Mutations in mitochondrial DNA associated with hypertension (Q84998195)

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13 February 2020

review article

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reason for deprecated rank

title

Mutations in mitochondrial DNA associated with hypertension (English)

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Crossref

DOI

https://api.crossref.org/works/10.3724/SP.J.1005.2011.00911

13 December 2024

Min-Xin Guan

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13 December 2024

Ling Xue

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13 February 2020

Hong Chen

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13 February 2020

Yan-Zi Meng

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13 February 2020

Yan Wang

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13 February 2020

Zhong-Qiu Lu

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13 February 2020

Jian-Xin Lu

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13 February 2020

language of work or name

Chinese

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National Center for Biotechnology Information

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13 December 2024

publication date

1 September 2011

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13 February 2020

September 2011

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21951790

full work available at URL

13 December 2024

http://www.chinagene.cn/CN/article/downloadArticleFile.do?attachType=PDF&id=2353

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13 December 2024

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13 February 2020

volume

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page(s)

911-918

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In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness

13 February 2020

cites work

1 reference

https://api.crossref.org/works/10.3724/SP.J.1005.2011.00911

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy

13 December 2024

1 reference

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Mitochondrial diseases in man and mouse

13 December 2024

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Human mitochondrial tRNAs in health and disease.

13 December 2024

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Diseases of the mitochondrial DNA.

13 December 2024

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Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease

13 December 2024

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A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathy.

13 December 2024

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Mitochondrial dysfunction in the hypertensive rat brain: respiratory complexes exhibit assembly defects in hypertension

13 December 2024

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Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation

13 December 2024

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Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness

13 December 2024

1 reference

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Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family

13 December 2024

1 reference

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Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population

13 December 2024

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Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.

13 December 2024

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Sequence and organization of the human mitochondrial genome

13 December 2024

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tRNA punctuation model of RNA processing in human mitochondria

13 December 2024

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A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

13 December 2024

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Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome

13 December 2024

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A Novel mtDNA Point Mutation in Maternally Inherited Cardiomyopathy

13 December 2024

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A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

13 December 2024

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Maternal inheritance of human mitochondrial DNA

13 December 2024

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RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme

13 December 2024

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A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

13 December 2024

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A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency

13 December 2024

1 reference

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Mitochondrial genome mutations in hypertensive individuals

13 December 2024

1 reference

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Sequence and organization of the human mitochondrial genome

13 December 2024

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A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations

13 December 2024

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Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G or A10044G mutation

13 December 2024

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Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

13 December 2024

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Compilation of tRNA sequences and sequences of tRNA genes

13 December 2024

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Mitochondrial defects in cardiomyopathy and neuromuscular disease

13 December 2024

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Actions of the anticodon arm in translation on the phenotypes of RNA mutants.

13 December 2024

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Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese family.

13 December 2024

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The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.

13 December 2024

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An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

13 December 2024

1 reference

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In vitro 3'-end endonucleolytic processing defect in a human mitochondrial tRNA(Ser(UCN)) precursor with the U7445C substitution, which causes non-syndromic deafness

13 December 2024

1 reference

https://api.crossref.org/works/10.3724/SP.J.1005.2011.00911

Mitochondrial mutation in fatal infantile cardiomyopathy

13 December 2024

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Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

13 December 2024

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Mitochondrial tRNA 3' end metabolism and human disease.

13 December 2024

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A novel combination of mitochondrial tRNA and ND1 gene mutations in a syndrome with MELAS, cardiomyopathy, and diabetes mellitus

13 December 2024

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Prevalence, awareness, treatment, and control of hypertension in china

13 December 2024

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Three modified nucleosides present in the anticodon stem and loop influence the in vivo aa-tRNA selection in a tRNA-dependent manner

13 December 2024

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A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy

13 December 2024

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Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree

13 December 2024

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Heteroplasmic mitochondrial DNA 3310 mutation in NADH dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation in a single patient

13 December 2024

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Mitochondrial DNA mutations and pathogenesis

13 December 2024

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Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

13 December 2024

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Hypermodified nucleosides in the anticodon of tRNALys stabilize a canonical U-turn structure

13 December 2024

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Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness

13 December 2024

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Possible role of mtDNA mutations in sudden infant death

13 December 2024

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Mitochondrial energy conversion disturbance with decrease in ATP production as a source of systemic arterial hypertension

13 December 2024

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Mitochondria and the heart

13 December 2024

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A case of cardiomyopathy showing progression from the hypertrophic to the dilated form: association of Mt8348A-->G mutation in the mitochondrial tRNA(Lys) gene with severe ultrastructural alterations of mitochondria in cardiomyocytes

13 December 2024

1 reference

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13 December 2024

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21951790%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

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