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The Journal of Biological Chemistry|May 5, 1991
Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1J G Conboy, J Y Chan, J A Chasis, et al.
Molecular and Cellular Biology|April 5, 2012
Deep intron elements mediate nested splicing events at consecutive AG dinucleotides to regulate alternative 3' splice site choice in vertebrate 4.1 genesMarilyn K Parra, Thomas L Gallagher, Sharon L Amacher, et al.
Nucleic Acids Research|May 29, 2001
Computational analysis of candidate intron regulatory elements for tissue-specific alternative pre-mRNA splicingM Brudno, M S Gelfand, S Spengler, et al.
Scientific Reports|October 13, 2020
Selective effects of protein 4.1N deficiency on neuroendocrine and reproductive systemsHua Wang, Marilyn Parra, John G Conboy, et al.
The Journal of Clinical Investigation|January 1, 1993
An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cellsJ G Conboy, J A Chasis, R Winardi, et al.
Genomics|May 23, 1998
Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene familyM Parra, P Gascard, L D Walensky, et al.
Blood|December 1, 1995
Evolutionarily conserved alternative pre-mRNA splicing regulates structure and function of the spectrin-actin binding domain of erythroid protein 4.1R Winardi, D Discher, C Kelley, et al.
The Journal of Cell Biology|August 1, 1995
Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengtheningD E Discher, R Winardi, P O Schischmanoff, et al.
The Journal of Biological Chemistry|September 15, 1992
Human erythroid 5-aminolevulinate synthase. Gene structure and species-specific differences in alternative RNA splicingJ G Conboy, T C Cox, S S Bottomley, et al.
Blood|November 1, 1991
Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1J G Conboy, R Shitamoto, M Parra, et al.
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