未登录Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition
Siebzehnrubl, Florian A.; Reber, Kerstin A.; Urbach, Yvonne K.; Schulze-Krebs, Anja; Canneva, Fabio; Moceri, Sandra; Habermeyer, Johanna; Achoui, Dalila; Gupta, Bhavana; Steindler, Dennis A.; Stephan, Michael; Huu Phuc Nguyen; Bonin, Michael; Riess, Olaf; Bauer, Andreas; Aigner, Ludwig; Couillard-Despres, Sebastien; Paucar, Martin Arce; Svenningsson, Per; Osmand, Alexander; Andreew, Alexander; Zabel, Claus; Weiss, Andreas; Kuhn, Rainer; Moussaoui, Saliha; Blockx, Ines; Van der Linden, Annemie; Cheong, Rachel Y.; Roybon, Laurent; Petersen, Asa; von Hoersten, Stephan .png)
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收藏分享 收藏 分享 收藏 Coexistence of Huntington's disease and amyotrophic lateral sclerosis: a clinicopathologic studyTada, Mari; Coon, Elizabeth A.; Osmand, Alexander P.; Kirby, Patricia A.; Martin, Wayne; Wieler, Marguerite; Shiga, Atsushi; Shirasaki, Hiroe; Tada, Masayoshi; Makifuchi, Takao; Yamada, Mitsunori; Kakita, Akiyoshi; Nishizawa, Masatoyo; Takahashi, Hitoshi; Paulson, Henry L. 分享 收藏 ACCUMULATION AND AGGREGATION OF HUMAN MUTANT HUNTINGTIN AND NEURON ATROPHY IN BAC-HD TRANSGENIC RATYu, L.; Metzger, S.; Clemens, L. E.; Ehrismann, J.; Ott, T.; Gu, X.; Gray, M.; Yang, W.; Osmand, A. P.; Riess, O.; Nguyen, H. P. 分享 收藏 Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's diseaseNguyen, Huu Phuc; Kobbe, Philipp; Rahne, Henning; Woerpel, Till; Jaeger, Burkard; Stephan, Michael; Pabst, Reinhard; Holzmann, Carsten; Riess, Olaf; Korr, Hubert; Kantor, Orsolya; Petrasch-Parwez, Elisabeth; Wetzel, Ronald; Osmand, Alexander; von Hoersten, Stephan 分享 收藏 Absence of behavioral abnormalities and neurodegeneration in vivo despite widespread neuronal huntingtin inclusionsSlow, EJ; Graham, RK; Osmand, AP; Devon, RS; Lu, G; Deng, Y; Pearson, J; Vaid, K; Bissada, N; Wetzel, R; Leavitt, BR; Hayden, MR 分享 收藏 分享 收藏 
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