(Q33894661)

English

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

Muscle expression of mutant androgen receptor accounts for systemic and motor neuron disease phenotypes in spinal and bulbar muscular atrophy (English)

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

motor neuron disease

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

Don W. Cleveland

12

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Europe PubMed Central

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14 March 2020

author name string

Constanza J Cortes

1

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14 March 2020

Shuo-Chien Ling

2

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14 March 2020

Ling T Guo

3

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14 March 2020

Gene Hung

4

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14 March 2020

Taiji Tsunemi

5

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14 March 2020

Linda Ly

6

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14 March 2020

Seiya Tokunaga

7

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14 March 2020

Edith Lopez

8

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14 March 2020

Bryce L Sopher

9

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14 March 2020

C Frank Bennett

10

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14 March 2020

G Diane Shelton

11

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14 March 2020

Albert R La Spada

13

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14 March 2020

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1 April 2014

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14 March 2020

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

82

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14 March 2020

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

295-307

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14 March 2020

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4096235/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Peripheral androgen receptor gene suppression rescues disease in mouse models of spinal and bulbar muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Motor neuron involvement in multisystem proteinopathy: implications for ALS

1 reference

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5 July 2018

Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis.

1 reference

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5 July 2018

ALS-linked TDP-43 mutations produce aberrant RNA splicing and adult-onset motor neuron disease without aggregation or loss of nuclear TDP-43.

1 reference

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5 July 2018

Skeletal muscle degenerative diseases and strategies for therapeutic muscle repair

1 reference

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5 July 2018

Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Pathogenesis and therapy of spinal and bulbar muscular atrophy (SBMA).

1 reference

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5 July 2018

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1 reference

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5 July 2018

Intercellular (mis)communication in neurodegenerative disease.

1 reference

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5 July 2018

Neurogenic and myogenic contributions to hereditary motor neuron disease

1 reference

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5 July 2018

Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Increased IGF-1 in muscle modulates the phenotype of severe SMA mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Disrupted transforming growth factor-beta signaling in spinal and bulbar muscular atrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Insulin-like growth factors (IGFs), IGF receptors, and IGF-binding proteins: roles in skeletal muscle growth and differentiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Repeat expansion disease: progress and puzzles in disease pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Recovery of function in a myogenic mouse model of spinal bulbar muscular atrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Astrocytes as determinants of disease progression in inherited amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Overexpression of wild-type androgen receptor in muscle recapitulates polyglutamine disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression

1 reference

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5 July 2018

Gene transfer demonstrates that muscle is not a primary target for non-cell-autonomous toxicity in familial amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Androgen-dependent pathology demonstrates myopathic contribution to the Kennedy disease phenotype in a mouse knock-in model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Onset and progression in inherited ALS determined by motor neurons and microglia

1 reference

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1 reference

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5 July 2018

Muscle expression of a local Igf-1 isoform protects motor neurons in an ALS mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

5 July 2018

Androgen receptor YAC transgenic mice recapitulate SBMA motor neuronopathy and implicate VEGF164 in the motor neuron degeneration

1 reference

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5 July 2018

Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport.

1 reference

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1 reference

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4096235

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1 reference

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1 reference

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Reversible molecular pathology of skeletal muscle in spinal muscular atrophy

1 reference

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Skeletal Muscle Is a Primary Target of SOD1G93A-Mediated Toxicity

1 reference

https://pubmed.ncbi.nlm.nih.gov/24742458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulation of SOD1 mutants in postnatal motoneurons does not cause motoneuron pathology or motoneuron disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/24742458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.NEURON.2014.03.001

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24742458%20AND%20SRC:MED&resulttype=core&format=json

14 March 2020

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