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

Enhancing cardiac serine biosynthesis mitigates the progression of dilated cardiomyopathy in mice

增强心脏丝氨酸生物合成可减轻小鼠扩张型心肌病的进展。

Kay, Maryam; Samuelsson, Anne-Maj; Bharucha, Nike; Li, Xueyi; Ramchandani, Rohin; Baum, Rachel E; Ruiz Arvizo, Diego; Laguerre, Aurélie; Lajevardi, Sherin; Kambhampati, Shrikaar; Metallo, Christian M; Kapiloff, Michael S; Karakikes, Ioannis

Connexin-43 Restoration Alleviates Desmosomal Arrhythmogenic Cardiomyopathy

连接蛋白-43的恢复可缓解桥粒性致心律失常性心肌病

Zhang, Jing; Zanella, Fabian; Ellis, Matthew W; Bradford, William H; Gutierrez-Lara, Erika Joana; Wang, Tsui-Min; Fujita, Kyohei; Duron, Charlize; Karakikes, Ioannis; Lyon, Robert C; Mezzano, Valeria; Roberts, Jason D; Carromeu, Cassiano; Gu, Yusu; Martin, Jody L; Muotri, Alysson R; Scheinman, Melvin M; Peterson, Kirk L; Sheikh, Farah

CRISPR-MiX: A pooled single-stranded donor strategy to enhance HDR efficiency in human iPSCs

CRISPR-MiX:一种用于提高人类iPSCs中HDR效率的单链供体混合策略

Baum, Rachel; Telugu, Narasimha; Bruyneel, Arne A N; Kay, Maryam; Nair, Pooja; Perea-Gil, Isaac; Termglinchan, Vittavat; Bharucha, Nike; Lee, Edina; Mercola, Mark; Diecke, Sebastian; Karakikes, Ioannis

Gastruloids enable modeling of the earliest stages of human cardiac and hepatic vascularization

原肠胚可以模拟人类心脏和肝脏血管化的早期阶段。

Abilez, Oscar J; Yang, Huaxiao; Guan, Yuan; Shen, Mengcheng; Yildirim, Zehra; Zhuge, Yan; Venkateshappa, Ravichandra; Zhao, Shane R; Gomez, Angello H; El-Mokahal, Marcel; Dunkenberger, Logan; Ono, Yoshikazu; Shibata, Masafumi; Nwokoye, Peter N; Tian, Lei; Wilson, Kitchener D; Lyall, Evan H; Jia, Fangjun; Wo, Hung Ta; Zhou, Gao; Aldana, Bryan; Karakikes, Ioannis; Obal, Detlef; Peltz, Gary; Zarins, Christopher K; Wu, Joseph C

Decoding human cardiovascular development and disease through single-cell transcriptomic and epigenomic profiling

通过单细胞转录组和表观基因组分析解码人类心血管发育和疾病

Dunkenberger, Logan; Li, Daniel Y; Karakikes, Ioannis; Quertermous, Thomas

Carboxypeptidase D deficiency causes hearing loss amenable to treatment

羧肽酶D缺乏症会导致听力损失,但这种损失可以通过治疗得到改善。

Memoona Ramzan ,Natalie Ortiz-Vega ,Mohammad Faraz Zafeer ,Amanda G Lobato ,Tahir Atik ,Clemer Abad ,Nirmal Vadgama ,Duygu Duman ,Nazım Bozan ,Enise Avcı Durmuşalioǧlu ,Sunny Greene ,Shengru Guo ,Suna Tokgöz-Yılmaz ,Merve Koç Yekedüz ,Fatma Tuba Eminoğlu ,Mehmet Aydın ,Serhat Seyhan ,Ioannis Karakikes ,Vladimir Camarena ,Maria Camila Robayo ,Tijana Canic ,Güney Bademci ,Gaofeng Wang ,Amjad Farooq ,Mei-Ling Joiner ,Katherina Walz ,Daniel F Eberl ,Jamal Nasir ,R Grace Zhai ,Mustafa Tekin

Light-evoked activity and BDNF regulate mitochondrial dynamics and mitochondrial localized translation in CNS axons

光诱发活动和脑源性神经营养因子(BDNF)调节中枢神经系统轴突中的线粒体动力学和线粒体局部翻译

Alexander Kreymerman ,Jessica E Weinstein ,Nirmal Vadgama ,Sahil H Shah ,Michael M Nahmou ,Kinsley C Belle ,Marco H Ji ,Xin Xia ,Anne Faust ,Yolandi Van Der Merwe ,David N Buickians ,In-Jae Cho ,Star K Huynh ,Sonya Verma ,Kristina Russano ,Xiao-Lu Jin ,Ioannis Karakikes ,Michael B Steketee ,Jeffrey L Goldberg

Correction: De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies

更正:遗传性心肌病中编码区和调控区的新生变异和遗传变异

Vadgama, Nirmal; Ameen, Mohamed; Sundaram, Laksshman; Gaddam, Sadhana; Gifford, Casey; Nasir, Jamal; Karakikes, Ioannis

Genetic analysis and multimodal imaging confirm m.12148 T > C mitochondrial variant pathogenicity leading to multisystem dysfunction

基因分析和多模态成像证实了线粒体变异 m.12148 T > C 的致病性,导致多系统功能障碍。

Kinsley Belle ,Alexander Kreymerman ,Jill L Young ,Nirmal Vadgama ,Marco H Ji ,Sandeep Randhawa ,Juan Caicedo ,Megan Wong ,Stephanie P Muscat ,Casey A Gifford ,Richard T Lee ,Jamal Nasir ,Gregory M Enns ,Ioannis Karakikes ,Andrew M Schaefer ,Robert W Taylor ,Mark Mercola ,Dwight Koeberl ,Edward H Wood

Generation of human induced pluripotent stem cell lines from patients with PHACE syndrome

从PHACE综合征患者中生成人类诱导多能干细胞系

Ramchandani, Rohin; Cheawsamoot, Chanatjit; Torres, Giovanni A; Arthur Ataam, Jennifer; Siegel, Dawn; Karakikes, Ioannis