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LUC7L2
Analysis of Trans Esnps Infers Regulatory Network Architecture
Molecular Effects of Isoflavone Supplementation Human Intervention Studies and Quantitative Models for Risk Assessment
Aneuploidy: Using Genetic Instability to Preserve a Haploid Genome?
The H3K9 Methylation Writer SETDB1 and Its Reader MPP8 Cooperate to Silence Satellite DNA Repeats in Mouse Embryonic Stem Cells
Deep Multiomics Profiling of Brain Tumors Identifies Signaling Networks
Mutations in Splicing Factor Genes in Myeloid Malignancies: Significance and Impact on Clinical Features
Putative RNA-Splicing Gene LUC7L2 on 7Q34 Represents a Candidate Gene in Pathogenesis of Myeloid Malignancies
Functional Study of Mir-27A in Human Hepatic Stellate Cells by Proteomic Analysis: Comprehensive View and a Role in Myogenic Tans-Differentiation
MRTFB Suppresses Colorectal Cancer Development Through Regulating SPDL1 and MCAM
Cell-Type, Single-Cell, and Spatial Signatures of Brain-Region Specific
Recurrent Genetic Defects on Chromosome 7Q in Myeloid Neoplasms
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
I This Thesis Has Been Submitted in Fulfilment of the Requirements for A
Primepcr™Assay Validation Report
Sheet1 Page 1 Gene Symbol Gene Description Entrez Gene ID
Identification of High-Confidence RNA Regulatory Elements By
Functional Analysis of a Chromosomal Deletion Associated with Myelodysplastic Syndromes Using Isogenic Human Induced Pluripotent Stem Cells
Role of Glycogen Synthase Kinase-3 Beta in the Transition to Excessive Consumption
Top View
Conditional Resampling Improves Calibration and Sensitivity in Single-Cell CRISPR Screen Analysis
Promoterless Transposon Mutagenesis Drives Solid Cancers Via Tumor Suppressor Inactivation
Evidence for a Direct Role of the Disease Modifier SCNM1 in Splicing
Gene Trap Cassettes for Random and Targeted
LUC7L2 Shrna (M) Lentiviral Particles: Sc-149140-V
Supplemental Figure 1. Proliferation Status of Lung Cancer Cell Lines in 3D Lrecm
The Glomerular Transcriptome and a Predicted Protein–Protein Interaction Network
Structure-Function Relationships of Rna and Protein in Synaptic Plasticity
Using Massively Parallel Sequencing to Determine the Genetic Basis of Leigh Syndrome, the Most Common Mitochondrial Disorder Affecting Children
Comprehensive in Vivo Identification of the C-Myc Mrna Interactome Using Hypr-MS
Putative RNA-Splicing Gene LUC7L2 on 7Q34 Represents a Candidate Gene in Pathogenesis of Myeloid Malignancies
Supplementary Table 8. Genes Expressed in HNSCC and That Map to Regions Exhibiting Recurrent Genomic Amplification in Head and Neck Carcinomas
Loss of LUC7L2 and U1 Snrnp Subunits Shifts Energy Metabolism from Glycolysis to OXPHOS
A Pooled Genome-Wide Screening Strategy to Identify and Rank
Genetic Abnormalities and Pathophysiology of MDS
1 Functional Evidence Implicating Chromosome 7Q22 Haploinsufficiency In
View of Collapsing Methods
Longitudinal Dynamics of Clonal Hematopoiesis Identifies Gene-Specific Fitness Effects