Bilaketaren emaitzak - Tan, Tuantuan

RETRACTED ARTICLE: Human Umbilical Cord Mesenchymal Stem Cells-Derived Exosomal MicroRNA-18b-3p Inhibits the Occurrence of Preeclampsia by Targeting LEP nork Huang, Qin, Gong, Meng, Tan, Tuantuan, Lin, Yunong, Bao, Yan, Fan, Cuifang

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Transthoracic ultrasound-guided percutaneous intramyocardial injection combined with ultrasound-targeted microbubble destruction-mediated angiogenin 1 gene therapy in canine myocar... nork Cao, Sheng, Deng, Qing, Tan, Tuantuan, Zhou, Yanxiang, Wang, Yijia, Zhou, Qing

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Enhancement of Angiogenesis by Ultrasound-Targeted Microbubble Destruction Combined with Nuclear Localization Signaling Peptides in Canine Myocardial Infarction nork Cui, Jingjing, Deng, Qing, Zhou, Qing, Cao, Sheng, Jiang, Nan, Wang, Yijia, Chen, Jinling, Hu, Bo, Tan, Tuantuan

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Cardiospecific CD36 suppression by lentivirus-mediated RNA interference prevents cardiac hypertrophy and systolic dysfunction in high-fat-diet induced obese mice nork Zhang, Yijie, Bao, Mingwei, Dai, Mingyan, Wang, Xin, He, Wenbo, Tan, Tuantuan, Lin, Dandan, Wang, Wei, Wen, Ying, Zhang, Rui

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Evaluating the morphology of the left atrial appendage by a transesophageal echocardiographic 3-dimensional printed model nork Song, Hongning, Zhou, Qing, Zhang, Lan, Deng, Qing, Wang, Yijia, Hu, Bo, Tan, Tuantuan, Chen, Jinling, Pan, Yiteng, He, Fazhi

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Mitochondrial Respiration Defects in Single-Ventricle Congenital Heart Disease nork Xu, Xinxiu, Lin, Jiuann-Huey Ivy, Bais, Abha S., Reynolds, Michael John, Tan, Tuantuan, Gabriel, George C., Kondos, Zoie, Liu, Xiaoqin, Shiva, Sruti S., Lo, Cecilia W.

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Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability nork Teekakirikul, Polakit, Zhu, Wenjuan, Xu, Xinxiu, Young, Cullen B., Tan, Tuantuan, Smith, Amanda M., Wang, Chengdong, Peterson, Kevin A., Gabriel, George C., Ho, Sebastian, Sheng, Yi, Moreau de Bellaing, Anne, Sonnenberg, Daniel A., Lin, Jiuann-huey, Fotiou, Elisavet, Tenin, Gennadiy, Wang, Michael X., Wu, Yijen L., Feinstein, Timothy, Devine, William, Gou, Honglan, Bais, Abha S., Glennon, Benjamin J., Zahid, Maliha, Wong, Timothy C., Ahmad, Ferhaan, Rynkiewicz, Michael J., Lehman, William J., Keavney, Bernard, Alastalo, Tero-Pekka, Freckmann, Mary-Louise, Orwig, Kyle, Murray, Steve, Ware, Stephanie M., Zhao, Hui, Feingold, Brian, Lo, Cecilia W.

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Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease nork Teekakirikul, Polakit, Zhu, Wenjuan, Gabriel, George C., Young, Cullen B., Williams, Kylia, Martin, Lisa J., Hill, Jennifer C., Richards, Tara, Billaud, Marie, Phillippi, Julie A., Wang, Jianbin, Wu, Yijen, Tan, Tuantuan, Devine, William, Lin, Jiuann-huey, Bais, Abha S., Klonowski, Jonathan, de Bellaing, Anne Moreau, Saini, Ankur, Wang, Michael X., Emerel, Leonid, Salamacha, Nathan, Wyman, Samuel K., Lee, Carrie, Li, Hung Sing, Miron, Anastasia, Zhang, Jingyu, Xing, Jianhua, McNamara, Dennis M., Fung, Erik, Kirshbom, Paul, Mahle, William, Kochilas, Lazaros K., He, Yihua, Garg, Vidu, White, Peter, McBride, Kim L., Benson, D. Woodrow, Gleason, Thomas G., Mital, Seema, Lo, Cecilia W.

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