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Classification of the disorders of hemoglobin

Cold Spring Harbor perspectives in medicine, 2013-02, Vol.3 (2), p.a011684-a011684

2013

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Erythroid and Nonerythroid Spectrins

Blood, 1993-06, Vol.81 (12), p.3173-3185

1993

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Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Haematologica (Roma), 2014-09, Vol.99 (9), p.e168

2014

Volltextzugriff (PDF)

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Nature genetics, 1996-06, Vol.13 (2), p.214-218

1996

Volltextzugriff (PDF)

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter

Blood, 2000-08, Vol.96 (3), p.1136-1143

2000

Volltextzugriff (PDF)

Full-length sequence of the cDNA for human erythroid beta-spectrin

The Journal of biological chemistry, 1990-07, Vol.265 (20), p.11827-11832

1990

Volltextzugriff (PDF)

An Olfactory Receptor Gene Is Located in the Extended Human β-Globin Gene Cluster and Is Expressed in Erythroid Cells

Genomics (San Diego, Calif.), 1999-10, Vol.61 (1), p.15-23

1999

Volltextzugriff (PDF)

Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

Blood, 1997-06, Vol.89 (12), p.4628-4635

1997

Volltextzugriff (PDF)

The Gene for the Human Erythropoietin Receptor: Analysis of the Coding Sequence and Assignment to Chromosome 19p

Blood, 1990-07, Vol.76 (1), p.24-30

1990

Volltextzugriff (PDF)

Ankyrin Binds to the 15th Repetitive Unit of Erythroid and Nonerythroid β-Spectrin

The Journal of cell biology, 1991-10, Vol.115 (1), p.267-277

1991

Volltextzugriff (PDF)

Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3' beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus

The Journal of biological chemistry, 1990-11, Vol.265 (33), p.20449-20454

1990

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A partial structural repeat forms the heterodimer self-association site of all beta-spectrins

The Journal of biological chemistry, 1994-04, Vol.269 (15), p.11400-11408

1994

Volltextzugriff (PDF)

YAC Transgenes: Bigger is Probably Better

Proceedings of the National Academy of Sciences - PNAS, 1993-09, Vol.90 (17), p.7909-7911

Forget, Bernard G.

1993

Volltextzugriff (PDF)

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

British journal of haematology, 1996-10, Vol.95 (1), p.57-66

1996

Volltextzugriff (PDF)

The Breakpoint of a Large Deletion Causing Hereditary Persistence of Fetal Hemoglobin Occurs Within an Erythroid DNA Domain Remote From the β-Globin Gene Cluster

Blood, 1989-11, Vol.74 (6), p.2178-2186

1989

Volltextzugriff (PDF)

High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin

Molecular and Cellular Biology, 1997-04, Vol.17 (4), p.2076-2089

1997

Volltextzugriff (PDF)

Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-association

The Journal of clinical investigation, 1990-09, Vol.86 (3), p.909-916

1990

Volltextzugriff (PDF)

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

American journal of hematology, 1997-03, Vol.54 (3), p.242-248

1997

Volltextzugriff (PDF)

Developmental Regulation of Human γ- and β-Globin Genes in the Absence of the Locus Control Region

Blood, 1994-09, Vol.84 (5), p.1656-1665

1994

Volltextzugriff (PDF)

β Spectrin kissimmee : a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1

The Journal of clinical investigation, 1993-08, Vol.92 (2), p.612-616

1993

Volltextzugriff (PDF)

A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain

The Journal of biological chemistry, 1991-08, Vol.266 (23), p.15154-15159

1991

Volltextzugriff (PDF)

Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell line

Molecular and Cellular Biology, 1991-07, Vol.11 (7), p.3528-3536

1991

Volltextzugriff (PDF)

Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase

Gene, 1990-04, Vol.88 (2), p.293-296

1990

Volltextzugriff (PDF)

Spectrin genes in health and disease

Seminars in hematology, 1993-01, Vol.30 (1), p.4-20

1993

Volltextzugriff (PDF)

Characterization of the calmodulin-binding site of nonerythroid alpha-spectrin. Recombinant protein and model peptide studies

The Journal of biological chemistry, 1989-04, Vol.264 (10), p.5826-5830

1989

Volltextzugriff (PDF)

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Classification of the disorders of hemoglobin

Erythroid and Nonerythroid Spectrins

Severe nondominant hereditary spherocytosis due to uniparental isodisomy at the SPTA1 locus

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter

Full-length sequence of the cDNA for human erythroid beta-spectrin

An Olfactory Receptor Gene Is Located in the Extended Human β-Globin Gene Cluster and Is Expressed in Erythroid Cells

Familial Erythrocytosis Associated With a Short Deletion in the Erythropoietin Receptor Gene

The Gene for the Human Erythropoietin Receptor: Analysis of the Coding Sequence and Assignment to Chromosome 19p

Ankyrin Binds to the 15th Repetitive Unit of Erythroid and Nonerythroid β-Spectrin

Beta spectrin in human skeletal muscle. Tissue-specific differential processing of 3' beta spectrin pre-mRNA generates a beta spectrin isoform with a unique carboxyl terminus

A partial structural repeat forms the heterodimer self-association site of all beta-spectrins

YAC Transgenes: Bigger is Probably Better

Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin

The Breakpoint of a Large Deletion Causing Hereditary Persistence of Fetal Hemoglobin Occurs Within an Erythroid DNA Domain Remote From the β-Globin Gene Cluster

High levels of human gamma-globin gene expression in adult mice carrying a transgene of deletion-type hereditary persistence of fetal hemoglobin

Point mutation in the β-spectrin gene associated with αI/74 hereditary elliptocytosis : implications for the mechanism of spectrin dimer self-association

Ankyrin Bugey: A de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosis

Developmental Regulation of Human γ- and β-Globin Genes in the Absence of the Locus Control Region

β Spectrin kissimmee : a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1

A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain

Negative regulation of globin gene expression during megakaryocytic differentiation of a human erythroleukemic cell line

Reverse transcription and direct amplification of cellular RNA transcripts by Taq polymerase

Spectrin genes in health and disease

Characterization of the calmodulin-binding site of nonerythroid alpha-spectrin. Recombinant protein and model peptide studies

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