DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» SF3B5
SF3B5
SF3B2-Mediated RNA Splicing Drives Human Prostate Cancer Progression
Supplementary Files for Understanding the Functional Impact of Copy Number Alterations in Breast Cancers Using a Network Modeling Approach
Noelia Díaz Blanco
WO 2012/174282 A2 20 December 2012 (20.12.2012) P O P C T
Mrna Editing, Processing and Quality Control in Caenorhabditis Elegans
P53 and Sp1 Associated Rnas Act As Non-Coding Transcriptional Regulators at Homologous Loci
Encoded on Chromosome 6P21.33 in Human Breast Cancers Revealed by Transcrip- Tome Analysis Yan A
Variation in Protein Coding Genes Identifies Information Flow
Using Network Inference to Discover Molecular Pathways Underlying Cytokine Synergism and Age-Related Neurodegeneration by Bryce Hwang S.B., M.I.T
Quantitative Trait Loci Mapping of Macrophage Atherogenic Phenotypes
(A) Schematic Representation of the Secondary Assays Done to Control for Promoter Or Luciferase Specific Effects
Olea Europaea L
PHF5A Epigenetically Inhibits Apoptosis to Promote Breast Cancer Progression
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Prion Characterization Using Cell Based Approaches
S41467-021-25596-2.Pdf
Network-Based Metaanalysis Identifies HNF4A and PTBP1 As Longitudinally Dynamic Biomarkers for Parkinson’S Disease
Identification and Mechanistic Investigation of Recurrent Functional Genomic and Transcriptional Alterations in Advanced Prostat
Top View
HIV Tat Controls RNA Polymerase II and the Epigenetic Landscape
Extensive Cargo Identification Reveals Distinct Biological Roles of the 12 Importin Pathways Makoto Kimura1,*, Yuriko Morinaka1
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Towards the Identification of Novel Interferon-Alpha Induced Anti
Nucleomorph Genome Sequences of Two Chlorarachniophytes, Amorphochlora Amoebiformis and Lotharella Vacuolata
Β-Actin Dependent Chromatin Remodeling Mediates Compartment Level Changes in 3D Genome Architecture
View U.S. Patent No. 10131950 in PDF
Supplementary Data
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Universidade De Lisboa Faculdade De Ciências
Whole-Genome Sequencing Is More Powerful Than Whole-Exome Sequencing for Detecting Exome Variants
Splicing Modulators Act at the Branch Point Adenosine Binding Pocket Defined by the PHF5A–Sf3b Complex
Platelet Transcriptome Heterogeneity: a Role for RNA Uptake in Vascular Health and Disease
Rearrangements Within Human Spliceosomes Captured After Exon Ligation
The Extracellular Bone Marrow Microenvironment – a Proteomic Comparison of Constitutive Protein Release by in Vitro Cultured Osteoblasts and Mesenchymal Stem Cells