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Blood Cells, Molecules & Diseases|May 19, 2001
Gene expression profiling during erythroid differentiation of K562 cellsT Mitchell, M Plonczynski, A McCollum, et al.
British Journal of Haematology|December 1, 1978
Erythrocyte calcium abnormalities and the clinical severity of sickling disordersM H Steinberg, J W Eaton, E Berger, et al.
Hemoglobin|November 1, 1994
Delta beta-thalassemia in an African-American: identification of the deletion endpoints and PCR-based diagnosisJ S Waye, B Eng, M B Coleman, et al.
British Journal of Haematology|September 6, 2000
Effect of nitric oxide and nitric oxide donors on red blood cell oxygen transportB W Hrinczenko, A I Alayash, D A Wink, et al.
Archives of Neurology|January 1, 1988
Brain glucose metabolism in neurologically normal patients with sickle cell disease. Regional alterationsG P Rodgers, C M Clark, S M Larson, et al.
The British Journal of Ophthalmology|August 1, 1985
Conjunctival sign in sickle cell anaemia: an in-vivo correlate of the extent of red cell heterogeneityM S Roy, G P Rodgers, M J Podgor, et al.
The American Journal of Medicine|April 1, 1986
Hemoglobin SC disease and alpha-thalassemia. Prolonged survival and mild clinical courseG P Rodgers, E A Sahovic, L E Pierce, et al.
The American Journal of Physiology|January 1, 1990
Microcirculatory adaptations in sickle cell anemia: reactive hyperemia responseG P Rodgers, A N Schechter, C T Noguchi, et al.
The New England Journal of Medicine|December 13, 1984
Periodic microcirculatory flow in patients with sickle-cell diseaseG P Rodgers, A N Schechter, C T Noguchi, et al.
Science in China. Series B, Chemistry, Life Sciences & Earth Sciences|October 1, 1992
Study of the RNA splicing defect in the common Chinese beta-thalassemia gene, IVS-II nt. 654 C-->T by using mRNA/PCRS Z Huang, Z R Ren, Y T Zeng, et al.
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