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Journal Articles

Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adult [see comments]

A Palena, A Blau, G Stamatoyannopoulos, NP Anagnou

Blood (1994) 83 (12): 3738–3745.

https://doi.org/10.1182/blood.V83.12.3738.3738

Published: 1994

Journal Articles

Expression of embryonic globins by erythroid cells in juvenile chronic myelocytic leukemia

T Papayannopoulou, B Nakamoto, NP Anagnou, D Chui, L Dow, J Sanders

Blood (1991) 77 (12): 2569–2576.

https://doi.org/10.1182/blood.V77.12.2569.2569

Published: 1991

Journal Articles

Laotian (delta beta) degree-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin

JW Zhang, G Stamatoyannopoulos, NP Anagnou

Blood (1988) 72 (3): 983–988.

https://doi.org/10.1182/blood.V72.3.983.983

Published: 1988

Journal Articles

A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait

MH Steinberg, MB Coleman, JG 3d Adams, RC Hartmann, H Saba, NP Anagnou

Blood (1986) 67 (2): 469–473.

https://doi.org/10.1182/blood.V67.2.469.469

Published: 1986

Journal Articles

Structurally diverse molecular deletions in the beta-globin gene cluster exhibit an identical phenotype on interaction with the beta S- gene

NP Anagnou, T Papayannopoulou, G Stamatoyannopoulos, AW Nienhuis

Blood (1985) 65 (5): 1245–1251.

https://doi.org/10.1182/blood.V65.5.1245.1245

Published: 1985

Journal Articles

Regulatory factors specific for adult and embryonic globin genes may govern their expression in erythroleukemia cells

NP Anagnou, TY Yuan, E Lim, J Helder, S Wieder, D Glaister, B Marks, A Wang, D Colbert, A Deisseroth

Blood (1985) 65 (3): 705–712.

https://doi.org/10.1182/blood.V65.3.705.705

Published: 1985

Journal Articles

Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability

RK Humphries, TJ Ley, NP Anagnou, AW Baur, AW Nienhuis

Blood (1984) 64 (1): 23–32.

https://doi.org/10.1182/blood.V64.1.23.23

Published: 1984

Journal Articles

Advances in thalassemia research

AW Nienhuis, NP Anagnou, TJ Ley

Blood (1984) 63 (4): 738–758.

https://doi.org/10.1182/blood.V63.4.738.738

Published: 1984

Journal Articles

Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemia

P Fessas, NP Anagnou, D Loukopoulos

Blood (1980) 55 (4): 564–569.

https://doi.org/10.1182/blood.V55.4.564.564

Published: 1980

NARROW

Eastern European (delta beta) zero-thalassemia: molecular characterization of a novel 9.1-kb deletion resulting in high levels of fetal hemoglobin in the adult [see comments]

Expression of embryonic globins by erythroid cells in juvenile chronic myelocytic leukemia

Laotian (delta beta) degree-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin

A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait

Structurally diverse molecular deletions in the beta-globin gene cluster exhibit an identical phenotype on interaction with the beta S- gene

Regulatory factors specific for adult and embryonic globin genes may govern their expression in erythroleukemia cells

Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability

Advances in thalassemia research

Glycerol-3-phosphate dehydrogenase activity in the red cells of patients with thalassemia

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American Society of Hematology

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ASH Publications

American Society of Hematology

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