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Interleukin (IL)-22, a Novel Human Cytokine That Signals through the Interferon Receptor-related Proteins CRF2–4 and IL-22R
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Outgoing claims: the papers this work cites, builds on, or argues with.
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The family of the IL-6-Type cytokines: Specificity and promiscuity of the receptor complexes
inferredcites →https://doi.org/10.1002/jlb.61.4.389openalex-snapshot
Studies with IL-10-/- mice: an overview
inferredcites →https://doi.org/10.1006/cyto.1999.0485openalex-snapshot
FGF-19, A NOVEL FIBROBLAST GROWTH FACTOR WITH UNIQUE SPECIFICITY FOR FGFR4
inferredcites →https://doi.org/10.1006/geno.1993.1199openalex-snapshot
A New Member of the Cytokine Receptor Gene Family Maps on Chromosome 21 at Less Than 35 kb from IFNAR
inferredcites →https://doi.org/10.1016/0014-5793(96)00990-8openalex-snapshot
IL‐10 induces DNA binding activity of three STAT proteins (Stat1, Stat3, and Stat5) and their distinct combinatorial assembly in the promoters of selected genes
inferredcites →https://doi.org/10.1016/0092-8674(93)80068-popenalex-snapshot
Interleukin-10-deficient mice develop chronic enterocolitis
inferredcites →https://doi.org/10.1016/1359-6101(96)00007-xopenalex-snapshot
Cardiotrophin-1: a multifunctional cytokine that signals via LIF receptor gp130 dependent pathways
inferredcites →https://doi.org/10.1016/s0378-1119(96)00690-7openalex-snapshot
CRF2-4: isolation of cDNA clones encoding the human and mouse proteins
inferredcites →https://doi.org/10.1016/s0898-6568(98)00023-0openalex-snapshot
Regulation of Proliferation, Differentiation and Survival by the IL-3/IL-5/GM-CSF Receptor Family
inferredcites →https://doi.org/10.1016/s0962-8924(99)01709-2openalex-snapshot
Association of STATs with relatives and friends
inferredcites →https://doi.org/10.1042/bj3340297openalex-snapshot
Interleukin-6-type cytokine signalling through the gp130/Jak/STAT pathway
inferredcites →https://doi.org/10.1073/pnas.92.12.5292openalex-snapshot
Distinct regions of c-Mpl cytoplasmic domain are coupled to the JAK-STAT signal transduction pathway and Shc phosphorylation.
inferredcites →https://doi.org/10.1084/jem.187.4.571openalex-snapshot
The Orphan Receptor CRF2-4 Is an Essential Subunit of the Interleukin 10 Receptor
inferredcites →https://doi.org/10.1093/emboj/16.19.5894openalex-snapshot
Identification and functional characterization of a second chain of the interleukin‐10 receptor complex
inferredcites →https://doi.org/10.1615/critrevimmunol.v18.i6.20openalex-snapshot
The Structure and Function of γс-Dependent Cytokines and Receptors: Regulation of T Lymphocyte Development and Homeostasis
inferredcites →https://doi.org/10.4049/jimmunol.155.3.1079openalex-snapshot
IL-10 induces the tyrosine phosphorylation of tyk2 and Jak1 and the differential assembly of STAT1 α and STAT3 complexes in human T cells and monocytes
inferredcites →https://doi.org/10.4049/jimmunol.164.4.1814openalex-snapshot
Cloning and Characterization of IL-10-Related T Cell-Derived Inducible Factor (IL-TIF), a Novel Cytokine Structurally Related to IL-10 and Inducible by IL-9
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/art.20965openalex-snapshot
Expression of interleukin‐22 in rheumatoid arthritis: Potential role as a proinflammatory cytokine
inferred← citeshttps://doi.org/10.1002/art.22866openalex-snapshot
Distinct regulation of interleukin‐17 in human T helper lymphocytes
inferred← citeshttps://doi.org/10.1002/art.33446openalex-snapshot
Interleukin‐22 promotes osteoclastogenesis in rheumatoid arthritis through induction of RANKL in human synovial fibroblasts
inferred← citeshttps://doi.org/10.1002/bit.27375openalex-snapshot
Off‐target glycans encountered along the synthetic biology route toward humanized N ‐glycans in Pichia pastoris
