BACE knockout mice are healthy despite lacking the primary β-secretase activity in brain: implications for Alzheimer's disease therapeutics von ROBERDS, Steven L, ANDERSON, John, JOHNSON-WOOD, Kelly, KAPPENMAN, Karl E, KAWABE, Thomas T, KOLA, Ismail, KUEHN, Ralf, LEE, Michael, LIU, Weiqun, MOTTER, Ruth, NICHOLS, Nanette F, POWER, Michael, BASI, Guriqbal, ROBERTSON, David W, SCHENK, Dale, SCHOOR, Michael, SHOPP, George M, SHUCK, Mary E, SINHA, Sukanto, SVENSSON, Kjell A, TATSUNO, Gwen, TINTRUP, Hartmut, WIJSMAN, John, BIENKOWSKI, Michael J, WRIGHT, Sarah, MCCONLOGUE, Lisa, BRANSTETTER, Daniel G, CHEN, Karen S, FREEDMAN, Stephen B, FRIGON, Normand L, GAMES, Dora, KANG HU

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Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin) von ROBERDS, S. L, ANDERSON, R. D, IBRAGHIMOV-BESKROVNAYA, O, CAMPBELL, K. P

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Cloning and Tissue-Specific Expression of Five Voltage-Gated Potassium Channel cDNAs Expressed in Rat Heart von Roberds, Steven L., Tamkun, Michael M.

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Time-, voltage-, and state-dependent block by quinidine of a cloned human cardiac potassium channel von SNYDERS, D. J, KNOTH, K. M, ROBERDS, S. L, TAMKUN, M. M

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity von Piccolo, F, Chaouch, M, Jeanpierre, M, Romero, N.B, Campbell, K.P, Voit, T, Kaplan, J-C, El Kerch, F, Collin, H, Roberds, S.L, Eymard, B, Fardeau, M, Leturcq, F, Beckmann, J.S, Sefiani, A, Tomé, F.M.S, Azibi, K, Récan, D, Reghis, A, Merlini, L, Beldjord, C, Carrié, A

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Disruption of the dystrophin-glycoprotein complex in the cardiomyopathic hamster von ROBERDS, S. L, ERVASTI, J. M, ANDERSON, R. D, OHLENDIECK, K, KAHL, S. D, ZOLOTO, D, CAMPBELL, K. P

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Clustering and Immobilization of Acetylcholine Receptors by the 43-kD Protein: A Possible Role for Dystrophin-Related Protein von Phillips, William D., Noakes, Peter G., Roberds, Steven L., Campbell, Kevin P., Merlie, John P.

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Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord von Olsen, Mary K., Roberds, Steven L., Ellerbrock, Brenda R., Fleck, Timothy J., McKinley, Denise K., Gurney, Mark E.

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A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy von Bueno, M.Rita Passos, Moreira, Eloísa S., Vainzof, Mariz, Chamberlain, Jeffrey, Marle, Suely K., Pereira, Lygia, Akiyama, Jeanne, Roberds, Steven L., Campbell, Kevin P., Zatz, Mayana

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Non-Muscle α-Dystroglycan Is Involved in Epithelial Development von Durbeej, Madeleine, Larsson, Erik, Ibraghimov-Beskrovnaya, Oxana, Roberds, Steven L., Campbell, Kevin P., Ekblom, Peter

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A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering von Campanelll, James T., Roberds, Steven L., Campbell, Kevin P., Scheller, Richard H.

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A cluster of novel serotonin receptor 3-like genes on human chromosome 3 von Karnovsky, Alla M., Gotow, Lisa F., McKinley, Denise D., Piechan, Julie L., Ruble, Cara L., Mills, Cynthia J., Schellin, Kathleen A.B., Slightom, Jerry L., Fitzgerald, Laura R., Benjamin, Christopher W., Roberds, Steven L.

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Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy von Roberds, Steven L., Leturcq, France, Allamand, Valérie, Piccolo, Federica, Jeanpierre, Marc, Anderson, Richard D., Lim, Leland E., Lee, Jane C., Tomé, Fernando M.S., Romero, Norma B., Fardeau, Michel, Beckmann, Jacques S., Kaplan, Jean-Claude, Campbell, Kevin P.

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Rapsyn may function as a link between the acetylcholine receptor and the agrin-binding dystrophin-associated glycoprotein complex von Apel, Elizabeth D., Roberds, Steven L., Campbell, Kevin P., Merlie, John P.

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Functional characterization of RK5, a voltage-gated K + channel cloned from the rat cardiovascular system von Blair, T.Ann, Roberds, Steven L., Tamkun, Michael M., Hartshorne, Robert P.

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Developmental expression of cloned cardiac potassium channels von Roberds, Steven L., Tamkun, Michael M.

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Adhalin gene polymorphism von Allamand, V., Leturcq, F., Piccoto, F., Jeanpierre, M., Azibi, K., Roberds, S.L., Lim, L.E., Campbell, K.P., Beckmann, J.S., Kaplan, J.C.

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The Expression of Dystrophin-associated Glycoproteins During Skeletal Muscle Degeneration and Regeneration. An Immunofluorescence Study von VATER, RUTH, HARRIS, JOHN B, ANDERSON, LOUISE V. B, ROBERDS, STEVEN L, CAMPBELL, KEVIN P, CULLEN, MICHAEL J

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Expression of deletion-containing dystrophins in mdx muscle : implications for gene therapy and dystrophin function von FRITZ, J. D, DANKO, I, ROBERDS, S. L, CAMPBELL, K. P, LATENDRESSE, J. S, WOLFF, J. A

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Applying genomics tools to identify therapeutic targets for asthma von Roberds, Steven L

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