High levels of human γ-globin are expressed in adult mice carrying a transgene of the Brazilian type of hereditary persistence of fetal hemoglobin (Aγ -195)

Hemoglobin

Volumn 33, Issue 6, 2009, Pages 439-447

  Da Cunha, Anderson F ^a,b   Brugnerotto, Ana F ^a   Finzi Corat, Marcus A ^a   Devlin, Emily E ^c   Gimenes, Ana P ^a   Barbosa De Melo, Mnica ^a   Corra Passos, Luiz A ^a   Bodine, David ^c   Saad, Sara T O ^a   Costa, Fernando F ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b FEDERAL UNIVERSITY OF SÃO CARLOS   (Brazil)

^c NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

Globin; 195 Mutation; Hb F; Hereditary persistence of fetal hemoglobin (HPFH); Transgenic mice

Indexed keywords

GAMMA GLOBIN; HEMOGLOBIN F; MESSENGER RNA; RIBONUCLEASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BETA THALASSEMIA; BIOASSAY; BLOOD DISEASE; CONTROLLED STUDY; FLOW CYTOMETRY; GENE EXPRESSION; HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN; MOUSE; MUTATIONAL ANALYSIS; NONHUMAN; PHENOTYPE; SEQUENCE ANALYSIS; SICKLE CELL ANEMIA; TRANSGENE;

ANEMIA, SICKLE CELL; ANIMALS; BETA-THALASSEMIA; BRAZIL; FETAL HEMOGLOBIN; GAMMA-GLOBINS; HUMANS; MICE; MICE, TRANSGENIC; MUTATION; PHENOTYPE; RNA, MESSENGER; TRANSGENES;

MUS; MUS MUSCULUS;

EID: 72049086207     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.3109/03630260903344176     Document Type: Article

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