(Q45019171)

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SAGE analysis of genes differentially expressed in presymptomatic TgSOD1G93A transgenic mice identified cellular processes involved in early stage of ALS pathology

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scholarly article

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Europe PubMed Central

PubMed publication ID

8 December 2017

SAGE analysis of genes differentially expressed in presymptomatic TgSOD1G93A transgenic mice identified cellular processes involved in early stage of ALS pathology (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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amyotrophic lateral sclerosis

1 reference

based on heuristic

inferred from title

4

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Europe PubMed Central

PubMed publication ID

8 December 2017

Hamish S. Scott

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Hamish S Scott

7

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object named as

Gordon K Smyth

5

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Colin L. Masters

6

object named as

Colin L Masters

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

author name string

Michel Guipponi

1

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Europe PubMed Central

PubMed publication ID

8 December 2017

Qiao-Xin Li

2

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Europe PubMed Central

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8 December 2017

Lavinia Hyde

3

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Europe PubMed Central

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8 December 2017

publication date

2 December 2009

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Europe PubMed Central

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8 December 2017

Journal of Molecular Neuroscience

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Europe PubMed Central

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8 December 2017

41

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Europe PubMed Central

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8 December 2017

1

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Europe PubMed Central

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8 December 2017

172-182

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Europe PubMed Central

PubMed publication ID

8 December 2017

https://scigraph.springernature.com/pub.10.1007/s12031-009-9317-1

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Activated p38MAPK is a novel component of the intracellular inclusions found in human amyotrophic lateral sclerosis and mutant SOD1 transgenic mice.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-009-9317-1

21 January 2018

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

1 reference

https://api.crossref.org/works/10.1007%2FS12031-009-9317-1

21 January 2018

Progressive loss of motor neuron function in wasted mice: effects of a spontaneous null mutation in the gene for the eEF1 A2 translation factor

1 reference

https://api.crossref.org/works/10.1007%2FS12031-009-9317-1

21 January 2018

No widespread induction of cell death genes occurs in pure motoneurons in an amyotrophic lateral sclerosis mouse model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Using the transcriptome to annotate the genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteomic identification of proteins oxidized by Abeta(1-42) in synaptosomes: implications for Alzheimer's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Astrocytes expressing ALS-linked mutated SOD1 release factors selectively toxic to motor neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toxicity of familial ALS-linked SOD1 mutants from selective recruitment to spinal mitochondria.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transgenic mice overexpressing glutathione peroxidase 4 are protected against oxidative stress-induced apoptosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prosaposin: a myelinotrophic protein that promotes expression of myelin constituents and is secreted after nerve injury

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of SOD1 in ALS: a gain of a loss of function

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ALS: a disease of motor neurons and their nonneuronal neighbors

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced creatine kinase activity in transgenic amyotrophic lateral sclerosis mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pyruvate slows disease progression in a G93A SOD1 mutant transgenic mouse model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinal cord mRNA profile in patients with ALS: comparison with transgenic mice expressing the human SOD-1 mutant.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-cell autonomous effect of glia on motor neurons in an embryonic stem cell-based ALS model

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow component of axonal transport is impaired in the proximal axon of transgenic mice with a G93A mutant SOD1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteomic analysis of 4-hydroxy-2-nonenal-modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serial analysis of gene expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

UCHL1 is a Parkinson's disease susceptibility gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased glycolytic metabolism contributes to but is not the inducer of apoptosis following IL-3-starvation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microarray analysis of the cellular pathways involved in the adaptation to and progression of motor neuron injury in the SOD1 G93A mouse model of familial ALS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein nitration in a mouse model of familial amyotrophic lateral sclerosis: possible multifunctional role in the pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Controlling the false discovery rate in behavior genetics research

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TDP-43 A315T mutation in familial motor neuron disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unraveling the mechanisms involved in motor neuron degeneration in ALS

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis-associated SOD1 mutant proteins bind and aggregate with Bcl-2 in spinal cord mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial dysfunction and its role in motor neuron degeneration in ALS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informatics-assisted protein profiling in a transgenic mouse model of amyotrophic lateral sclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studying the effects of actin cytoskeletal destabilization on cell cycle by cofilin overexpression

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAD and glucokinase reside in a mitochondrial complex that integrates glycolysis and apoptosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuroprotective effects of creatine in a transgenic animal model of amyotrophic lateral sclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of MMS19 domains with distinct functions in NER and transcription.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19953340

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12031-009-9317-1

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 December 2017

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