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RBM26
Nuclear PTEN Safeguards Pre-Mrna Splicing to Link Golgi Apparatus for Its Tumor Suppressive Role
Proteomic Characterization of Transcription and Splicing Factors Associated with a Metastatic Phenotype in Colorectal Cancer
Single Cell Derived Clonal Analysis of Human Glioblastoma Links
Breeding Against Infectious Diseases in Animals
Thesis Front Matter
A Catalogue of Stress Granules' Components
A High Throughput, Functional Screen of Human Body Mass Index GWAS Loci Using Tissue-Specific Rnai Drosophila Melanogaster Crosses Thomas J
Systems Genetics Analysis of the LXS Recombinant Inbred Mouse Strains:Genetic and Molecular Insights Into Acute Ethanol Tolerance
Genetic Interaction Mapping and Exon-Resolution Functional Genomics with a Hybrid Cas9–Cas12a Platform
The Changing Chromatome As a Driver of Disease: a Panoramic View from Different Methodologies
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Nanopore Direct RNA Sequencing Detects DUX4-Activated Repeats and Isoforms in Human Muscle Cells
RADX Sustains POT1 Function at Telomeres to Counteract RAD51 Binding, Which Triggers Telomere Fragility
Developing a Network View of Type 2 Diabetes Risk Pathways Through Integration of Genetic, Genomic and Functional Data Juan Fernández-Tajes1†, Kyle J
Robust Sampling of Defective Pathways in Multiple Myeloma
Genetic Investigation in Non-Obstructive Azoospermia: from the X Chromosome to The
Figure S1 the Pipeline of Calling and Filtering Rare Variants from RNA-Seq Data in This Study
Antibodies Targeting Histone Marks Associated with Transcriptional Ac
Top View
SUPPLEMENTARY MATERIAL Differential Expression Profile Of
Supplementary Materials For
Platelet Transcriptome Heterogeneity: a Role for RNA Uptake in Vascular Health and Disease
Robust Sampling of Defective Pathways in Multiple Myeloma
INSTITUTO CARLOS CHAGAS Doutorado Em Biociências E Biotecnologia
Thomas Hennig
Supplementary Table 1. a Full List of Cancer Genes
Deciphering the Genetic Heterogeneity in Acute Myeloid Leukemia: Association of Gene Mutations with Distinct Chromosomal Aberrations