Mice Lacking COX10 in Skeletal Muscle Recapitulate the Phenotype of Progressive Mitochondrial Myopathies Associated With Cytochrome C Oxidase Deficiency

Human Molecular Genetics - United Kingdom
doi 10.1093/hmg/ddi307
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Oxford University Press (OUP)

Related search

Deficiency of Muscle Cytochrome C Oxidase (Co) in Leigh's Disease

Pediatric Research
Child HealthPediatricsPerinatology
1984English

Cytochrome C Oxidase Deficiency Associated With the First Stop-Codon Point Mutation in Human mtDNA

American Journal of Human Genetics
Genetics
1998English

Oxidation of Ferrocytochrome C by Mitochondrial Cytochrome C Oxidase.

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
1976English

119 CYTOCHROME C OXIDASE IN THE DEVELOPING HUMAN HEART. CORRELATION WITH MITOCHONDRIAL ULTRASTRUCTURE

Pediatric Research
Child HealthPediatricsPerinatology
1985English

Defective Mitochondrial Morphology and Bioenergetic Function in Mice Lacking the Transcription Factor Yin Yang 1 in Skeletal Muscle

Molecular and Cellular Biology
Cell BiologyMolecular Biology
2012English

Protein Kinase C- Coimmunoprecipitates With Cytochrome Oxidase Subunit IV and Is Associated With Improved Cytochrome-C Oxidase Activity and Cardioprotection

American Journal of Physiology - Heart and Circulatory Physiology
Cardiovascular MedicinePhysiologyCardiology
2007English

Human Cytochrome Oxidase Deficiency

Pediatric Research
Child HealthPediatricsPerinatology
2000English

Ultrastructure of Skeletal Muscles in Mice Lacking Muscle-Specific VEGF Expression

Anatomical Record
EvolutionEcologySystematicsAnatomyHistologyBehaviorBiotechnology
2017English

Table 1: Cytochrome C Oxidase I Mitochondrial Gene Primers.

English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy