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Journal of the American Chemical Society
|
February 10, 2012
Conformational transition and energy landscape of ErbB4 activated by neuregulin1β: one microsecond molecular dynamics simulations
Yun Du, Huaiyu Yang, Yechun Xu, et al.
Iscience
|
August 21, 2023
Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1
Lingxiao Tong, Jia Rao, Chenxi Yang, et al.
The Journal of Biological Chemistry
|
December 11, 2019
Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA<sup>His</sup> mutation
Shasha Gong, Xiaoqiong Wang, Feilong Meng, et al.
The Journal of Biological Chemistry
|
January 5, 2017
Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation
Feilong Meng, Xiaohui Cang, Yanyan Peng, et al.
Nucleic Acids Research
|
January 5, 2021
A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation
Feilong Meng, Mi Zhou, Yun Xiao, et al.
Frontiers in Cell and Developmental Biology
|
January 23, 2026
XPNPEP2 regulates angiogenesis via modulation of mitochondrial function through SLC25A6
Chenxi Yang, Yijun Lu, Yu Xia, et al.
The Journal of Biological Chemistry
|
November 6, 2019
Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNA<sup>Ser(UCN)</sup> 7511A>G mutation
Wenlu Fan, Jing Zheng, Wanzhong Kong, et al.
Frontiers in Cell and Developmental Biology
|
January 27, 2023
Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China
Fan Tong, Yuchen Zhang, Chi Chen, et al.
Iscience
|
October 27, 2022
A novel NF2 splicing mutant causes neurofibromatosis type 2 via liquid-liquid phase separation with large tumor suppressor and Hippo pathway
Zexiao Jia, Shuxu Yang, Mengyao Li, et al.
JCI Insight
|
April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia
Chengxian Xu, Lingxiao Tong, Jia Rao, et al.
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Search research articles
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Journal of the American Chemical Society
|
February 10, 2012
Conformational transition and energy landscape of ErbB4 activated by neuregulin1β: one microsecond molecular dynamics simulations
Yun Du, Huaiyu Yang, Yechun Xu, et al.
Iscience
|
August 21, 2023
Mutational burden of XPNPEP3 leads to defects in mitochondrial complex I and cilia in NPHPL1
Lingxiao Tong, Jia Rao, Chenxi Yang, et al.
The Journal of Biological Chemistry
|
December 11, 2019
Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA<sup>His</sup> mutation
Shasha Gong, Xiaoqiong Wang, Feilong Meng, et al.
The Journal of Biological Chemistry
|
January 5, 2017
Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation
Feilong Meng, Xiaohui Cang, Yanyan Peng, et al.
Nucleic Acids Research
|
January 5, 2021
A deafness-associated tRNA mutation caused pleiotropic effects on the m1G37 modification, processing, stability and aminoacylation of tRNAIle and mitochondrial translation
Feilong Meng, Mi Zhou, Yun Xiao, et al.
Frontiers in Cell and Developmental Biology
|
January 23, 2026
XPNPEP2 regulates angiogenesis via modulation of mitochondrial function through SLC25A6
Chenxi Yang, Yijun Lu, Yu Xia, et al.
The Journal of Biological Chemistry
|
November 6, 2019
Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNA<sup>Ser(UCN)</sup> 7511A>G mutation
Wenlu Fan, Jing Zheng, Wanzhong Kong, et al.
Frontiers in Cell and Developmental Biology
|
January 27, 2023
Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China
Fan Tong, Yuchen Zhang, Chi Chen, et al.
Iscience
|
October 27, 2022
A novel NF2 splicing mutant causes neurofibromatosis type 2 via liquid-liquid phase separation with large tumor suppressor and Hippo pathway
Zexiao Jia, Shuxu Yang, Mengyao Li, et al.
JCI Insight
|
April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemia
Chengxian Xu, Lingxiao Tong, Jia Rao, et al.
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of 4