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SCO1
Supl Table 1 for Pdf.Xlsx
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Output Results of CLIME (Clustering by Inferred Models of Evolution)
Novel Pathogenic COX20 Variants Causing Dysarthria, Ataxia, and Sensory Neuropathy
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
030626 Mitochondrial Respiratory-Chain Diseases
Elesclomol Restores Mitochondrial Function in Genetic Models of Copper Deficiency
Loop Recognition and Copper-Mediated Disulfide Reduction Underpin Metal Site Assembly of Cua in Human Cytochrome Oxidase
Functions of Cytochrome C Oxidase Assembly Factors
Copper Chaperones for Cytochrome C Oxidase and Human Disease
The Role of Cox20 in Cox2 Maturation and Cytochrome C Oxidase Assembly
Mutation Screening in Patients with Isolated Cytochrome C Oxidase Deficiency
The Multifaceted Roles of Copper in Cancer: a Trace Metal Element with Dysregulated Metabolism, but Also a Target Or a Bullet for Therapy
Transfer from Cox17 to Sco1 Is Coupled to Electron Transfer
Blueprint Genetics SCO1 Single Gene Test
Bits and Bytes and Eukaryotes
Top View
Modeling Leigh Syndrome Using Patient-Specific Induced Pluripotent Stem Cells
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
1Wp0 Lichtarge Lab 2006
32-13398: SCO1 Human Description Product Info
REVIEW ARTICLE Human Cytochrome Oxidase Deficiency
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?
Human Sco1 Functional Studies and Pathological Implications of the P174L Mutant
Mapping the Functional Interaction of Sco1 and Cox2 in Cytochrome Oxidase Biogenesis Kevin Rigby University of Utah Health Sciences Center
Mutations of the SCO1 Gene in Mitochondrial Cytochrome C
A Sco Protein Among the Hypothetical Proteins of Bacillus Lehensis G1: Its
Impaired Complex IV Activity in Response to Loss of LRPPRC
Cytochrome C Oxidase Deficiency Due to a Novel SCO2 Mutation Mimics Werdnig-Hoffmann Disease
UC San Francisco Electronic Theses and Dissertations