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

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

Hypertension (Dallas, Tex. : 1979) - 1 Jun 2009

Liu Yuqi, Li Ronghua, Li Zongbin, Wang Xin-Jian, Yang Li, Wang Shiwen, Guan Min-Xin

Abstract excerpt

Mitochondrial DNA mutations have been associated with cardiovascular disease. We report here the clinical, genetic, and molecular characterization of 1 Han Chinese family with suggestively maternally transmitted hypertension. Matrilineal relatives in this family exhibited the variable degree of hypertension at the age at onset of 44 to 55 years old. Sequence analysis of entire mitochondrial DNA in this pedigree...

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 Blood Pressure Determination

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA, Mitochondrial

Share to Heterozygote

Share to Hypertension

Share to Mitochondrial Proteins

Share to Risk Assessment

Share to RNA, Transfer

Source

Open in PubMed Open full text

Identifiers

PMID: 19398658
DOI: 10.1161/HYPERTENSIONAHA.109.128702
PMCID: PMC2907152

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.PMID 19398658Read ↗

The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.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 pedigree carrying the hypertension‑associated mitochondrial tRNAGln T4363C mutation.Semantic proximity Read ↗

Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family.Semantic proximity Read ↗

Mitochondrial tRNA mutations in 2070 Chinese Han subjects 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 are associated with maternally inherited hypertension in two Han Chinese pedigrees.Semantic proximity Read ↗

Mitochondrial transfer RNA mutations and hypertension.Semantic proximity Read ↗

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

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

Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension.Semantic proximity Read ↗

A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).Semantic proximity Read ↗

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