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Publications by Dayami Hernandez
Mice Lacking COX10 in Skeletal Muscle Recapitulate the Phenotype of Progressive Mitochondrial Myopathies Associated With Cytochrome C Oxidase Deficiency
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
Related publications
Deficiency of Muscle Cytochrome C Oxidase (Co) in Leigh's Disease
Pediatric Research
Child Health
Pediatrics
Perinatology
Cytochrome C Oxidase Deficiency Associated With the First Stop-Codon Point Mutation in Human mtDNA
American Journal of Human Genetics
Genetics
Oxidation of Ferrocytochrome C by Mitochondrial Cytochrome C Oxidase.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
119 CYTOCHROME C OXIDASE IN THE DEVELOPING HUMAN HEART. CORRELATION WITH MITOCHONDRIAL ULTRASTRUCTURE
Pediatric Research
Child Health
Pediatrics
Perinatology
Defective Mitochondrial Morphology and Bioenergetic Function in Mice Lacking the Transcription Factor Yin Yang 1 in Skeletal Muscle
Molecular and Cellular Biology
Cell Biology
Molecular Biology
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 Medicine
Physiology
Cardiology
Human Cytochrome Oxidase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Ultrastructure of Skeletal Muscles in Mice Lacking Muscle-Specific VEGF Expression
Anatomical Record
Evolution
Ecology
Systematics
Anatomy
Histology
Behavior
Biotechnology
Table 1: Cytochrome C Oxidase I Mitochondrial Gene Primers.