Amanote Research
Register
Sign In
Negative Regulation Contributes to Tissue Specificity of the Immunoglobulin Heavy-Chain Enhancer.
Molecular and Cellular Biology
- United States
doi 10.1128/mcb.7.7.2558
Full Text
Open PDF
Abstract
Available in
full text
Categories
Cell Biology
Molecular Biology
Date
July 1, 1987
Authors
J L Imler
C Lemaire
C Wasylyk
B Wasylyk
Publisher
American Society for Microbiology
Related search
Proteins Binding to Site C2 (muE3) in the Immunoglobulin Heavy-Chain Enhancer Exist in Multiple Oligomeric Forms.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Selective Utilization of Basic Helix-Loop-Helix-Leucine Zipper Proteins at the Immunoglobulin Heavy-Chain Enhancer.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Developmental Regulation of DNA Cytosine Methylation at the Immunoglobulin Heavy Chain Constant Locus
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Combinatorial Control of DNase I-Hypersensitive Site Formation and Erasure by Immunoglobulin Heavy Chain Enhancer-Binding Proteins
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Tissue Specificity of the Initiation of Immunoglobulin κGene Transcription
Hoppe-Seyler´s Zeitschrift für physiologische Chemie
Regulation of B Cell Fate Commitment and Immunoglobulin Heavy-Chain Gene Rearrangements by Ikaros
Nature Immunology
Allergy
Immunology
A Three-Protein-Dna Complex on a B Cell-Specific Domain of the Immunoglobulin Μ Heavy Chain Gene Enhancer
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Trans-Silencing Effect of the 3′RR Immunoglobulin Heavy Chain Enhancer on Igκ Transcription at the Pro-B Cell Stage
Cellular and Molecular Immunology
Infectious Diseases
Medicine
Allergy
Immunology
GATA Elements Are Necessary for the Activity and Tissue Specificity of the T-Cell Receptor Beta-Chain Transcriptional Enhancer.
Molecular and Cellular Biology
Cell Biology
Molecular Biology