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MBNL2
MBNL1 Regulates Essential Alternative RNA Splicing Patterns in MLL-Rearranged Leukemia
Role and Regulation of the P53-Homolog P73 in the Transformation of Normal Human Fibroblasts
Identification of Protein Features Encoded by Alternative Exons Using Exon Ontology
ID AKI Vs Control Fold Change P Value Symbol Entrez Gene Name *In
Towards Personalized Medicine in Psychiatry: Focus on Suicide
Parental-To-Embryo Switch of Chromosome Organization in Early
Muscleblind-Like 2-Mediated Alternative Splicing in the Developing Brain and Dysregulation in Myotonic Dystrophy
Dynamics of Alternative Splicing During Somatic Cell Reprogramming Reveals Functions for RNA-Binding Proteins CPSF3, Hnrnp UL1 and TIA1
Mouse Mbnl2 Knockout Project (CRISPR/Cas9)
Network Pharmacology-Based Approach Uncovers the Mechanism of Guanxinning Tablet for Treating Thrombus by Mapks Signal Pathway
Supplementary Material Peptide-Conjugated Oligonucleotides Evoke Long-Lasting Myotonic Dystrophy Correction in Patient-Derived C
A Computational Analysis of Alternative Splicing Across Mammalian Tissues Reveals Circadian and Ultradian Rhythms in Splicing Events
Muscleblind-Like 2 Controls the Hypoxia Response of Cancer Cells
Muscleblind-Like 2 Controls the Hypoxia Response of Cancer Cells
Transcriptome Landscape of the Human Placenta Jinsil Kim1†, Keyan Zhao2†, Peng Jiang2†, Zhi-Xiang Lu2, Jinkai Wang2, Jeffrey C Murray3,4,5* and Yi Xing2,6,7*
Dynamics of Alternative Splicing During Somatic
Genome-Wide Transcriptome Analysis Identifies Alternative Splicing
Consequences of Aneuploidy in Human Fibroblasts with Trisomy 21
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29733 MBNL2 Antibody
Discovery and Validation of Blood Biomarkers for Suicidality
Sensory Neuropathy Affects Cardiac Mirna Expression Network Targeting
Microrna Binding Microrna Binding Probe Set Entrez Gene Gene
Decoding Differential Gene Expression
Data Mining for Identifying Key Genes in Biological Processes Using
Related Rnas Affecting Abiraterone E Cacy In
Transcriptional Maturation of the Mouse Auditory Forebrain Troy A
Modeling Microcephaly Caused by Inactivation of the Minor
Transcriptional Changes and Developmental Abnormalities in a Zebrafish Model of Myotonic Dystrophy Type 1 Peter K
RNA Structure Drives Interaction with Proteins
Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation