Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population.

Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis - 1 Sept 2016

Meng Xing, Pei Hui, Lan Chao

Abstract excerpt

We reported here the possible role of a mitochondrial tRNA mutation: T4353C in clinical expression of essential hypertension in Chinese population. The human mammalian mitochondrial tRNA database was used to analyze the conservation index of this mutation between different species. Moreover, phylogenetic analysis showed that the T4353C mutation belonged to human mitochondrial haplogroup HV, a West Eurasian...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Asian People
Share to China
Share to Essential Hypertension

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Mitochondrial

Share to Hypertension

Share to Maternal Inheritance

Share to RNA, Transfer

Share to RNA, Transfer, Gln

Source

Identifiers

PMID: 25693701
DOI: 10.3109/19401736.2015.1018199

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The mitochondrial tRNA(Gln) T4353C mutation may not be associated with essential hypertension in Han Chinese population.PMID 25693701Read ↗

The mitochondrial tRNA(Met) 4454T > C variant may not be associated with essential hypertension in Han Chinese population.Semantic proximity Read ↗

Molecular characterization of a pedigree carrying the hypertension‑associated mitochondrial tRNAGln T4363C mutation.Semantic proximity Read ↗

Mitochondrial tRNAAla C5601T mutation may modulate the clinical expression of tRNAMet A4435G mutation in a Han Chinese family with hypertension.Semantic proximity Read ↗

Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes.Semantic proximity Read ↗

Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertension.Semantic proximity Read ↗

The Mitochondrial tRNAAsp T7561C, tRNAHis C12153T, and A12172G Mutations May Be Associated with Essential Hypertension in a Han Chinese Pedigree.Semantic proximity Read ↗

[The mitochondrial tRNAMet/tRNAGlnA4401G and tRNACysG5821A mutations may be associated with hypertension in two Han Chinese families].Semantic proximity Read ↗

Mitochondrial transfer RNA mutations and hypertension.Semantic proximity Read ↗

Mitochondrial tRNAThr 15909A>G mutation associated with hypertension in a Chinese Han pedigree.Semantic proximity Read ↗

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.Semantic proximity Read ↗

Assessment of mitochondrial DNA mutations in Chinese family with essential hypertension.Semantic proximity Read ↗

Mitochondrial tRNASer(UCN) 7471delC may be a novel mutation associated with maternally transmitted hypertension.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.