(Q43628011)

25 November 2017

Silencing mutant SOD1 using RNAi protects against neurodegeneration and extends survival in an ALS model (English)

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amyotrophic lateral sclerosis

25 November 2017

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13

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25 November 2017

G Scott Ralph

1

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25 November 2017

Pippa A Radcliffe

2

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25 November 2017

Denise M Day

3

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25 November 2017

Janine M Carthy

4

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25 November 2017

Marie A Leroux

5

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25 November 2017

Debbie C P Lee

6

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25 November 2017

Liang-Fong Wong

7

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25 November 2017

Lynsey G Bilsland

8

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25 November 2017

Linda Greensmith

9

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25 November 2017

Susan M Kingsman

10

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25 November 2017

Kyriacos A Mitrophanous

11

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25 November 2017

Nicholas D Mazarakis

12

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25 November 2017

language of work or name

English

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publication date

13 March 2005

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25 November 2017

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25 November 2017

11

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25 November 2017

429-433

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25 November 2017

4

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https://scigraph.springernature.com/pub.10.1038/nm1205

25 November 2017

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cites work

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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RNA interference-mediated silencing of mutant superoxide dismutase rescues cyclosporin A-induced death in cultured neuroblastoma cells

21 January 2018

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Selective silencing by RNAi of a dominant allele that causes amyotrophic lateral sclerosis

21 January 2018

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RNAi suppresses polyglutamine-induced neurodegeneration in a model of spinocerebellar ataxia.

21 January 2018

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siRNA-mediated gene silencing in vitro and in vivo.

21 January 2018

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Local gene knockdown in the brain using viral-mediated RNA interference.

21 January 2018

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Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery

21 January 2018

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VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model.

21 January 2018

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An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

21 January 2018

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

21 January 2018

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

21 January 2018

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A system for stable expression of short interfering RNAs in mammalian cells

21 January 2018

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Testosterone reduction prevents phenotypic expression in a transgenic mouse model of spinal and bulbar muscular atrophy

21 January 2018

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Leuprorelin rescues polyglutamine-dependent phenotypes in a transgenic mouse model of spinal and bulbar muscular atrophy

21 January 2018

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Transgenic mice with an expanded CAG repeat controlled by the human AR promoter show polyglutamine nuclear inclusions and neuronal dysfunction without neuronal cell death

21 January 2018

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Retrograde viral delivery of IGF-1 prolongs survival in a mouse ALS model.

21 January 2018

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Wild-Type Nonneuronal Cells Extend Survival of SOD1 Mutant Motor Neurons in ALS Mice

21 January 2018

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Stable gene transfer to the nervous system using a non-primate lentiviral vector

21 January 2018

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New methods to titrate EIAV-based lentiviral vectors

21 January 2018

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Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

21 January 2018

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7 January 2021

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

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7 January 2021

Transduction Patterns of Pseudotyped Lentiviral Vectors in the Nervous System

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7 January 2021

A transient three-plasmid expression system for the production of high titer retroviral vectors

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7 January 2021

Estimation of nuclear population from microtome sections

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7 January 2021

Identifiers

DOI

10.1038/NM1205

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25 November 2017

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