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A connection between the ribosome and two S. pombe tRNA modification mutants subject to rapid tRNA decay
De Zoysa, Thareendra, Hauke, Alayna C., Iyer, Nivedita R., Marcus, Erin, Ostrowski, Sarah M., Stegemann, Franziska, Ermolenko, Dmitri N., Fay, Justin C., Phizicky, Eric M.
Published in PLoS genetics (31.01.2024)
Published in PLoS genetics (31.01.2024)
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Direct sequencing of total Saccharomyces cerevisiae tRNAs by LC–MS/MS
Jones, Joshua D, Simcox, Kaley M, Kennedy, Robert T, Koutmou, Kristin S
Published in RNA (Cambridge) (01.08.2023)
Published in RNA (Cambridge) (01.08.2023)
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The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss
Han, Dongyi, Dai, Pu, Zhu, Qingwen, Liu, Xin, Huang, Deliang, Yuan, Yongyi, Yuan, Huijun, Wang, Xinjian, Qian, Yaping, Young, Wie-Yen, Guan, Min-Xin
Published in Biochemical and biophysical research communications (01.06.2007)
Published in Biochemical and biophysical research communications (01.06.2007)
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Metabolic rewiring during bone development underlies tRNA m7G–associated primordial dwarfism
Li, Qiwen, Jiang, Shuang, Lei, Kexin, Han, Hui, Chen, Yaqian, Lin, Weimin, Xiong, Qiuchan, Qi, Xingying, Gan, Xinyan, Sheng, Rui, Wang, Yuan, Zhang, Yarong, Ma, Jieyi, Li, Tao, Lin, Shuibin, Zhou, Chenchen, Chen, Demeng, Yuan, Quan
Published in The Journal of clinical investigation (10.09.2024)
Published in The Journal of clinical investigation (10.09.2024)
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POS0807 A TRANSCRIPTIONAL PROFILE OF FATIGUE IN PRECLINICAL AUTOIMMUNITY WHICH IS PRESERVED IN SLE AND SJOGREN'S SYNDROME
Carter, L.M., MD Yusof, M.Y., Plant, D., Bauer, J., Wenlock, S., Alase, A., Psarras, A., Wigston, Z., Vital, E.
Published in Annals of the rheumatic diseases (01.06.2023)
Published in Annals of the rheumatic diseases (01.06.2023)
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Aminoglycoside tolerance in Vibrio cholerae engages translational reprogramming associated with queuosine tRNA modification
Fruchard, Louna, Babosan, Anamaria, Carvalho, Andre, Lang, Manon, Li, Blaise, Duchateau, Magalie, Giai Gianetto, Quentin, Matondo, Mariette, Bonhomme, Frederic, Hatin, Isabelle, Arbes, Hugo, Fabret, Céline, Corler, Enora, Sanchez, Guillaume, Marchand, Virginie, Motorin, Yuri, Namy, Olivier, de Crécy-Lagard, Valérie, Mazel, Didier, Baharoglu, Zeynep
Published in eLife (06.01.2025)
Published in eLife (06.01.2025)
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Lost in Translation: Defects in Transfer RNA Modifications and Neurological Disorders
Bednářová, Andrea, Hanna, Marley, Durham, Isabella, VanCleave, Tara, England, Alexis, Chaudhuri, Anathbandhu, Krishnan, Natraj
Published in Frontiers in molecular neuroscience (09.05.2017)
Published in Frontiers in molecular neuroscience (09.05.2017)
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Metabolomics and Lipidomics Studies in Pediatric Type 1 Diabetes: Biomarker Discovery for the Early Diagnosis and Prognosis
Liu, Yaru, Dong, Guanping, Huang, Ke, Hong, Ye, Chen, Xuefeng, Zhu, Mingqiang, Hao, Xiaoqiang, Ni, Yan, Fu, Junfen
Published in Pediatric diabetes (2023)
Published in Pediatric diabetes (2023)
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tRNA and tsRNA: From Heterogeneity to Multifaceted Regulators
Li, Yun, Yu, Zongyu, Jiang, Wenlin, Lyu, Xinyi, Guo, Ailian, Sun, Xiaorui, Yang, Yiting, Zhang, Yunfang
Published in Biomolecules (Basel, Switzerland) (01.10.2024)
Published in Biomolecules (Basel, Switzerland) (01.10.2024)
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Aminoglycoside tolerance in Vibrio cholerae engages translational reprogramming associated to queuosine tRNA modification
Fruchard, Louna, Babosan, Anamaria, Carvalho, Andre, Lang, Manon, Li, Blaise, Duchateau, Magalie, Gianetto, Quentin Giai, Matondo, Mariette, Bonhomme, Frederic, Hatin, Isabelle, Arbes, Hugo, Fabret, Celine, Sanchez, Guillaume, Marchand, Virginie, Motorine, Yuri, Namy, Olivier, Valerie De Crecy-Lagard, Mazel, Didier, Baharoglu, Zeynep
Published in bioRxiv (08.02.2024)
Published in bioRxiv (08.02.2024)
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Mechanistic insights into mitochondrial tRNAAla 3’-end metabolism deficiency
Ji, Yanchun, Nie, Zhipeng, Meng, Feilong, Hu, Cuifang, Chen, Hui, Jin, Lihao, Chen, Mengquan, Zhang, Minglian, Zhang, Juanjuan, Liang, Min, Wang, Meng, Guan, Min-Xin
Published in The Journal of biological chemistry (01.07.2021)
Published in The Journal of biological chemistry (01.07.2021)
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Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension
Xue, Ling, Wang, Meng, Li, Haiying, Wang, Heng, Jiang, Feng, Hou, Lingling, Geng, Junwei, Lin, Zhi, Peng, Yanyan, Zhou, Hong, Yu, Han, Jiang, Pingping, Mo, Jun Qin, Guan, Min-Xin
Published in Mitochondrion (01.09.2016)
Published in Mitochondrion (01.09.2016)
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Mitochondrial tRNA mutations in Chinese hypertensive individuals
Liu, Yuqi, Li, Yang, Wang, Xin, Ma, Qinha, Zhu, Chao, Li, Zongbin, Yin, Tong, Yang, Jie, Chen, Yundai, Guan, Minxin
Published in Mitochondrion (01.05.2016)
Published in Mitochondrion (01.05.2016)
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Screening of mitochondrial tRNA mutations in 300 infants with hearing loss
Tang, Kai, Gao, Ziying, Han, Chunling, Zhao, Suolin, Du, Xiaoyun, Wang, Wenjuan
Published in Mitochondrial DNA. Part A. DNA mapping, sequencing, and analysis (17.02.2019)
Published in Mitochondrial DNA. Part A. DNA mapping, sequencing, and analysis (17.02.2019)
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Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutation
Zhu, Yuhua, Li, Qi, Chen, Zhengyi, Kun, Yao, Liu, Lijia, Liu, Xin, Yuan, Huijun, Zhai, Suoqiang, Han, Dongyi, Dai, Pu
Published in Mitochondrion (01.11.2009)
Published in Mitochondrion (01.11.2009)
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Mutational analysis of mitochondrial tRNA genes in patients with lung cancer
He, ZF, Zheng, LC, Xie, DY, Yu, SS, Zhao, J
Published in Balkan journal of medical genetics (01.12.2016)
Published in Balkan journal of medical genetics (01.12.2016)
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