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NDUFS3
Supplement 1 Overview of Dystonia Genes
Assessment of a Targeted Gene Panel for Identification of Genes Associated with Movement Disorders
1 Metabolic Dysfunction Is Restricted to the Sciatic Nerve in Experimental
Supplemental Table 10
Association of Gene Ontology Categories with Decay Rate for Hepg2 Experiments These Tables Show Details for All Gene Ontology Categories
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Growth and Gene Expression Profile Analyses of Endometrial Cancer Cells Expressing Exogenous PTEN
(12) Patent Application Publication (10) Pub. No.: US 2003/0082511 A1 Brown Et Al
Gene Expression Profiling Analysis of Lung Adenocarcinoma
Laser Microdissection-Based Microproteomics of the Hippocampus of a Rat Epilepsy Model Reveals Regional Diferences in Protein Abundances Amanda M
The Diabetic Brain and Cognition
Coupling Mitochondrial Respiratory Chain to Cell Death: an Essential Role of Mitochondrial Complex I in the Interferon-B and Retinoic Acid-Induced Cancer Cell Death
Biogenesis of NDUFS3-Less Complex I Indicates TMEM126A/OPA7 As an Assembly Factor of the ND4-Module
Downregulation of Carnitine Acyl-Carnitine Translocase by Mirnas
Pathogenetic and Prognostic Implications of Increased Mitochondrial Content in Multiple Myeloma
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
A Human-Mouse Conserved Sex Bias in Amygdala Gene Expression Related to Circadian Clock and Energy Metabolism Li-Chun Lin, David a Lewis and Etienne Sibille*
Integration of Multi-Omics Approaches for Functional Characterization Of
Top View
Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared Amongst Δγ T, Innate Lymphoid, and Th Cells
Using Machine Intelligence to Uncover Alzheimer's Disease Progression
Supplemental Figures 04 12 2017
Protective Effects of Flavonoids Against Mitochondriopathies and Associated Pathologies: Focus on the Predictive Approach and Personalized Prevention
The Crosstalk Between Hifs and Mitochondrial Dysfunctions in Cancer Development
Discovery of Pharmaceutically-Targetable Pathways and Prediction of Survivorship for Pneumonia and Sepsis Patients from the View Point of Ensemble Gene Noise
Analysis of the Expression and Single-Nucleotide Variant Frequencies of the Buyrophilin-Like 2 Gene in Patients with Uveal Melanoma
Pink1 Regulates the Oxidative Phosphorylation Machinery Via Mitochondrial fission
Characterization of Mitochondrial Health from Human Peripheral Blood
Enhanced Autophagic-Lysosomal Activity and Increased BAG3- Mediated Selective Macroautophagy As Adaptive Response of Neuronal Ce
Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's
From Genetics to Genomics of Epilepsy
Supplementary Figure (Legends in the Main Text): S1
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Identification and Mechanistic Investigation of Recurrent Functional Genomic and Transcriptional Alterations in Advanced Prostat
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Wasin Vol. 9 N. 4 2558.Pmd
Supplemental Materials Integrative Metabolomic and Transcriptomic
The Role of Microrna-23B-5P in Regulating Brown Adipogenesis and Thermogenic Program
Genomic Unity® Prenatal Analysis
Selective Antagonism of Muscarinic Receptors Is Neuroprotective in Peripheral Neuropathy
Altered Skeletal Muscle Lipase Expression and Activity Contribute to Insulin Resistance in Humans
Abordagens Diferentes, Um Único Objetivo: Compreender Os
Mutant NDUFS3 Subunit of Mitochondrial Complex I Causes Leigh Syndrome
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Arginine Starvation Elicits Chromatin Leakage and Cgas-STING Activation Via Epigenetic Silencing of Metabolic and DNA-Repair Genes
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Responsive Nuclear Proteins in Collecting Duct Cells
NDUFA10 Mutations Cause Complex I Deficiency in a Patient with Leigh Disease
Individual Genome Sequence Gene List (By Disease)
Supplementary File 2B Revised
Analysis of Differentially Expressed Mitochondrial Proteins in Chromo- Phobe Renal Cell Carcinomas and Renal Oncocytomas by 2-D Gel Electro- Phoresis Maria V
Supplementary Table 1; List of Analyzed Genes
Downloaded from Sequence Read Archive
Networks Predicted by Ingenuity Pathway Analysis in Atg7 Deficient Skeletal Muscle of Septic
Accession Gene Name Description Coverage
Acute Wheeze-Specific Gene Module Shows Correlation with Vitamin D and Asthma Medication
Mutant Plasticity Related Gene 1 (PRG1) Acts As a Potential Modifier in SCN1A Related Epilepsy
Recessive Gene List V2.0