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Biologic properties and enucleation of red blood cells from human embryonic stem cells

Blood, 2008-12, Vol.112 (12), p.4475-4484

2008

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Clotting-Factor Concentrations 5 Days After Discontinuation of Warfarin

Regional anesthesia and pain medicine, 2018-08, Vol.43 (6), p.616-620

2018

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Bone morphogenetic protein 4 induces efficient hematopoietic differentiation of rhesus monkey embryonic stem cells in vitro

Blood, 2001-07, Vol.98 (2), p.335-342

2001

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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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Hemostatic Factors and Shortened Sleep

Blood, 2012-11, Vol.120 (21), p.5137-5137

2012

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D-Dimer in the Months Leading up to Acute Coronary Events: A Case Crossover Study

Blood, 2014-12, Vol.124 (21), p.2864-2864

2014

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CD34+CD38- hematopoietic precursors derived from human embryonic stem cells exhibit an embryonic gene expression pattern

Blood, 2004-06, Vol.103 (11), p.4134-4141

2004

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Biologic properties and enucleation of red blood cells from human embryonic stem cells. Commentary

Blood, 2008, Vol.112 (12)

2008

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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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Hematopoietic Progenitor Cells Derived from Embryonic Stem Cells: Analysis of Gene Expression

Stem cells (Dayton, Ohio), 2002-01, Vol.20 (5), p.428-437

2002

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Comparative gene expression in hematopoietic progenitor cells derived from embryonic stem cells

Experimental hematology, 2002, Vol.30 (1), p.58-66

2002

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Aspirin acetylation of βLys-82 of human hemoglobin

Biochemical pharmacology, 2000-10, Vol.60 (7), p.917-922

2000

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Aspirin acetylation of βLys-82 of human hemoglobin: NMR study of acetylated hemoglobin tsurumai

Biochemical pharmacology, 2000-10, Vol.60 (7), p.917-922

2000

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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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610 α-THALASSEMIA SILENT CARRIER WITH HEMOGLOBINS S AND C

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

1978

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Biologic properties and enucleation of red blood cells from human embryonic stem cells

Clotting-Factor Concentrations 5 Days After Discontinuation of Warfarin

Bone morphogenetic protein 4 induces efficient hematopoietic differentiation of rhesus monkey embryonic stem cells in vitro

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

Hemostatic Factors and Shortened Sleep

D-Dimer in the Months Leading up to Acute Coronary Events: A Case Crossover Study

CD34+CD38- hematopoietic precursors derived from human embryonic stem cells exhibit an embryonic gene expression pattern

Biologic properties and enucleation of red blood cells from human embryonic stem cells. Commentary

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

Hematopoietic Progenitor Cells Derived from Embryonic Stem Cells: Analysis of Gene Expression

Comparative gene expression in hematopoietic progenitor cells derived from embryonic stem cells

Aspirin acetylation of βLys-82 of human hemoglobin

Aspirin acetylation of βLys-82 of human hemoglobin: NMR study of acetylated hemoglobin tsurumai

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

610 α-THALASSEMIA SILENT CARRIER WITH HEMOGLOBINS S AND C

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