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

[Expression and significance of respiratory chain enzyme of cells in urine sediment in MELAS syndrome].

Zhonghua yi xue za zhi - 23 Apr 2013

Wu Hai-rong, Ma Yi-nan, Qi Yu, Liu Hong-gang

Abstract excerpt

OBJECTIVE: To explore the expression and significance of respiratory chain enzyme of cells in urine sediment in mitochondrial encephalopathy myopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome. METHODS: Through enzyme histochemistry, the authors analyzed the changes of respiratory chain enzyme in urine sediment in 20 MELAS patients due to mitochondrial A3243G mutation (MELAS group) and 20 health...

Read the complete abstract on PubMed

Topics

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

Share to Cell Nucleus
Share to Child, Preschool
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electron Transport

Share to Electron Transport Complex IV

Share to MELAS Syndrome

Share to Mitochondrial Membranes

Share to Young Adult

Source

Identifiers

PMID: 23902617

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

[Expression and significance of respiratory chain enzyme of cells in urine sediment in MELAS syndrome].PMID 23902617Read ↗

[G14453A mutation in mitochondrial myopathy encephalomyopathy with lactic acidosis and stroke-like episodes].Semantic proximity Read ↗

When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?Semantic proximity Read ↗

Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome: A case-report and literature review (CARE-complaint).Semantic proximity Read ↗

[A3243G mitochondrial DNA mutation and heterogeneous phenotypic expression].Semantic proximity Read ↗

A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients.Semantic proximity Read ↗

["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].Semantic proximity Read ↗

[MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].Semantic proximity Read ↗

[Clinical case of MELAS syndrom].Semantic proximity Read ↗

[MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes)].Semantic proximity Read ↗

Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation.Semantic proximity Read ↗

Identification of miRNA, lncRNA and mRNA-associated ceRNA networks and potential biomarker for MELAS with mitochondrial DNA A3243G mutation.Semantic proximity Read ↗

[A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes].Semantic proximity Read ↗

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