Inducible nuclear factors binding the IgM heavy chain pre-mRNA secretory poly(A) site
- 1 December 1996
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 26 (12) , 3144-3152
- https://doi.org/10.1002/eji.1830261247
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Regulation of Poly(A) Site Use during Mouse B-Cell Development Involves a Change in the Binding of a General Polyadenylation Factor in a B-Cell Stage-Specific MannerMolecular and Cellular Biology, 1995
- Identification of an Activity in B-Cell Extracts That Selectively Impairs the Formation of an Immunoglobulin μs Poly(A) Site Processing ComplexMolecular and Cellular Biology, 1995
- Regulated immunoglobulin (Ig) RNA processing does not require specific cis-acting sequences: non-Ig RNA can be alternatively processed in B cells and plasma cells.Molecular and Cellular Biology, 1994
- Exon size affects competition between splicing and cleavage-polyadenylation in the immunoglobulin mu gene.Molecular and Cellular Biology, 1994
- Alternative poly(A) site utilization during adenovirus infection coincides with a decrease in the activity of a poly(A) site processing factor.Molecular and Cellular Biology, 1993
- An RNA-binding protein specifically interacts with a functionally important domain of the downstream element of the simian virus 40 late polyadenylation signal.Molecular and Cellular Biology, 1991
- The developmentally regulated shift from membrane to secreted mu mRNA production is accompanied by an increase in cleavage-polyadenylation efficiency but no measurable change in splicing efficiency.Molecular and Cellular Biology, 1991
- The regulated production of mu m and mu s mRNA is dependent on the relative efficiencies of mu s poly(A) site usage and the c mu 4-to-M1 splice.Molecular and Cellular Biology, 1989
- Polyadenylation of mRNA precursorsBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1988
- Transcriptional control of μ- and и-Gene expression in resting and bacterial lipopolysaccharide-activated normal B cellsImmunobiology, 1987