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COQ7
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Table S2.Up Or Down Regulated Genes in Tcof1 Knockdown Neuroblastoma N1E-115 Cells Involved in Differentbiological Process Anal
Electronic Supplementary Material (ESI) for Metallomics
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Metabolic Targets of Coenzyme Q10 in Mitochondria
CLK-1/Coq7p Is a DMQ Mono-Oxygenase and a New Member of the Di-Iron Carboxylate Protein Family
Supplementary Table 1
Human Mitochondrial Pathologies of the Respiratory Chain and ATP Synthase: Contributions from Studies of Saccharomyces Cerevisiae
Engineered Type 1 Regulatory T Cells Designed for Clinical Use Kill Primary
Paramagnetic States of Diiron Carboxylate Proteins
Instability in NAD Metabolism Leads to Impaired Cardiac Mitochondrial
Mitochondrial Diseases: Expanding the Diagnosis in the Era of Genetic Testing
Minimal Mitochondrial Respiration Is Required to Prevent Cell Death by Inhibition of Mtor Signaling in Coq-Deficient Cells ✉ Ying Wang 1 and Siegfried Hekimi1
SANTA CRUZ BIOTECHNOLOGY, INC. COQ7 Sirna (M): Sc-62147
S41467-020-16918-X.Pdf
Additional Tables.Xlsx
Supplemental Figures 04 12 2017
Fungal and Host Transcriptome Analysis of Ph-Regulated Genes
Top View
Supplementary Table S1. Relative Change in Proteins Associated with Heme Biosynthesis and Degradation
Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity
Primary and Secondary Antibodies & Reagents for Laboratory Research 2017
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Molecular Epidemiology of Mitochondrial Cardiomyopathy:A Search Among Mitochondrial and Nuclear Genes
Rescue of Primary Ubiquinone Deficiency Due to a Novel COQ7 Defect Using 2,4–Dihydroxybensoic Acid
The in Vivo Endothelial Cell Translatome Is Highly Heterogeneous Across Vascular Beds
Expression Profiling of Macrophages Reveals Multiple Populations With
Metalloproteins in the Biology of Heterocysts
Are Shown B Gene Numbera
Identification of GPCR-Interacting Cytosolic Proteins Using HDL Particles and Mass Spectrometry-Based Proteomic Approach
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
Neurometabolic Implications of Coenzyme Q10 Deficiency: Pathogenesis, Detection and Treatment 1
Negative Result Does Not Rule out a Genetic Basis for a Diagnosis of a Mitochondrial Disorder in This Patient
Ubiquinol-Binding Site in the Alternative Oxidase: Mutagenesis Reveals Features Important for Substrate Binding and Inhibition
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Blueprint Genetics Comprehensive Metabolism Panel
Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice Piotr Zabie
Recombinant Human 5-Demethoxyubiquinone Hydroxylase, Mitochondrial/COQ7 (C-6His)
Generated by SRI International Pathway Tools Version 25.0 on Mon
Mitochondrial COQ9 Is a Lipid-Binding Protein That Associates with COQ7
Mitochondrial COQ9 Is a Lipid-Binding Protein That Associates with COQ7 to Enable Coenzyme Q Biosynthesis
Nuclear Receptor Errα and Coactivator PGC-1Β Are Effectors of IFN
Pptc7 Is an Essential Phosphatase for Promoting Mammalian
Cell Survival from Chemotherapy Depends on NF-Kb Transcriptional Up-Regulation of Coenzyme Q Biosynthesis
Supplementary File 2B Revised
Assessing the Association of Mitochondrial Genetic Variation
Mitochondrial Ubiquinone-Mediated Longevity Is Marked by Reduced Cytoplasmic Protein Translation
ROS-Based Lethality of Caenorhabditis Elegans Mitochondrial Electron Transport Mutants Grown on Escherichia Coli Siderophore Iron Release Mutants
Positive Control Is Provided for Testing of a Specific Variant Identified at Another Laboratory
Supp Table 2.Pdf
Generated by SRI International Pathway Tools Version 24.0 on Thu
Supplementary Materials PDF File Includes: • Supplementary Figures 1-3 • Supplementary Tables 1-2
Genomic Unity® Neurology Analysis
Expression Profiling of Macrophages Reveals Multiple Populations With
Supplementary Information For
Impaired Mitochondrial Biogenesis in Adipose Tissue in Acquired Obesity Running Title: Impaired Mitochondrial Function in Obesity
Gene Expression Study of Mycobacterium Avium Subspecies
Supplementary Table 4-10