Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis von Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr

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Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis von CUDKOWICZ, M. E, MCKENNA-YASEK, D, SAPP, P. E, CHIN, W, GETTER, B, HAYDEN, D. L, SCHOENFELD, D. A, HOSLER, B. A, HORVITZ, H. R, BROWN, R. H

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Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis von Aoki, Masashi, Lin, Chien-Liang G., Rothstein, Jeffrey D., Geller, Brian A., Hosler, Besty A., Munsat, Theodore L., Horvitz, H. Robert, Brown Jr, Robert H.

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 von Hadano, Shinji, Hand, Collette K., Osuga, Hitoshi, Yanagisawa, Yoshiko, Otomo, Asako, Devon, Rebecca S., Miyamoto, Natsuki, Showguchi-Miyata, Junko, Okada, Yoshinori, Singaraja, Roshni, Figlewicz, Denise A., Kwiatkowski, Thomas, Hosler, Betsy A., Sagie, Tally, Skaug, Jennifer, Nasir, Jamal, Brown, Robert H., Scherer, Stephen W., Rouleau, Guy A., Hayden, Michael R., Ikeda, Joh-E

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Specific expression of a retinoic acid-regulated, zinc-finger gene, Rex-1, in preimplantation embryos, trophoblast and spermatocytes von ROGERS, M. B, HOSLER, B. A, GUDAS, L. J

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Expression of REX-1, a gene containing zinc finger motifs, is rapidly reduced by retinoic acid in F9 teratocarcinoma cells von HOSLER, B. A, LAROSA, G. J, GRIPPO, J. F, GUDAS, L. J

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Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22 von Hosler, Betsy A, Siddique, Teepu, Sapp, Peter C, Sailor, Wen, Huang, Michael C, Hossain, Anwar, Daube, Jasper R, Nance, Martha, Fan, Chaohong, Kaplan, Jocelyn, Hung, Wu-Yen, McKenna-Yasek, Diane, Haines, Jonathan L, Pericak-Vance, Margaret A, Horvitz, H. Robert, Brown, Jr, Robert H

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy von Liu, Jing, Aoki, Masashi, Illa, Isabel, Wu, Chenyan, Fardeau, Michel, Angelini, Corrado, Serrano, Carmen, Urtizberea, J. Andoni, Hentati, Faycal, Hamida, Mongi Ben, Bohlega, Saeed, Culper, Edward J., Amato, Anthony A., Bossie, Karen, Oeltjen, Joshua, Bejaoui, Khemissa, McKenna-Yasek, Diane, Hosler, Betsy A., Schurr, Erwin, Arahata, Kiichi, de Jong, Pieter J., Brown, Robert H.

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Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22 von BEJAOUI, K, MCKENNA-YASEK, D, HOSLER, B. A, BURNS-DEATER, E, DEATER, L. M, O'NEILL, G, HAINES, J. L, BROWN, R. H

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An octamer motif contributes to the expression of the retinoic acid-regulated zinc finger gene Rex-1 (Zfp-42) in F9 teratocarcinoma cells von HOSLER, B. A, ROGERS, M. B, KOZAK, C. A, GUDAS, L. J

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Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13 von Liu, Jing, Wu, Chenyan, Bossie, Karen, Bejaoui, Khemissa, Hosler, Betsy A., Gingrich, Jeffrey C., Hamida, Mongi Ben, Hentati, Faycal, Schurr, Erwin, de Jong, Pieter J., Brown, Robert H.

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Cross-reactivity between herpes simplex virus glycoprotein B and a 63,000-dalton varicella-zoster virus envelope glycoprotein von EDSON, C. M, HOSLER, B. A, RESPESS, R. A, WATERS, D. J, THORLEY-LAWSON, D. A

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CuZn Superoxide Dismutase (SOD-1):Tetanus Toxin Fragment C Hybrid Protein for Targeted Delivery of SOD-1 to Neuronal Cells (∗) von Francis, Jonathan W., Hosler, Betsy A., Brown, Robert H., Fishman, Paul S.

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Varicella-zoster virus envelope glycoproteins: Biochemical characterization and identification in clinical material von Edson, Clark M., Hosler, Betsy A., Poodry, Clifton A., Schooley, Robert T., Waters, David J., Thorley-Lawson, David A.

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy von JING LIU, AOKI, M, BOHLEGA, S, CULPER, E. J, AMATO, A. A, BOSSIE, K, OELTJEN, J, BEJAOUI, K, MCKENNA-YASEK, D, HOSLER, B. A, SCHURR, E, ARAHATA, K, ILLA, I, DE JONG, P. J, BROWN, R. H, CHENYAN WU, FARDEAU, M, ANGELINI, C, SERRANO, C, URTIZBEREA, J. A, HENTATI, F, MONGI BEN HAMIDA

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Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis von Sapp, Peter C., Hosler, Betsy A., McKenna-Yasek, Diane, Chin, Wendy, Gann, Amity, Genise, Hilary, Gorenstein, Julie, Huang, Michael, Sailer, Wen, Scheffler, Meg, Valesky, Marianne, Haines, Jonathan L., Pericak-Vance, Margaret, Siddique, Teepu, Horvitz, H. Robert, Brown, Robert H.

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Superoxide dismutase and oxygen radical neurotoxicity von Hosler, B A, Brown, Jr, R H

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Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis von Hosler, Betsy A., Nicholson, Garth A., Sapp, Peter C., Chin, Wendy, Orrell, Richard W., De Belleroche, Jackie S., Esteban, Jesus, Hayward, Lawrence J., McKenna-Yasek, Diane, Yeung, Leone, Cherryson, Annia K., Dench, Joanne E., Wilton, Steve D., Laing, Nigel G., Horvitz, H.Robert, Brown, Robert H.

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Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33 von Hosler, B A, Sapp, P C, Berger, R, O'Neill, G, Bejaoui, K, Hamida, M B, Hentati, F, Chin, W, McKenna-Yasek, D, Haines, J L, Patterson, D, Horvitz, H R, Brown, Jr, R H, Day, C B

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Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis von Cudkowicz, M. E., McKenna-Yasek, D., Sapp, P. E., Chin, W., Geller, B., Hayden, D. L., Schoenfeld, D. A., Hosler, B. A., Horvitz, H. R., Brown, R. H.

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