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A Novel Mutation in the SCO2 Gene in a Neonate With Early-Onset ...
A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy ...
ClustalW results showing alignment of mutated human SCO2 gene sequence ...
The TP gene overlaps with the SCO2 gene. (a) Chromosomal positions of ...
(PDF) Analysis of reported SCO2 gene mutations affecting cytochrome c ...
The germline 4A>G mutation in the SHOC2 gene causes a distinctive ...
(PDF) A Human SCO2 Mutation Helps Define the Role of Sco1p in the ...
Table 2 from Analysis of reported SCO2 gene mutations affecting ...
(PDF) A hemizygous SCO2 mutation in an early onset rapidly progressive ...
Regulation of SCO2 and TIGAR gene expression in hypoxia mimicking ...
Mitochondrial Cardioencephalomyopathy Due to a Novel SCO2 Mutation in a ...
A Human SCO2 Mutation Helps Define the Role of Sco1p in the Cytochrome ...
Detection of SCO2 mutations in cardioencephalomyopathy patients ...
Figure 1 from SCO2 mutations cause early-onset axonal Charcot-Marie ...
Mutations in SCO2 and COA6 Affect Protein Association (A) After ...
Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome ...
b: A model depicting the mechanism of p53-mediated regulation of SCO2 ...
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease ...
Association of Mutations in SCO2, a Cytochrome c Oxidase Assembly Gene ...
The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have ...
Mutations in SCO1 and SCO2 Produce Cellular Copper-Deficiency ...
Association of Mutations in SCO2, a Cytochrome C Oxidase Assembly Gene ...
SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper ...
Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in ...
Proposed model of SCO1 and SCO2 function in Cu A site assembly. COX17 ...
(PDF) Mutations in SCO2 are associated with a distinct form of ...
SCO2 - Wikipedia
Human Sco1 and Sco2 Function as Copper-binding Proteins* - Journal of ...
Mutations in SCO2 Are Associated with Autosomal-Dominant High-Grade ...
Complementation analysis in SCO1 and SCO2 patient cell lines trans ...
The SCO2 protein disulphide isomerase is required for thylakoid ...
Complementation analysis in SCO1 and SCO2 patient fibroblasts ...
SCO2 mutations result in a specific defect in CO II expression ...
Deficiency of Sco2 protein in fibroblasts and myoblasts of patients ...
SCO2 is required as a chaperone for newly synthesized CO II. Control ...
(PDF) Mutations in SCO2 Are Associated with Autosomal-Dominant High ...
SCO1 and SCO2 patient cells contain reduced levels of fully assembled ...
(PDF) A novel homozygous SCO2 mutation, p.G193S, causing fatal ...
SCO2 induces expression of apoptotic genes in tumor xenografts. A PCR ...
(PDF) Cytochrome c oxidase deficiency due to mutations in SCO2 ...
Fig. Morphology of muscle sections of SURF-1 Patient 4, SCO2 Patient 2 ...
Uptake mechanism of PTD-IVT-mRNA of SCO2 in SCO2/COXdeficient ...
Hybrids between cyo1 and sco2 showed reduced growth and hybrid vigor at ...
SCO1 and SCO2 redox state and copper binding are regulated by COX11 ...
Unexpected Vascular Enrichment of SCO1 over SCO2 in Mammalian Tissues ...
Complementation analysis in SCO1 and SCO2 patient cells transduced with ...
Reconciled gene tree of Sco1/Sco2 (see Suppl. Figure S5 for the full ...
SCO1, SCO2 and COX11 all exist in higher order, homo-oligomeric ...
Human eye tissues expression. CCDC102B, COL8A1 and SCO2 genes were ...
Bulk and Single-Cell Transcriptomics Reveal That SCO2 Drives Psoriasis ...
-Elevated SCS2 gene dosage overcomes the dominant effect of the ...
Identification of the corresponding genes for the mutant phenotypes ...
Development of a novel PTD-mediated IVT-mRNA delivery platform for ...
Figure 1 from Analysis of mouse models of cytochrome c oxidase ...
Large copy number variations in combination with point mutations in the ...
Snowy cotyledon 2: the identification of a zinc finger domain protein ...
Schematic illustration of potential mechanisms of SCO-dependent ...
Proposed mechanism of SCO-dependent regulation of cellular copper ...
Genetic alterations in fatty acid transport and metabolism genes are ...
Protein Transduction Domain-Mediated Delivery of Recombinant Proteins ...
Fatal infantile cardioencephalomyopathy with COX deficiency and ...
Figure 1 from Remodelling of skeletal muscle cells in children with ...
Copper and bezafibrate cooperate to rescue cytochrome c oxidase ...
A Structural Characterization of Human SCO2: Structure
SCO-dependent regulation of CO II synthesis and maturation. Pro- posed ...
Three dimensional structures of human SCO1 and SCO2. PyMOL-derived ...
The Scoop on Sco: Molecular Cell
Figure 1 from Molecular Pathogenesis of Genetic and Inherited Diseases ...
Overexpression of a SCO1/SCO2 chimeric protein results in a ...
(PDF) Analysis of mouse models of cytochrome c oxidase deficiency owing ...
(PDF) Tissue-specific cytochrome c oxidase assembly defects due to ...
Figure 10 from Remodelling of skeletal muscle cells in children with ...
In vivo biodistribution study of TAT-L-Sco2 fusion protein, developed ...
(PDF) Fatal infantile cardioencephalomyopathy with COX deficiency and ...
cyt c oxidase.ppt
Low, medium and high magnifications of FJB-stained brain coronal ...
Model depicting the mechanism of SCO2-induced apoptosis in can ...
Figure 1 from Tissue-specific cytochrome c oxidase assembly defects due ...
Seeking the determinants of the elusive functions of Sco proteins ...
Genetic modulation of mitochondrial respiration affects nuclear O 2 ...
The Many Clinical Faces Of Cytochrome C Oxidase Deficiency – UBMU
Characterization of the human C-terminal portion of wild-type and ...
(PDF) Large copy number variations in combination with point mutations ...
Mapping the Functional Interaction of Sco1 and Cox2 in Cytochrome ...
Inactivating Mutations in ESCO2 Cause SC Phocomelia and Roberts ...
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