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PMID: 9346488 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease.

Science (New York, N.Y.) ·Vol. 278 ·No. 5339 ·1997-10-31 ·Pages 876-8

Pászty C, Brion CM, Manci E, Witkowska HE, Stevens ME, Mohandas N, Rubin EM

Abstract

To create mice expressing exclusively human sickle hemoglobin (HbS), transgenic mice expressing human alpha-, gamma-, and betaS-globin were generated and bred with knockout mice that had deletions of the murine alpha- and beta-globin genes. These sickle cell mice have the major features (irreversibly sickled red cells, anemia, multiorgan pathology) found in humans with sickle cell disease and, as such, represent a useful in vivo system to accelerate the development of improved therapies for this common genetic disease.

MeSH Terms
Anemia, Sickle Cell/genetics,pathology Animals Disease Models, Animal Female Globins/genetics Hemoglobin, Sickle/genetics Humans Male Mice Mice, Inbred C57BL Mice, Knockout Mice, Transgenic
Chemicals
Hemoglobin, Sickle Globins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Pászty C
Human Genome Center and Department of Subcellular Structure, Lawrence Berkeley National Laboratory, 1 Cyclotron Road (MS 74-157), University of California, Berkeley, CA 94720, USA. [email protected]
Brion C M
Manci E
Witkowska H E
Stevens M E
Mohandas N
Rubin E M
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1997-10-31
Pages
876-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NHLBI NIH HHS · HL20985 · United States
NHLBI NIH HHS · HL31579 · United States
NHLBI NIH HHS · N01-HB-07086 · United States
Corrections
CommentIn
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