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NDUFS1
Proteomic and Metabolomic Analyses of Mitochondrial Complex I-Deficient
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Abstracts from the 50Th European Society of Human Genetics Conference: Electronic Posters
Fatal Neonatal-Onset Mitochondrial Respiratory Chain Disease with T Cell Immunodeficiency
A High-Fat Diet Coordinately Downregulates Genes Required for Mitochondrial Oxidative Phosphorylation in Skeletal Muscle Lauren M
Anti-NDUFS1 Polyclonal Antibody Cat: K110186P Summary
Impaired Mitochondrial Fatty Acid Synthesis Leads to Neurodegeneration in Mice
Inositol Phosphate in the Basidiomycete Fungus Schizophyllum Commune
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
Epigenetic Programming by Prenatal Stress in Female Serotonin Transporter Deficient Mice
Analysis of Human Mutations in the Supernumerary Subunits of Complex I
PRAVEEN KUMAR DHANDAPANI: Expressing Alternative Oxidase
Activation of the Endogenous Renin-Angiotensin- Aldosterone System Or Aldosterone Administration Increases Urinary Exosomal Sodium Channel Excretion
Epididymal V-Atpase-Rich Cell Proteome Database
Effect of Redox-Cycling Agents on Nitric Oxide Synthase Activity In
Anti-NDUFS1 (Aa 88-137) Polyclonal Antibody (DPABH-28859) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Complex I Assembly Into Supercomplexes Determines Differential Mitochondrial ROS Production in Neurons and Astrocytes
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Histone Methyltransferase Smyd1 Regulates Mitochondrial Energetics in the Heart
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency Due to a Novel Mutation in the NDUFS1 Gene
Annual Symposium of the Society for the Study of Inborn Errors of Metabolism Istanbul, Turkey, 31 August– 3 September 2010
Distinct Requirements for Energy Metabolism in Mouse Primordial Germ Cells and Their Reprogramming to Embryonic Germ Cells
Supporting Information
Mutations in NDUFS1 Cause Metabolic Reprogramming and Disruption of the Electron Transfer
Critical Role of C-Jun N-Terminal Protein Kinase in Promoting Mitochondrial Dysfunction and Acute Liver Injury
Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1
Mutant NDUFS3 Subunit of Mitochondrial Complex I Causes Leigh Syndrome
Tnfa-Induced Lysosomal Membrane Permeability Is Downstream of MOMP and Triggered by Caspase
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Supporting Information
Genetic Variant in NDUFS1 Gene Is Associated with Schizophrenia and Negative Symptoms in Han Chinese
Genetic Features of Mitochondrial Respiratory Chain Disorders
Cytoglobin Protects Cancer Cells from Apoptosis by Regulation of Mitochondrial Cardiolipin Lorna S
Mitochondrial Complex I Activity and Oxidative Damage to Mitochondrial Proteins in the Prefrontal Cortex of Patients with Bipolar Disorder
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
NDUFS1 Rabbit Pab