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FBXO38
Inherited Neuropathies
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Appendix 2. Significantly Differentially Regulated Genes in Term Compared with Second Trimester Amniotic Fluid Supernatant
Genomic Diagnostics Within a Medically Underserved Population: Efficacy and Implications
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
A Genetic Investigation of the Muscle and Neuronal Channelopathies: from Sanger to Next – Generation Sequencing
Somatic Mutations in the Human Brain: Implications for Psychiatric Research
1 the Identification of Colorectal Cancer Susceptibility Genes Using
Supplemental Figures
Blueprint Genetics Spinal Muscular Atrophy Panel
1 Supplementary Material Figure S1. Volcano Plot of Differentially
Polarity Gene Alterations in Pure Invasive Micropapillary Carcinomas
Delineation of the Genome-Wide Recruitment of Hepatitis B Virus Trans-Activator Protein Hbx, in Primary Hepatocytes and Liver Cancer Cells
Computational Approaches for Disease Gene Identification
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Interactions and Functions of the Ubiquitin Specific Protease 7 in Human Cells
Analysis of Genetically Driven Alternative Splicing Identifies FBXO38 As a Novel COPD
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Whole Exome Sequencing to Identify Disease-Causing Mutations in Lower Motor Neuron Disease and Peripheral Neuropathy
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
Late-Onset Spinal Motor Neuronopathy – a New Neuromuscular Disease
Two-Stage Comprehensive Evaluation of Genetic Susceptibility of Common
Analysis of Genetically Driven Alternative Splicing Identifies