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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

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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

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The exon-intron organization of the human erythroid [beta]-spectrin gene

Genomics (San Diego, Calif.), 1993-10, Vol.18:1

1993

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The gene for human erythrocyte membrane protein band 7. 2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region

Genomics (San Diego, Calif.), 1993-10, Vol.18:1

1993

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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

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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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Cloning of a portion of the chromosomal gene and cDNA for human [beta]-fodrin, the nonerythroid form of [beta]-spectrin

Genomics (San Diego, Calif.), 1993-08, Vol.17:2

1993

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Increased Expression of the Gγ and Aγ Globin Genes Associated With a Mutation in the Aγ Enhancer

Blood, 1994-06, Vol.83 (12), p.3727-3737

1994

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Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization

Cytogenetics and cell genetics, 1994, Vol.66 (1), p.39

1994

Volltextzugriff (PDF)

Spectrin Jendouba: An α1I/31 Spectrin Variant That Is Associated With Elliptocytosis and Carries a Mutation Distant From the Dimer Self-Association Site

Blood, 1992-08, Vol.80 (3), p.809-815

1992

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Three RFLPs are detected by an alpha spectrin genomic clone

Nucleic acids research, 1987-06, Vol.15 (11), p.4696-4696

1987

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Evidence that expression of Sp?I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous ?-spectrin allele

Human genetics, 1990-10, Vol.85 (6)

1990

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Spectrin Tunis (Spαl/78), an Elliptocytogenic Variant, Is Due to the CGG → TGG Codon Change (Arg -→ Trp) at Position 35 of the αl Domain

Blood, 1989-08, Vol.74 (2), p.828-832

1989

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Molecular Basis of Sp αI/6S Hereditary Elliptocytosis in North Africa: Insertion of a TTG Triplet Between Codons 147 and 149 in the α-Spectrin Gene From Five Unrelated Families

Blood, 1989-06, Vol.73 (8), p.2196-2201

1989

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Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization

Cytogenetics and cell genetics, 1990, Vol.53 (4), p.232

1990

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Nucleotide sequence of the coding portion of human alpha globin messenger RNA

The Journal of biological chemistry, 1980-04, Vol.255 (7), p.2807-2815

1980

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Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin

Cell, 1976-03, Vol.7 (3), p.323-329

1976

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Partial nucleotide sequence of human alpha globin mRNA derived from analysis of 32P-labeled cRNA and 125I-labeled mRNA; correlation with a globin cDNA sequence

The Journal of biological chemistry, 1980-04, Vol.255 (7), p.2814-2815

1980

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STRUCTURES IN INTERGENIC DNA OF NON-ALPHA GLOBIN GENES OF MAN

Developmental Biology Using Purified Genes, 1981, p.71-84

1981

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STRUCTURE OF THE HUMAN GLOBIN GENES

Eucaryotic Gene Regulation, 1979, p.367-381

1979

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

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

The exon-intron organization of the human erythroid [beta]-spectrin gene

The gene for human erythrocyte membrane protein band 7. 2 (EPB72) maps to 9q33-q34 centromeric to the Philadelphia chromosome translocation breakpoint region

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

Isolation and chromosomal localization of a novel nonerythroid ankyrin gene

Cloning of a portion of the chromosomal gene and cDNA for human [beta]-fodrin, the nonerythroid form of [beta]-spectrin

Increased Expression of the Gγ and Aγ Globin Genes Associated With a Mutation in the Aγ Enhancer

Localization of the human alpha-fodrin gene (SPTAN1) to 9q33-->q34 by fluorescence in situ hybridization

Spectrin Jendouba: An α1I/31 Spectrin Variant That Is Associated With Elliptocytosis and Carries a Mutation Distant From the Dimer Self-Association Site

Three RFLPs are detected by an alpha spectrin genomic clone

Evidence that expression of Sp?I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous ?-spectrin allele

Spectrin Tunis (Spαl/78), an Elliptocytogenic Variant, Is Due to the CGG → TGG Codon Change (Arg -→ Trp) at Position 35 of the αl Domain

Molecular Basis of Sp αI/6S Hereditary Elliptocytosis in North Africa: Insertion of a TTG Triplet Between Codons 147 and 149 in the α-Spectrin Gene From Five Unrelated Families

Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridization

Nucleotide sequence of the coding portion of human alpha globin messenger RNA

Absence of messenger RNA and gene DNA for β-globin chains in hereditary persistence of fetal hemoglobin

Partial nucleotide sequence of human alpha globin mRNA derived from analysis of 32P-labeled cRNA and 125I-labeled mRNA; correlation with a globin cDNA sequence

STRUCTURES IN INTERGENIC DNA OF NON-ALPHA GLOBIN GENES OF MAN

STRUCTURE OF THE HUMAN GLOBIN GENES

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