(Q34625379)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

title

Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for X linked hypopituitarism (English)

1 reference

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26 February 2020

3

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26 February 2020

author name string

James Hughes

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

Sandra Piltz

2

1 reference

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26 February 2020

Dale McAninch

4

1 reference

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26 February 2020

Lynn Rowley

5

1 reference

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26 February 2020

Paul Thomas

6

1 reference

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26 February 2020

publication date

7 March 2013

1 reference

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26 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

volume

9

1 reference

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26 February 2020

issue

3

1 reference

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26 February 2020

page(s)

e1003290

1 reference

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Creative Commons Attribution 4.0 International

26 February 2020

copyright license

start time

7 March 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Limb skeletal malformations - what the HOX is going on?

1 reference

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Sox3 functions in a cell-autonomous manner to regulate spermatogonial differentiation in mice.

7 July 2018

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ARX spectrum disorders: making inroads into the molecular pathology

7 July 2018

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Repeat expansion disease: progress and puzzles in disease pathogenesis

7 July 2018

1 reference

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X-linked isolated growth hormone deficiency: expanding the phenotypic spectrum of SOX3 polyalanine tract expansions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591313

A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment

7 July 2018

1 reference

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The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism

7 July 2018

1 reference

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Minimization of exogenous signals in ES cell culture induces rostral hypothalamic differentiation.

7 July 2018

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A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons.

7 July 2018

1 reference

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The other trinucleotide repeat: polyalanine expansion disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591313

Over- and underdosage of SOX3 is associated with infundibular hypoplasia and hypopituitarism

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591313

A polyalanine tract expansion in Arx forms intranuclear inclusions and results in increased cell death

7 July 2018

1 reference

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SOX3 is required during the formation of the hypothalamo-pituitary axis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591313

FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation

7 July 2018

1 reference

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Conversion of embryonic stem cells into neuroectodermal precursors in adherent monoculture

7 July 2018

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Transcription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiency

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3591313

Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA

7 July 2018

1 reference

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Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

7 July 2018

1 reference

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Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model

7 July 2018

1 reference

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Polyalanine expansion mutations in the X-linked hypopituitarism gene SOX3 result in aggresome formation and impaired transactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003290

A molecular pathogenesis for transcription factor associated poly-alanine tract expansions

21 January 2018

1 reference

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Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.

21 January 2018

1 reference

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Increased transactivation associated with SOX3 polyalanine tract deletion in a patient with hypopituitarism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003290

10.1371/JOURNAL.PGEN.1003290

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json

26 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23505376%20AND%20SRC:MED&resulttype=core&format=json