压肾病相关。

Chen, Yuqing; Rao, Fangwen; Wen, Gen; Gayen, Jiaur R; Zhang, Kuixing; Vaingankar, Sucheta M; Biswas, Nilima; Mahata, Manjula; Friese, Ryan S; Fung, Maple M; Salem, Rany M; Nievergelt, Caroline; Bhatnagar, Vibha; Hook, Vivian Y; Ziegler, Michael G; Mahata, Sushil K; Hamilton, Bruce A; O'Connor, Daniel T

Urocortin 2 lowers blood pressure and reduces plasma catecholamine levels in mice with hyperadrenergic activity.

尿皮质素 2 可降低高肾上腺素能活性小鼠的血压并降低其血浆儿茶酚胺水平

Gu Yusu, Zhang Kuixing, Biswas Nilima, Friese Ryan S, Lin Dennis H, Mahata Sushil K, Hoshijima Masahiko, O'Connor Daniel T, Peterson Kirk L, Brar Bhawanjit K

Conserved regulatory motifs at phenylethanolamine N-methyltransferase (PNMT) are disrupted by common functional genetic variation: an integrated computational/experimental approach

苯乙醇胺N-甲基转移酶(PNMT)的保守调控基序会被常见的遗传功能变异破坏:一种整合计算/实验的方法

Rodríguez-Flores, Juan L; Zhang, Kuixing; Kang, Sun Woo; Wen, Gen; Ghosh, Sajalendu; Friese, Ryan S; Mahata, Sushil K; Subramaniam, Shankar; Hamilton, Bruce A; O'Connor, Daniel T

Global metabolic consequences of the chromogranin A-null model of hypertension: transcriptomic detection, pathway identification, and experimental verification

嗜铬粒蛋白A缺失型高血压模型的全球代谢后果:转录组学检测、通路鉴定和实验验证

Friese, Ryan S; Gayen, Jiaur R; Mahapatra, Nitish R; Schmid-Schönbein, Geert W; O'Connor, Daniel T; Mahata, Sushil K

Catecholamine storage vesicles and the metabolic syndrome: The role of the chromogranin A fragment pancreastatin

儿茶酚胺储存囊泡与代谢综合征:嗜铬粒蛋白A片段胰抑素的作用

Zhang, Kuixing; Rao, Fangwen; Wen, Gen; Salem, Rany M; Vaingankar, Sucheta; Mahata, Manjula; Mahapatra, Nitish R; Lillie, Elizabeth O; Cadman, Peter E; Friese, Ryan S; Hamilton, Bruce A; Hook, Vivian Y; Mahata, Sushil K; Taupenot, Laurent; O'Connor, Daniel T