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Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators

Physiological genomics, 2006-12, Vol.28 (1), p.114-128

2006

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Organization of the gene for platelet glycoprotein IIb

Biochemistry (Easton), 1990-02, Vol.29 (5), p.1232-1244

1990

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53 EARLY EXPOSURE TO BUTYRATE INCREASES FETAL HEMOGLOBIN DURING ADULT ERYTHROID DEVELOPMENT IN VITRO

Journal of investigative medicine, 2006-03, Vol.54 (2), p.S352-S352

2006

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Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

Human molecular genetics, 1997-09, Vol.6 (9), p.1605-1609

1997

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Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements

Physiological genomics, 2004-09, Vol.19 (1), p.117-130

2004

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Identification of the Nucleotide Change (CAC→CGC) Responsible for Hb P-Galveston [β117(G19)His→Arg]

Hemoglobin, 2000-01, Vol.24 (2), p.165-167

2000

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Early Exposure to Butyrate Increases Fetal Hemoglobin during Adult Erythroid Development in Vitro

Journal of investigative medicine, 2006-03, Vol.54 (2_suppl), p.352-352

2006

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Identification of APC gene mutations in colorectal cancer using universal microarray‐based combinatorial sequencing‐by‐hybridization

Human mutation, 2004-09, Vol.24 (3), p.261-271

2004

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A > 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish Descent

Hemoglobin, 1991, Vol.15 (1-2), p.23-41

1991

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Detection of a novel DNA polymorphism in the beta-globin gene cluster

The Journal of biological chemistry, 1984-05, Vol.259 (10), p.6045-6048

1984

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Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia

The Journal of biological chemistry, 1985-06, Vol.260 (11), p.6507-6510

1985

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Simple two-color array-based approach for mutation detection

European journal of human genetics : EJHG, 2000-11, Vol.8 (11), p.884-894

2000

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Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy

Journal of pediatric hematology/oncology, 2002-08, Vol.24 (6), p.499-502

2002

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A Single-Base Change at Position - 175 in the 5’-Flanking Region of the Gγ-Globin Gene From a Black With Gγ-β+HPFH

Blood, 1988-03, Vol.71 (3), p.807-810

1988

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DNA sequence changes in the 5'-flanking region of G gamma-globin genes in a black with beta S and a non-deletional form of G gamma-beta+ HPFH

Progress in clinical and biological research, 1987, Vol.251, p.363

1987

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Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humans

Progress in clinical and biological research, 1989, Vol.316B, p.151

1989

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Interaction of a rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of α thalassemia

Blood, 1994-06, Vol.83 (11), p.3356-3362

1994

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Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

Blood, 1994-06, Vol.83 (11), p.3356-3362

1994

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The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions

Cell, 1984-01, Vol.39 (1), p.123-128

1984

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The – 175T → C Mutation Increases Promoter Strength in Erythroid Cells: Correlation With Evolutionary Conservation of Binding Sites for Two Trans-Acting Factors

Blood, 1990-02, Vol.75 (3), p.756-761

1990

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A large deletion encompassing the entire α-like globin gene cluster in a family of Northern European extraction

Nucleic acids research, 1988-12, Vol.16 (23), p.11223-11235

1988

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A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH

Blood, 1988-03, Vol.71 (3), p.807-810

1988

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DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2)

Nucleic acids research, 1987-07, Vol.15 (13), p.5169-5179

1987

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A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent

Hemoglobin, 1991, Vol.15 (1-2), p.23-41

1991

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The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors

Blood, 1990-02, Vol.75 (3), p.756-761

1990

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Transcriptional regulatory network analysis of developing human erythroid progenitors reveals patterns of coregulation and potential transcriptional regulators

Organization of the gene for platelet glycoprotein IIb

53 EARLY EXPOSURE TO BUTYRATE INCREASES FETAL HEMOGLOBIN DURING ADULT ERYTHROID DEVELOPMENT IN VITRO

Connexin26 Mutations Associated with the Most Common Form of Non-Syndromic Neurosensory Autosomal Recessive Deafness (DFNB1) in Mediterraneans

Erythroid-induced commitment of K562 cells results in clusters of differentially expressed genes enriched for specific transcription regulatory elements

Identification of the Nucleotide Change (CAC→CGC) Responsible for Hb P-Galveston [β117(G19)His→Arg]

Early Exposure to Butyrate Increases Fetal Hemoglobin during Adult Erythroid Development in Vitro

Identification of APC gene mutations in colorectal cancer using universal microarray‐based combinatorial sequencing‐by‐hybridization

A > 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish Descent

Detection of a novel DNA polymorphism in the beta-globin gene cluster

Functional analysis of a beta-globin gene containing a TATA box mutation from a Kurdish Jew with beta thalassemia

Simple two-color array-based approach for mutation detection

Interpretation of fetal hemoglobin only on newborn screening for hemoglobinopathy

A Single-Base Change at Position - 175 in the 5’-Flanking Region of the Gγ-Globin Gene From a Black With Gγ-β+HPFH

DNA sequence changes in the 5'-flanking region of G gamma-globin genes in a black with beta S and a non-deletional form of G gamma-beta+ HPFH

Large deletions encompassing the entire alpha- and beta-like globin gene clusters in humans

Interaction of a rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of α thalassemia

Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia

The silent carrier allele: β thalassemia without a mutation in the β-globin gene or its immediate flanking regions

The – 175T → C Mutation Increases Promoter Strength in Erythroid Cells: Correlation With Evolutionary Conservation of Binding Sites for Two Trans-Acting Factors

A large deletion encompassing the entire α-like globin gene cluster in a family of Northern European extraction

A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH

DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2)

A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent

The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors

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