Transgenic knockout mice exclusively expressing human hemoglobin S after transfer of a 240-kb s-globin yeast artificial chromosome: A mouse model of sickle cell anemia-Reference-Cited by-同舟云学术

Transgenic knockout mice exclusively expressing human hemoglobin S after transfer of a 240-kb s-globin yeast artificial chromosome: A mouse model of sickle cell anemia

Published:1998-12-08 Issue:25 Volume:95 Page:14886-14890
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Chang J. C.,Lu R.,Lin C.,Xu S.-M.,Kan Y. W.,Porcu S.,Carlson E.,Kitamura M.,Yang S.,Flebbe-Rehwaldt L.,Gaensler K. M. L.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference35 articles.

1. Sickle Cell Anemia, a Molecular Disease

2. A Specific Chemical Difference Between the Globins of Normal Human and Sickle-Cell Anæmia Hæmoglobin

3. Human Sickle Hemoglobin in Transgenic Mice

4. A transgenic mouse model of sickle cell disorder

5. A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severity

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