Works matching IS 00778923 AND DT 1998 AND VI 850 AND IP 1
Results: 86
Silencing and Activation of Embryonic Globin Gene Expression.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 70, doi. 10.1111/j.1749-6632.1998.tb10464.x
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Improved Amphotropic Retrovirus-Mediated Gene Transfer into Hematopoietic Stem Cells.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 139, doi. 10.1111/j.1749-6632.1998.tb10471.x
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Reduced β-Globin Gene Expression in Adult Mice Containing Deletions of Locus Control Region 5′ HS-2 or 5′ HS-3<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 45, doi. 10.1111/j.1749-6632.1998.tb10461.x
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PREFACE.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. xiii, doi. 10.1111/j.1749-6632.1998.tb10455.x
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Molecular Basis of Hereditary Persistence of Fetal Hemoglobin.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 38, doi. 10.1111/j.1749-6632.1998.tb10460.x
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The Psychosocial Burden of Cooley's Anemia in Affected Children and Their Parents.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 512, doi. 10.1111/j.1749-6632.1998.tb10536.x
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Audit of Prenatal Diagnosis for Hemoglobin Disorders in the United Kingdom: The First Twenty Years.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 420, doi. 10.1111/j.1749-6632.1998.tb10509.x
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Regulation of Glucose Disturbances with Glibenclamide in Patients with Thalassemia.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 471, doi. 10.1111/j.1749-6632.1998.tb10525.x
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Approaches to Working with Adult Thalassemia Patients in Pediatric Settings.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 516, doi. 10.1111/j.1749-6632.1998.tb10538.x
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Impact of Asian Immigration on Thalassemia in California.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 442, doi. 10.1111/j.1749-6632.1998.tb10515.x
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The Social Impact of Migration on Disease: Cooley's Anemia, Thalassemia, and New Asian Immigrants.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 509, doi. 10.1111/j.1749-6632.1998.tb10535.x
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Future Orientation and Life Expectations of Adolescents and Young Adults with Thalassemia Major<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 361, doi. 10.1111/j.1749-6632.1998.tb10494.x
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Bone Metabolism in Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 475, doi. 10.1111/j.1749-6632.1998.tb10526.x
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Detection of Fetal Hemoglobin in Erythrocytes by Flow Cytometry.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 446, doi. 10.1111/j.1749-6632.1998.tb10516.x
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Enhancement by Ubiquitin Aldehyde of Proteolysis of Hemoglobin α-Subunits in β-Thalassemic Hemolysates<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 394, doi. 10.1111/j.1749-6632.1998.tb10501.x
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Relationship between Genotype and Phenotype: Thalassemia Intermedia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 325, doi. 10.1111/j.1749-6632.1998.tb10489.x
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Global Epidemiology of Hemoglobin Disorders.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 251, doi. 10.1111/j.1749-6632.1998.tb10482.x
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Selective Loss of Anterior Pituitary Volume with Severe Pituitary-Gonadal Insufficiency in Poorly Compliant Male Thalassemic Patients with Pubertal Arrest.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 479, doi. 10.1111/j.1749-6632.1998.tb10527.x
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α- and β-Thalassemia in Thailand.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 412, doi. 10.1111/j.1749-6632.1998.tb10507.x
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An α-2 Globin Gene Initiation Codon Mutation in a Vietnamese Patient with Hb H Disease.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 398, doi. 10.1111/j.1749-6632.1998.tb10502.x
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Spectrum of β-Thalassemia Mutations in Guadeloupe (French West Indies) and Interactions with Other Hemoglobinopathies.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 423, doi. 10.1111/j.1749-6632.1998.tb10510.x
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Targeted Integration of a Recombinant Globin Gene Adeno-Associated Viral Vector into Human Chromosome 19<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 163, doi. 10.1111/j.1749-6632.1998.tb10473.x
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Hemoglobin Switching Protocols in Thalassemia: Experience with Sodium Phenylbutyrate and Hydroxyurea<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 80, doi. 10.1111/j.1749-6632.1998.tb10465.x
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The Montreal Thalassemia Screening Program: Response of the High School Students.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 401, doi. 10.1111/j.1749-6632.1998.tb10503.x
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Treatment of Two Infants with Cooley's Anemia with Sodium Phenylbutyrate.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 452, doi. 10.1111/j.1749-6632.1998.tb10518.x
