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Peters, Luanne L; Swearingen, Rebecca A; Andersen, Sabra G et al. (2004) Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency. Blood 103:3233-40
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Eber, Stefan; Lux, Samuel E (2004) Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin Hematol 41:118-41
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Tse, W T; Tang, J; Jin, O et al. (2001) A new spectrin, beta IV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix. J Biol Chem 276:23974-85
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Peters, L L; Jindel, H K; Gwynn, B et al. (1999) Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice. J Clin Invest 103:1527-37
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Cho, M R; Eber, S W; Liu, S C et al. (1998) Regulation of band 3 rotational mobility by ankyrin in intact human red cells. Biochemistry 37:17828-35
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Hoock, T C; Peters, L L; Lux, S E (1997) Isoforms of ankyrin-3 that lack the NH2-terminal repeats associate with mouse macrophage lysosomes. J Cell Biol 136:1059-70
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Lu, F M; Lux, S E (1996) Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element. Proc Natl Acad Sci U S A 93:5663-7
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Eber, S W; Gonzalez, J M; Lux, M L et al. (1996) Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nat Genet 13:214-8
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Peters, L L; Shivdasani, R A; Liu, S C et al. (1996) Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell 86:917-27
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