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Items: 1 to 20 of 38

1.

Common denominator of Cu/Zn superoxide dismutase mutants associated with amyotrophic lateral sclerosis: decreased stability of the apo state.

Lindberg MJ, Tibell L, Oliveberg M.

Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16607-12. Epub 2002 Dec 13.

2.

Insights into Lou Gehrig's disease from the structure and instability of the A4V mutant of human Cu,Zn superoxide dismutase.

Cardoso RM, Thayer MM, DiDonato M, Lo TP, Bruns CK, Getzoff ED, Tainer JA.

J Mol Biol. 2002 Nov 22;324(2):247-56.

PMID:
12441104
3.

Sequence-dependent denaturation energetics: A major determinant in amyloid disease diversity.

Hammarström P, Jiang X, Hurshman AR, Powers ET, Kelly JW.

Proc Natl Acad Sci U S A. 2002 Dec 10;99 Suppl 4:16427-32. Epub 2002 Sep 25.

4.
5.

Amyotrophic lateral sclerosis: a proposed mechanism.

Okado-Matsumoto A, Fridovich I.

Proc Natl Acad Sci U S A. 2002 Jun 25;99(13):9010-4. Epub 2002 Jun 11.

6.

Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases.

Bucciantini M, Giannoni E, Chiti F, Baroni F, Formigli L, Zurdo J, Taddei N, Ramponi G, Dobson CM, Stefani M.

Nature. 2002 Apr 4;416(6880):507-11.

PMID:
11932737
7.

Familial amyotrophic lateral sclerosis-associated mutations decrease the thermal stability of distinctly metallated species of human copper/zinc superoxide dismutase.

Rodriguez JA, Valentine JS, Eggers DK, Roe JA, Tiwari A, Brown RH Jr, Hayward LJ.

J Biol Chem. 2002 May 3;277(18):15932-7. Epub 2002 Feb 19.

8.

From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS.

Cleveland DW, Rothstein JD.

Nat Rev Neurosci. 2001 Nov;2(11):806-19. Review. No abstract available.

PMID:
11715057
9.

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

Kato S, Takikawa M, Nakashima K, Hirano A, Cleveland DW, Kusaka H, Shibata N, Kato M, Nakano I, Ohama E.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):163-84. Review.

PMID:
11464950
10.

Superoxide dismutase-1 mutation-related neurotoxicity in familial amyotrophic lateral sclerosis.

Shibata N, Hirano A, Yamamoto T, Kato Y, Kobayashi M.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):143-61. Review.

PMID:
11464949
11.

Protein misfolding and disease; protein refolding and therapy.

Soto C.

FEBS Lett. 2001 Jun 8;498(2-3):204-7. Review.

12.

Amyotrophic lateral sclerosis.

Rowland LP, Shneider NA.

N Engl J Med. 2001 May 31;344(22):1688-700. Review. No abstract available.

PMID:
11386269
13.

Partially folded intermediates as critical precursors of light chain amyloid fibrils and amorphous aggregates.

Khurana R, Gillespie JR, Talapatra A, Minert LJ, Ionescu-Zanetti C, Millett I, Fink AL.

Biochemistry. 2001 Mar 27;40(12):3525-35.

PMID:
11297418
14.
15.

Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded.

Julien JP.

Cell. 2001 Feb 23;104(4):581-91. Review. No abstract available.

16.
17.

Mutational analysis of the propensity for amyloid formation by a globular protein.

Chiti F, Taddei N, Bucciantini M, White P, Ramponi G, Dobson CM.

EMBO J. 2000 Apr 3;19(7):1441-9.

18.

Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations.

Orrell RW.

Neuromuscul Disord. 2000 Jan;10(1):63-8. Review.

PMID:
10677867
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