scholarly article | Q13442814 |
P50 | author | Min-Xin Guan | Q88150569 |
Ye Zhang | Q90429786 | ||
P2093 | author name string | Qiang Li | |
Yuqi Liu | |||
Meng Wang | |||
Zidong Jia | |||
Xiaohui Cang | |||
Changzhu Fu | |||
Zhenzhen Ye | |||
P2860 | cites work | Projections of global mortality and burden of disease from 2002 to 2030 | Q21144688 |
Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome | Q24546324 | ||
Human umbilical vein endothelial cells and human dermal microvascular endothelial cells offer new insights into the relationship between lipid metabolism and angiogenesis | Q26250150 | ||
UCSF Chimera--a visualization system for exploratory research and analysis | Q27860666 | ||
The Amber biomolecular simulation programs | Q27860745 | ||
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA | Q27860870 | ||
Understanding and preventing mitochondrial oxidative damage | Q28080331 | ||
Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data | Q28242645 | ||
Tissue-specific differences in human transfer RNA expression | Q28469081 | ||
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine | Q29547303 | ||
Mitochondria: in sickness and in health | Q29614825 | ||
ROS function in redox signaling and oxidative stress | Q29615229 | ||
tRNA punctuation model of RNA processing in human mitochondria | Q29616348 | ||
Apoptosis: controlled demolition at the cellular level | Q29620114 | ||
Physiological roles of mitochondrial reactive oxygen species | Q29620297 | ||
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression. | Q33780674 | ||
A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential. | Q33843127 | ||
A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis | Q33916058 | ||
Factors affecting wound healing | Q33993981 | ||
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families | Q34000668 | ||
Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree | Q34007628 | ||
Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family | Q34007647 | ||
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. | Q34551734 | ||
Mitochondrial-nuclear communications | Q34574082 | ||
The human mitochondrial transcriptome | Q35178219 | ||
Evaluation of chemiluminescence and flow cytometry as tools in assessing production of hydrogen peroxide and superoxide anion in human spermatozoa. | Q46423888 | ||
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. | Q46515103 | ||
Contribution of the tRNAIle 4317A>G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A>G mutation | Q47653533 | ||
Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T>C mutation altered the assembly and function of complex I, apoptosis and mitophagy. | Q51734734 | ||
A natural non-Watson-Crick base pair in human mitochondrial tRNAThr causes structural and functional susceptibility to local mutations. | Q52691120 | ||
Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family. | Q53257295 | ||
CO2-sensitive tRNA modification associated with human mitochondrial disease. | Q55332430 | ||
Genes, Environment, and Cardiovascular Disease | Q61829183 | ||
Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function. | Q64916501 | ||
Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family | Q80451072 | ||
T7 RNA polymerase transcription of Escherichia coli isoacceptors tRNA(Leu) | Q81826225 | ||
Pathogenesis of atherosclerosis | Q83187658 | ||
Mitochondrial genetics and human systemic hypertension | Q83759195 | ||
Mitochondrial diseases | Q83827338 | ||
Human mitochondrial tRNAs in health and disease. | Q35207430 | ||
MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention | Q35234097 | ||
Endothelial cell tube formation assay for the in vitro study of angiogenesis | Q35255024 | ||
The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree | Q35406187 | ||
An introduction to the wound healing assay using live-cell microscopy | Q35497608 | ||
A Matrigel-based tube formation assay to assess the vasculogenic activity of tumor cells | Q35591218 | ||
Cytochrome C-mediated apoptosis | Q35799945 | ||
The intersection between aging and cardiovascular disease | Q36006533 | ||
Mitochondrial dysfunction in cardiovascular disease | Q36108165 | ||
Mitochondrial reactive oxygen species-mediated signaling in endothelial cells | Q36712703 | ||
Endothelial mitochondria: contributing to vascular function and disease | Q36803365 | ||
A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. | Q37073167 | ||
Coronary heart disease is associated with a mutation in mitochondrial tRNA. | Q37193896 | ||
An integrated, structure- and energy-based view of the genetic code | Q37294856 | ||
A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial function. | Q37507554 | ||
Mitochondrial tRNA variants in Chinese subjects with coronary heart disease | Q37648407 | ||
Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases | Q37930666 | ||
Mitochondria and heart disease | Q37991639 | ||
Mitochondria in vascular health and disease | Q38060230 | ||
Mitochondrial cytopathies and cardiovascular disease | Q38180688 | ||
Mitochondrial disease associated with complex I (NADH-CoQ oxidoreductase) deficiency | Q38249965 | ||
Mitochondria: a pathogenic paradigm in hypertensive renal disease | Q38268844 | ||
Oxidative stress in inherited mitochondrial diseases | Q38527423 | ||
A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. | Q38752245 | ||
The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation | Q38813517 | ||
Genetics and Genomics of Coronary Artery Disease | Q38944185 | ||
Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart | Q39017553 | ||
Universal rules and idiosyncratic features in tRNA identity | Q39725604 | ||
A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR). | Q40146692 | ||
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 | Q40386722 | ||
A novel system for assigning the mode of inheritance in mitochondrial disorders using cybrids and rhodamine 6G. | Q40936504 | ||
Analysis of aminoacylation of human mitochondrial tRNAs | Q41244333 | ||
Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells | Q41253074 | ||
Mitochondrial membrane potential monitored by JC-1 dye. | Q41386010 | ||
Assessing bioenergetic function in response to oxidative stress by metabolic profiling | Q41816998 | ||
Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells | Q44797361 | ||
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination | Q46099938 | ||
A hypertension-associated mitochondrial DNA mutation introduces an m1G37 modification into tRNAMet, altering its structure and function | Q46244954 | ||
Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension | Q46274125 | ||
Mitochondria and Angiogenesis | Q46359827 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 4 | |
P921 | main subject | angiogenesis | Q539568 |
P304 | page(s) | 2056-2074 | |
P577 | publication date | 2019-02-01 | |
P1433 | published in | Nucleic Acids Research | Q135122 |
P1476 | title | A coronary artery disease-associated tRNAThr mutation altered mitochondrial function, apoptosis and angiogenesis | |
P478 | volume | 47 |
Q96303204 | Cellular Mechanisms of Human Atherogenesis: Focus on Chronification of Inflammation and Mitochondrial Mutations |
Q92647056 | Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism |
Q90029316 | Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript |
Q89824003 | Maternally Inherited Diabetes Mellitus Associated with a Novel m.15897G>A Mutation in Mitochondrial tRNAThr Gene |
Q92015808 | Maternally inherited coronary heart disease is associated with a novel mitochondrial tRNA mutation |
Q92198280 | Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family |
Q89463179 | Reply to comments on: "Obesity associated with a novel mitochondrial tRNACys 5802A>G mutation in a Chinese family" |
Search more.