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DHX36
Chronic Exposure of Humans to High Level Natural Background Radiation Leads to Robust Expression of Protective Stress Response Proteins S
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Exploring the Role of a PYHIN Protein and Involvement of Caspase-8 in the Regulation and Activation of Inflammasomes
The RNA Helicase RHAU (DHX36) Unwinds a G4-Quadruplex in Human Telomerase RNA and Promotes the Formation of the P1 Helix Template Boundary E
Highlights of the Advances in Basic Immunology in 2011
Supplementary Data.Xlsx
Supplemental Table 1A. Differential Gene Expression Profile of Adehcd40l and Adehnull Treated Cells Vs Untreated Cells
Human Proteins That Interact with RNA/DNA Hybrids
Understanding the Molecular Mechanisms of The
Genome-Wide CRISPR Screen for PARKIN Regulators Reveals Transcriptional Repression As a Determinant of Mitophagy
Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors
DHX36 Prevents the Accumulation of Translationally Inactive Mrnas with G4-Structures in Untranslated Regions
Supplemental Solier
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
Glucagon-Like Peptide-1 Receptor Agonists Increase Pancreatic Mass by Induction of Protein Synthesis
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Microrna-203 Represses Selection and Expansion of Oncogenic Hras Transformed Tumor Initiating Cells
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses by a Synthetic TLR3 Ligand Mitigates
Top View
Mrna Translation Control by Dhx36 Binding to 5'UTR G-Quadruplex
Identification of DHX36 As a Tumour Suppressor Through Modulating The
Original Article Identification of DHX36 As a Tumour Suppressor Through
Unveiling Comparative Genomic Trajectories of Selection and Key Candidate Genes in Egg-Type Russian White and Meat-Type White Cornish Chickens
Enhanced Autophagic-Lysosomal Activity and Increased BAG3- Mediated Selective Macroautophagy As Adaptive Response of Neuronal Ce
Exploring Novel Triggers for Messenger Rna Decay in Eukaryotes
The RNA Helicase DHX36/G4R1 Modulates C9orf72 GGGGCC Repeat- Associated Translation
Downloaded from to Pre-Chilled 1.5 Ml Tubes
A Master Autoantigen-Ome Links Alternative Splicing, Female Predilection, and COVID-19 to Autoimmune Diseases
Exome Sequencing Enhanced Package Department of Pathology and Laboratory Medicine Feb 2012 UCLA Molecular Diagnostics Laboratories Page:1
613 Up-Regulated Genes in SOS Compared to Control Livers (FDR Adjusted P-Value ≤ 0.05) Fold- Chang Adjusted P-Value E (SOS P-Value Gene Symbol Name (SOS Vs
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Immunity Resolution of Inflammation and Airway Diversity in Expression with Critical Roles in Macrophage Populations Reveals
Supplementary Table 1
Sequence List Acetylome-Acetyltransferase JPT
How to Untie G-Quadruplex Knots and Why? Pauline Lejault, Jérémie Mitteaux, Francesco Sperti, David Monchaud
SUPPLEMENTARY MATERIAL Differential Expression Profile Of
Approaching Protein Barriers: Emerging Mechanisms of Replication Pausing in Eukaryotes
Modeling Gene Regulation from Paired Expression and Chromatin Accessibility Data
Responsive Nuclear Proteins in Collecting Duct Cells
Table SI. Targets of Berberine. Gene Symbol Gene Name ABL1 ABO
Translational Control by DHX36 Binding to 5′UTR G-Quadruplex Is Essential for Muscle Stem-Cell Regenerative Functions
Identification and Characterization of the RIG-I Helicase Partners Involved in the Balance Proliferation / Cell Differentiation
RNA G-Quadruplex Is Resolved by Repetitive and ATP-Dependent Mechanism of DHX36
RNA–Protein Analysis Using a Conditional CRISPR Nuclease
Quantitative Proteomics Identifies Vasopressin- Responsive Nuclear Proteins in the Collecting Duct”
Responsive Nuclear Proteins in Collecting Duct Cells
DHX36 Binding at G-Rich Sites in Mrna Untranslated Regions Promotes Translation
Supp Tables S1-S7.Pdf
S1- Alphabetical List of Aging-Related Genes
Bidirectional Genome-Wide CRISPR Screens Reveal Host Factors Regulating SARS-Cov-2, MERS-Cov and Seasonal Hcovs