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8篇 您的检索式:作者名="Lux SE"
    题名 作者 年代 出处 被引量
1Constitutively active human Notchl binds to the transcription factor CBFI and stimulates transcription through a promoter containing a CBFl-responsive element 显示文摘Lu FM Lux SE 1996Proc Natl Acad Sci USA1996,93,11:1
2Simultaneous (AC) nmicrosateilite polymorphism analysis and single - stranded con-formation polymorphism screening is an efficient strategy for de-tecting ankyrin - 1 mutations in dominant hereditary spherocy-tosis 显示文摘Ozcan R Jarolim P Lux SE 2003B J Haematol2003,122,4:1
3Expression,purification,and characterization of the functional demerit cytoplasmic domain of human erythrocyte band 3 in Escherichia coli 显示文摘Wang CC Badylak JA Lux SE 1992Protein Science1992,1,:1
4Isoforrm of ankyrin-3 that lack the NH2-terminal repeats associate with mouse macrophage lysosomes显示文摘Hoock TC Peters LL Lux SE 1997J Cell Biol1997,136,5:1
5Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element显示文摘Lu FM Lux SE 1996Proc Natl Acad Sci USA1996,93,11:1
6Hereditar-y spherocytosis associated with deletion of human ankyrin gene on chromosome 8显示文摘Lux SE William T T Menninger J C 0,,:1
7Hereditary spherocytosis-defects in proteins that connect the membrane skeleton to the lipid bilayer显示文摘Eber S Lux SE 2004Semin Hematol2004,41,:1
8Constitutively active human Notch 1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1 - responsive element 显示文摘Lu FM Lux SE 1996Proc Natl Acad Sci USA1996,93,11:1
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