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

[Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Feb 2005

Zhang Xiao-ai, Wu Hua-cheng, Zhang Bing-feng, Yu Wen, Fan Qi-shi

Abstract excerpt

OBJECTIVE: To examine mitochondrial DNA mutations in mitochondrial myopathy. METHODS: Three suspected cases of mitochondrial myopathy were examined by HE staining, histochemical staining methods and electron microscopy. The mutations in all 22 tRNA genes of mitochondrial genome were screened by polymerase chain reaction-single strand conformation polymorphism and DNA sequencing. RESULTS: The three cases were...

Read the complete abstract on PubMed

Topics

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

Share to DNA, Mitochondrial
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Microscopy, Electron, Transmission

Share to Mitochondrial Myopathies

Share to Muscle Fibers, Skeletal

Share to Polymerase Chain Reaction

Share to Polymorphism, Single-Stranded Conformational

Share to Young Adult

Source

Identifiers

PMID: 15696472

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy].PMID 15696472Read ↗

A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function.Semantic proximity Read ↗

[Human pathologies associated with mutations of mitochondrial genome].Semantic proximity Read ↗

Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM gene.Semantic proximity Read ↗

[Mutations in mitochondrial DNA associated with hypertension].Semantic proximity Read ↗

"Myo-neuropathy" is commonly associated with mitochondrial tRNALysine mutation.Semantic proximity Read ↗

[Mitochondrial liver disease caused by TRMU gene mutation].Semantic proximity Read ↗

MELAS syndrome associated with a new mitochondrial tRNA-Val gene mutation (m.1616A>G).Semantic proximity Read ↗

Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.Semantic proximity Read ↗

[Nucleotide modification of mitochondrial tRNA and mitochondrial diseases].Semantic proximity Read ↗

A new mitochondrial tRNA(Met) gene mutation in a patient with dystrophic muscle and exercise intolerance.Semantic proximity Read ↗

Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) gene.Semantic proximity Read ↗

Molecular Epidemiology of Childhood Mitochondrial Encephalomyopathies in a Finnish Population: Sequence Analysis of Entire mtDNA of 17 Children Reveals Heteroplasmic Mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) GenesSemantic proximity Read ↗

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