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MEGF10
Supplementary Table 1: Adhesion Genes Data Set
Detailed Characterization of Human Induced Pluripotent Stem Cells Manufactured for Therapeutic Applications
Brain Region-Specific Gene Signatures Revealed by Distinct Astrocyte Subpopulations Unveil Links to Glioma and Neurodegenerative
Identification of Shared and Unique Gene Families Associated with Oral
Regulation of Muscle Stem Cell Function by the Transcription Factor Pax7
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita
Computational Evaluation of Exome Sequence Data Using Human and Model Organism Phenotypes Improves Diagnostic Efficiency
SARS-Cov-2 Infected Pediatric Cerebral Cortical Neurons: Transcriptomic Analysis and Potential Role of Toll-Like Receptors in Pathogenesis
PARKINSON DISEASE LOCI in the MID-WESTERN AMISH by Mary
Fine Mapping of a Linkage Peak with Integration of Lipid Traits Identifies
Differentially Expressed Genes in Aneurysm Tissue Compared With
The Role of MEGF10 in Skeletal Muscle Myopathy
Genome-Wide DNA Methylation Analysis Identifies MEGF10 As a Novel Epigenetically Repressed Candidate Tumour Suppressor Gene in Neuroblastoma
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
An Integrative Genomic Analysis of the Longshanks Selection Experiment for Longer Limbs in Mice
Single-Cell Transcriptomics of the Developing Lateral PNAS PLUS Geniculate Nucleus Reveals Insights Into Circuit Assembly and Refinement
The Influence of Notch Over-Stimulation on Muscle Stem Cell Quiescence Versus Proliferation, and on Muscle Regeneration Can Ding
Modeling Pulmonary Fibrosis by AAV-Mediated Tgfβ1 Expression – a Proof of Concept Study for AAV-Based Disease Modeling and Riboswitch-Controlled Vector Production
Top View
A Novel Duplication Confirms the Involvement of 5Q23.2 in Autosomal Dominant Leukodystrophy
Genetic Variants in the Transcription Regulatory Region of MEGF10 Are
Genome-Scale Profiling Reveals a Subset of Genes Regulated by DNA
Mutations in the Satellite Cell Gene MEGF10 Cause a Recessive Congenital Myopathy with Minicores
Transcriptome of the Eastern Oyster Crassostrea Virginica in Response to Bacterial Challenge
Supplementary Methods
Degenerative and Regenerative Pathways Underlying Duchenne Muscular Dystrophy Revealed by Single-Nucleus RNA Sequencing
Genome-Wide DNA Methylation Analysis Identifies MEGF10 As a Novel Epigenetically
Single-Cell and Single-Nucleus RNA-Seq Uncovers Shared
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Fa
Gene Expression Profiling and Functional Studies of Astrocytes in SOD1-Related Amyotrophic Lateral Sclerosis
Supporting Information Appendix SI Materials and Methods
Evaluation and Optimization of the Translational Potential of Array
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
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ACTA MYOLOGICA (Myopathies, Cardiomyopathies and Neuromyopathies)
Comprehensive Identification of Mrna Isoforms Reveals the Diversity of Neural Cell-Surface Molecules with Roles in Retinal Devel
Identification of Candidate Tumor Oncogenes by Integrative Molecular Analysis of Choroidal Melanoma Fine-Needle Aspiration Biopsy Specimens