Red blood cell membrane disorders von Tse, William T., Lux, Samuel E.

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Notch1 inhibits neurite outgrowth in postmitotic primary neurons von Berezovska, O., McLean, P., Knowles, R., Frosh, M., Lu, F.M., Lux, S.E., Hyman, B.T.

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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis von Eber, Stefan W, Gonzalez, Jennifer M, Lux, Marcia L, Scarpa, Alphonse L, Tse, William T, Dornwell, Marion, Herbers, Jutta, Kugler, Wilfried, Ozcan, Refik, Pekrun, Arnulf, Gallagher, Patrick G, Schroter, Werner, Forget, Bernard G, Lux, Samuel E

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Cloning and Characterization of Band 3, the Human Erythrocyte Anion-Exchange Protein (AE1) von Lux, Samuel E., John, Kathryn M., Kopito, Ron R., Lodish, Harvey F.

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Analysis of cDNA for human erythrocyte ankyrin indicates a repeated structure with homology to tissue-differentiation and cell-cycle control proteins von Lux, Samuel E, John, Kathryn M, Bennett, Vann

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The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter von GALLAGHER, P. G, ROMANA, M, TSE, W. T, LUX, S. E, FORGET, B. G

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Positional cloning of zebrafish ferroportin1 identifies a conserved vertebrate iron exporter von Zon, Leonard I, Donovan, Adriana, Brownlie, Alison, Zhou, Yi, Shepard, Jennifer, Pratt, Stephen J, Moynihan, John, Paw, Barry H, Drejer, Anna, Barut, Bruce, Zapata, Agustin, Law, Terence C, Brugnara, Carlo, Lux, Samuel E, Pinkus, Geraldine S, Pinkus, Jack L, Kingsley, Paul D, Palis, James, Fleming, Mark D, Andrews, Nancy C

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Differential expression of Na(+)-K(+)-ATPase, ankyrin, fodrin, and E-cadherin along the kidney nephron von Piepenhagen, P. A, Peters, L. L, Lux, S. E, Nelson, W. J

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Constitutively Active Human Notch1 Binds to the Transcription Factor CBF1 and Stimulates Transcription through a Promoter Containing a CBF1-Responsive Element von Lu, Frederick M., Lux, Samuel E.

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Dependence of Nodal Sodium Channel Clustering on Paranodal Axoglial Contact in the Developing CNS von Rasband, Matthew N, Peles, Elior, Trimmer, James S, Levinson, S. Rock, Lux, Samuel E, Shrager, Peter

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Immunolocalization of AE2 Anion Exchanger in Rat and Mouse Epididymis von JENSEN, L. J, STUART-TILLEY, A. K, PETERS, L. L, LUX, S. E, ALPER, S. L, BRETON, S

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Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia von SHINAR, E, RACHMILEWITZ, E. A, LUX, S. E

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Mapping the ankyrin-binding site of the human erythrocyte anion exchanger von Davis, L, Lux, S E, Bennett, V

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Complex patterns of sequence variation and multiple 5' and 3' ends are found among transcripts of the erythroid ankyrin gene von BIRKENMEIER, C. S, WHITE, R. A, PETERS, L. L, HALL, E. J, LUX, S. E, BARKER, J. E

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Combined spectrin and ankyrin deficiency is common in autosomal dominant hereditary spherocytosis von SAVVIDES, P, SHALEV, O, JOHN, K. M, LUX, S. E

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A highly conserved region of human erythrocyte ankyrin contains the capacity to bind spectrin von PLATT, O. S, LUX, S. E, FALCONE, J. F

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Ankyrin and the Hemolytic Anemia Mutation, nb, Map to Mouse Chromosome 8: Presence of the nb Allele is Associated with a Truncated Erythrocyte Ankyrin von White, Robert A., Birkenmeier, Connie S., Lux, Samuel E., Barker, Jane E.

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Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8 von Lux, Samuel E, Tse, William T, Menninger, Joan C, John, Kathryn M, Harris, Peter, Shalev, Oded, Chilcote, Robert R, Marchesi, Sally L, Watkins, Paul C, Bennett, Vann, Mclntosh, Sue, Collins, Francis S, Francke, Uta, Ward, David C, Forget, Bernard G

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Platelet membrane glycoprotein IIIa contains target antigens that bind anti-platelet antibodies in immune thrombocytopenias von BEARDSLEY, D. S, SPIEGEL, J. E, JACOBS, M. M, HANDIN, R. I, LUX, S. E. IV

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β Spectrin kissimmee : a spectrin variant associated with autosomal dominant hereditary spherocytosis and defective binding to protein 4.1 von BECKER, P. S, TSE, W. T, LUX, S. E, FORGET, B. G

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