Heme degradation and oxidative stress in murine models for hemoglobinopathies: Thalassemia, sickle cell disease and hemoglobin C disease

Blood Cells, Molecules, and Diseases

Volumn 41, Issue 1, 2008, Pages 60-66

  Nagababu, Enika ^a   Fabry, Mary E ^b   Nagel, Ronald L ^b   Rifkind, Joseph M ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

Fluorescence; Heme degradation; Hemoglobin; Sickle cell; Thalassemia; Transgenic mice

Indexed keywords

HEME; HEMOGLOBIN F; HYDROGEN PEROXIDE; IMMUNOGLOBULIN G;

ANIMAL EXPERIMENT; ARTICLE; AUTOOXIDATION; CONTROLLED STUDY; ERYTHROCYTE; FLUORESCENCE; GENE DELETION; HEMOGLOBIN C DISEASE; HEMOGLOBINOPATHY; MOUSE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; SICKLE CELL ANEMIA; THALASSEMIA;

ANEMIA, SICKLE CELL; ANIMALS; ERYTHROCYTES; HEME; HEMOGLOBIN C; HEMOGLOBIN C DISEASE; HEMOGLOBINOPATHIES; IMMUNOGLOBULIN G; MICE; MICE, TRANSGENIC; OXIDATIVE STRESS; THALASSEMIA;

MURINAE; MUS; MUS MUSCULUS;

EID: 44649126828     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2007.12.003     Document Type: Article

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