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Intestinal tumor suppression in ApcMin/+ mice by prostaglandin D2 receptor PTGDR
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The role of IL ‐22 in the resolution of sterile and nonsterile inflammation
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Regulation of T cells and cytokines by the interleukin‐10 (IL‐10)‐family cytokines IL‐19, IL‐20, IL‐22, IL‐24 andIL‐26
inferred← citeshttps://doi.org/10.1002/eji.200535503openalex-snapshot
IL‐22 regulates the expression of genes responsible for antimicrobial defense, cellular differentiation, and mobility in keratinocytes: a potential role in psoriasis
inferred← citeshttps://doi.org/10.1002/eji.200837718openalex-snapshot
Differential signaling of cmvIL‐10 through common variants of the IL‐10 receptor 1
inferred← citeshttps://doi.org/10.1002/eji.200838655openalex-snapshot
IL‐22 and inflammation: Leukin' through a glass onion
inferred← citeshttps://doi.org/10.1002/eji.200939687openalex-snapshot
The Th17 cytokine IL‐22 induces IL‐20 production in keratinocytes: A novel immunological cascade with potential relevance in psoriasis
inferred← citeshttps://doi.org/10.1002/hep.20184openalex-snapshot
Interleukin 22 (IL-22) plays a protective role in T cell-mediated murine hepatitis: IL-22 is a survival factor for hepatocytes via STAT3 activation
inferred← citeshttps://doi.org/10.1002/hep.24486openalex-snapshot
Interleukin-22 promotes human hepatocellular carcinoma by activation of STAT3
inferred← citeshttps://doi.org/10.1002/ibd.20315openalex-snapshot
Linking genetic susceptibility to Crohnʼs disease with Th17 cell function: IL-22 serum levels are increased in Crohnʼs disease and correlate with disease activity and IL23R genotype status
inferred← citeshttps://doi.org/10.1002/ibd.21473openalex-snapshot
DMBT1 is a novel gene induced by IL-22 in ulcerative colitis
inferred← citeshttps://doi.org/10.1002/ijc.29305openalex-snapshot
Metformin decreases IL ‐22 secretion to suppress tumor growth in an orthotopic mouse model of hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1002/iub.2295openalex-snapshot
Interleukin‐22 and intestinal homeostasis: Protective or destructive?
inferred← citeshttps://doi.org/10.1002/prp2.434openalex-snapshot
Nonclinical safety assessment of a human interleukin‐22 FC IG fusion protein demonstrates in vitro to in vivo and cross‐species translatability
inferred← citeshttps://doi.org/10.1006/cyto.2001.0905openalex-snapshot
SO MANY LIGANDS, SO FEW TRANSCRIPTION FACTORS: A NEW PARADIGM FOR SIGNALING THROUGH THE STAT TRANSCRIPTION FACTORS
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Type I-interferon signalling in fish
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The mucosal inflammatory response. Cytokines and chemokines
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The mucosal inflammatory response. Cytokines and chemokines
inferred← citeshttps://doi.org/10.1007/978-1-4419-0170-5_4openalex-snapshot
IL-24 in Regulation of Antitumor Immune Response and in Signaling
inferred← citeshttps://doi.org/10.1007/978-1-4419-0170-5_5openalex-snapshot
IL-28 and IL-29 in Regulation of Antitumor Immune Response and Induction of Tumor Regression
inferred← citeshttps://doi.org/10.1007/978-1-4419-6102-0_11openalex-snapshot
Interleukin-24 Gene Therapy for Melanoma
inferred← citeshttps://doi.org/10.1007/978-1-4419-9371-7_24openalex-snapshot
The Roles of IL-22 and Its Related Family Members in the Pathogenesis of Psoriasis
inferred← citeshttps://doi.org/10.1007/978-3-031-21358-8_12openalex-snapshot
Influence of the Gut Microbiota on Neuroendocrine-Immune Interactions
inferred← citeshttps://doi.org/10.1007/978-3-0348-0522-3_2openalex-snapshot
IL-22 and IL-17: An Overview
inferred← citeshttps://doi.org/10.1007/978-3-0348-0522-3_21openalex-snapshot
Role of IL-23, IL-17, and IL-22 in Psoriasis
inferred← citeshttps://doi.org/10.1007/978-3-0348-0522-3_22openalex-snapshot
Contribution of IL-22 to Experimental Skin Inflammation
