scholarly journals Hemoglobin H Disease

2020 ◽  
Author(s):  
Keyword(s):  

Blood ◽  
2003 ◽  
Vol 101 (3) ◽  
pp. 791-800 ◽  
Author(s):  
David H. K. Chui ◽  
Suthat Fucharoen ◽  
Vivian Chan


1995 ◽  
Vol 26 (11) ◽  
pp. 736-742 ◽  
Author(s):  
Robert B. Hall ◽  
Jo A. Haga ◽  
Cynthia G. Guerra ◽  
Silvia M. Castleberry ◽  
John R. Hickman
Keyword(s):  


1968 ◽  
Vol 20 (3) ◽  
pp. 381-385 ◽  
Author(s):  
S. Rahbar
Keyword(s):  


1981 ◽  
Vol 305 (11) ◽  
pp. 607-612 ◽  
Author(s):  
D. J. Weatherall ◽  
D. R. Higgs ◽  
C. Bunch ◽  
J. M. Old ◽  
D. M. Hunt ◽  
...  


Blood ◽  
1996 ◽  
Vol 88 (5) ◽  
pp. 1846-1851 ◽  
Author(s):  
J Chang ◽  
RH Lu ◽  
SM Xu ◽  
J Meneses ◽  
K Chan ◽  
...  

We have disrupted the 5′ locus of the duplicated adult alpha-globin genes by gene targeting in the mouse embryonic stem cells and created mice with alpha-thalassemia syndromes. The heterozygous knockout mice (.alpha/alpha alpha) are asymptomatic like the silent carriers in humans whereas the homozygous knockout mice (.alpha/.alpha) show hemolytic anemia. Mice with three dysfunctional alpha-globin genes generated by breeding the 5′ alpha-globin knockouts (.alpha/alpha alpha) and the deletion type alpha-thalassemia mice (../alpha alpha) produce severe hemoglobin H disease and they die in utero. These results indicate that the 5′ alpha-globin gene is the predominant locus in mice, and suggest that it is even more dominant than its human homologue.



2018 ◽  
Vol 93 (7) ◽  
pp. 963-964 ◽  
Author(s):  
Michael Spencer-Chapman ◽  
Asad Luqmani ◽  
D. Mark Layton ◽  
Barbara J. Bain
Keyword(s):  


2011 ◽  
Vol 78 (2) ◽  
pp. 101-104
Author(s):  
Takahiro Ueda ◽  
Makoto Migita ◽  
Miho Yamanishi ◽  
Miho Maeda ◽  
Keiko Harano ◽  
...  
Keyword(s):  


2019 ◽  
Vol 46 (5) ◽  
pp. 5041-5048 ◽  
Author(s):  
Mostafa Paridar ◽  
Ebrahim Azizi ◽  
Bijan Keikhaei ◽  
Vahideh Takhviji ◽  
Iman Baluchi ◽  
...  




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