Integration-free induced pluripotent stem cells derived from schizophrenia patients with a DISC1 mutation von Chiang, C-H, Su, Y, Wen, Z, Yoritomo, N, Ross, C A, Margolis, R L, Song, H, Ming, G-l

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Differential effects of prenatal and postnatal expressions of mutant human DISC1 on neurobehavioral phenotypes in transgenic mice: evidence for neurodevelopmental origin of major p... von Ayhan, Y, Abazyan, B, Nomura, J, Kim, R, Ladenheim, B, Krasnova, I N, Sawa, A, Margolis, R L, Cadet, J L, Mori, S, Vogel, M W, Ross, C A, Pletnikov, M V

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A comparison of nine scales to detect depression in Parkinson disease: Which scale to use? von WILLIAMS, J. R, HIRSCH, E. S, PONTONE, G, WEISS, H, RABINS, P, MARSH, L, ANDERSON, K, BUSH, A. L, GOLDSTEIN, S. R, GRILL, S, LEHMANN, S, LITTLE, J. T, MARGOLIS, R. L, PALANCI, J

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Onset and rate of striatal atrophy in preclinical Huntington disease von AYLWARD, E. H, SPARKS, B. F, MARGOLIS, R. L, ROSS, C. A, FIELD, K. M, YALLAPRAGADA, V, SHPRITZ, B. D, ROSENBLATT, A, BRANDT, J, GOURLEY, L. M, LIANG, K, ZHOU, H

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SP600125 suppresses Cdk1 and induces endoreplication directly from G2 phase, independent of JNK inhibition von Kim, J A, Lee, J, Margolis, R L, Fotedar, R

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A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder von Sachs, N A, Sawa, A, Holmes, S E, Ross, C A, DeLisi, L E, Margolis, R L

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The association of CAG repeat length with clinical progression in huntington disease von ROSENBLATT, A, LIANG, K.-Y, ZHOU, H, ABBOTT, M. H, GOURLEY, L. M, MARGOLIS, R. L, BRANDT, J, ROSS, C. A

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Tetraploid state induces p53-dependent arrest of nontransformed mammalian cells in G1 von Andreassen, P R, Lohez, O D, Lacroix, F B, Margolis, R L

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Distinct specificity in the recognition of phosphoinositides by the pleckstrin homology domains of dynamin and Bruton's tyrosine kinase von Salim, K, Bottomley, M. J, Querfurth, E, Zvelebil, M. J, Gout, I, Scaife, R, Margolis, R. L, Gigg, R, Smith, C. I, Driscoll, P. C, Waterfield, M. D, Panayotou, G

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Quantitative Susceptibility Mapping Suggests Altered Brain Iron in Premanifest Huntington Disease von van Bergen, J M G, Hua, J, Unschuld, P G, Lim, I A L, Jones, C K, Margolis, R L, Ross, C A, van Zijl, P C M, Li, X

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The clinical and genetic spectrum of spinocerebellar ataxia 14 von CHEN, D.-H, CIMINO, P. J, WOLFF, J, MORGAN, C, LAU, D, FERNANDEZ, M, SASAKI, H, RASKIND, W. H, BIRD, T. D, RANUM, L. P. W, ZOGHBI, H. Y, YABE, I, SCHUT, L, MARGOLIS, R. L, LIPE, H. P, FELEKE, A, MATSUSHITA, M

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Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant von Earnshaw, W. C, Allshire, R. C, Black, B. E, Bloom, K, Brinkley, B. R, Brown, W, Cheeseman, I. M, Choo, K. H. A, Copenhaver, G. P, DeLuca, J. G, Desai, A, Diekmann, S, Erhardt, S, Fitzgerald-Hayes, M, Foltz, D, Fukagawa, T, Gassmann, R, Gerlich, D. W, Glover, D. M, Gorbsky, G. J, Harrison, S. C, Heun, P, Hirota, T, Jansen, L. E. T, Karpen, G, Kops, G. J. P. L, Lampson, M. A, Lens, S. M, Losada, A, Luger, K, Maiato, H, Maddox, P. S, Margolis, R. L, Masumoto, H, McAinsh, A. D, Mellone, B. G, Meraldi, P, Musacchio, A, Oegema, K, O’Neill, R. J, Salmon, E. D, Scott, K. C, Straight, A. F, Stukenberg, P. T, Sullivan, B. A, Sullivan, K. F, Sunkel, C. E, Swedlow, J. R, Walczak, C. E, Warburton, P. E, Westermann, S, Willard, H. F, Wordeman, L, Yanagida, M, Yen, T. J, Yoda, K, Cleveland, D. W

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Huntington's disease-like 2 can present as chorea-acanthocytosis von WALKER, R. H, RASMUSSEN, A, RUDNICKI, D, HOLMES, S. E, ALONSO, E, MATSUURA, T, ASHIZAWA, T, DAVIDOFF-FELDMAN, B, MARGOLIS, R. L

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SCA-12 : Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion von O'HEARN, E, HOLMES, S. E, CALVERT, P. C, ROSS, C. A, MARGOLIS, R. L

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Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions von Engelender, Simone, Kaminsky, Zachary, Guo, Xin, Sharp, Alan H., Amaravi, Ravi K., Kleiderlein, John J., Margolis, Russell L., Troncoso, Juan C., Lanahan, Anthony A., Worley, Paul F., Dawson, Valina L., Dawson, Ted M., Ross, Christopher A.

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Expansion explosion: new clues to the pathogenesis of repeat expansion neurodegenerative diseases von Margolis, Russell L, Ross, Christopher A

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CAG/CTG repeat expansions at the Huntington's disease: like 2 locus are rare in Huntington's disease patients von STEVANIN, G, CAMUZAT, A, BRICE, A, HOLMES, S. E, JULIEN, C, SAHLOUL, R, DODE, C, HAHN-BARMA, V, ROSS, C. A, MARGOLIS, R. L, DURR, A

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A mutation in NPAS3 segregates with mental illness in a small family von Yu, L, Arbez, N, Nucifora, L G, Sell, G L, DeLisi, L E, Ross, C A, Margolis, R L, Nucifora, F C

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Purification of the Centromere-Specific Protein CENP-A and Demonstration that it is a Distinctive Histone von Palmer, D K, O'Day, K, Trong, H L, Charbonneau, H, Margolis, R L

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Familial influence on age of onset among siblings with Huntington disease von Rosenblatt, Adam, Brinkman, R.R., Liang, K.Y., Almqvist, E.W., Margolis, R.L., Huang, C.Y., Sherr, M., Franz, M.L., Abbott, M.H., Hayden, M.R., Ross, C.A.

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