Sco2 Gene Mutation

A Novel Mutation in the SCO2 Gene in a Neonate With EarlyOnset

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 4AG 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

Regulation of SCO2 and TIGAR gene expression in hypoxia mimicking

Detection of SCO2 mutations in cardioencephalomyopathy patients

Figure 1 from SCO2 mutations cause earlyonset axonal CharcotMarie

Mutations in SCO2 and COA6 Affect Protein Association A After

Detection of SCO2 mutations in cardioencephalomyopathy patients

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

b A model depicting the mechanism of p53mediated regulation of SCO2

SCO2 mutations cause earlyonset axonal CharcotMarieTooth disease

Mutations in SCO2 and COA6 Affect Protein Association A After

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 CopperDeficiency

Association of Mutations in SCO2 a Cytochrome C Oxidase Assembly Gene

SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper

b A model depicting the mechanism of p53mediated regulation of SCO2

Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

Proposed model of SCO1 and SCO2 function in Cu A site assembly COX17

Mutations in SCO2 and COA6 Affect Protein Association A After

PDF Mutations in SCO2 are associated with a distinct form of

SCO2 Wikipedia

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

Human Sco1 and Sco2 Function as Copperbinding Proteins Journal of

Mutations in SCO2 Are Associated with AutosomalDominant HighGrade

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

Mutations in SCO2 Are Associated with AutosomalDominant HighGrade

SCO2 Wikipedia

SCO2 mutations cause earlyonset axonal CharcotMarieTooth disease

Mutations in SCO2 Are Associated with AutosomalDominant HighGrade

SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper

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 AutosomalDominant High

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

SCO1 and SCO2 patient cells contain reduced levels of fully assembled

Human Sco1 and Sco2 Function as Copperbinding Proteins Journal of

PDF A novel homozygous SCO2 mutation pG193S causing fatal

SCO1 and SCO2 patient cells contain reduced levels of fully assembled

SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper

SCO2 induces expression of apoptotic genes in tumor xenografts A PCR

PDF Cytochrome c oxidase deficiency due to mutations in SCO2

SCO2 Wikipedia

SCO2 induces expression of apoptotic genes in tumor xenografts A PCR

Association of Mutations in SCO2 a Cytochrome c Oxidase Assembly Gene

Fig Morphology of muscle sections of SURF1 Patient 4 SCO2 Patient 2

Complementation analysis in SCO1 and SCO2 patient cell lines trans

Uptake mechanism of PTDIVTmRNA of SCO2 in SCO2COXdeficient

Hybrids between cyo1 and sco2 showed reduced growth and hybrid vigor at

SCO1 and SCO2 redox state and copper binding are regulated by COX11

The SCO2 protein disulphide isomerase is required for thylakoid

Unexpected Vascular Enrichment of SCO1 over SCO2 in Mammalian Tissues

Association of Mutations in SCO2 a Cytochrome c Oxidase Assembly Gene

Complementation analysis in SCO1 and SCO2 patient cells transduced with

Reconciled gene tree of Sco1Sco2 see Suppl Figure S5 for the full

SCO1 SCO2 and COX11 all exist in higher order homooligomeric

Human eye tissues expression CCDC102B COL8A1 and SCO2 genes were

Bulk and SingleCell Transcriptomics Reveal That SCO2 Drives Psoriasis

SCO1 and SCO2 Act as High Copy Suppressors of a Mitochondrial Copper

SCO2 induces expression of apoptotic genes in tumor xenografts A PCR

Elevated SCS2 gene dosage overcomes the dominant effect of the

Identification of the corresponding genes for the mutant phenotypes

Development of a novel PTDmediated IVTmRNA 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 SCOdependent

Proposed mechanism of SCOdependent regulation of cellular copper

Genetic alterations in fatty acid transport and metabolism genes are

Protein Transduction DomainMediated 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

SCOdependent regulation of CO II synthesis and maturation Pro posed

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

The Scoop on Sco Molecular Cell

Figure 1 from Molecular Pathogenesis of Genetic and Inherited Diseases

Overexpression of a SCO1SCO2 chimeric protein results in a

PDF Analysis of mouse models of cytochrome c oxidase deficiency owing

PDF Tissuespecific cytochrome c oxidase assembly defects due to

Figure 10 from Remodelling of skeletal muscle cells in children with

In vivo biodistribution study of TATLSco2 fusion protein developed

PDF Fatal infantile cardioencephalomyopathy with COX deficiency and

cyt c oxidaseppt

Low medium and high magnifications of FJBstained brain coronal

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

Fatal infantile cardioencephalomyopathy with COX deficiency and

Model depicting the mechanism of SCO2induced apoptosis in can

Figure 1 from Tissuespecific cytochrome c oxidase assembly defects due

A Structural Characterization of Human SCO2 Structure

Seeking the determinants of the elusive functions of Sco proteins

Genetic modulation of mitochondrial respiration affects nuclear O 2

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

The Many Clinical Faces Of Cytochrome C Oxidase Deficiency UBMU

Development of a novel PTDmediated IVTmRNA delivery platform for

Figure 1 from Molecular Pathogenesis of Genetic and Inherited Diseases

Characterization of the human Cterminal portion of wildtype 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

TP53 Signaling Pathway

SCO2 与电子呼吸链

Hexokinase II

Protein Gene Expression

PDHA1 Gene

Glycolysis and Oxidative Phosphorylation

SCO2 Border

Sub1 Gene

Ceruloplasmin

Glycolysis vs Oxidative Phosphorylation

P53 Gene and PTEN Gene

Materials SCO2 Shingledecker

Cytochrome Oxidase Deficiency

P53 Mitochondria

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