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HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

Human mutation, 2002-03, Vol.19 (3), p.225-233

2002

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Persistent γ-globin expression in adult transgenic mice is mediated by HPFH-2, HPFH-3, and HPFH-6 breakpoint sequences

Blood, 2003-11, Vol.102 (9), p.3412-3419

2003

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Dynamic retrotransposition of ERV-9 LTR and L1 in the β-globin gene locus during primate evolution

Molecular phylogenetics and evolution, 2004-03, Vol.30 (3), p.867-871

2004

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5-azacytidine selectively increases gamma-globin synthesis in a patient with beta+ thalassemia

The New England journal of medicine, 1982-12, Vol.307 (24), p.1469-1475

1982

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Activation of Developmentally Mutated Human Globin Genes by Cell Fusion

Science (American Association for the Advancement of Science), 1988-11, Vol.242 (4881), p.1056-1058

1988

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Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the β-globin gene cluster

Human genetics, 1997-09, Vol.100 (3-4), p.441-445

1997

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An embryonic-specific repressor element located 3' to the Agamma-globin gene influences transcription of the human beta-globin locus in transgenic mice

Experimental hematology, 2004-02, Vol.32 (2), p.224-233

2004

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Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice

The Journal of biological chemistry, 1995-04, Vol.270 (17), p.10256-10263

1995

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Functional role of the four different types of (AT)(x)T(y) motifs 5' to the beta-globin gene and their distribution in the Greek population

Blood cells, molecules, & diseases, 2002-01, Vol.28 (1), p.39-46

2002

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Advances in Thalassemia Research

Blood, 1984-04, Vol.63 (4), p.738-758

1984

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Expression of Embryonic Globins by Erythroid Cells in Juvenile Chronic Myelocytic Leukemia

Blood, 1991-06, Vol.77 (12), p.2569-2576

1991

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RNA Processing Errors in Patients with β -thalassemia

Proceedings of the National Academy of Sciences - PNAS, 1982-08, Vol.79 (15), p.4775-4779

1982

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Laotian (δβ)°-Thalassemia: Molecular Characterization of a Novel Deletion Associated With Increased Production of Fetal Hemoglobin

Blood, 1988-09, Vol.72 (3), p.983-988

1988

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β-Thalassemia resulting from a single nucleotide substitution in an acceptor splice site

Nucleic acids research, 1985-02, Vol.13 (3), p.777-790

1985

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Structurally Diverse Molecular Deletions in the β-Globin Gene Cluster Exhibit an Identical Phenotype on Interaction With the βS-Gene

Blood, 1985-05, Vol.65 (5), p.1245-1251

1985

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DNA Methylation and Regulation of the Human β -globin-Like Genes in Mouse Erythroleukemia Cells Containing Human Chromosome 11

Proceedings of the National Academy of Sciences - PNAS, 1984-11, Vol.81 (21), p.6618-6622

1984

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A β -globin Gene, Inactive in the K562 Leukemic Cell, Functions Normally in a Heterologous Expression System

Proceedings of the National Academy of Sciences - PNAS, 1984-07, Vol.81 (14), p.4485-4489

1984

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Regulatory Regions Flanking the Human Fetal γ-Globin Genes

Annals of the New York Academy of Sciences, 1989-01, Vol.565 (1), p.13-22

1989

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Acquired α -thalassemia in Preleukemia is due to Decreased Expression of All Four α -globin Genes

Proceedings of the National Academy of Sciences - PNAS, 1983-10, Vol.80 (19), p.6051-6055

1983

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Butyrate induces expression of transfected human fetal and endogenous mouse embryonic globin genes in GM 979 erythroleukemia cells

Developmental genetics, 1990, Vol.11 (2), p.168-174

1990

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HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

Persistent γ-globin expression in adult transgenic mice is mediated by HPFH-2, HPFH-3, and HPFH-6 breakpoint sequences

Dynamic retrotransposition of ERV-9 LTR and L1 in the β-globin gene locus during primate evolution

5-azacytidine selectively increases gamma-globin synthesis in a patient with beta+ thalassemia

Activation of Developmentally Mutated Human Globin Genes by Cell Fusion

Molecular cloning of the breakpoints of the hereditary persistence of fetal hemoglobin type-6 (HPFH-6) deletion and sequence analysis of the novel juxtaposed region from the 3' end of the β-globin gene cluster

An embryonic-specific repressor element located 3' to the Agamma-globin gene influences transcription of the human beta-globin locus in transgenic mice

Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice

Functional role of the four different types of (AT)(x)T(y) motifs 5' to the beta-globin gene and their distribution in the Greek population

Advances in Thalassemia Research

Expression of Embryonic Globins by Erythroid Cells in Juvenile Chronic Myelocytic Leukemia

RNA Processing Errors in Patients with β -thalassemia

Laotian (δβ)°-Thalassemia: Molecular Characterization of a Novel Deletion Associated With Increased Production of Fetal Hemoglobin

β-Thalassemia resulting from a single nucleotide substitution in an acceptor splice site

Structurally Diverse Molecular Deletions in the β-Globin Gene Cluster Exhibit an Identical Phenotype on Interaction With the βS-Gene

DNA Methylation and Regulation of the Human β -globin-Like Genes in Mouse Erythroleukemia Cells Containing Human Chromosome 11

A β -globin Gene, Inactive in the K562 Leukemic Cell, Functions Normally in a Heterologous Expression System

Regulatory Regions Flanking the Human Fetal γ-Globin Genes

Acquired α -thalassemia in Preleukemia is due to Decreased Expression of All Four α -globin Genes

Butyrate induces expression of transfected human fetal and endogenous mouse embryonic globin genes in GM 979 erythroleukemia cells

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