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SCO2
Mitochondrial Dysfunction and Its Role in Tissue-Specific Cellular Stress
Exome Sequencing Reveals SCO2 Mutations in a Family Presented with Fatal Infantile Hyperthermia
Regulation of COX Assembly and Function by Twin CX9C Proteins—Implications for Human Disease
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Novel Pathogenic COX20 Variants Causing Dysarthria, Ataxia, and Sensory Neuropathy
SCO2 Sequencing Indication
Structural Models and Considerations on the COA6, COX18 and COX20 Factors That Assist Assembly of Human Cytochrome C Oxidase Subunit II
Observation of Novel COX20 Mutations Related to Autosomal Recessive Axonal Neuropathy and Static Encephalopathy
Near Infrared Spectroscopy Evaluated Cerebral Oxygenation During Anesthesia
Fatal Infantile Cardioencephalomyopathy Due to Cytochrome C Oxidase Deficiency Sco2 Gene Sequencing
Elesclomol Restores Mitochondrial Function in Genetic Models of Copper Deficiency
Respiratory Chain Activity and Protein Expression in Skeletal Muscles from High and Low Feed Efficient Swine Within the Same Genetic Line
Loop Recognition and Copper-Mediated Disulfide Reduction Underpin Metal Site Assembly of Cua in Human Cytochrome Oxidase
Functions of Cytochrome C Oxidase Assembly Factors
Blueprint Genetics SCO2 Single Gene Test
The Role of Cox20 in Cox2 Maturation and Cytochrome C Oxidase Assembly
Mutation Screening in Patients with Isolated Cytochrome C Oxidase Deficiency
Pyrimidine Biosynthesis Links Mitochondrial Respiration to the P53 Pathway
Top View
Leigh Syndrome
Association of Mutations in SCO2, a Cytochrome C Oxidase Assembly Gene, with Early Fetal Lethality
BBA - Molecular Cell Research 1865 (2018) 323–333
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
COA6 Facilitates Cytochrome C Oxidase Biogenesis As Thiol-Reductase for Copper Metallochaperones in Mitochondria
Mutation Analysis of COX18 in 29 Patients with Isolated Cytochrome C Oxidase Deficiency
Molecular Basis of Leigh Syndrome: a Current Look Manuela Schubert Baldo* and Laura Vilarinho
Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade Myopia
REVIEW ARTICLE Human Cytochrome Oxidase Deficiency
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Mitochondrial Respiration Protects Against Oxygen-Associated DNA Damage
What Role Does COA6 Play in Cytochrome C Oxidase Biogenesis: a Metallochaperone Or Thiol Oxidoreductase, Or Both?
What Role Does COA6 Play in Cytochrome C Oxidase Biogenesis: a Metallochaperone Or Thiol Oxidoreductase, Or Both?
Diagnostic Work up in a Patient with a Progressive Cardio
The Significance of Mitochondrial Dysfunction in Cancer
Cytochrome C Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease
Mitochondrial Recoupling: a Novel Therapeutic Strategy for Cancer&Quest;