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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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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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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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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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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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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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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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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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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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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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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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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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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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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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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

Volltextzugriff (PDF)

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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Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis

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

1993

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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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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

Volltextzugriff (PDF)

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

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

1988

Volltextzugriff (PDF)

Ebola RNA Persistence in Semen of Ebola Virus Disease Survivors — Final Report

The New England journal of medicine, 2017-10, Vol.377 (15), p.1428-1437

2017

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Persistence of Ebola virus in semen among Ebola virus disease survivors in Sierra Leone: A cohort study of frequency, duration, and risk factors

PLoS medicine, 2021-02, Vol.18 (2), p.e1003273-e1003273

2021

Volltextzugriff (PDF)

Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1989, Vol.308 (2), p.43

1989

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

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

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

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

Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (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

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

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

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene

Molecular Cloning of the cDNA for Human Erythrocyte β-Spectrin

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

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

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

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

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

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

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

Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis

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

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

Molecular cloning of the cDNA for human erythrocyte beta-spectrin

Ebola RNA Persistence in Semen of Ebola Virus Disease Survivors — Final Report

Persistence of Ebola virus in semen among Ebola virus disease survivors in Sierra Leone: A cohort study of frequency, duration, and risk factors

Research on genetic abnormality in the hemolytic form of hereditary elliptocytosis with homozygosity for the spectrin alpha I/74 variant

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