Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse model (Q36218785)

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31 January 2020

title

Molecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse model (English)

1 reference

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amyotrophic lateral sclerosis

31 January 2020

main subject

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author

Daniele Capitanio

1

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31 January 2020

Michele Vasso

2

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31 January 2020

Manuela Volta

5

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31 January 2020

Manuela Moriggi

6

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31 January 2020

Caterina Bendotti

8

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31 January 2020

Vincenzo Silani

9

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31 January 2020

Cecilia Gelfi

10

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31 January 2020

author name string

Antonia Ratti

3

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31 January 2020

Giuliano Grignaschi

4

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31 January 2020

Cristina Daleno

7

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31 January 2020

publication date

13 June 2012

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Antioxidants & Redox Signaling

31 January 2020

published in

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31 January 2020

volume

17

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31 January 2020

issue

10

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31 January 2020

page(s)

1333-1350

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Mitochondria in motor nerve terminals: function in health and in mutant superoxide dismutase 1 mouse models of familial ALS

31 January 2020

cites work

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1 October 2017

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1 October 2017

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Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons

1 October 2017

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Neuromuscular junction destruction during amyotrophic lateral sclerosis: insights from transgenic models

1 October 2017

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Changes in the spinal cord proteome of an amyotrophic lateral sclerosis murine model determined by differential in-gel electrophoresis

1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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PGC-1alpha regulates the neuromuscular junction program and ameliorates Duchenne muscular dystrophy.

1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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29 June 2018

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29 June 2018

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29 June 2018

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29 June 2018

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Dysregulation of iron homeostasis in the CNS contributes to disease progression in a mouse model of amyotrophic lateral sclerosis.

22 September 2018

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22 September 2018

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Bicarbonate-dependent peroxidase activity of human Cu,Zn-superoxide dismutase induces covalent aggregation of protein: intermediacy of tryptophan-derived oxidation products

22 September 2018

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22 September 2018

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22 September 2018

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Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity.

22 September 2018

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Age-dependent penetrance of disease in a transgenic mouse model of familial amyotrophic lateral sclerosis

22 September 2018

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Amyotrophic lateral sclerosis

22 September 2018

1 reference

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Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts

5 December 2018

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12 December 2020

Gene profiling of skeletal muscle in an amyotrophic lateral sclerosis mouse model

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12 December 2020

PGC-1α protects neurons and alters disease progression in an amyotrophic lateral sclerosis mouse model

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12 December 2020

Ultrastructural mitochondrial abnormalities in patients with sporadic amyotrophic lateral sclerosis

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12 December 2020

Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease

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12 December 2020

Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man

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12 December 2020

Type 1, 2A, and 2B myosin heavy chain electrophoretic analysis of rat muscle fibers

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Metabolic capacity of individual muscle fibers from different anatomic locations

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12 December 2020

Ultrastructural evidence for altered calcium in motor nerve terminals in amyotropic lateral sclerosis

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12 December 2020

Elevated levels of albumin in soleus and diaphragm muscles of mdx mice

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Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

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12 December 2020

Redox proteomics analysis of oxidatively modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis

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12 December 2020

Complete dissociation of motor neuron death from motor dysfunction by Bax deletion in a mouse model of ALS

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12 December 2020

Identifiers

DOI

10.1089/ARS.2012.4524

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22563797%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22563797%20AND%20SRC:MED&resulttype=core&format=json

31 January 2020

PubMed publication ID

22563797

1 reference