inferred← citeshttps://doi.org/10.1007/978-3-0348-0522-3_4openalex-snapshot
Contributions of IL-22 to TH17 Responses: Repairing and Protecting Peripheral Tissues
inferred← citeshttps://doi.org/10.1007/978-3-319-29785-9_15openalex-snapshot
Cytokines and Chemokines
inferred← citeshttps://doi.org/10.1007/978-3-642-39432-4_9openalex-snapshot
9 Mucosal Immunology in Candida albicans Infection
inferred← citeshttps://doi.org/10.1007/978-3-662-43492-5_10openalex-snapshot
Role of IL-22 in Microbial Host Defense
inferred← citeshttps://doi.org/10.1007/978-3-662-43492-5_9openalex-snapshot
The Molecular Basis of IL-10 Function: from Receptor Structure to the Onset of Signaling
inferred← citeshttps://doi.org/10.1007/978-3-7643-8681-8_2openalex-snapshot
IL-22 and IL-17: Common and different properties
inferred← citeshttps://doi.org/10.1007/978-3-7643-8681-8_4openalex-snapshot
Contributions of IL-22 to Th17 responses: Repairing and protecting peripheral tissues
inferred← citeshttps://doi.org/10.1007/978-4-431-54442-5_6openalex-snapshot
Interleukin-22: A Bridge Between Epithelial Innate Host Defense and Immune Cells
inferred← citeshttps://doi.org/10.1007/978-90-481-2289-9_4openalex-snapshot
Recombinant proteins and genomics in cancer therapy
inferred← citeshttps://doi.org/10.1007/978-94-017-2757-0_4openalex-snapshot
Recombinant proteins and genomics in cancer therapy
inferred← citeshttps://doi.org/10.1007/978-94-017-3000-6_10openalex-snapshot
IFNS and STATs, an Incestuous Relationship
inferred← citeshttps://doi.org/10.1007/978-94-017-9487-9_8openalex-snapshot
The Biology and Functions of Th22 Cells
inferred← citeshttps://doi.org/10.1007/978-981-10-2425-2_14openalex-snapshot
Novel Inflammatory and Immunomodulatory Mediators in Sepsis
inferred← citeshttps://doi.org/10.1007/s00005-015-0362-xopenalex-snapshot
Targeting Th17 Effector Cytokines for the Treatment of Autoimmune Diseases
inferred← citeshttps://doi.org/10.1007/s00018-010-0380-0openalex-snapshot
Structure and function of interleukin-22 and other members of the interleukin-10 family
inferred← citeshttps://doi.org/10.1007/s00018-016-2289-8openalex-snapshot
Cytokine responses and epithelial function in the intestinal mucosa
inferred← citeshttps://doi.org/10.1007/s00103-002-0563-4openalex-snapshot
Zytokine in der Dermatologie
inferred← citeshttps://doi.org/10.1007/s00109-009-0457-0openalex-snapshot
IL-22 and IL-20 are key mediators of the epidermal alterations in psoriasis while IL-17 and IFN-γ are not
inferred← citeshttps://doi.org/10.1007/s00109-016-1391-6openalex-snapshot
Biological and pathological activities of interleukin-22
inferred← citeshttps://doi.org/10.1007/s00251-008-0326-yopenalex-snapshot
Comparative study and expression analysis of the interferon gamma gene locus cytokines in Xenopus tropicalis
inferred← citeshttps://doi.org/10.1007/s00262-012-1241-5openalex-snapshot
Increased intratumoral IL-22-producing CD4+ T cells and Th22 cells correlate with gastric cancer progression and predict poor patient survival
inferred← citeshttps://doi.org/10.1007/s00281-021-00854-zopenalex-snapshot
The good and the bad about separation anxiety: roles of IL-22 and IL-22BP in liver pathologies
inferred← citeshttps://doi.org/10.1007/s00281-022-00917-9openalex-snapshot
Th17 cells in the liver: balancing autoimmunity and pathogen defense
inferred← citeshttps://doi.org/10.1007/s00535-017-1401-7openalex-snapshot
Clinical importance of IL-22 cascade in IBD
inferred← citeshttps://doi.org/10.1007/s00592-022-02024-5openalex-snapshot
Relationship between IL-22 and IL-22BP in diabetic cognitive dysfunction
inferred← citeshttps://doi.org/10.1007/s00894-004-0195-8openalex-snapshot
Molecular modeling of the interleukin-19 receptor complex
inferred← citeshttps://doi.org/10.1007/s10875-010-9368-7openalex-snapshot
Th17 Cytokines and the Gut Mucosal Barrier
inferred← citeshttps://doi.org/10.1007/s10875-011-9540-8openalex-snapshot
