Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter (Q44674289)

5 December 2017

Molecular signature of late-stage human ALS revealed by expression profiling of postmortem spinal cord gray matter (English)

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amyotrophic lateral sclerosis

5 December 2017

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8

Robert H Brown

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5 December 2017

5

Matthew P Frosch

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5 December 2017

Fernando Dangond

1

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5 December 2017

Daehee Hwang

2

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5 December 2017

Sandra Camelo

3

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5 December 2017

Piera Pasinelli

4

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5 December 2017

Gregory Stephanopoulos

6

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5 December 2017

George Stephanopoulos

7

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5 December 2017

Steven R Gullans

9

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5 December 2017

15 January 2004

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5 December 2017

Physiological Genomics

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5 December 2017

16

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5 December 2017

2

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5 December 2017

229-239

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Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease.

5 December 2017

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Exploring the metabolic and genetic control of gene expression on a genomic scale

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Discovery and analysis of inflammatory disease-related genes using cDNA microarrays

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Determination of minimum sample size and discriminatory expression patterns in microarray data

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Cytoskeletal abnormalities in amyotrophic lateral sclerosis: beneficial or detrimental effects?

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Disruption of dynein/dynactin inhibits axonal transport in motor neurons causing late-onset progressive degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Ubiquitin deposits in anterior horn cells in motor neurone disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Expression monitoring by hybridization to high-density oligonucleotide arrays

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Interleukin-7 is trophic for embryonic neurons and is expressed in developing brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

A comparative review of statistical methods for discovering differentially expressed genes in replicated microarray experiments

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Brain superoxide dismutase, catalase, and glutathione peroxidase activities in amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Genetics of amyotrophic lateral sclerosis

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Pitfalls in the use of DNA microarray data for diagnostic and prognostic classification

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

21 January 2018

Autoimmunity and ALS.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

An efficient and robust statistical modeling approach to discover differentially expressed genes using genomic expression profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Bax and Bcl-2 interaction in a transgenic mouse model of familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

A gain-of-function of an amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutant: An enhancement of free radical formation due to a decrease in Km for hydrogen peroxide

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Possible involvement of folate cycle in the pathogenesis of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00087.2001

10.1152/PHYSIOLGENOMICS.00087.2001

21 January 2018

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DOI

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5 December 2017

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