IPEX as a result of mutations in FOXP3 (Q21342967)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

review article

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title

IPEX as a result of mutations in FOXP3 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

9 references

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12 October 2019

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autoimmune polyendocrine syndrome

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hemic and immune systems

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18 October 2019

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11 December 2019

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22 December 2019

1

Hans J J van der Vliet

author given names

Hans J J

author last names

van der Vliet

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Edward E Nieuwenhuis

2

Edward E

Nieuwenhuis

1 reference

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3 January 2020

language of work or name

English

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publication date

1 January 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

Clinical and Developmental Immunology

3 January 2020

published in

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22 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

volume

2007

1 reference

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3 January 2020

page(s)

89017

1 reference

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Creative Commons Attribution 3.0 Unported

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copyright license

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on focus list of Wikimedia project

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copyright status

copyrighted

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ScienceSource

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cites work

Analysis of FOXP3 reveals multiple domains required for its function as a transcriptional repressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

FOXP3 controls regulatory T cell function through cooperation with NFAT

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse

19 March 2017

1 reference

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Specific recruitment of regulatory T cells in ovarian carcinoma fosters immune privilege and predicts reduced survival

19 March 2017

1 reference

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Naturally arising Foxp3-expressing CD25+CD4+ regulatory T cells in immunological tolerance to self and non-self

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

FOXP3 modifies the phenotypic and functional properties of regulatory T cells

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Regulatory T cells in human autoimmune diseases

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Defective regulatory and effector T cell functions in patients with FOXP3 mutations.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

12 September 2017

FOXP3: of mice and men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Clinical and molecular findings in IPEX syndrome

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Enhancement of vaccine-mediated antitumor immunity in cancer patients after depletion of regulatory T cells

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Regulation of immunity by self-reactive T cells

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

IPEX and the role of Foxp3 in the development and function of human Tregs

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2248278

An X-linked syndrome of diarrhea, polyendocrinopathy, and fatal infection in infancy.

30 May 2018

1 reference

https://api.crossref.org/works/10.1155%2F2007%2F89017

A potential screening tool for IPEX syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2007%2F89017

Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2007%2F89017

Successful bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2007%2F89017

Treatment of the Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (IPEX) by Allogeneic Bone Marrow Transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1155%2F2007%2F89017

A long-term survivor with the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

21 January 2018

1 reference

12 December 2020

A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome

1 reference

12 December 2020

A Japanese family of X-linked auto-immune enteropathy with haemolytic anaemia and polyendocrinopathy

1 reference

12 December 2020

Combination therapy with tacrolimus and betamethasone for a patient with X-linked auto-immune enteropathy

1 reference

12 December 2020

Identifiers

DOI

10.1155/2007/89017

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18317533%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

2 references