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FARS2
Supplemental Information to Mammadova-Bach Et Al., “Laminin Α1 Orchestrates VEGFA Functions in the Ecosystem of Colorectal Carcinogenesis”
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
A Common Analgesic Enhances the Anti-Tumour Activity of 5-Aza-2’- Deoxycytidine Through Induction of Oxidative Stress
Aminoacyl-Trna Synthetase Deficiencies in Search of Common Themes
Hereditary Spastic Paraplegia: from Genes, Cells and Networks to Novel Pathways for Drug Discovery
Identification of Genetic Modifiers in Hereditary Spastic Paraplegias Due to SPAST/SPG4 Mutations Livia Parodi
Downloaded Per Proteome Cohort Via the Web- Site Links of Table 1, Also Providing Information on the Deposited Spectral Datasets
New Insights Into the Phenotype of FARS2 Deficiency
Supplementary Data
Oxidized Phospholipids Regulate Amino Acid Metabolism Through MTHFD2 to Facilitate Nucleotide Release in Endothelial Cells
Massive Sequencing of 70 Genes Reveals a Myriad of Missing Genes Or Mechanisms to Be Uncovered in Hereditary Spastic Paraplegias
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Blueprint Genetics Spastic Paraplegia Panel
STAT3 Targets Suggest Mechanisms of Aggressive Tumorigenesis in Diffuse Large B Cell Lymphoma
FARS2 Mutations Presenting with Pure Spastic Paraplegia and Lesions of the Dentate Nuclei
Mitochondrial Dysfunction and Its Role in Tissue-Specific Cellular Stress
Clinical and Genetic Studies in Paediatric Mitochondrial Disease
Top View
Genetic Types of HSP* Autosomal Dominant
A Gene–Environment Interaction Between Smoking and Gene Polymorphisms Provides a High Risk of Two Subgroups of Sarcoidosis Natalia V
Biological Characterization of Adult MYC-Translocation-Positive Mature
Genes and Variants Underlying Human Congenital Lactic Acidosis—From Genetics to Personalized Treatment
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
Novel FARS2 Variants in Patients with Early Onset Encephalopathy with Or Without Epilepsy
TP53 Target Genes from Chea NR3C1 Target Genes From
Gain-Of-Function P53 Mutants Have Widespread Genomic Locations Partially Overlapping with P63
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Newborndxtm Advanced Sequencing Evaluation Disorders List
Supplementary File 1B Revised-Förslag
Dichloroacetate Prevents Cisplatin-Induced Nephrotoxicity Without Compromising Cisplatin Anticancer Properties
Multi-Omics Database Analysis of Aminoacyl-Trna Synthetases in Cancer
Db171195supplementarydata2.Pdf
Calmodulin Inhibition of E2A Differentiation Into Plasma Cells by Initiation of Antigen Receptor-Dependent
Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
Table of Contents List of Investigators
A Novel Homozygous YARS2 Mutation Causes Severe Myopathy, Lactic Acidosis, and Sideroblastic Anemia 2