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Analyses of in vitro nonenzymatic glycation of normal and variant hemoglobins by MALDI-TOF mass spectrometry

Journal of biomolecular techniques, 2011-09, Vol.22 (3), p.90-94

2011

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α-Thalassemia-Like Globin Gene Expression by Primitive Erythrocytes Derived from Human Embryonic Stem Cells

Hemoglobin, 2010-04, Vol.34 (2), p.145-150

2010

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Fetal hemoglobin expression in transplant recipients of placental blood hematopoietic progenitor cells

Pediatric research, 1995-04, Vol.37 (4), p.432-436

1995

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Effects in vitro of the proposed antisickling agent DBA

Nature (London), 1978-04, Vol.272 (5656), p.833-834

1978

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Hb RAMPA [α95(G2)Pro→Ser (α2)] IN A FAMILY OF EUROPEAN ANCESTRY: DNA ANALYSIS CONFIRMS THE C CG→T CG MUTATION AT CODON 95 OF THE α2-GLOBIN GENE; CLINICAL AND LABORATORY FEATURES

Hemoglobin, 2002, Vol.26 (4), p.397-403

2002

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Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C

Pediatric research, 1979-10, Vol.13 (10), p.1109-1111

1979

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Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe β thalassemia

American journal of hematology, 1998-05, Vol.58 (1), p.67-71

1998

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Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease

Blood, 1997-03, Vol.89 (6), p.2155-2158

1997

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Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clinical and laboratory features

Hemoglobin, 2002-11, Vol.26 (4), p.397-403

2002

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Iron deficiency and sickle cell anemia

Archives of internal medicine (1960), 1983-05, Vol.143 (5), p.1030

1983

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Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression

American journal of hematology, 1989-09, Vol.32 (1), p.36-41

1989

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Hemoglobin Lincoln Park: A β δ Fusion (Anti-Lepore) Variant with an Amino Acid Deletion in the δ Chain-Derived Segment

Proceedings of the National Academy of Sciences - PNAS, 1978-03, Vol.75 (3), p.1475-1479

1978

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Sickle cell syndromes

The Journal of pediatrics, 1978-04, Vol.92 (4), p.556-561

1978

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Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome

The Journal of pediatrics, 1978-04, Vol.92 (4), p.556-561

1978

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611 UNBALANCED GLOBIN SYNTHESIS IN ANTI-LEPORE HEMOGLOBIN Oil ERYTHROID CELLS

Pediatric research, 1978-04, Vol.12, p.465-465

1978

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610 α-THALASSEMIA SILENT CARRIER WITH HEMOGLOBINS S AND C

Pediatric research, 1978-04, Vol.12, p.465-465

1978

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Hemoglobin Nigeria (α-81 Ser→CysJiA New Variant Associated With α-Thalassemia

Blood, 1980-01, Vol.55 (1), p.131-137

1980

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The Primary Structure and Functional Properties of the Hemoglobins of a Ground Squirrel (Spermophilus townsendii, Rodentia)

Biological chemistry Hoppe-Seyler, 1985-01, Vol.366 (2), p.971-978

1985

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Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes

Blood, 1972-06, Vol.39 (6), p.778-784

1972

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Three new variants of glucose‐6‐phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G‐6‐PD Lincoln Park, G‐6‐PD arlington heights, and G‐6‐PD West Town

American journal of hematology, 1979, Vol.6 (4), p.353-360

1979

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Homozygous sickle cell disease with coexistent hereditary spherocytosis in three siblings

The Journal of pediatrics, 1972-02, Vol.80 (2), p.235-242

1972

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Unbalanced globin chain synthesis by Hb lincoln park (anti‐lepore) reticulocytes

American journal of hematology, 1978, Vol.5 (4), p.335-340

1978

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Hemoglobin Abraham Lincoln, β32 (B14) Leucine → Proline AN UNSTABLE VARIANT PRODUCING SEVERE HEMOLYTIC DISEASE

The Journal of clinical investigation, 1973-07, Vol.52 (7), p.1746-1755

1973

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Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia

Pediatric research, 1976-06, Vol.10 (6), p.613-620

1976

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Two New Sickle Cell Syndromes: HbS, Hb Camden, and α-Thalassemia; and HbS in Combination With Hb Tacoma

Blood, 1980-04, Vol.55 (4), p.655-660

1980

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Analyses of in vitro nonenzymatic glycation of normal and variant hemoglobins by MALDI-TOF mass spectrometry

α-Thalassemia-Like Globin Gene Expression by Primitive Erythrocytes Derived from Human Embryonic Stem Cells

Fetal hemoglobin expression in transplant recipients of placental blood hematopoietic progenitor cells

Effects in vitro of the proposed antisickling agent DBA

Hb RAMPA [α95(G2)Pro→Ser (α2)] IN A FAMILY OF EUROPEAN ANCESTRY: DNA ANALYSIS CONFIRMS THE C CG→T CG MUTATION AT CODON 95 OF THE α2-GLOBIN GENE; CLINICAL AND LABORATORY FEATURES

Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C

Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe β thalassemia

Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease

Hb Rampa [alpha 95(G2)pro-->Ser (alpha 2)] in a family of European ancestry: DNA analysis confirms the CCG-->TCG mutation at codon 95 of the alpha 2-globin gene; clinical and laboratory features

Iron deficiency and sickle cell anemia

Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression

Hemoglobin Lincoln Park: A β δ Fusion (Anti-Lepore) Variant with an Amino Acid Deletion in the δ Chain-Derived Segment

Sickle cell syndromes

Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome

611 UNBALANCED GLOBIN SYNTHESIS IN ANTI-LEPORE HEMOGLOBIN Oil ERYTHROID CELLS

610 α-THALASSEMIA SILENT CARRIER WITH HEMOGLOBINS S AND C

Hemoglobin Nigeria (α-81 Ser→CysJiA New Variant Associated With α-Thalassemia

The Primary Structure and Functional Properties of the Hemoglobins of a Ground Squirrel (Spermophilus townsendii, Rodentia)

Similarities of the Erythrocytes in Juvenile Chronic Myelogenous Leukemia to Fetal Erythrocytes

Three new variants of glucose‐6‐phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G‐6‐PD Lincoln Park, G‐6‐PD arlington heights, and G‐6‐PD West Town

Homozygous sickle cell disease with coexistent hereditary spherocytosis in three siblings

Unbalanced globin chain synthesis by Hb lincoln park (anti‐lepore) reticulocytes

Hemoglobin Abraham Lincoln, β32 (B14) Leucine → Proline AN UNSTABLE VARIANT PRODUCING SEVERE HEMOLYTIC DISEASE

Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia

Two New Sickle Cell Syndromes: HbS, Hb Camden, and α-Thalassemia; and HbS in Combination With Hb Tacoma

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