Evidence map›Paper›PMID 27799162›Full record

ArticleBlood2016

Protein stabilization improves STAT3 function in autosomal dominant hyper-IgE syndrome.

Claire E Bocchini, Karen Nahmod, Panagiotis Katsonis, Sang Kim, Moses M Kasembeli, Alexandra Freeman, Olivier Lichtarge, George Makedonas, David J Tweardy

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 33 citations in OpenAlex.

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  17. A deep intronic splice mutation ofProceedings of the National Academy of Sciences of the United States of America · 2019
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Claire E BocchiniDepartment of Pediatrics and.
Karen NahmodDepartment of Pediatrics and.
Panagiotis KatsonisDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
Sang KimDivision of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX; and.
Moses M KasembeliDivision of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX; and.
Alexandra FreemanNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Olivier LichtargeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX.
George MakedonasDepartment of Pediatrics and.
David J TweardyDivision of Internal Medicine, University of Texas MD Anderson Cancer Center, Houston, TX; and.ORCID 0000-0001-8492-8460
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · USNational Institutes of Health · US

Funding

Functional Determinnats in G Protein-coupled ReceptorsR01GM066099 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2003 to 2022
$7.5M
Comparative genomics of protein structure and functionR01GM079656 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI LICHTARGE, OLIVIER · 2007 to 2019
$4.3M
Baylor CHRC: Pediatrics Mentored Research ProgramK12HD041648 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI KLINE, MARK · 2002 to 2011
$4.2M
Center for Protein Folding Machinery (RMI)PN1EY016525 · NEI · BAYLOR COLLEGE OF MEDICINE · PI CHIU, WAH · 2004 to 2004
$67k
NEI NIH HHS PN1 EY016525NICHD NIH HHS K12 HD041648NIGMS NIH HHS R01 GM066099NIGMS NIH HHS R01 GM079656
6 · The paper itself

Abstract

Autosomal dominant hyper-IgE syndrome (AD-HIES) is caused by dominant-negative mutations in STAT3; however, the molecular basis for mutant STAT3 allele dysfunction is unclear and treatment remains supportive. We hypothesized that AD-HIES mutations decrease STAT3 protein stability and that mutant STAT3 activity can be improved by agents that increase chaperone protein activity. We used computer modeling to characterize the effect of STAT3 mutations on protein stability. We measured STAT3 protein half-life (t

Indexed as

AnimalsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCytokinesDiterpenesDNA-Binding ProteinsHalf-LifeHeat Shock Transcription FactorsHerpesvirus 4, HumanHumansInterleukin-17Job SyndromeMiceModels, MolecularMutant ProteinsMutationCytokinesDiterpenesDNA-Binding ProteinsgeranylgeranylacetoneHeat Shock Transcription FactorsInterleukin-17Mutant ProteinsPhosphotyrosineSTAT3 Transcription FactorTranscription Factors

Identifiers

PMID27799162
PMCPMC5201093
OpenAlexW2542557406

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.