(Q46321148)

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Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation

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Europe PubMed Central

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21 December 2017

http://europepmc.org/abstract/MED/24916357

Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation (English)

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Europe PubMed Central

PubMed publication ID

21 December 2017

http://europepmc.org/abstract/MED/24916357

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7 June 2020

1

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7 June 2020

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7 June 2020

Myriam Ricarda Lorenz

8

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Myriam Lorenz

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7 June 2020

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Ilka Schulze

2

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7 June 2020

Elif Karakoç Aydıner

4

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7 June 2020

Emel Altuncu

5

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7 June 2020

Gulsun Tezcan Karasu

6

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7 June 2020

Nilufer Ozturk

7

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7 June 2020

Klaus Schwarz

9

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7 June 2020

Thomas Vraetz

10

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7 June 2020

Isil B Barlan

12

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7 June 2020

publication date

12 June 2014

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21 December 2017

http://europepmc.org/abstract/MED/24916357

Journal of Clinical Immunology

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7 June 2020

34

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7 June 2020

6

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7 June 2020

601-606

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7 June 2020

https://scigraph.springernature.com/pub.10.1007/s10875-014-0059-7

0 references

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Immune dysregulation, polyendocrinopathy, enteropathy, x-linked syndrome: a paradigm of immunodeficiency with autoimmunity

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Clinical and molecular characteristics of immunodysregulation, polyendocrinopathy, enteropathy, X-linked syndrome in China.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

The immunogenetics of immune dysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

An update on pulmonary complications of hematopoietic stem cell transplantation

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Large functional repertoire of regulatory T-cell suppressible autoimmune T cells in scurfy mice

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

FOXP3 is a homo-oligomer and a component of a supramolecular regulatory complex disabled in the human XLAAD/IPEX autoimmune disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

Genome-wide analysis of Foxp3 target genes in developing and mature regulatory T cells.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

FOXP3 orchestrates H4K16 acetylation and H3K4 trimethylation for activation of multiple genes by recruiting MOF and causing displacement of PLU-1.

1 reference

https://api.crossref.org/works/10.1007%2FS10875-014-0059-7

21 January 2018

FOXP3 forkhead domain mutation and regulatory T cells in the IPEX syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24916357

12 December 2020

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10.1007/S10875-014-0059-7

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24916357%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

release_fvw7x3k7yvhlrck7o7v7afirgu

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24 November 2022

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24916357%20AND%20SRC:MED&resulttype=core&format=json

7 June 2020

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