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NDUFS2
Proteomic and Metabolomic Analyses of Mitochondrial Complex I-Deficient
Supplementary Materials
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Supercomplexes of Prokaryotic Aerobic Respiratory Chains Escherichia Coli and Bacillus Subtilis Supramolecular Assemblies Pedro M.F
Munkácsy E. & Rea, S. L. the Paradox Of
Integrated Proteomic and Mirna Transcriptional Analysis Reveals the Hepatotoxicity Mechanism of PFNA Exposure in Mice
Blueprint Genetics NDUFS2 Single Gene Test
Proteome Characteristics of Liver Tissue from Patients with Parenteral
A Novel Mutation in NDUFS4 Causes Leigh Syndrome in an Ashkenazi Jewish Family
Supplementary Table S1. Relative Change in Proteins Associated with Heme Biosynthesis and Degradation
Reveals of Candidate Active Ingredients in Justicia and Its Anti-Thrombotic Action of Mechanism Based on Network Pharmacology Ap
Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Effect of Redox-Cycling Agents on Nitric Oxide Synthase Activity In
Mitochondrial and Autophagic Regulation of Adult Neurogenesis in the Healthy and Diseased Brain
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency Due to a Novel Mutation in the NDUFS1 Gene
Bioenergetic Regulation of Microglia
Distinct Requirements for Energy Metabolism in Mouse Primordial Germ Cells and Their Reprogramming to Embryonic Germ Cells
Top View
Quality Improvement of Mitochondrial Respiratory Chain Complex Enzyme Assays Using Caenorhabditis Elegans Xiulian Chen, MD, Phd1, David R
Supporting Information
Identification of P450 Oxidoreductase As a Major Determinant of Sensitivity to Hypoxia-Activated Prodrugs
Recombinant Human Ndufs2 Protein Catalog Number: ATGP2463
Mutations in NDUFS1 Cause Metabolic Reprogramming and Disruption of the Electron Transfer
Mutant NDUFS3 Subunit of Mitochondrial Complex I Causes Leigh Syndrome
Edematous Severe Acute Malnutrition Is Characterized by Hypomethylation of DNA
WO 2013/078372 Al 30 May 2013 (30.05.2013) W P O P C T
Airway Inflammation Mitochondrial Dysfunction Increases Allergic
Datasheet: VMA00279 Product Details
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
List for Testing Done out of Québec LABORATOIRE CLINIQUES CUSM MUHC CLINICAL LABS
Diabetes Susceptibility Genes Pdx1 and Clec16a Function in a Pathway Regulating Mitophagy in B-Cells
Db171195supplementarydata2.Pdf
NDUFS2 Mitochondrial Complex I Deficiency Induces Adipose Tissue Degeneration Via IIS in a Drosophila Melanogaster Model
Supplementary File 1
Granzyme B-Induced Mitochondrial ROS Are Required for Apoptosis
A Systems Approach to Identify Genetic and Environmental Regulators of Metabolism