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Search results 201 to 237 out of 237 for Irak4

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0.019s
Type Details Score
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
UniProt Feature
Begin: 209
Description: Phosphothreonine; by IRAK4
Type: modified residue
End: 209
Allele  
Name: interleukin-1 receptor-associated kinase 4; targeted mutation 1, Hermann Gram
Allele Type: Targeted
Allele
Name: interleukin-1 receptor-associated kinase 4; targeted mutation 1, Xiaoxia Li
Allele Type: Targeted
Attribute String: Not Specified
Publication
First Author: Giménez N
Year: 2020
Journal: Leukemia
Title: Targeting IRAK4 disrupts inflammatory pathways and delays tumor development in chronic lymphocytic leukemia.
Volume: 34
Issue: 1
Pages: 100-114
Publication  
First Author: Wu X
Year: 2022
Journal: Pharmacol Res
Title: Pharmacological inhibition of IRAK1 and IRAK4 prevents endothelial inflammation and atherosclerosis in ApoE(-/-) mice.
Volume: 175
Pages: 106043
Publication
First Author: Cushing L
Year: 2017
Journal: J Biol Chem
Title: IRAK4 kinase activity controls Toll-like receptor-induced inflammation through the transcription factor IRF5 in primary human monocytes.
Volume: 292
Issue: 45
Pages: 18689-18698
Publication
First Author: Smith MA
Year: 2019
Journal: Nat Cell Biol
Title: U2AF1 mutations induce oncogenic IRAK4 isoforms and activate innate immune pathways in myeloid malignancies.
Volume: 21
Issue: 5
Pages: 640-650
Publication  
First Author: Bourn JR
Year: 2021
Journal: Cancer Lett
Title: Tumor cell intrinsic RON signaling suppresses innate immune responses in breast cancer through inhibition of IRAK4 signaling.
Volume: 503
Pages: 75-90
Publication  
First Author: Celhar T
Year: 2019
Journal: Front Immunol
Title: TLR7 Protein Expression in Mild and Severe Lupus-Prone Models Is Regulated in a Leukocyte, Genetic, and IRAK4 Dependent Manner.
Volume: 10
Pages: 1546
Allele
Name: C-C motif chemokine ligand 24; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Publication
First Author: Hoarau C
Year: 2007
Journal: J Immunol
Title: TLR9 activation induces normal neutrophil responses in a child with IRAK-4 deficiency: involvement of the direct PI3K pathway.
Volume: 179
Issue: 7
Pages: 4754-65
Protein Domain
Type: Domain
Description: IRAK4 is a serine/threonine-protein kinase that plays a critical role in initiating innate immune response against foreign pathogens []. It is required for the efficient recruitment of IRAK1 to the interleukin-1 (IL-1) receptor complex following IL-1 engagement, triggering intracellular signalling cascades leading to transcriptional up-regulation and mRNA stabilisation [, ]. IRAK4 phosphorylates IRAK1. Pellino-2 may be a substrate for both IRAK1 and IRAK4 [].This entry represents the Death domain of IRAK4.DDs (Death domains) are protein-protein interaction domains found in a variety of domain architectures. Their common feature is that they form homodimers by self-association or heterodimers by associating with other members of the DD superfamily including CARD (Caspase activation and recruitment domain), DED (Death Effector Domain), and PYRIN. They serve as adaptors in signaling pathways and can recruit other proteins into signaling complexes [, ].
Protein
Organism: Mus musculus/domesticus
Length: 197  
Fragment?: false
Publication
First Author: Ohba T
Year: 2012
Journal: FEBS J
Title: Identification of interleukin-1 receptor-associated kinase 1 as a critical component that induces post-transcriptional activation of IκB-ζ.
Volume: 279
Issue: 2
Pages: 211-22
Publication
First Author: Honda K
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: Role of a transductional-transcriptional processor complex involving MyD88 and IRF-7 in Toll-like receptor signaling.
Volume: 101
Issue: 43
Pages: 15416-21
HT Experiment  
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: ArrayExpress
Publication
First Author: Mirza MK
Year: 2010
Journal: Am J Pathol
Title: Caveolin-1 deficiency dampens Toll-like receptor 4 signaling through eNOS activation.
Volume: 176
Issue: 5
Pages: 2344-51
Publication  
First Author: Kato T
Year: 2019
Journal: Front Immunol
Title: Interleukin-1/-33 Signaling Pathways as Therapeutic Targets for Endometriosis.
Volume: 10
Pages: 2021
Publication
First Author: Li J
Year: 2018
Journal: J Immunol
Title: Small Molecule Mimetics of α-Helical Domain of IRAK2 Attenuate the Proinflammatory Effects of IL-33 in Asthma-like Mouse Models.
Volume: 200
Issue: 12
Pages: 4036-4043
Publication
First Author: Heinz LX
Year: 2012
Journal: Cell Death Differ
Title: The death domain-containing protein Unc5CL is a novel MyD88-independent activator of the pro-inflammatory IRAK signaling cascade.
Volume: 19
Issue: 4
Pages: 722-31
Publication
First Author: Li Z
Year: 2015
Journal: J Clin Invest
Title: Inhibition of IRAK1/4 sensitizes T cell acute lymphoblastic leukemia to chemotherapies.
Volume: 125
Issue: 3
Pages: 1081-97
Publication
First Author: Srivastav S
Year: 2015
Journal: Eur J Immunol
Title: IRAK-M regulates the inhibition of TLR-mediated macrophage immune response during late in vitro Leishmania donovani infection.
Volume: 45
Issue: 10
Pages: 2787-97
Publication
First Author: Zhang D
Year: 2018
Journal: Cancer Res
Title: Tumor-Stroma IL1β-IRAK4 Feedforward Circuitry Drives Tumor Fibrosis, Chemoresistance, and Poor Prognosis in Pancreatic Cancer.
Volume: 78
Issue: 7
Pages: 1700-1712
Publication  
First Author: Nanda SK
Year: 2019
Journal: Life Sci Alliance
Title: Distinct signals and immune cells drive liver pathology and glomerulonephritis in ABIN1[D485N] mice.
Volume: 2
Issue: 6
Publication
First Author: McCrory EH
Year: 2022
Journal: Biochem J
Title: Identification of ester-linked ubiquitylation sites during TLR7 signalling increases the number of inter-ubiquitin linkages from 8 to 12.
Volume: 479
Issue: 23
Pages: 2419-2431
Publication
First Author: Banerjee M
Year: 2020
Journal: Arterioscler Thromb Vasc Biol
Title: Platelets Endocytose Viral Particles and Are Activated via TLR (Toll-Like Receptor) Signaling.
Volume: 40
Issue: 7
Pages: 1635-1650
Publication
First Author: Emmerich CH
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Activation of the canonical IKK complex by K63/M1-linked hybrid ubiquitin chains.
Volume: 110
Issue: 38
Pages: 15247-52
Publication
First Author: Kissner TL
Year: 2011
Journal: PLoS One
Title: Activation of MyD88 signaling upon staphylococcal enterotoxin binding to MHC class II molecules.
Volume: 6
Issue: 1
Pages: e15985
Publication
First Author: Feinstein E
Year: 1995
Journal: Trends Biochem Sci
Title: The death domain: a module shared by proteins with diverse cellular functions.
Volume: 20
Issue: 9
Pages: 342-4
Publication  
First Author: Park HH
Year: 2007
Journal: Annu Rev Immunol
Title: The death domain superfamily in intracellular signaling of apoptosis and inflammation.
Volume: 25
Pages: 561-86
Publication      
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China