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Tissue-Specific Targeting of Retroviral Vectors Through Ligand-Receptor Interactions

Science (American Association for the Advancement of Science), 1994-11, Vol.266 (5189), p.1373-1376

1994

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Tissue-specific targeting of retroviral vectors via ligand-receptor interactions

Advanced drug delivery reviews, 1995-12, Vol.17 (3), p.227-234

1995

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Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia

The New England journal of medicine, 1982-02, Vol.306 (5), p.270-274

1982

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Identification of a nondeletion defect in alpha-thalassemia

The New England journal of medicine, 1977-11, Vol.297 (20), p.1081-1084

1977

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Prenatal diagnosis of alpha-thalassemia. Clinical application of molecular hybridization

The New England journal of medicine, 1976-11, Vol.295 (21), p.1165-1167

1976

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Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia

The New England journal of medicine, 1975-05, Vol.292 (21), p.1096-1099

1975

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Construction of a functional human suppressor tRNA gene: an approach to gene therapy for β -thalassaemia

Nature (London), 1982-04, Vol.296 (5857), p.537-540

1982

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Triplicated α -globin Loci in Humans

Proceedings of the National Academy of Sciences - PNAS, 1980-01, Vol.77 (1), p.518-521

1980

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Antenatal Diagnosis of Sickle-Cell Anaemia by D. N. A. Analysis of Amniotic-Fluid Cells

Obstetrical & gynecological survey, 1979-05, Vol.34 (5), p.364

1979

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Polymorphism of DNA Sequence Adjacent to Human β -globin Structural Gene: Relationship to Sickle Mutation

Proceedings of the National Academy of Sciences - PNAS, 1978-11, Vol.75 (11), p.5631-5635

1978

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Detection of the sickle gene in the human fetus. Potential for intrauterine diagnosis of sickle-cell anemia

The New England journal of medicine, 1972-07, Vol.287 (1), p.1-5

1972

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Prenatal diagnosis of homozygous alpha-thalassemia

JAMA : the journal of the American Medical Association, 1979-04, Vol.241 (15), p.1610

1979

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Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts

The New England journal of medicine, 1978-03, Vol.298 (12), p.669-670

1978

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Assignment of Human $\beta $-, $\gamma $-, and $\delta $-globin Genes to the Short Arm of Chromosome 11 by Chromosome Sorting and DNA Restriction Enzyme Analysis

Proceedings of the National Academy of Sciences - PNAS, 1979-11, Vol.76 (11), p.5804-5808

1979

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Evidence for Multiple Structural Genes for the γ Chain of Human Fetal Hemoglobin

Proceedings of the National Academy of Sciences - PNAS, 1968-06, Vol.60 (2), p.537-544

1968

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ANTENATAL DIAGNOSIS OF SICKLE-CELL ANÆMIA BY D.N.A. ANALYSIS OF AMNIOTIC-FLUID CELLS

The Lancet (British edition), 1978-10, Vol.312 (8096), p.910-912

1978

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Globin Chain Synthesis in Haemoglobin New York (β 113 Valine→Glutamic acid

British journal of haematology, 1980-12, Vol.46 (4), p.557-564

1980

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Hemoglobin C in newborn sheep and goats: a possible explanation for its function and biosynthesis

Pediatric research, 1969-05, Vol.3 (3), p.189-198

1969

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Studies on the heterogeneity of hemoglobin : IV. Chromatographic behavior of different human hemoglobins on anion-exchange cellulose (DEAE-cellulose)

Journal of Chromatography A, 1962, Vol.7, p.180-203

1962

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MOLECULAR MECHANISMS IN α THALASSEMIA: RACIAL DIFFERENCES IN α-GLOBIN GENE ORGANIZATION

Annals of the New York Academy of Sciences, 1980-05, Vol.344 (1), p.31-40

1980

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Modification of hemoglobin H disease by sickle trait

The Journal of clinical investigation, 1979-10, Vol.64 (4), p.1024-1032

1979

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Characterization of β-thalassemia mutations by denaturing gradient gel electrophoresis: patterns in the Mediterranean mutations

Clinical genetics, 1994-05, Vol.45 (5), p.221-227

1994

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Studies on the heterogeneity of hemoglobin

Journal of Chromatography A, 1962, Vol.7, p.180-203

1962

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A new frameshift mutation, insertion of ATCT, at codon 48 in the β-globin gene causes β-thalassemia in an Indian proband

Human mutation, 1994, Vol.3 (4), p.397-398

1994

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Quantitative determination of the minor hemoglobin component Hb-A 2 by DEAE-cellulose chromatography

Analytical biochemistry, 1961, Vol.2 (4), p.400-403

1961

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Tissue-Specific Targeting of Retroviral Vectors Through Ligand-Receptor Interactions

Tissue-specific targeting of retroviral vectors via ligand-receptor interactions

Concurrent sickle-cell anemia and alpha-thalassemia: effect on severity of anemia

Identification of a nondeletion defect in alpha-thalassemia

Prenatal diagnosis of alpha-thalassemia. Clinical application of molecular hybridization

Successful application of prenatal diagnosis in a pregnancy at risk for homozygous beta-thalassemia

Construction of a functional human suppressor tRNA gene: an approach to gene therapy for β -thalassaemia

Triplicated α -globin Loci in Humans

Antenatal Diagnosis of Sickle-Cell Anaemia by D. N. A. Analysis of Amniotic-Fluid Cells

Polymorphism of DNA Sequence Adjacent to Human β -globin Structural Gene: Relationship to Sickle Mutation

Detection of the sickle gene in the human fetus. Potential for intrauterine diagnosis of sickle-cell anemia

Prenatal diagnosis of homozygous alpha-thalassemia

Diagnosis of homozygous alpha-thalassemia in cultured amniotic-fluid fibroblasts

Assignment of Human $\beta $-, $\gamma $-, and $\delta $-globin Genes to the Short Arm of Chromosome 11 by Chromosome Sorting and DNA Restriction Enzyme Analysis

Evidence for Multiple Structural Genes for the γ Chain of Human Fetal Hemoglobin

ANTENATAL DIAGNOSIS OF SICKLE-CELL ANÆMIA BY D.N.A. ANALYSIS OF AMNIOTIC-FLUID CELLS

Globin Chain Synthesis in Haemoglobin New York (β 113 Valine→Glutamic acid

Hemoglobin C in newborn sheep and goats: a possible explanation for its function and biosynthesis

Studies on the heterogeneity of hemoglobin : IV. Chromatographic behavior of different human hemoglobins on anion-exchange cellulose (DEAE-cellulose)

MOLECULAR MECHANISMS IN α THALASSEMIA: RACIAL DIFFERENCES IN α-GLOBIN GENE ORGANIZATION

Modification of hemoglobin H disease by sickle trait

Characterization of β-thalassemia mutations by denaturing gradient gel electrophoresis: patterns in the Mediterranean mutations

Studies on the heterogeneity of hemoglobin

A new frameshift mutation, insertion of ATCT, at codon 48 in the β-globin gene causes β-thalassemia in an Indian proband

Quantitative determination of the minor hemoglobin component Hb-A 2 by DEAE-cellulose chromatography

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