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NDUFS8
High-Throughput, Pooled Sequencing Identifies Mutations in NUBPL And
Health Effects Support Document for Perfluorooctanoic Acid (PFOA)
Supplementary Materials
THE FUNCTIONAL SIGNIFICANCE of MITOCHONDRIAL SUPERCOMPLEXES in C. ELEGANS by WICHIT SUTHAMMARAK Submitted in Partial Fulfillment
NDUFS8 Antibody Cat
Higher NDUFS8 Serum Levels Correlate with Better Insulin Sensitivity in Type 1 Diabetes
Colon Cancer and Its Molecular Subsystems: Network Approaches to Dissecting Driver Gene Biology
Supercomplexes of Prokaryotic Aerobic Respiratory Chains Escherichia Coli and Bacillus Subtilis Supramolecular Assemblies Pedro M.F
Indoxyl Sulfate and P-Cresyl Sulfate Promote Vascular Calcification and Associate with Glucose Intolerance
TAT-Conjugated NDUFS8 Can Be Transduced Into Mitochondria in a Membrane-Potential-Independent Manner and Rescue Complex I Defici
Integrated Proteomic and Mirna Transcriptional Analysis Reveals the Hepatotoxicity Mechanism of PFNA Exposure in Mice
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
Clinical and Genetic Studies in Paediatric Mitochondrial Disease
Epigenetic Programming by Prenatal Stress in Female Serotonin Transporter Deficient Mice
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
Top View
Table 2. List of 113 Potential Blastocystis Mitochondrial Proteins and Proteins Associated with Mitochondria with Their EST Accession Numbers
NDUFS8 (A-6): Sc-515527
Cellular Features Predicting Susceptibility to Ferroptosis: Insights from Cancer Cell-Line Profiling
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency Due to a Novel Mutation in the NDUFS1 Gene
Research Article Sodium Butyrate-Modulated Mitochondrial Function in High-Insulin Induced Hepg2 Cell Dysfunction
The First Nuclear-Encoded Complex I Mutation in a Patient with Leigh
Bioenergetic Regulation of Microglia
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism Istanbul, Turkey, 31 August– 3 September 2010
Differential Transcriptome Profile of Peripheral White Cells to Identify Biomarkers Involved in Oxaliplatin Induced Neuropathy
Targeting FGFR Signalling to Disrupt Cellular Cross-Talk in Pancreatic Cancer
Distinct Requirements for Energy Metabolism in Mouse Primordial Germ Cells and Their Reprogramming to Embryonic Germ Cells
NDUFS8 Rabbit Pab
Supporting Information
Mammalian Mitochondrial Complex I Structure and Disease-Causing Mutations
A Salvage Pathway Maintains Highly Functional Respiratory Complex I
Regulation of Alzheimer's Disease-Associated Proteins During Epileptogenesis
Mutant NDUFS3 Subunit of Mitochondrial Complex I Causes Leigh Syndrome
Dynamic Interplay Between Copper Toxicity and Mitochondrial Dysfunction in Alzheimer’S Disease
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
NDUFS8 (D-5): Sc-515537
Genetic Features of Mitochondrial Respiratory Chain Disorders
Membrane Disruption, but Not Metabolic Rewiring, Is the Key Mechanism of Anticancer‑Action of FASN‑Inhibitors: a Multi‑Omics Analysis in Ovarian Cancer Thomas W
WO 2013/078372 Al 30 May 2013 (30.05.2013) W P O P C T
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
Db171195supplementarydata2.Pdf
Rapid Mendelian Sequencing Gene List December 2018
Myocardial Gene Expression Associated with Genetic Cardiac Hypertrophy in the Absence of Hypertension
Impaired Mitochondrial Fat Oxidation Induces Adaptive Remodeling of Muscle Metabolism
Wo2018/191558
Indices Disorders Index
Ovarian Tumor Mitochondria Exhibit Abnormal Phenotypes and Blunted Associations with Biobehavioral Factors