Cleveland DW - Search Results

1

Mutant SOD1 in cell types other than motor neurons and oligodendrocytes accelerates onset of disease in ALS mice.

Yamanaka K, Boillee S, Roberts EA, Garcia ML, McAlonis-Downes M, Mikse OR, Cleveland DW, Goldstein LS. Yamanaka K, et al. Among authors: cleveland dw. Proc Natl Acad Sci U S A. 2008 May 27;105(21):7594-9. doi: 10.1073/pnas.0802556105. Epub 2008 May 20. Proc Natl Acad Sci U S A. 2008. PMID: 18492803 Free PMC article.

2

Superoxide dismutase is an abundant component in cell bodies, dendrites, and axons of motor neurons and in a subset of other neurons.

Pardo CA, Xu Z, Borchelt DR, Price DL, Sisodia SS, Cleveland DW. Pardo CA, et al. Among authors: cleveland dw. Proc Natl Acad Sci U S A. 1995 Feb 14;92(4):954-8. doi: 10.1073/pnas.92.4.954. Proc Natl Acad Sci U S A. 1995. PMID: 7862672 Free PMC article.

3

Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.

Borchelt DR, Lee MK, Slunt HS, Guarnieri M, Xu ZS, Wong PC, Brown RH Jr, Price DL, Sisodia SS, Cleveland DW. Borchelt DR, et al. Among authors: cleveland dw. Proc Natl Acad Sci U S A. 1994 Aug 16;91(17):8292-6. doi: 10.1073/pnas.91.17.8292. Proc Natl Acad Sci U S A. 1994. PMID: 8058797 Free PMC article.

4

Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease.

Cleveland DW, Bruijn LI, Wong PC, Marszalek JR, Vechio JD, Lee MK, Xu XS, Borchelt DR, Sisodia SS, Price DL. Cleveland DW, et al. Neurology. 1996 Oct;47(4 Suppl 2):S54-61; discussion S61-2. doi: 10.1212/wnl.47.4_suppl_2.54s. Neurology. 1996. PMID: 8858052 Review.

5

Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis.

Vechio JD, Bruijn LI, Xu Z, Brown RH Jr, Cleveland DW. Vechio JD, et al. Among authors: cleveland dw. Ann Neurol. 1996 Oct;40(4):603-10. doi: 10.1002/ana.410400410. Ann Neurol. 1996. PMID: 8871580

6

Mechanisms of selective motor neuron death in ALS: insights from transgenic mouse models of motor neuron disease.

Bruijn LI, Cleveland DW. Bruijn LI, et al. Among authors: cleveland dw. Neuropathol Appl Neurobiol. 1996 Oct;22(5):373-87. doi: 10.1111/j.1365-2990.1996.tb00907.x. Neuropathol Appl Neurobiol. 1996. PMID: 8930947 Review.

7

ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.

Bruijn LI, Becher MW, Lee MK, Anderson KL, Jenkins NA, Copeland NG, Sisodia SS, Rothstein JD, Borchelt DR, Price DL, Cleveland DW. Bruijn LI, et al. Among authors: cleveland dw. Neuron. 1997 Feb;18(2):327-38. doi: 10.1016/s0896-6273(00)80272-x. Neuron. 1997. PMID: 9052802 Free article.

8

Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superoxide dismutase 1 mutant.

Bruijn LI, Beal MF, Becher MW, Schulz JB, Wong PC, Price DL, Cleveland DW. Bruijn LI, et al. Among authors: cleveland dw. Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7606-11. doi: 10.1073/pnas.94.14.7606. Proc Natl Acad Sci U S A. 1997. PMID: 9207139 Free PMC article.

9

CENP-E is a plus end-directed kinetochore motor required for metaphase chromosome alignment.

Wood KW, Sakowicz R, Goldstein LS, Cleveland DW. Wood KW, et al. Among authors: cleveland dw. Cell. 1997 Oct 31;91(3):357-66. doi: 10.1016/s0092-8674(00)80419-5. Cell. 1997. PMID: 9363944 Free article.

10

Chaperone-facilitated copper binding is a property common to several classes of familial amyotrophic lateral sclerosis-linked superoxide dismutase mutants.

Corson LB, Strain JJ, Culotta VC, Cleveland DW. Corson LB, et al. Among authors: cleveland dw. Proc Natl Acad Sci U S A. 1998 May 26;95(11):6361-6. doi: 10.1073/pnas.95.11.6361. Proc Natl Acad Sci U S A. 1998. PMID: 9600970 Free PMC article.

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