Literature DB >> 7477368

Toxic mutants in Charcot's sclerosis.

D W Cleveland, N Laing, P V Hurse, R H Brown.   

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Year:  1995        PMID： 7477368     DOI： 10.1038/378342a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  16 in total

1.  Caspase-1 and -3 are sequentially activated in motor neuron death in Cu,Zn superoxide dismutase-mediated familial amyotrophic lateral sclerosis.

Authors:  P Pasinelli; M K Houseweart; R H Brown; D W Cleveland
Journal:  Proc Natl Acad Sci U S A       Date:  2000-12-05       Impact factor: 11.205

2.  Pathological characterization of astrocytic hyaline inclusions in familial amyotrophic lateral sclerosis.

Authors:  S Kato; H Hayashi; K Nakashima; E Nanba; M Kato; A Hirano; I Nakano; K Asayama; E Ohama
Journal:  Am J Pathol       Date:  1997-08       Impact factor: 4.307

Review 3.  Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features.

Authors:  A Radunovíc; P N Leigh
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-12       Impact factor: 10.154

4.  Genome-wide siRNA screening reveals that DCAF4-mediated ubiquitination of optineurin stimulates autophagic degradation of Cu,Zn-superoxide dismutase.

Authors:  Kengo Homma; Hiromitsu Takahashi; Naomi Tsuburaya; Isao Naguro; Takao Fujisawa; Hidenori Ichijo
Journal:  J Biol Chem       Date:  2020-02-03       Impact factor: 5.157

5.  Novel mutations in an otherwise strictly conserved domain of CuZn superoxide dismutase.

Authors:  R M Luche; R Maiwald; E J Carlson; C J Epstein
Journal:  Mol Cell Biochem       Date:  1997-03       Impact factor: 3.396

Review 6.  Decoding ALS: from genes to mechanism.

Authors:  J Paul Taylor; Robert H Brown; Don W Cleveland
Journal:  Nature       Date:  2016-11-10       Impact factor: 49.962

7.  Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.

Authors:  Ralf Giess; Bettina Holtmann; Massimiliano Braga; Tiemo Grimm; Bertram Müller-Myhsok; Klaus V Toyka; Michael Sendtner
Journal:  Am J Hum Genet       Date:  2002-04-09       Impact factor: 11.025

8.  SOD1 deficiency: a novel syndrome distinct from amyotrophic lateral sclerosis.

Authors:  Julien H Park; Christiane Elpers; Janine Reunert; Michael L McCormick; Julia Mohr; Saskia Biskup; Oliver Schwartz; Stephan Rust; Marianne Grüneberg; Anja Seelhöfer; Ulrike Schara; Eugen Boltshauser; Douglas R Spitz; Thorsten Marquardt
Journal:  Brain       Date:  2019-08-01       Impact factor: 13.501

9.  Variation in the vulnerability of mice expressing human superoxide dismutase 1 to prion-like seeding: a study of the influence of primary amino acid sequence.

Authors:  Jacob I Ayers; Guilian Xu; Kristy Dillon; Qing Lu; Zhijuan Chen; John Beckman; Alma K Moreno-Romero; Diana L Zamora; Ahmad Galaleldeen; David R Borchelt
Journal:  Acta Neuropathol Commun       Date:  2021-05-20       Impact factor: 7.578

10.  Ligand binding and aggregation of pathogenic SOD1.

Authors:  Gareth S A Wright; Svetlana V Antonyuk; Neil M Kershaw; Richard W Strange; S Samar Hasnain
Journal:  Nat Commun       Date:  2013       Impact factor: 14.919
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