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SMN2
Systemic Restoration of UBA1 Ameliorates Disease in Spinal Muscular Atrophy
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Mitochondrial Heat Shock Protein 60: Evaluation of Its Role As a Neuroprotectant in Familial ALS and Its Mutation As a Cause of Hereditary Spastic Paraplegia
Supplementary Table S1. Correlation Between the Mutant P53-Interacting Partners and PTTG3P, PTTG1 and PTTG2, Based on Data from Starbase V3.0 Database
The Ubiquitin Proteasome System in Neuromuscular Disorders: Moving Beyond Movement
FARE2021WINNERS Sorted by Institute
SPINAL MUSCULAR ATROPHY: PATHOLOGY, DIAGNOSIS, CLINICAL PRESENTATION, THERAPEUTIC STRATEGIES & TREATMENTS Content
Supplementary Material Contents
Hnrnp C1/C2 May Regulate Exon 7 Splicing in the Spinal Muscular Atrophy Gene SMN1
Newborn Screening for Spinal Muscular Atrophy (SMA): Phase I Update of the Evidence Review
Genome-Wide Identification of Mrnas Associated with the Protein SMN Whose Depletion Decreases Their Axonal Localization
Role of Dcps in Mammalian RNA Regulation and Human Diseases
Mechanistic Studies of a Small-Molecule Modulator of SMN2 Splicing
ML372 Blocks SMN Ubiquitination and Improves Spinal Muscular Atrophy Pathology in Mice
Spinal Muscular Atrophy Testing
SMN2 Gene Survival of Motor Neuron 2, Centromeric
Noncoding Rnas in Glioblastoma: Emerging Biological Concepts and Potential Therapeutic Implications
Dysregulation of Ubiquitin Homeostasis and Β-Catenin Signaling Promote Spinal Muscular Atrophy Thomas M
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Microarray Analyses Reveal Strong Influence of DNA Copy Number
Graduate Students Alphabetical by Graduate Student Last Name
Proteomic Assessment of a Cell Model of Spinal Muscular Atrophy
Genetic Analysis of ALS Cases in the Isolated Island Population of Malta
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Transcriptome Profiling of Spinal Muscular Atrophy Motor Neurons Derived from Mouse Embryonic Stem Cells
Mechanistic Studies of a Small-Molecule Modulator of SMN2 Splicing
Supplemental Table 3 Two-Class Paired Significance Analysis of Microarrays Comparing Gene Expression Between Paired
Correlation Between SMA Type and SMN2 Copy Number Revisited: An
SMN1 and Spinal Muscular Atrophy Description Spinal Muscular Atrophy Is a Genetic Disorder That Affects the Control of Muscle Movement
Supplementary Data
LCM-Seq Reveals Unique Transcriptional Adaptation Mechanisms of Resistant Neurons and Identifies Protective Pathways in Spinal Muscular Atrophy
Spinal Muscular Atrophy
Genetic Testing for Hereditary and Multifactorial Conditions
Stress-Responsive MDM2 Alternative Splicing: Regulation and Consequences
Sumoylation Regulates the Assembly and Activity of the SMN Complex
Differential Gene Expression During Placentation in Pregnancies Conceived with Different Fertility Treatments Compared with Spontaneous Pregnancies
Example Report Indicating Abnormal Screening
The Importance of Digging Into the Genetics of SMN Genes in the Therapeutic Scenario of Spinal Muscular Atrophy
Lysine-Less Variants of Spinal Muscular Atrophy SMN and SMN7
Systemic Restoration of UBA1 Ameliorates Disease in Spinal Muscular Atrophy
Full Disclosure Forms
Geisinger Health Plan Policies and Procedure Manual
A Crucial Role for the Protein Quality Control System in Motor Neuron Diseases
Towards Improved Therapies, Model Systems and Understanding of Spinocerebellar Ataxia Type 3
SMN Deficiency in Severe Models of Spinal Muscular Atrophy Causes
A Single Amino Acid Residue Regulates PTEN-Binding and Stability of the Spinal Muscular Atrophy Protein SMN
The Prior Authorization List
1. Introduction 1.1
Discovery of a CNS Penetrant Small Molecule SMN2 Splicing Modulator
Identification of Modifiers of Spinal Muscular Atrophy
SMN Deficiency in Severe Models of Spinal Muscular Atrophy Causes
Multi-Study Proteomic Identification of Conserved Disease Mechanisms In
Systematic Analysis of Dark and Camouflaged Genes: Disease-Relevant Genes Hiding in Plain 2 Sight 3 4 Mark T
Removal of the Polyglutamine Repeat of Ataxin-3 by Redirecting Pre-Mrna Processing
Label-Free Proteomics Identifies Calreticulin and GRP75/Mortalin As Peripherally Accessible Protein Biomarkers for Spinal Muscul
New Insights on the Evolution of the SMN1 and SMN2 Region: Simulation and Meta-Analysis for Allele and Haplotype Frequency Calculations
Prenatal Cytogenetics Requisition
Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
957 AIM Genetic Testing Management Program CPT and HCPCS Codes
Dysregulation of Mdm2 and Mdm4 Alternative Splicing Underlies Motor Neuron Death in Spinal Muscular Atrophy
Supplementary Information
Cure Sma Care Series Booklet Guide for Healthcare Providers What You Need to Know and Do About an Sma Diagnosis
Evidence for Gene Conversion from SMN2 to SMN1
Supplementary Table 1. a Full List of Cancer Genes
The Role of Muscle and Nerve in Spinal Muscular Atrophy
Proteomic Assessment of a Cell Model of Spinal Muscular Atrophy
1 Combining Multi-Omics and Drug Perturbation Profiles to Identify Novel Treatments That Improve Disease Phenotypes in Spinal Mu