Literature DB >> 4441462

Studies of red-cell membrane function in heterozygous beta thalassaemia and other hypochromic anaemias.

H H Knox-Macaulay, D J Weatherall.   

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Year:  1974        PMID: 4441462     DOI: 10.1111/j.1365-2141.1974.tb00809.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


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  2 in total

1.  Epistatic interactions between genetic disorders of hemoglobin can explain why the sickle-cell gene is uncommon in the Mediterranean.

Authors:  Bridget S Penman; Oliver G Pybus; David J Weatherall; Sunetra Gupta
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-01       Impact factor: 11.205

2.  The erythrocyte membrane properties of beta thalassaemia heterozygotes and their consequences for Plasmodium falciparum invasion.

Authors:  Viola Introini; Alejandro Marin-Menendez; Guilherme Nettesheim; Yen-Chun Lin; Silvia N Kariuki; Adrian L Smith; Letitia Jean; John N Brewin; David C Rees; Pietro Cicuta; Julian C Rayner; Bridget S Penman
Journal:  Sci Rep       Date:  2022-05-27       Impact factor: 4.996

  2 in total

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