(Q82605242)

English

Destructive pulmonary staphylococcal infection in a boy with hyper-IgE syndrome: a novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene (p.Y657S)

scientific article published on 24 November 2010

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Destructive pulmonary staphylococcal infection in a boy with hyper-IgE syndrome: a novel mutation in the signal transducer and activator of transcription 3 (STAT3) gene (p.Y657S) (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

hyper-IgE syndrome

1 reference

based on heuristic

inferred from title

staphylococcal infection

1 reference

based on heuristic

inferred from title

author name string

Jin-yan Liu

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Qiang Li

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Ting-ting Chen

3

1 reference

Europe PubMed Central

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17 January 2020

Xia Guo

4

1 reference

Europe PubMed Central

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17 January 2020

Jiao Ge

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Li-xing Yuan

6

1 reference

Europe PubMed Central

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17 January 2020

publication date

24 November 2010

1 reference

Europe PubMed Central

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17 January 2020

European Journal of Pediatrics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21107604%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

170

1 reference

Europe PubMed Central

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17 January 2020

5

1 reference

Europe PubMed Central

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17 January 2020

661-666

1 reference

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17 January 2020

https://scigraph.springernature.com/pub.10.1007/s00431-010-1349-6

0 references

Insights into the role of STAT3 in human lymphocyte differentiation as revealed by the hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human beta-defensin 3 inhibits cell wall biosynthesis in Staphylococci

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Job's Syndrome. Recurrent, "cold", staphylococcal abscesses

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperimmunoglobulin E syndrome and tyrosine kinase 2 deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic granulomatous disease. Report on a national registry of 368 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extreme hyperimmunoglobulinemia E and undue susceptibility to infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

STAT3 mutations in the hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chemical probes that competitively and selectively inhibit Stat3 activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple liver abscesses in a patient with the hyper IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of hyper-IgE syndrome to chromosome 4.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined immunodeficiency associated with DOCK8 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral chloramphenicol therapy for multiple liver abscesses in hyperimmunoglobulinemia E syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular explanation for the contradiction between systemic Th17 defect and localized bacterial infection in hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21107604

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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