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Disruption of the Mouse μ-Calpain Gene Reveals an Essential Role in Platelet Function

Molecular and Cellular Biology, 2001-03, Vol.21 (6), p.2213-2220

2001

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Using a histone yellow fluorescent protein fusion for tagging and tracking endothelial cells in ES cells and mice

Genesis (New York, N.Y. : 2000), 2005-07, Vol.42 (3), p.162-171

2005

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Acceleration of mesoderm development and expansion of hematopoietic progenitors in differentiating ES cells by the mouse Mix-like homeodomain transcription factor

Blood, 2006-04, Vol.107 (8), p.3122-3130

2006

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Identification of the proximal erythroid promoter region of the mouse anion exchanger gene

Blood, 1996-12, Vol.88 (12), p.4500-4509

1996

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Deletion in Erythrocyte Band 3 Gene in Malaria-Resistant Southeast Asian Ovalocytosis

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (24), p.11022-11026

1991

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Mutations of the Red Blood Cell Membrane Proteins: From Clinical Evaluation to Detection of the Underlying Genetic Defect

Blood, 1992-07, Vol.80 (2), p.308-330

1992

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Complete Deficiency of Glycophorin A in Red Blood Cells From Mice With Targeted Inactivation of the Band 3 (AE1) Gene

Blood, 1998-03, Vol.91 (6), p.2146-2151

1998

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The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin

The Journal of biological chemistry, 1990-03, Vol.265 (8), p.4434-4443

1990

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The Structure and Organization of the Human Erythroid Anion Exchanger (AE1) Gene

Genomics (San Diego, Calif.), 1994-12, Vol.24 (3), p.491-501

1994

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Band 3 memphis : a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG→GAG (Lys→Glu) in codon 56

Blood, 1992-09, Vol.80 (6), p.1592-1598

1992

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Asynchronous Synthesis of Membrane Skeletal Proteins During Terminal Maturation of Murine Erythroblasts

Blood, 1992-07, Vol.80 (2), p.530-539

1992

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A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis

The Journal of clinical investigation, 1994-08, Vol.94 (2), p.643-648

1994

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Identification of the mouse homologue of human discs large and rat SAP97 genes

Biochimica et biophysica acta, 1997-11, Vol.1362 (1), p.1-5

1997

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Complete Genomic Organization of the Human Erythroid p55 Gene (MPP1), a Membrane-Associated Guanylate Kinase Homologue

Genomics (San Diego, Calif.), 1996-01, Vol.31 (2), p.223-229

1996

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Molecular Basis of Spectrin Deficiency in Hereditary Pyropoikilocytosis

Blood, 1993-09, Vol.82 (5), p.1652-1660

1993

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Spectrin cagliari. an Ala–>Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

The Journal of biological chemistry, 1993-10, Vol.268 (30), p.22656-22662

1993

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Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect

Blood, 1992-07, Vol.80 (2), p.308-330

1992

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Sequence and exon-intron organization of the DNA encoding the αI domain of human spectrin: application to the study of mutations causing hereditary elliptocytosis

The Journal of clinical investigation, 1989-10, Vol.84 (4), p.1243-1252

1989

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Isolation and chromosomal localization of a novel nonerythroid ankyrin gene

Genomics (San Diego, Calif.), 1991-08, Vol.10 (4), p.858-866

1991

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Molecular Cloning of the cDNA for Human Erythrocyte β-Spectrin

Blood, 1988-07, Vol.72 (1), p.328-334

1988

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Erythropoietin enhances the assembly of alpha,beta spectrin heterodimers on the murine erythroblast membranes by increasing beta spectrin synthesis

The Journal of biological chemistry, 1991-08, Vol.266 (24), p.15626-15630

1991

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Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis

Blood, 1993-09, Vol.82 (5), p.1652-1660

1993

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SpαI/78: a mutation of the αI spectrin domain in a white kindred with HE and HPP phenotypes

Blood, 1989-08, Vol.74 (3), p.1126-1133

1989

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Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts

Blood, 1992-07, Vol.80 (2), p.530-539

1992

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Spectrin Cagliari: An Ala arrow right Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

The Journal of biological chemistry, 1993-01, Vol.268 (30), p.22656-22662

1993

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Disruption of the Mouse μ-Calpain Gene Reveals an Essential Role in Platelet Function

Using a histone yellow fluorescent protein fusion for tagging and tracking endothelial cells in ES cells and mice

Acceleration of mesoderm development and expansion of hematopoietic progenitors in differentiating ES cells by the mouse Mix-like homeodomain transcription factor

Identification of the proximal erythroid promoter region of the mouse anion exchanger gene

Deletion in Erythrocyte Band 3 Gene in Malaria-Resistant Southeast Asian Ovalocytosis

Mutations of the Red Blood Cell Membrane Proteins: From Clinical Evaluation to Detection of the Underlying Genetic Defect

Complete Deficiency of Glycophorin A in Red Blood Cells From Mice With Targeted Inactivation of the Band 3 (AE1) Gene

The complete cDNA and polypeptide sequences of human erythroid alpha-spectrin

The Structure and Organization of the Human Erythroid Anion Exchanger (AE1) Gene

Band 3 memphis : a widespread polymorphism with abnormal electrophoretic mobility of erythrocyte band 3 protein caused by substitution AAG→GAG (Lys→Glu) in codon 56

Asynchronous Synthesis of Membrane Skeletal Proteins During Terminal Maturation of Murine Erythroblasts

A novel mobile element inserted in the alpha spectrin gene: spectrin dayton. A truncated alpha spectrin associated with hereditary elliptocytosis

Identification of the mouse homologue of human discs large and rat SAP97 genes

Complete Genomic Organization of the Human Erythroid p55 Gene (MPP1), a Membrane-Associated Guanylate Kinase Homologue

Molecular Basis of Spectrin Deficiency in Hereditary Pyropoikilocytosis

Spectrin cagliari. an Ala–>Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect

Sequence and exon-intron organization of the DNA encoding the αI domain of human spectrin: application to the study of mutations causing hereditary elliptocytosis

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene

Molecular Cloning of the cDNA for Human Erythrocyte β-Spectrin

Erythropoietin enhances the assembly of alpha,beta spectrin heterodimers on the murine erythroblast membranes by increasing beta spectrin synthesis

Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis

SpαI/78: a mutation of the αI spectrin domain in a white kindred with HE and HPP phenotypes

Asynchronous synthesis of membrane skeletal proteins during terminal maturation of murine erythroblasts

Spectrin Cagliari: An Ala arrow right Gly substitution in helix 1 of beta spectrin repeat 17 that severely disrupts the structure and self-association of the erythrocyte spectrin heterodimer

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