Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis by Ticozzi, N., Vance, C., LeClerc, A.L., Keagle, P., Glass, J.D., McKenna-Yasek, D., Sapp, P.C., Silani, V., Bosco, D.A., Shaw, C.E., Brown Jr, R.H., Landers, J.E.

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis by 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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SOD1 A4V-mediated ALS: Absence of a closely linked modifier gene and origination in Asia by Broom, W.J., Johnson, D.V., Auwarter, K.E., Iafrate, A.J., Russ, C., Al-Chalabi, A., Sapp, P.C., McKenna-Yasek, D., Andersen, P.M., Brown, R.H.

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SOD1A4V-mediated ALS : Absence of a closely linked modifier gene and origination in Asia by BROOM, W. J, JOHNSON, D. V, AUWARTER, K. E, IAFRATE, A. J, RUSS, C, AL-CHALABI, A, SAPP, P. C, MCKENNA-YASEK, D, ANDERSEN, P. M, BROWN, R. H

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Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1 by Rosen, D.R., Sapp, P.C., O'Regan, J., Horvitz, H.R., Donaldson, D.H., Nussbaum, C., Gusella, J.F., Haines, J.L., Pestka, S., Jung, V., Patterson, D., Brown, R.H.

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Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1) by Donaldson, D.H., Rosen, D.R., O'Regan, J., Sapp, P.C., Horvitz, H.R., Gusella, J.F., Haines, J.L., Pestka, S., Jung, V., Nusbaum, C., Patterson, D., Brown, R.H.

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Mechanism of low-temperature copper-to-copper direct bonding for 3D TSV package interconnection by Cho, J., Yu, S., Roma, M. P. C., Maganty, S., Park, S., Bersch, E., Kim, C., Sapp, B.

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