Wheeler V - Search Results

1

Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG).

Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, MacDonald ME, Gusella JF, Myers RH. Hendricks AE, et al. Among authors: wheeler v. Am J Med Genet A. 2009 Jul;149A(7):1375-81. doi: 10.1002/ajmg.a.32901. Am J Med Genet A. 2009. PMID: 19507258 Free PMC article.

2

Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse.

Wheeler VC, Auerbach W, White JK, Srinidhi J, Auerbach A, Ryan A, Duyao MP, Vrbanac V, Weaver M, Gusella JF, Joyner AL, MacDonald ME. Wheeler VC, et al. Hum Mol Genet. 1999 Jan;8(1):115-22. doi: 10.1093/hmg/8.1.115. Hum Mol Genet. 1999. PMID: 9887339

3

Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in mice.

Wheeler VC, White JK, Gutekunst CA, Vrbanac V, Weaver M, Li XJ, Li SH, Yi H, Vonsattel JP, Gusella JF, Hersch S, Auerbach W, Joyner AL, MacDonald ME. Wheeler VC, et al. Hum Mol Genet. 2000 Mar 1;9(4):503-13. doi: 10.1093/hmg/9.4.503. Hum Mol Genet. 2000. PMID: 10699173

4

Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells.

Trettel F, Rigamonti D, Hilditch-Maguire P, Wheeler VC, Sharp AH, Persichetti F, Cattaneo E, MacDonald ME. Trettel F, et al. Among authors: wheeler vc. Hum Mol Genet. 2000 Nov 22;9(19):2799-809. doi: 10.1093/hmg/9.19.2799. Hum Mol Genet. 2000. PMID: 11092756

5

The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin.

Auerbach W, Hurlbert MS, Hilditch-Maguire P, Wadghiri YZ, Wheeler VC, Cohen SI, Joyner AL, MacDonald ME, Turnbull DH. Auerbach W, et al. Among authors: wheeler vc. Hum Mol Genet. 2001 Oct 15;10(22):2515-23. doi: 10.1093/hmg/10.22.2515. Hum Mol Genet. 2001. PMID: 11709539

6

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice.

Wheeler VC, Gutekunst CA, Vrbanac V, Lebel LA, Schilling G, Hersch S, Friedlander RM, Gusella JF, Vonsattel JP, Borchelt DR, MacDonald ME. Wheeler VC, et al. Hum Mol Genet. 2002 Mar 15;11(6):633-40. doi: 10.1093/hmg/11.6.633. Hum Mol Genet. 2002. PMID: 11912178

7

Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice.

Fossale E, Wheeler VC, Vrbanac V, Lebel LA, Teed A, Mysore JS, Gusella JF, MacDonald ME, Persichetti F. Fossale E, et al. Among authors: wheeler vc. Hum Mol Genet. 2002 Sep 15;11(19):2233-41. doi: 10.1093/hmg/11.19.2233. Hum Mol Genet. 2002. PMID: 12217951

8

The HD mutation does not alter neuronal death in the striatum of Hdh(Q92) knock-in mice after mild focal ischemia.

Namura S, Hirt L, Wheeler VC, McGinnis KM, Hilditch-Maguire P, Moskowitz MA, MacDonald ME, Persichetti F. Namura S, et al. Neurobiol Dis. 2002 Oct;11(1):147-54. doi: 10.1006/nbdi.2002.0532. Neurobiol Dis. 2002. PMID: 12460554

9

Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.

Wheeler VC, Lebel LA, Vrbanac V, Teed A, te Riele H, MacDonald ME. Wheeler VC, et al. Hum Mol Genet. 2003 Feb 1;12(3):273-81. doi: 10.1093/hmg/ddg056. Hum Mol Genet. 2003. PMID: 12554681

10

Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice.

Gines S, Seong IS, Fossale E, Ivanova E, Trettel F, Gusella JF, Wheeler VC, Persichetti F, MacDonald ME. Gines S, et al. Hum Mol Genet. 2003 Mar 1;12(5):497-508. doi: 10.1093/hmg/ddg046. Hum Mol Genet. 2003. PMID: 12588797

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