相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Molecular characterization of two Chinese pedigrees with maternally inherited hypertension
Yu Ding et al.
JOURNAL OF GENE MEDICINE (2021)
The expanding world of tRNA modifications and their disease relevance
Tsutomu Suzuki
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2021)
Posttranscriptional modifications in mitochondria! tRNA and its implication in mitochondria! translation and disease
Tomizawa Kazuhito et al.
JOURNAL OF BIOCHEMISTRY (2020)
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function
Mi Zhou et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2018)
Synthesis and Multiple Incorporations of 2-O-Methyl-5-hydroxymethylcytidine, 5-Hydroxymethylcytidine and 5-Formylcytidine Monomers into RNA Oligonucleotides
Arun A. Tanpure et al.
CHEMBIOCHEM (2017)
Synthesis of RNA Containing 5-Hydroxymethyl-, 5-Formyl-, and 5-Carboxycytidine
Iacovos N. Michaelides et al.
CHEMISTRY-A EUROPEAN JOURNAL (2017)
Trm5 and TrmD: Two Enzymes from Distinct Origins Catalyze the Identical tRNA Modification, m1G37
Sakurako Goto-Ito et al.
BIOMOLECULES (2017)
NSUN3 methylase initiates 5-formylcytidine biogenesis in human mitochondrial tRNAMet
Saori Nakano et al.
NATURE CHEMICAL BIOLOGY (2016)
Expanded use of sense codons is regulated by modified cytidines in tRNA
William A. Cantara et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Stability of single-nucleotide bulge loops embedded in a GAAA RNA hairpin stem
Geoffrey F. S. Lim et al.
RNA (2012)
Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
Tsutomu Suzuki et al.
ANNUAL REVIEW OF GENETICS, VOL 45 (2011)
The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree
Zhongqiu Lu et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
The Human Mitochondrial tRNAMet: Structure/Function Relationship of a Unique Modification in the Decoding of Unconventional Codons
Yann Bilbille et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
Mitochondrial Transfer RNAMet 4435A>G Mutation Is Associated With Maternally Inherited Hypertension in a Chinese Pedigree
Yuqi Liu et al.
HYPERTENSION (2009)
Unconventional decoding of the AUA codon as methionine by mitochondrial tRNAMet with the anticodon f5CAU as revealed with a mitochondrial in vitro translation system
Chie Takemoto et al.
NUCLEIC ACIDS RESEARCH (2009)
Synthesis and investigation of the 5-formylcytidine modified, anticodon stem and loop of the human mitochondrial tRNAMet
Hrvoje Lusic et al.
NUCLEIC ACIDS RESEARCH (2008)
The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation
J Qu et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2006)
Mitochondrial genome polymorphisms associated with type-2 diabetes or obesity
LJ Guo et al.
MITOCHONDRION (2005)
An efficient preparation of protected ribonucleosides for phosphoramidite RNA synthesis
V Serebryany et al.
TETRAHEDRON LETTERS (2002)
Synthesis and properties of oligonucleotides containing 5-formyl-2′-deoxycytidine:: in vitro DNA polymerase reactions on DNA templates containing 5-formyl-2′-deoxycytidine
N Karino et al.
NUCLEIC ACIDS RESEARCH (2001)