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COX6A1
Mutation in the COX4I1 Gene Is Associated with Short Stature, Poor Weight Gain and Increased Chromosomal Breaks, Simulating Fanconi Anemia
Structure of the Intact 14-Subunit Human Cytochrome C Oxidase
A High-Resolution Genome-Wide CRISPR/Cas9 Viability Screen
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
Electron Transport Chain Activity Is a Predictor and Target for Venetoclax Sensitivity in Multiple Myeloma
Observation of Novel COX20 Mutations Related to Autosomal Recessive Axonal Neuropathy and Static Encephalopathy
Transcriptomic and Proteomic Landscape of Mitochondrial
Conserved in Situ Arrangement of Complex I and III2 in Mitochondrial Respiratory Chain Supercomplexes of Mammals, Yeast, and Plants
Mice Deficient in the Respiratory Chain Gene Cox6a2 Are Protected Against High-Fat Diet-Induced Obesity and Insulin Resistance
RNA-Seq and GSEA Identifies Suppression of Ligand-Gated
Functions of Cytochrome C Oxidase Assembly Factors
Novel Insights Into the Assembly and Function of Human Nuclear-Encoded
Mouse Cox6a1 Knockout Project (CRISPR/Cas9)
Charcot-Marie-Tooth Disease
The Enigma of the Respiratory Chain Supercomplex
Primepcr™Assay Validation Report
BMC Genomics Biomed Central
Top View
Differential Gene Expression in Human Abdominal Aortic Aneurysm and Aortic Occlusive Disease
Mouse Cox6a1 Conditional Knockout Project (CRISPR/Cas9)
COX6A1 (NM 004373) Human Recombinant Protein Product Data
High-Resolution Melting Analysis of 15 Genes in 60 Patients with Cytochrome-C Oxidase Deficiency
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
Quaternary Protein Modeling to Predict the Function of DNA Variation Found in Human Mitochondrial Cytochrome C Oxidase
Comparative Proteomic Analysis of the Effects of High-Concentrate Diet On
Integrated Omic Analysis of Lung Cancer Reveals Metabolism Proteome Signatures with Prognostic Impact
Mass-Spectrometry Based Proteomics Reveals Mitochondrial
Structural Organization of the Bovine Gene for the Heart/Muscle Isoform of Cytochrome C Oxidase Subunit Via
Loss of the Smallest Subunit of Cytochrome C Oxidase, COX8A, Causes Leigh-Like Syndrome and Epilepsy
COX6A1 Mouse Monoclonal Antibody [Clone ID: OTI3F1] – TA501397
Mitochondrial COA7 Is a Heme-Binding Protein Involved in the Early Stages of Complex 2 IV Assembly