Creation of an open-access, mutation-defined fibroblast resource for neurological disease research

Autor: Wray, S, Self, M, Lewis, PA, Taanman, JW, Ryan, NS, Mahoney, CJ, Liang, Y, Devine, MJ, Sheerin, UM, Houlden, H, Morris, HR, Healy, D, Marti-Masso, JF, Preza, E, Barker, S, Sutherland, M, Corriveau, RA, D'Andrea, M, Schapira, AHV, Uitti, RJ, Guttman, M, Opala, G, Jasinska-Myga, B, Puschmann, A, Nilsson, C, Espay, AJ, Slawek, J, Gutmann, L, Boeve, BF, Boylan, K, Jon Stoessl, A, Ross, OA, Maragakis, NJ, Van Gerpen, J, Gerstenhaber, M, Gwinn, K, Dawson, TM, Isacson, O, Marder, KS, Clark, LN, Przedborski, SE, Finkbeiner, S, Rothstein, JD, Wszolek, ZK, Rossor, MN, Hardy, J, Gusella, JF, MacDonald, ME, Wheeler, VC, Ross, CA, Akimov, S, Arjomand, J, Thompson, LM, King, A, Hermanowicz, N, Winokur, S, Svendsen, CN, Mattis, V, Onorati, M, Cattaneo, E, Allen, ND, Kemp, PJ, Kim, KS, Przedborski, S, Feng, J, Lee, VMY, Trojanowski, JQ, James Surmeier, D, Henderson, CE, Maniatis, T, Eggan, K, Cudowicz, ME

Publikováno v: Wray, S; Self, M; Lewis, PA; Taanman, JW; Ryan, NS; Mahoney, CJ; et al.(2012). Creation of an open-access, mutation-defined fibroblast resource for neurological disease research. PLoS ONE, 7(8). doi: 10.1371/journal.pone.0043099. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/0hr9m7bt

Our understanding of the molecular mechanisms of many neurological disorders has been greatly enhanced by the discovery of mutations in genes linked to familial forms of these diseases. These have facilitated the generation of cell and animal models

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::858a8a3006d4e18ea535d6f3ffd2375b
http://www.escholarship.org/uc/item/0hr9m7bt

Ingroups and Dropouts

Autor: Winokur, S.

Publikováno v: Science, 1964 Feb 01. 143(3606), 526-526.

Externí odkaz: https://www.jstor.org/stable/1713603

Immunosuppressive and cytotoxic chemotherapy: long-term complications.

Autor: Schein, Philip S., Winokur, Stanley H., Schein, P S, Winokur, S H

Publikováno v: Annals of Internal Medicine; Jan75, Vol. 82 Issue 1, p84-95, 12p

Oligonucleotide microarray expression analysis of genes whose expression is correlated with tumorigenic and non-tumorigenic phenotype of HeLaxhuman fibroblast hybrid cells

Autor: Nishizuka, S., Winokur, S. T., Simon, M., Martin, J., Tsujimoto, H., Stanbridge, E. J.

Publikováno v: Cancer Letters; 2001, Vol. 165 Issue: 2 p201-209, 9p

Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus

Autor: Haraguchi, Y., Chung, A. B., Torroni, A., Stepien, G., Shoffner, J. M., Wasmuth, J. J., Costigan, D. A., Polak, M., Altherr, M. R., Winokur, S. T., Wallace, D. C.

Publikováno v: Genomics; May 1993, Vol. 16 Issue: 2 p479-485, 7p