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

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

BMC medical genetics - 23 Jul 2014

Liu Yuqi, Li Yang, Gao Jinliao, Zhu Chao, Lan Yunfeng, Yang Jie, Li Zongbin, Guan Minxin, Chen Yundai

Abstract excerpt

BACKGROUND: Hypertension is a very common cardiovascular disease influenced by multiple genetic and environmental factors. More recently, there are some studies showed that mutations in mitochondrial DNA have been involved in its pathogenesis. In this study we did further investigations on this relationship. METHODS: Epidemiological research found a Han Chinese family with probable maternally transmitted...

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 Cytosine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Mitochondrial

Share to Guanine

Share to Hypertension

Share to Mitochondria

Share to Point Mutation

Share to RNA, Transfer, Gln

Source

Open in PubMed Open full text

Identifiers

PMID: 25056089
DOI: 10.1186/1471-2350-15-84
PMCID: PMC4120007

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

Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes.PMID 25056089Read ↗

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

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

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

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

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

Molecular characterization of two Chinese pedigrees with maternally inherited hypertension.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 ↗

Mitochondrial transfer RNA mutations and hypertension.Semantic proximity Read ↗

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

Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.Semantic proximity Read ↗

Mitochondrial tRNAMet mutation is associated with clinical and biochemical characteristics in primary hypertension.Semantic proximity Read ↗

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