Armstrong D - Search Results

1

Functional conservation of atonal and Math1 in the CNS and PNS.

Ben-Arie N, Hassan BA, Bermingham NA, Malicki DM, Armstrong D, Matzuk M, Bellen HJ, Zoghbi HY. Ben-Arie N, et al. Among authors: armstrong d. Development. 2000 Mar;127(5):1039-48. doi: 10.1242/dev.127.5.1039. Development. 2000. PMID: 10662643

2

Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals.

Servadio A, Koshy B, Armstrong D, Antalffy B, Orr HT, Zoghbi HY. Servadio A, et al. Among authors: armstrong d. Nat Genet. 1995 May;10(1):94-8. doi: 10.1038/ng0595-94. Nat Genet. 1995. PMID: 7647801

3

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome.

Moretti P, Levenson JM, Battaglia F, Atkinson R, Teague R, Antalffy B, Armstrong D, Arancio O, Sweatt JD, Zoghbi HY. Moretti P, et al. Among authors: armstrong d. J Neurosci. 2006 Jan 4;26(1):319-27. doi: 10.1523/JNEUROSCI.2623-05.2006. J Neurosci. 2006. PMID: 16399702 Free PMC article.

4

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.

Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H. Shahbazian M, et al. Among authors: armstrong d. Neuron. 2002 Jul 18;35(2):243-54. doi: 10.1016/s0896-6273(02)00768-7. Neuron. 2002. PMID: 12160743 Free article.

5

Impaired conditioned fear and enhanced long-term potentiation in Fmr2 knock-out mice.

Gu Y, McIlwain KL, Weeber EJ, Yamagata T, Xu B, Antalffy BA, Reyes C, Yuva-Paylor L, Armstrong D, Zoghbi H, Sweatt JD, Paylor R, Nelson DL. Gu Y, et al. Among authors: armstrong d. J Neurosci. 2002 Apr 1;22(7):2753-63. doi: 10.1523/JNEUROSCI.22-07-02753.2002. J Neurosci. 2002. PMID: 11923441 Free PMC article.

6

Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain?

Armstrong DD. Armstrong DD. Brain Dev. 2005 Nov;27 Suppl 1:S72-S76. doi: 10.1016/j.braindev.2004.10.009. Epub 2005 Sep 22. Brain Dev. 2005. PMID: 16182497 Review.

7

Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancy.

Moretti P, Blazo M, Garcia L, Armstrong D, Lewis RA, Roa B, Scaglia F. Moretti P, et al. Among authors: armstrong d. Am J Med Genet A. 2004 Feb 1;124A(4):392-6. doi: 10.1002/ajmg.a.20428. Am J Med Genet A. 2004. PMID: 14735588

8

Pathologic basis of the symptomatic epilepsies in childhood.

Armstrong DD, Mizrahi EM. Armstrong DD, et al. J Child Neurol. 1998 Aug;13(8):361-71. doi: 10.1177/088307389801300801. J Child Neurol. 1998. PMID: 9721890 Review.

9

The neurological mutant quaking(viable) is Parkin deficient.

Lorenzetti D, Antalffy B, Vogel H, Noveroske J, Armstrong D, Justice M. Lorenzetti D, et al. Among authors: armstrong d. Mamm Genome. 2004 Mar;15(3):210-7. doi: 10.1007/s00335-003-2333-5. Mamm Genome. 2004. PMID: 15014970

10

Expression patterns of cytochrome P4501B1 (Cyp1b1) in FVB/N mouse eyes.

Bejjani BA, Xu L, Armstrong D, Lupski JR, Reneker LW. Bejjani BA, et al. Among authors: armstrong d. Exp Eye Res. 2002 Sep;75(3):249-57. Exp Eye Res. 2002. PMID: 12384088

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