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GTF2I
Molecular Profile of Tumor-Specific CD8+ T Cell Hypofunction in a Transplantable Murine Cancer Model
Primary Driver Mutations in GTF2I Specific to the Development Of
Whole Genome Comparative Genomic Hybridization of Ewing Sarcoma Indicates Cytoskeleton, Migration and Protein Trafficking †
The Nuclear Localization Pattern and Interaction Partners of GTF2IRD1 Demonstrate a Role in Chromatin Regulation
The Tumor Suppressor Notch Inhibits Head and Neck Squamous Cell
Curcumin Alters Gene Expression-Associated DNA Damage, Cell Cycle, Cell Survival and Cell Migration and Invasion in NCI-H460 Human Lung Cancer Cells in Vitro
Supplementary Figure Legends
Characterization of Williams-Beuren Syndrome Mouse Models: Linking Genes with Cognition and Behaviour
Effects of Altered Gtf2i and Gtf2ird1 Expression on the Growth of Neural Progenitors and Organization of the Mouse Cortex
Supplementary Data
Molecular Targeting and Enhancing Anticancer Efficacy of Oncolytic HSV-1 to Midkine Expressing Tumors
WBSCR14, a Putative Transcription Factor Gene Deleted in Williams-Beuren Syndrome: Complete Characterisation of the Human Gene and the Mouse Ortholog
(12) Patent Application Publication (10) Pub. No.: US 2009/0269772 A1 Califano Et Al
Proteomic Profiling and Genome-Wide Mapping of O-Glcnac Chromatin
Mutant GTF2I Induces Cell Transformation and Metabolic Alterations in Thymic Epithelial Cells
Transcriptional Gene Expression Profiling of Small Cell Lung Cancer Cells1
RNA-Seq Analysis of Gtf2ird1 Knockout Epidermal Tissue Provides Potential Insights Into Molecular Mechanisms Underpinning Williams-Beuren Syndrome Susan M
Downloaded the Raw FASTQ Ously Published Genotype Data from 26 Microsatellites files from NCBI, and Reads Were Trimmed and Clipped with (Vonholdt Et Al
Top View
GTF2IRD2 Is Located in the Williams–Beuren Syndrome Critical Region 7Q11.23 and Encodes a Protein with Two TFII-I-Like Helix–Loop–Helix Repeats
S13229-020-00387-6.Pdf
Supplementary Table 1. HUGO Gene Nomenclature Committee (HGNC) Gene Symbols of Genes Included in the Targeted Next-Generation Sequencing Assay
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Mapping Gene Regulatory Circuitry of Pax6 During Neurogenesis
An Atypical 7Q11.23 Deletion in a Normal IQ Williams&Ndash
Generation of a Mouse Model for a Conditional Inactivation of Gtf2i Allele
GTF2IRD2 Is Located in the Williams–Beuren Syndrome Critical Region 7Q11.23 and Encodes a Protein with Two TFII-I-Like Helix–Loop–Helix Repeats
GTF2I Mutations Are Common in Thymic Epithelial Tumors but Not In
GTF2IRD1 Antibody Cat
Their Important Role in Wound Healing Supports Human
Mechanosensitive Mechanisms in Transcriptional Regulation
Data Set 1. Biological Analysis of the Genes Found to Be Significant in the Endotoxin Study
Supplementary Appendix
The Transcription Factor TCF-1 Initiates the Differentiation of TFH Cells During Acute Viral Infection
DNA Damage Response Defect in Williams‑Beuren Syndrome
GTF2I Gene General Transcription Factor Iii
Fine-Grained Temporal Mapping of Derived High-Frequency Variants