DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» COX15
COX15
Ncomms8214.Pdf
Alterations of Genetic Variants and Transcriptomic Features of Response to Tamoxifen in the Breast Cancer Cell Line
Supplementary Materials
Supplementary Data Table 1. Genes Upregulated in N-Myc-Overexpressing Mouse Mac1+/Gr1+ BM Cells
Gene Ontology Functional Annotations and Pleiotropy
MOCHI Enables Discovery of Heterogeneous Interactome Modules in 3D Nucleome
Regulation of COX Assembly and Function by Twin CX9C Proteins—Implications for Human Disease
Role of Cytochrome C Oxidase Nuclear-Encoded Subunits in Health and Disease
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Leigh Syndrome
(-)-Oleocanthal As a Dual C-MET-COX2 Inhibitor for The
COX15 Mouse Monoclonal Antibody [Clone ID: 6H2.B4] Product Data
Structure, Function, and Assembly of Heme Centers in Mitochondrial Respiratory Complexes Hyung J
Functions of Cytochrome C Oxidase Assembly Factors
Identification of a Novel Deletion in SURF1 Gene
Mutation Screening in Patients with Isolated Cytochrome C Oxidase Deficiency
Leigh Syndrome
COX15 Antibody Cat
Top View
Effects of Exercise Training on Quadriceps Muscle Gene Expression in Chronic Obstructive Pulmonary Disease
Defects in the Biosynthesis of Mitochondrial Heme C and Heme a in Yeast and Mammals
Retrospective, Multicentric Study of 180 Children with Cytochrome C Oxidase Deficiency
Understanding Metabolic and Stress Changes in Mitochondrial Disease
COX15 Mouse Monoclonal Antibody [Clone ID: 7H8.2C12] Product Data
From Synthesis to Utilization: the Ins and Outs of Mitochondrial Heme
Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways
Interplay Between Mitochondrial Protein Import and Respiratory Complexes Assembly in Neuronal Health and Degeneration
Supp Table S1.Pdf
Genetic Features of Mitochondrial Respiratory Chain Disorders
Evidence That Links Loss of Cyclooxygenase-2 With
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
Therapeutic Approaches to Treat Mitochondrial Diseases: “One-Size-Fits-All” and “Precision Medicine” Strategies
Hypertension
Responsive Nuclear Proteins in Collecting Duct Cells
Blueprint Genetics COX15 Single Gene Test
Novel Mutations in COX15 in a Long Surviving Leigh Syndrome Patient with Cytochrome C Oxidase Deficiency M Bugiani, V Tiranti, L Farina, G Uziel, M Zeviani