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Treatment of Iron Overload in the 'Ex-Thalassemic': Report from the Phlebotomy Program<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 288, doi. 10.1111/j.1749-6632.1998.tb10485.x
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High-Level Transfer and Long-Term Expression of the Human β-Globin Gene in a Mouse Transplant Model<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 178, doi. 10.1111/j.1749-6632.1998.tb10474.x
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Iron Overload and Antioxidant Status in Patients with β-Thalassemia Major.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 463, doi. 10.1111/j.1749-6632.1998.tb10522.x
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An in Vitro Model of Human Erythropoiesis for the Study of Hemoglobinopathies<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 382, doi. 10.1111/j.1749-6632.1998.tb10498.x
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Hydroxyurea and Hemin Affect Both the Transcriptional and Post-Transcriptional Mechanisms of Some Globin Genes in Human Adult Erythroid Cells<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 449, doi. 10.1111/j.1749-6632.1998.tb10517.x
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New Approaches to the Management of Hepatitis and Endocrine Disorders in Cooley's Anemia.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 232, doi. 10.1111/j.1749-6632.1998.tb10480.x
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Full Developmental Silencing of the Embryonic ζ-Globin Gene Reflects Instability of its mRNA.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 386, doi. 10.1111/j.1749-6632.1998.tb10499.x
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Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 100, doi. 10.1111/j.1749-6632.1998.tb10467.x
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Late Effects of Bone Marrow Transplantation for Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 294, doi. 10.1111/j.1749-6632.1998.tb10486.x
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Retroviral Vectors Aimed at the Gene Therapy of Human β-Globin Gene Disorders<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 151, doi. 10.1111/j.1749-6632.1998.tb10472.x
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Pathophysiology of Iron Overload<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 191, doi. 10.1111/j.1749-6632.1998.tb10475.x
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Current and Future Preparative Regimens for Bone Marrow Transplantation in Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 276, doi. 10.1111/j.1749-6632.1998.tb10484.x
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Developmental Control of ɛ- and γ- Globin Genes<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 10, doi. 10.1111/j.1749-6632.1998.tb10457.x
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Expression and Developmental Control of the Human α-Globin Gene Cluster.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 54, doi. 10.1111/j.1749-6632.1998.tb10462.x
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Cellular and Molecular Effects of a Pulse Butyrate Regimen and New Inducers of Globin Gene Expression and Hematopoiesis.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 87, doi. 10.1111/j.1749-6632.1998.tb10466.x
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The Dynamics of Globin Gene Expression and Gene Therapy Vectors.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 18, doi. 10.1111/j.1749-6632.1998.tb10458.x
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Patient Cultures: Thalassemia Service Delivery and Patient Compliance.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 521, doi. 10.1111/j.1749-6632.1998.tb10540.x
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Bone Marrow Transplantation in Thalassemia: A Role for Radiation?
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 503, doi. 10.1111/j.1749-6632.1998.tb10533.x
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Outreach Strategies for Asian Pacific Island (API) Communities.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 514, doi. 10.1111/j.1749-6632.1998.tb10537.x
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Spectrum of β-Thalassemia Mutations in Oman<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 404, doi. 10.1111/j.1749-6632.1998.tb10504.x
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From A Distance: Using Information Technologies to Overcome Geographic Boundaries in Thalassemia Service Delivery.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 518, doi. 10.1111/j.1749-6632.1998.tb10539.x
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Patient Psychosocial Perspectives<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 370, doi. 10.1111/j.1749-6632.1998.tb10495.x
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Homozygous Hemoglobin Constant Spring with Normal Electrophoresis: A Possible Cause for Under-Diagnosis.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 415, doi. 10.1111/j.1749-6632.1998.tb10508.x
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Erythropoietin Level and Effect of rHuEPO in Beta-Thalassemic Mice<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 455, doi. 10.1111/j.1749-6632.1998.tb10519.x
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Mixed Chimerism after Bone Marrow Transplantation in Thalassemia.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 495, doi. 10.1111/j.1749-6632.1998.tb10531.x
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