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Fox-2 Splicing Factor Binds to a Conserved Intron Motif to Promote Inclusion of Protein 4.1R Alternative Exon 16

The Journal of biological chemistry, 2006-05, Vol.281 (18), p.12468-12474

2006

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Decrease in hnRNP A/B expression during erythropoiesis mediates a pre-mRNA splicing switch

The EMBO journal, 2002-11, Vol.21 (22), p.6195-6204

2002

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Distinct distribution of specific members of protein 4.1 gene family in the mouse nephron

Kidney international, 2003-04, Vol.63 (4), p.1321-1337

2003

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Differential domain evolution and complex RNA processing in a family of paralogous EPB41 (protein 4.1) genes facilitate expression of diverse tissue-specific isoforms

Genomics (San Diego, Calif.), 2004-10, Vol.84 (4), p.637-646

2004

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Evolutionarily conserved coupling of transcription and alternative splicing in the EPB41 (protein 4.1R) and EPB41L3 (protein 4.1B) genes

Genomics (San Diego, Calif.), 2005-12, Vol.86 (6), p.701-707

2005

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Molecular and Functional Characterization of Protein 4.1B, a Novel Member of the Protein 4.1 Family with High Level, Focal Expression in Brain

The Journal of biological chemistry, 2000-02, Vol.275 (5), p.3247-3255

2000

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Alternative 5′ exons and differential splicing regulate expression of protein 4.1R isoforms with distinct N-termini

Blood, 2003-05, Vol.101 (10), p.4164-4171

2003

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Regulation of alternative pre-mRNA splicing during erythroid differentiation

Current opinion in hematology, 2001-03, Vol.8 (2), p.74-79

2001

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Neurobehavioral deficits in mice lacking the erythrocyte membrane cytoskeletal protein 4.1

Current biology, 1998-11, Vol.8 (23), p.1269,S1-1272,S1

1998

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Cell Shape-dependent Regulation of Protein 4.1 Alternative Pre-mRNA Splicing in Mammary Epithelial Cells

The Journal of biological chemistry, 1997-04, Vol.272 (15), p.10254-10259

1997

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Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding (∗)

The Journal of biological chemistry, 1995-09, Vol.270 (36), p.21243-21250

1995

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The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane

Trends in biochemical sciences (Amsterdam. Regular ed.), 1998-08, Vol.23 (8), p.281-282

1998

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The 13-kD FK506 Binding Protein, FKBP13, Interacts with a Novel Homologue of the Erythrocyte Membrane Cytoskeletal Protein 4.1

The Journal of cell biology, 1998-04, Vol.141 (1), p.143-153

1998

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Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities

The Journal of clinical investigation, 1999-02, Vol.103 (3), p.331-340

1999

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Ca(2+)-dependent and Ca(2+)-independent calmodulin binding sites in erythrocyte protein 4.1. Implications for regulation of protein 4.1 interactions with transmembrane proteins

The Journal of biological chemistry, 2000-03, Vol.275 (9), p.6360-6367

2000

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Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells

Seminars in hematology, 1993-01, Vol.30 (1), p.58-73

Conboy, J G

1993

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Mechanochemistry of Protein 4.1's Spectrin-Actin-Binding Domain: Ternary Complex Interactions, Membrane Binding, Network Integration, Structural Strengthening

The Journal of cell biology, 1995-08, Vol.130 (4), p.897-907

1995

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Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1

The Journal of biological chemistry, 1993-04, Vol.268 (10), p.7186-7195

1993

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Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1

The Journal of biological chemistry, 1991-05, Vol.266 (13), p.8273-8280

1991

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Alternative splicing of protein 4.1R exon 16: ordered excision of flanking introns ensures proper splice site choice

Blood, 2000-01, Vol.95 (2), p.692-699

2000

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Multiple Protein 4.1 Isoforms Produced by Alternative Splicing in Human Erythroid Cells

Proceedings of the National Academy of Sciences - PNAS, 1988-12, Vol.85 (23), p.9062-9065

1988

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Evolutionarily Conserved Alternative Pre-mRNA Splicing Regulates Structure and Function of the Spectrin-Actin Binding Domain of Erythroid Protein 4.1

Blood, 1995-12, Vol.86 (11), p.4315-4322

1995

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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 cells

The Journal of clinical investigation, 1993-01, Vol.91 (1), p.77-82

1993

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Differential Use of Protein 4.1 Translation Initiation Sites During Erythropoiesis: Implications for a Mutation-Induced Stage-Specific Deficiency of Protein 4.1 During Erythroid Development

Blood, 1996-06, Vol.87 (12), p.5324-5331

1996

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Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency

The New England journal of medicine, 1986-09, Vol.315 (11), p.680-685

1986

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Fox-2 Splicing Factor Binds to a Conserved Intron Motif to Promote Inclusion of Protein 4.1R Alternative Exon 16

Decrease in hnRNP A/B expression during erythropoiesis mediates a pre-mRNA splicing switch

Distinct distribution of specific members of protein 4.1 gene family in the mouse nephron

Differential domain evolution and complex RNA processing in a family of paralogous EPB41 (protein 4.1) genes facilitate expression of diverse tissue-specific isoforms

Evolutionarily conserved coupling of transcription and alternative splicing in the EPB41 (protein 4.1R) and EPB41L3 (protein 4.1B) genes

Molecular and Functional Characterization of Protein 4.1B, a Novel Member of the Protein 4.1 Family with High Level, Focal Expression in Brain

Alternative 5′ exons and differential splicing regulate expression of protein 4.1R isoforms with distinct N-termini

Regulation of alternative pre-mRNA splicing during erythroid differentiation

Neurobehavioral deficits in mice lacking the erythrocyte membrane cytoskeletal protein 4.1

Cell Shape-dependent Regulation of Protein 4.1 Alternative Pre-mRNA Splicing in Mammary Epithelial Cells

Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding (∗)

The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane

The 13-kD FK506 Binding Protein, FKBP13, Interacts with a Novel Homologue of the Erythrocyte Membrane Cytoskeletal Protein 4.1

Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities

Ca(2+)-dependent and Ca(2+)-independent calmodulin binding sites in erythrocyte protein 4.1. Implications for regulation of protein 4.1 interactions with transmembrane proteins

Structure, function, and molecular genetics of erythroid membrane skeletal protein 4.1 in normal and abnormal red blood cells

Mechanochemistry of Protein 4.1's Spectrin-Actin-Binding Domain: Ternary Complex Interactions, Membrane Binding, Network Integration, Structural Strengthening

Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1

Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1

Alternative splicing of protein 4.1R exon 16: ordered excision of flanking introns ensures proper splice site choice

Multiple Protein 4.1 Isoforms Produced by Alternative Splicing in Human Erythroid Cells

Evolutionarily Conserved Alternative Pre-mRNA Splicing Regulates Structure and Function of the Spectrin-Actin Binding Domain of Erythroid Protein 4.1

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 cells

Differential Use of Protein 4.1 Translation Initiation Sites During Erythropoiesis: Implications for a Mutation-Induced Stage-Specific Deficiency of Protein 4.1 During Erythroid Development

Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency

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