Copeland N - Search Results

1

Distinct behavioral and neuropathological abnormalities in transgenic mouse models of HD and DRPLA.

Schilling G, Jinnah HA, Gonzales V, Coonfield ML, Kim Y, Wood JD, Price DL, Li XJ, Jenkins N, Copeland N, Moran T, Ross CA, Borchelt DR. Schilling G, et al. Among authors: copeland n. Neurobiol Dis. 2001 Jun;8(3):405-18. doi: 10.1006/nbdi.2001.0385. Neurobiol Dis. 2001. PMID: 11442350

2

Hyperaccumulation of FAD-linked presenilin 1 variants in vivo.

Lee MK, Borchelt DR, Kim G, Thinakaran G, Slunt HH, Ratovitski T, Martin LJ, Kittur A, Gandy S, Levey AI, Jenkins N, Copeland N, Price DL, Sisodia SS. Lee MK, et al. Among authors: copeland n. Nat Med. 1997 Jul;3(7):756-60. doi: 10.1038/nm0797-756. Nat Med. 1997. PMID: 9212102

3

Efficient Cre-loxP-induced mitotic recombination in mouse embryonic stem cells.

Liu P, Jenkins NA, Copeland NG. Liu P, et al. Nat Genet. 2002 Jan;30(1):66-72. doi: 10.1038/ng788. Epub 2001 Dec 10. Nat Genet. 2002. PMID: 11740496

4

Accumulation of proteolytic fragments of mutant presenilin 1 and accelerated amyloid deposition are co-regulated in transgenic mice.

Borchelt DR, Lee MK, Gonzales V, Slunt HH, Ratovitski T, Jenkins NA, Copeland NG, Price DL, Sisodia SS. Borchelt DR, et al. Neurobiol Aging. 2002 Mar-Apr;23(2):171-7. doi: 10.1016/s0197-4580(01)00280-9. Neurobiol Aging. 2002. PMID: 11804700

5

Genomics. Mmu 16--comparative genomic highlights.

Copeland NG, Jenkins NA, O'Brien SJ. Copeland NG, et al. Science. 2002 May 31;296(5573):1617-8. doi: 10.1126/science.1073127. Science. 2002. PMID: 12040165 No abstract available.

6

Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice.

Lee MK, Stirling W, Xu Y, Xu X, Qui D, Mandir AS, Dawson TM, Copeland NG, Jenkins NA, Price DL. Lee MK, et al. Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):8968-73. doi: 10.1073/pnas.132197599. Proc Natl Acad Sci U S A. 2002. PMID: 12084935 Free PMC article.

7

Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding site.

Wang J, Xu G, Gonzales V, Coonfield M, Fromholt D, Copeland NG, Jenkins NA, Borchelt DR. Wang J, et al. Neurobiol Dis. 2002 Jul;10(2):128-38. doi: 10.1006/nbdi.2002.0498. Neurobiol Dis. 2002. PMID: 12127151

8

Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease.

Wilson SM, Bhattacharyya B, Rachel RA, Coppola V, Tessarollo L, Householder DB, Fletcher CF, Miller RJ, Copeland NG, Jenkins NA. Wilson SM, et al. Nat Genet. 2002 Nov;32(3):420-5. doi: 10.1038/ng1006. Epub 2002 Oct 7. Nat Genet. 2002. PMID: 12368914

9

A highly efficient recombineering-based method for generating conditional knockout mutations.

Liu P, Jenkins NA, Copeland NG. Liu P, et al. Genome Res. 2003 Mar;13(3):476-84. doi: 10.1101/gr.749203. Genome Res. 2003. PMID: 12618378 Free PMC article.

10

Identification of Vangl2 and Scrb1 as planar polarity genes in mammals.

Montcouquiol M, Rachel RA, Lanford PJ, Copeland NG, Jenkins NA, Kelley MW. Montcouquiol M, et al. Nature. 2003 May 8;423(6936):173-7. doi: 10.1038/nature01618. Epub 2003 Apr 30. Nature. 2003. PMID: 12724779

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