Sco2 Gene

The TP gene overlaps with the SCO2 gene a Chromosomal positions of

ClustalW results showing alignment of mutated human SCO2 gene sequence

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

SCO2 Gene Somatic Mutations in Cancer

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

PCAF regulates SCO2 gene expression SCO2 protein levels were followed

PDF Analysis of reported SCO2 gene mutations affecting cytochrome c

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

Table 2 from Analysis of reported SCO2 gene mutations affecting

Symptoms and Testing information for SCO2 Gene Cardioencephalomyopathy

SCO2 Gene Cardioencephalomyopathy fatal infantile due to cytochrome c

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

Regulation of SCO2 and TIGAR gene expression in hypoxia mimicking

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

Regulation of SCO2 and TIGAR gene expression in hypoxia mimicking

PDF Phenotypic Consequences of a Novel SCO2 Gene Mutation

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

Regulation of SCO2 and TIGAR gene expression in hypoxia mimicking

SCO2 Gene GeneCards SCO2 Protein SCO2 Antibody

PDF Phenotypic Consequences of a Novel SCO2 Gene Mutation

b A model depicting the mechanism of p53mediated regulation of SCO2

Detection of SCO2 mutations in cardioencephalomyopathy patients

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

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

Association of Mutations in SCO2 a Cytochrome c Oxidase Assembly Gene

Association of Mutations in SCO2 a Cytochrome C Oxidase Assembly Gene

SCO2 induces expression of apoptotic genes in tumor xenografts A PCR

SCO2 is required as a chaperone for newly synthesized CO II Control

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

Mutations in SCO1 and SCO2 Produce Cellular CopperDeficiency

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

PDF Mutations in SCO2 are associated with a distinct form of

SCO1 and SCO2 patient cells contain reduced levels of fully assembled

PDF Mutations in SCO2 are associated with a distinct form of

SCO2 Wikipedia

Leigh disease due to SCO2 mutations revealed at extended autopsy

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

A schematic of SCO2 Brayton cycle and its operating conditions

Regulation Of Gene Expression In Eukaryotes Notes at Erik Cox blog

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

Cytochrome c Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics

Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in

The assembly intermediate common to SCO1 SCO2 and SURF1 patient cells

Leigh disease due to SCO2 mutations revealed at extended autopsy

SCO2 mutations result in a specific defect in CO II expression

PDF Cooperation between COA6 and SCO2 in COX2 Maturation during

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote

MiR18396182 cluster downregulates SCO2 and PDHA1 through targeting

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

SCO1 SCO2 and COX11 all exist in higher order homooligomeric

SCO2 overexpression in TP53 mutation background A Bar graph showing

Cooperation between COA6 and SCO2 in COX2 Maturation during Cytochrome

SCO1 SCO2 and COX11 all exist in higher order homooligomeric

The SCO2 protein disulphide isomerase is required for thylakoid

Transient interactions between COX20 and SCO1 and SCO2 depend on COX2

Deficiency of Sco2 protein in fibroblasts and myoblasts of patients

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

Complementation analysis in SCO1 and SCO2 patient fibroblasts

Upregulation of the cellular levels of SCO2 protein in HuH7 cells by

Complementation analysis in SCO1 and SCO2 patient cells transduced with

PDF Mitochondrial disease genes COA6 COX6B and SCO2 have overlapping

SCO2 abrogation in HCT116 cells results in asymmetry in CAC

The SCO2 protein disulphide isomerase is required for thylakoid

SCO2 induces expression of apoptotic genes in tumor xenografts A PCR

SCO2 loss in HCT116 cells leads to activation of AKT and AMPK

Mutations in SCO2 and COA6 Affect Protein Association A After

Kinetic analysis of SCO2 translation in fibroblasts derived from a

A The role of SCO2 in inducing the activation of ASK1 downstream

Possible approaches for the combined system based on sCO2 cycles

The SCO2 protein disulphide isomerase is required for thylakoid

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

The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have

Functional analysis of dominant negative effects in SCO1 and SCO2

A Human SCO2 Mutation Helps Define the Role of Sco1p in the Cytochrome

Complementation analysis in SCO1 and SCO2 patient cell lines trans

Mutations in SCO2 and COA6 Affect Protein Association A After

Unexpected Vascular Enrichment of SCO1 over SCO2 in Mammalian Tissues

Sequence alignments of SCO proteins Alignments of mature SCO1 and SCO2

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

SCO2 induces dissociation of the ASK1Trx complex A The role of

SCO2 Mediates Oxidative StressInduced Glycolysis to Oxidative

Investigated sCO2 cycle configurations Download Scientific Diagram

The SCO2 protein disulphide isomerase is required for thylakoid

Upregulation of the cellular levels of SCO2 protein in HuH7 cells by

SCOdependent regulation of CO II synthesis and maturation Pro posed

Proposed mechanism of SCOdependent regulation of cellular copper

Schematic diagram illustrating the potential regulation of cellular

Ts diagram of the sCO2HeRo cycle including a simplified sketch

PDF Clinical biochemical and molecular analyses of six patients with

Mitochondria in cancer cells what is so special about them Trends in

Synthesis of cytochrome c oxidase 2 a p53dependent metabolic

The downstream function of SCO1 during CO II maturation is tightly

Model depicting the mechanism of SCO2induced apoptosis in can

SCO2 Proteins and Enzymes

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

Palmitate stimulations induce changes in mitochondria copper protein

Southern analysis of W303SCO2 genomic DNA The construction of the

Large copy number variations in combination with point mutations in the

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

SCO2induced expression of apoptotic genes is absent in ASK1 knockdown

Characterization of the human Cterminal portion of wildtype and

Histone Phosphorylation

A Structural Characterization of Human SCO2 Structure

2 Human disorders presenting with COX deficiency caused by mutations in

A Structural Characterization of Human SCO2 Structure

Three dimensional structures of human SCO1 and SCO2 PyMOLderived

Fatal infantile cardioencephalomyopathy with COX deficiency and

Mapping the Functional Interaction of Sco1 and Cox2 in Cytochrome

Investigating the cardiac pathology of SCO2mediated hypertrophic

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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