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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1991
Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-T J Vulliamy, A Othman, M Town, et al.
European Journal of Biochemistry|December 1, 1994
Promoter function of the human glucose-6-phosphate dehydrogenase gene depends on two GC boxes that are cell specifically controlledM Philippe, Y Larondelle, F Lemaigre, et al.
American Journal of Human Genetics|December 1, 1990
Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle EastB Kurdi-Haidar, P J Mason, A Berrebi, et al.
Blood|September 25, 1998
Early phagocytosis of glucose-6-phosphate dehydrogenase (G6PD)-deficient erythrocytes parasitized by Plasmodium falciparum may explain malaria protection in G6PD deficiencyM Cappadoro, G Giribaldi, E O'Brien, et al.
Il Giornale Di Chirurgia|January 16, 2004
[Telementoring in surgery]G Midiri, V Papaspiropoulos, M Coppola, et al.
Gene Therapy|June 20, 2008
Quantitative analysis of clinically relevant mutations occurring in lymphoid cells harboring gamma-retrovirus-encoded hsvtk suicide genesX Wang, M Olszewska, V Capacio, et al.
Human Genetics|March 1, 1992
Molecular heterogeneity underlying the G6PD Mediterranean phenotypeC M Corcoran, V Calabrò, G Tamagnini, et al.
The EMBO Journal|August 1, 1986
Structural analysis of the X-linked gene encoding human glucose 6-phosphate dehydrogenaseG Martini, D Toniolo, T Vulliamy, et al.
American Journal of Human Genetics|March 1, 1993
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysisV Calabrò, P J Mason, S Filosa, et al.
American Journal of Human Genetics|October 1, 1996
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiencyS Filosa, N Giacometti, C Wangwei, et al.
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