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AARS2
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Abstracts from the 50Th European Society of Human Genetics Conference: Electronic Posters
Supplementary Data.Xlsx
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
The Promise of Whole-Exome Sequencing in Medical Genetics
Hormone and Inhibitor Treatment T47DM Cells Were Used for All Experiments Unless Otherwise Stated
Anti-AARS2 (Internal Region) Polyclonal Antibody (DPAB-DC2592) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Impact of Exome Sequencing in Characterizing Mendelian Disorders
Overexpression of Human Mitochondrial Alanyl-Trna Synthetase Suppresses Biochemical Defects of the Mt-Trnaala Mutation in Cybrid
Supplementary Table S1. List of All the Proteins Identified by Itraq Analysis
Clinical and Genetic Studies in Paediatric Mitochondrial Disease
Molecular Epidemiology of Mitochondrial Cardiomyopathy:A Search Among Mitochondrial and Nuclear Genes
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the Babyseq Project
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Supplementary Table 2. List of the Genes Implicated in Known Gld and Early Onset Hereditary Spastic Paraplegia Tested in Our Series
1 Characterizing the Function of Alanyl-Trna Synthetase Activity In
Evaluating Differential Gene Expression Using Rna-Sequencing: a Case Study in Diet-Induced Mouse Model Associated with Non- Alco
Structural Modeling of Tissue-Specific Mitochondrial Alanyl-Trna Synthetase (AARS2) Defects Predicts Differential Effects On
Top View
Primate Specific Retrotransposons, Svas, in the Evolution of Networks That Alter Brain Function
Newborndxtm Advanced Sequencing Evaluation Disorders List
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Platform Abstracts
Structural Modeling of Tissue-Specific Mitochondrial Alanyl-Trna Synthetase (AARS2) Defects Predicts Differential Effects On
Mitochondria and Disease: Mutation and Expression Landscape of Mitochondri-Associated Genes in Different Disease Types
Mitochondrial/Metabolic Oligonucleotide Array CGH Analysis
Recessive VARS2 Mutation Underlies a Novel Syndrome with Epilepsy, Mental Retardation, Short Stature, Growth Hormone Deficiency
Poster Session I – Sunday, 23 June - 12.30-14.30
Generated by SRI International Pathway Tools Version 25.0 on Mon
Preclinical Modeling of Musculoskeletal Cancer Dissertation Presented in Partial Fulfillment of the Requirements for the Degree
Trna Metabolism and Neurodevelopmental Disorders
Mutations in ELAC2 Associated with Hypertrophic Cardiomyopathy Impair Mitochondrial Trna 3’-End Processing
Individual Genome Sequence Gene List (By Disease)
Mitochondrial Aminoacyl-Trna Synthetase and Disease: the Yeast Contribution for Functional Analysis of Novel Variants
Responsive Nuclear Proteins in Collecting Duct Cells
Research Article the Potential Protective Effect of Curcumin on Amyloid- -42 Induced Cytotoxicity in HT-22 Cells
Generated by SRI International Pathway Tools Version 24.0 on Thu
Molecular Genetics and Metabolism 117 (2016) 221–298
Exome Sequencing Greatly Expedites the Progressive Research of Mendelian Diseases
Submitochondrial Organization of Human Mitochondrial Aspartyl-Trna Synthetase and Its Implication in LBSL Disease Loukmane Karim
Recessive Gene List V2.0