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VARS2
Anti-VARS (Aa 994-1102) Polyclonal Antibody (DPAB-DC3179) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen
Supporting Information
Rabbit Anti-Valyl Trna/FITC Conjugated Antibody-SL10504R
Clinical, Biochemical, and Genetic Features Associated with VARS2-Related Mitochondrial Disease
Mouse Vars2 Knockout Project (CRISPR/Cas9)
Physiological and Molecular Consequences of Large Y Chromosome Long Arm Deletions in Mice
Gene Expression Imputation Across Multiple Brain Regions Provides Insights Into Schizophrenia Risk
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Skeletal Phenotypes Due to Abnormalities in Mitochondrial Protein Homeostasis and Import
Histocompatibility Complex
A Novel Compound Heterozygous Mutation in VARS2 in a Newborn
Recessive VARS2 Mutation Underlies a Novel Syndrome with Epilepsy, Mental Retardation, Short Stature, Growth Hormone Deficiency
The HLA Genomic Loci Map: Expression, Interaction, Diversity and Disease
Biallelic VARS Variants Cause Developmental Encephalopathy with Microcephaly That Is Recapitulated in Vars Knockout Zebrafish
Multi-Omics Database Analysis of Aminoacyl-Trna Synthetases in Cancer
Identification and Functional Validation of New Mtdna and Nuclear Gene Variants Responsible for Mitochondrial Disorders
Top View
The Complex Genetics of Multiple Sclerosis a Preliminary Study of MS-Associated Snps Prior to a Larger Genotyping Project
CENPL, ISG20L2, LSM4, MRPL3 Are Four Novel Hub Genes And
MRNA Transcription, Translation, and Defects in Developmental Cognitive and Behavioral Disorders
Diversity Outbred Mice Reveal the Quantitative Trait Locus and Regulatory Cells of HER2 Immunity
Trna Metabolism and Neurodevelopmental Disorders
A Mitochondrial Trna Mutation Causes Axonal Charcot-Marie-Tooth Disease in a Large Family from the Venezuelan Andes
Genome-Wide Meta-Analysis of Brain Volume Identifies Genomic Loci And
A Non-Negative Matrix Factorization Network Analysis Method for Identifying Communities and Characteristic Genes from Pancreatic Cancer Data
Mitochondrial Aminoacyl-Trna Synthetase and Disease: the Yeast Contribution for Functional Analysis of Novel Variants
Gene Section Review
Overview of Inactivating Mutations in the Protein-Coding Genome of the Mouse Reference Strain C57BL/6J