A07 CircHTT, a novel circular rna molecule from the huntington’s disease gene locus: functional characterization and pathophysiological implications
Morandell, J, Döring, J, Monziani, A, Oss Pegorar, C, Ferrari, S, Bergonzoni, G, Tripathi, T, Di Leva, F, Kerschbamer, E, Mattis, VB, Rosati, J, Dieterich, C, Dassi, E, Wheeler, VC, Hansíková, H, Ellederová, Z, Wilusz, JE, Biagioli, M
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
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Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells
Trettel, F, Rigamonti, D, Hilditch-Maguire, P, Wheeler, V C, Sharp, A H, Persichetti, F, Cattaneo, E, MacDonald, M E
Published in Human molecular genetics (22.11.2000)
Published in Human molecular genetics (22.11.2000)
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Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice
Wheeler, Vanessa C., Gutekunst, Claire-Anne, Vrbanac, Vladimir, Lebel, Lori-Anne, Schilling, Gabriele, Hersch, Steven, Friedlander, Robert M., Gusella, James F., Vonsattel, Jean-Paul, Borchelt, David R., MacDonald, Marcy E.
Published in Human molecular genetics (15.03.2002)
Published in Human molecular genetics (15.03.2002)
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Journal Article
Length-Dependent Gametic CAG Repeat Instability in the Huntington's Disease Knock-in Mouse
Wheeler, Vanessa C., Auerbach, Wojtek, White, Jacqueline K., Srinidhi, Jayalakshmi, Auerbach, Anna, Ryan, Angela, Duyao, Mabel P., Vrbanac, Vladimir, Weaver, Meredith, Gusella, James F., Joyner, Alexandra L., MacDonald, Marcy E.
Published in Human molecular genetics (01.01.1999)
Published in Human molecular genetics (01.01.1999)
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Journal Article
A Genome Scan for Modifiers of Age at Onset in Huntington Disease: The HD MAPS Study
Li, Jian-Liang, Hayden, Michael R., Almqvist, Elisabeth W., Brinkman, Ryan R., Durr, Alexandra, Dodé, Catherine, Morrison, Patrick J., Suchowersky, Oksana, Ross, Christopher A., Margolis, Russell L., Rosenblatt, Adam, Gómez-Tortosa, Estrella, Cabrero, David Mayo, Novelletto, Andrea, Frontali, Marina, Nance, Martha, Trent, Ronald J.A., McCusker, Elizabeth, Jones, Randi, Paulsen, Jane S., Harrison, Madeline, Zanko, Andrea, Abramson, Ruth K., Russ, Ana L., Knowlton, Beth, Djoussé, Luc, Mysore, Jayalakshmi S., Tariot, Suzanne, Gusella, Michael F., Wheeler, Vanessa C., Atwood, Larry D., Cupples, L. Adrienne, Saint-Hilaire, Marie, Cha, Jang-Ho J., Hersch, Steven M., Koroshetz, Walter J., Gusella, James F., MacDonald, Marcy E., Myers, Richard H.
Published in American journal of human genetics (01.09.2003)
Published in American journal of human genetics (01.09.2003)
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Journal Article
The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin
AUERBACH, Wojtek, HURLBERT, Marc S, HILDITCH-MAGUIRE, Paige, WADGHIRI, Youssef Zaim, WHEELER, Vanessa C, COHEN, Sara I, JOYNER, Alexandra L, MACDONALD, Marcy E, TURNBULL, Daniel H
Published in Human molecular genetics (15.10.2001)
Published in Human molecular genetics (15.10.2001)
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Journal Article
A11 Induced pluripotent stem cells for basic and translational research on HD
Mattis, VB, Svendsen, SP, Ebert, A, Svendsen, CN, King, AR, Casale, M, Winokur, ST, Batugedara, G, Vawter, M, Donovan, PJ, Lock, LF, Thompson, LM, Zhu, Y, Fossale, E, Atwal, RS, Gillis, T, Mysore, J, Li, J-h, Seong, IS, Shen, Y, Chen, X, Wheeler, VC, MacDonald, Marcy E, Gusella, JF, Akimov, S, Arbez, N, Juopperi, T, Ratovitski, T, Chiang, JH, Kim, WR, Chighladze, E, Watkin, E, Zhong, C, Makri, G, Cole, RN, Margolis, RL, Song, H, Ming, G, Ross, CA, Kaye, JA, Daub, A, Sharma, P, Mason, AR, Finkbeiner, S, Yu, J, Thomson, JA, Rushton, D, Brazier, SP, Battersby, AA, Redfern, A, Tseng, H-E, Harrison, AW, Kemp, PJ, Allen, ND, Onorati, M, Castiglioni, V, Cattaneo, E, Arjomand, J
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2012)
Published in Journal of neurology, neurosurgery and psychiatry (01.09.2012)
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Journal Article
Huntington's disease
MacDonald, Marcy E, Gines, Silvia, Gusella, James F, Wheeler, Vanessa C
Published in Neuromolecular medicine (01.01.2003)
Published in Neuromolecular medicine (01.01.2003)
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Journal Article
Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice
Fossale, Elisa, Wheeler, Vanessa C., Vrbanac, Vladimir, Lebel, Lori-Anne, Teed, Allison, Mysore, Jayalakshmi S., Gusella, James F., MacDonald, Marcy E., Persichetti, Francesca
Published in Human molecular genetics (15.09.2002)
Published in Human molecular genetics (15.09.2002)
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Journal Article
Neocortical neurons cultured from mice with expanded cag repeats in the huntingtin gene: unaltered vulnerability to excitotoxins and other insults
Snider, B.J, Moss, J.L, Revilla, F.J, Lee, C.-S, Wheeler, V.C, Macdonald, M.E, Choi, D.W
Published in Neuroscience (01.01.2003)
Published in Neuroscience (01.01.2003)
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Journal Article
The HD mutation does not alter neuronal death in the striatum of Hdh(Q92) knock-in mice after mild focal ischemia
Namura, Shobu, Hirt, Lorenz, Wheeler, Vanessa C, McGinnis, Kim M, Hilditch-Maguire, Paige, Moskowitz, Michael A, MacDonald, Marcy E, Persichetti, Francesca
Published in Neurobiology of disease (01.10.2002)
Published in Neurobiology of disease (01.10.2002)
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Journal Article
Synthesis of a modified gene encoding human ornithine transcarbamylase for expression in mammalian mitochondrial and universal translation systems: a novel approach towards correction of a genetic defect
Wheeler, Vanessa C., Prodromou, Chrisostomos, Pearl, Laurence H., Williamson, Robert, Coutelle, Charles
Published in Gene (09.03.1996)
Published in Gene (09.03.1996)
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Use of an operon fusion to induce expression and crystallisation of a Bacillus thuringiensis delta-endotoxin encoded by a cryptic gene
Crickmore, N. (Cambridge Univ. (United Kingdom). Dept. of Biochemistry), Wheeler, V.C, Ellar, D.J
Published in Molecular & general genetics (01.02.1994)
Published in Molecular & general genetics (01.02.1994)
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