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

Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder

TRMT1基因的双等位致病变异会破坏tRNA修饰并诱发神经发育障碍。

Efthymiou, Stephanie; Leo, Cailyn P; Deng, Chenghong; Lin, Sheng-Jia; Maroofian, Reza; Lin, Renee; Karagoz, Irem; Zhang, Kejia; Kaiyrzhanov, Rauan; Scardamaglia, Annarita; Owrang, Daniel; Turchetti, Valentina; Jahnke, Friederike; Huang, Kevin; Petree, Cassidy; Derrick, Anna V; Rees, Mark I; Alvi, Javeria Raza; Sultan, Tipu; Li, Chumei; Jacquemont, Marie-Line; Tran-Mau-Them, Frederic; Valenzuela-Palafoll, Maria; Sidlow, Rich; Yoon, Grace; Morrow, Michelle M; Carere, Deanna Alexis; O'Connor, Mary; Fleischer, Julie; Gerkes, Erica H; Phornphutkul, Chanika; Isidor, Bertrand; Rivier-Ringenbach, Clotilde; Philippe, Christophe; Kurul, Semra Hiz; Soydemir, Didem; Kara, Bulent; Sunnetci-Akkoyunlu, Deniz; Bothe, Viktoria; Platzer, Konrad; Wieczorek, Dagmar; Koch-Hogrebe, Margarete; Rahner, Nils; Thuresson, Ann-Charlotte; Matsson, Hans; Frykholm, Carina; Bozdoğan, Sevcan Tuğ; Bisgin, Atil; Chatron, Nicolas; Lesca, Gaetan; Cabet, Sara; Tümer, Zeynep; Hjortshøj, Tina D; Rønde, Gitte; Marquardt, Thorsten; Reunert, Janine; Afzal, Erum; Zamani, Mina; Azizimalamiri, Reza; Galehdari, Hamid; Nourbakhsh, Pardis; Chamanrou, Niloofar; Chung, Seo-Kyung; Suri, Mohnish; Benke, Paul J; Zaki, Maha S; Gleeson, Joseph G; Calame, Daniel G; Pehlivan, Davut; Yilmaz, Halil I; Gezdirici, Alper; Rad, Aboulfazl; Abumansour, Iman Sabri; Oprea, Gabriela; Bereketoğlu, Muhammed Burak; Banneau, Guillaume; Julia, Sophie; Zeighami, Jawaher; Ashoori, Saeed; Shariati, Gholamreza; Sedaghat, Alireza; Sabri, Alihossein; Hamid, Mohammad; Parvas, Sahere; Tajudin, Tajul Arifin; Abdullah, Uzma; Baig, Shahid Mahmood; Chung, Wendy K; Glazunova, Olga O; Sabine, Sigaudy; Cheema, Huma Arshad; Zifarelli, Giovanni; Bauer, Peter; Sidpra, Jai; Mankad, Kshitij; Vona, Barbara; Fry, Andrew E; Varshney, Gaurav K; Houlden, Henry; Fu, Dragony

Human TRMT1 and TRMT1L paralogs ensure the proper modification state, stability, and function of tRNAs.

人类 TRMT1 和 TRMT1L 旁系同源物确保 tRNA 的正确修饰状态、稳定性和功能

Zhang Kejia, Manning Aidan C, Lentini Jenna M, Howard Jonathan, Dalwigk Felix, Maroofian Reza, Efthymiou Stephanie, Chan Patricia, Eliseev Sergei I, Yang Zi, Chang Hayley, Karimiani Ehsan Ghayoor, Bakhshoodeh Behnoosh, Houlden Henry, Kaiser Stefanie M, Lowe Todd M, Fu Dragony

Epileptic encephalopathy linked to a DALRD3 missense variant that impairs tRNA modification

与DALRD3错义变异相关的癫痫性脑病,该变异会损害tRNA修饰

Zhang, Kejia; Löhner, Katharina; Lemmink, Henny H; Boon, Maartje; Lentini, Jenna M; de Silva, Naduni; Fu, Dragony

tRNA modification enzyme-dependent redox homeostasis regulates synapse formation and memory

tRNA修饰酶依赖的氧化还原稳态调节突触形成和记忆

Madhwani, Kimberly R; Sayied, Shanzeh; Ogata, Carlson H; Hogan, Caley A; Lentini, Jenna M; Mallik, Moushami; Dumouchel, Jennifer L; Storkebaum, Erik; Fu, Dragony; O'Connor-Giles, Kate M

Proteolytic cleavage and inactivation of the TRMT1 tRNA modification enzyme by SARS-CoV-2 main protease

SARS-CoV-2 主蛋白酶对 TRMT1 tRNA 修饰酶进行蛋白水解和失活

Kejia Zhang, Patrick Eldin, Jessica H Ciesla, Laurence Briant, Jenna M Lentini, Jillian Ramos, Justin Cobb, Joshua Munger, Dragony Fu

Structural impact of 3-methylcytosine modification on the anticodon stem of a neuronally-enriched arginine tRNA

3-甲基胞嘧啶修饰对神经元富集精氨酸tRNA反密码子茎的结构影响

Berger, Kyle D; Puthenpeedikakkal, Anees M K; Mathews, David H; Fu, Dragony

Proteolytic cleavage and inactivation of the TRMT1 tRNA modification enzyme by SARS-CoV-2 main protease

SARS-CoV-2 主蛋白酶对 TRMT1 tRNA 修饰酶进行蛋白水解和失活

Kejia Zhang, Patrick Eldin, Jessica H Ciesla, Laurence Briant, Jenna M Lentini, Jillian Ramos, Justin Cobb, Joshua Munger, Dragony Fu

Expanded tRNA methyltransferase family member TRMT9B regulates synaptic growth and function

扩增的 tRNA 甲基转移酶家族成员 TRMT9B 调节突触生长和功能

Caley A Hogan #, Scott J Gratz #, Jennifer L Dumouchel #, Rajan S Thakur, Ambar Delgado, Jenna M Lentini, Kimberly R Madhwani, Dragony Fu, Kate M O'Connor-Giles

ADATscan - A flexible tool for scanning exomes for wobble inosine-dependent codons reveals a neurological bias for genes enriched in such codons in humans and mice

ADATscan——一种用于扫描外显子组中摆动肌苷依赖性密码子的灵活工具,揭示了人类和小鼠中富含此类密码子的基因存在神经系统偏好。

Longan, Emery R; Ramos, Jillian; Fu, Dragony

tRNA modification enzyme-dependent redox homeostasis regulates synapse formation and memory

tRNA修饰酶依赖的氧化还原稳态调节突触形成和记忆

Kimberly R Madhwani, Shanzeh Sayied, Carlson H Ogata, Caley A Hogan, Jenna M Lentini, Moushami Mallik, Jennifer L Dumouchel, Erik Storkebaum, Dragony Fu, Kate M O'Connor-Giles