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Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia

European journal of haematology, 2014-01, Vol.92 (1), p.66-72

2014

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Desensitization to hydroxycarbamide following long‐term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients

British journal of haematology, 2010-12, Vol.151 (5), p.509-515

2010

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Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients

Hemoglobin, 2015-07, Vol.39 (4), p.225-229

2015

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Efficacy of Ruxolitinib as Inducer of Fetal Hemoglobin in Primary Erythroid Cultures from Sickle Cell and Beta-Thalassemia Patients

Thalassemia reports, 2019-04, Vol.9 (1), p.8101

2019

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A genetic strategy to treat sickle cell anemia by coregulating globin transgene expression and RNA interference

Nature biotechnology, 2006-01, Vol.24 (1), p.89-94

2006

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Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures

Hematology reports, 2016-12, Vol.8 (4), p.6678-60

2016

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Treatment with hydroxycarbamide for intermedia thalassaemia: decrease of efficacy in some patients during long‐term follow up

British journal of haematology, 2006-04, Vol.133 (1), p.105-106

2006

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Study on the Efficacy of a JAK Inhibitor Pharmacological Agent As Inducer of Fetal Hemoglobin Production in Cultured Erythroid Precursors from Sickle Cell and Beta-Thalassemia Patients

Blood, 2015-12, Vol.126 (23), p.2048-2048

2015

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Lower Levels of LPI in Thalassemia Major Patients Treated with Deferasirox

Blood, 2016-12, Vol.128 (22), p.4821-4821

2016

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The Autoinflammatory Diseases Alliance Registry of monogenic autoinflammatory diseases

Frontiers in medicine, 2022-09, Vol.9, p.980679-980679

2022

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Quantification of HBG m RNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta‐thalassemia

European journal of haematology, 2014-01, Vol.92 (1), p.66-72

2014

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Induction of gamma‐globin gene transcription by hydroxycarbamide in primary erythroid cell cultures from Lepore patients

British journal of haematology, 2008-06, Vol.141 (5), p.720-727

2008

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The Sea Urchin sns5 Insulator Protects Retroviral Vectors From Chromosomal Position Effects by Maintaining Active Chromatin Structure

Molecular therapy, 2009-08, Vol.17 (8), p.1434-1441

2009

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Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and δβ° thalassemia patients

Experimental hematology, 2005-11, Vol.33 (11), p.1363-1370

2005

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Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients

Experimental hematology, 2005-11, Vol.33 (11), p.1363-1370

2005

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Hydroxyurea-Mediated Reactivation of Fetal Genes in Primary Erythroid Cell Cultures from Beta-Thalassemia Patients

Blood, 2006-11, Vol.108 (11), p.3809-3809

2006

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Functional characterization of the sea urchin sns chromatin insulator in erythroid cells

Blood cells, molecules, & diseases, 2005-11, Vol.35 (3), p.339-344

2005

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321. Sea Urchin sns Chromatin Insulator Prevents Silencing and Positional Effect Variegation of Oncoretroviral Vectors Transgene Expression in Murine Erythroid Cell Line

Molecular therapy, 2006-05, Vol.13 (S1), p.S122-S123

2006

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A Region Upstream of the Human δ-Globin Gene Shows a Stage-Specific Interaction with Globin Promoters in Erythroid Cell Lines

Blood cells, molecules, & diseases, 2001-09, Vol.27 (5), p.874-881

2001

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The spectrum of β-thalassaemia mutations in Sicily

British journal of haematology, 1988-07, Vol.69 (3), p.393-397

1988

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Evidence for a Globin Promoter-Specific Silencer Element Located Upstream of the Human δ-Globin Gene

Biochemical and biophysical research communications, 1994-10, Vol.204 (1), p.413-418

1994

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Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

Human genetics, 1995-05, Vol.95 (5), p.526-530

1995

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The spectrum of β‐thalassaemia mutations in Sicily

British journal of haematology, 1988-07, Vol.69 (3), p.393-397

1988

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C-ets-2 protoonoogene expression in human leukemias

Cell biology international reports, 1990-09, Vol.14, p.88-88

1990

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Different micrococcal nuclease cleavage patterns characterize transcriptionally active and inactive sea‐urchin histone genes

European journal of biochemistry, 1986-04, Vol.156 (2), p.367-374

1986

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Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia

Desensitization to hydroxycarbamide following long‐term treatment of thalassaemia intermedia as observed in vivo and in primary erythroid cultures from treated patients

Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients

Efficacy of Ruxolitinib as Inducer of Fetal Hemoglobin in Primary Erythroid Cultures from Sickle Cell and Beta-Thalassemia Patients

A genetic strategy to treat sickle cell anemia by coregulating globin transgene expression and RNA interference

Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures

Treatment with hydroxycarbamide for intermedia thalassaemia: decrease of efficacy in some patients during long‐term follow up

Study on the Efficacy of a JAK Inhibitor Pharmacological Agent As Inducer of Fetal Hemoglobin Production in Cultured Erythroid Precursors from Sickle Cell and Beta-Thalassemia Patients

Lower Levels of LPI in Thalassemia Major Patients Treated with Deferasirox

The Autoinflammatory Diseases Alliance Registry of monogenic autoinflammatory diseases

Quantification of HBG m RNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta‐thalassemia

Induction of gamma‐globin gene transcription by hydroxycarbamide in primary erythroid cell cultures from Lepore patients

The Sea Urchin sns5 Insulator Protects Retroviral Vectors From Chromosomal Position Effects by Maintaining Active Chromatin Structure

Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and δβ° thalassemia patients

Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients

Hydroxyurea-Mediated Reactivation of Fetal Genes in Primary Erythroid Cell Cultures from Beta-Thalassemia Patients

Functional characterization of the sea urchin sns chromatin insulator in erythroid cells

321. Sea Urchin sns Chromatin Insulator Prevents Silencing and Positional Effect Variegation of Oncoretroviral Vectors Transgene Expression in Murine Erythroid Cell Line

A Region Upstream of the Human δ-Globin Gene Shows a Stage-Specific Interaction with Globin Promoters in Erythroid Cell Lines

The spectrum of β-thalassaemia mutations in Sicily

Evidence for a Globin Promoter-Specific Silencer Element Located Upstream of the Human δ-Globin Gene

Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancer

The spectrum of β‐thalassaemia mutations in Sicily

C-ets-2 protoonoogene expression in human leukemias

Different micrococcal nuclease cleavage patterns characterize transcriptionally active and inactive sea‐urchin histone genes

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