Elevated Th22 Cells Correlated with Th17 Cells in Patients with Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1007/s10875-022-01376-5openalex-snapshot
Fulminant Viral Hepatitis in Two Siblings with Inherited IL-10RB Deficiency
inferred← citeshttps://doi.org/10.1007/s10928-023-09888-2openalex-snapshot
Population pharmacokinetics and pharmacodynamics of efmarodocokin alfa (IL-22Fc)
inferred← citeshttps://doi.org/10.1007/s10989-024-10636-4openalex-snapshot
Utilization of Antiviral Peptides in Treating Coronavirus Infection: An Overview
inferred← citeshttps://doi.org/10.1007/s11010-011-0772-yopenalex-snapshot
Th22 in inflammatory and autoimmune disease: prospects for therapeutic intervention
inferred← citeshttps://doi.org/10.1007/s11010-012-1430-8openalex-snapshot
Interleukin-22 protects rat PC12 pheochromocytoma cells from serum deprivation-induced cell death
inferred← citeshttps://doi.org/10.1007/s11010-024-05179-7openalex-snapshot
Interleukin-22 promotes endometrial carcinoma cell proliferation and cycle progression via ERK1/2 and p38 activation
inferred← citeshttps://doi.org/10.1007/s12016-014-8465-4openalex-snapshot
Cytokine-Mediated Immunopathogenesis of Hepatitis B Virus Infections
inferred← citeshttps://doi.org/10.1007/s12026-007-8014-9openalex-snapshot
Th17 cells: a new fate for differentiating helper T cells
inferred← citeshttps://doi.org/10.1007/s12026-020-09149-1openalex-snapshot
The role of Th17 cells in psoriasis
inferred← citeshttps://doi.org/10.1007/s12026-022-09325-5openalex-snapshot
Role of IL-22 in intestinal microenvironment and potential targeted therapy through diet
inferred← citeshttps://doi.org/10.1007/s12032-024-02481-8openalex-snapshot
The role of IL-22 in cancer
inferred← citeshttps://doi.org/10.1007/s12072-012-9361-8openalex-snapshot
Relevance of interleukin-10RB to chronic hepatitis B virus infection and biological activities of interferon-λ and interleukin-22
inferred← citeshttps://doi.org/10.1016/b978-0-12-381290-2.00003-3openalex-snapshot
Progress in the Development of Small Molecule Therapeutics Targeting Th17 Cell Function for the Treatment of Immune-Inflammatory Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-381300-8.00001-0openalex-snapshot
Functional Biology of the IL-22-IL-22R Pathway in Regulating Immunity and Inflammation at Barrier Surfaces
inferred← citeshttps://doi.org/10.1016/b978-0-12-801121-8.00002-6openalex-snapshot
Interleukin-1 Superfamily and Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-801121-8.00006-3openalex-snapshot
Interleukin-10 Superfamily and Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-823318-4.00024-xopenalex-snapshot
T cells in kidney injury and regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-443-40483-2.00040-6openalex-snapshot
Role of the gut microbiome in the development of colorectal cancer
inferred← citeshttps://doi.org/10.1016/b978-012689663-3/50030-2openalex-snapshot
The IL-10 family [Interleukin-19,-20,-22,-24 and-26]
inferred← citeshttps://doi.org/10.1016/bs.acr.2015.04.014openalex-snapshot
Tumor-Elicited Inflammation and Colorectal Cancer
inferred← citeshttps://doi.org/10.1016/j.achaem.2014.04.017openalex-snapshot
The role of Th17 cells in tumor immunity
inferred← citeshttps://doi.org/10.1016/j.ajpath.2012.08.043openalex-snapshot
Protective and Pathological Properties of IL-22 in Liver Disease
inferred← citeshttps://doi.org/10.1016/j.ajpath.2015.08.015openalex-snapshot
Differential Requirements for IL-17A and IL-22 in Cecal versus Colonic Inflammation Induced by Helicobacter hepaticus
inferred← citeshttps://doi.org/10.1016/j.antiviral.2017.03.006openalex-snapshot
IL-22 suppresses the infection of porcine enteric coronaviruses and rotavirus by activating STAT3 signal pathway
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2012.08.006openalex-snapshot
Expression of IL-22, IL-22R and IL-23 in the peri-implant soft tissues of patients with peri-implantitis
inferred← citeshttps://doi.org/10.1016/j.autrev.2017.10.004openalex-snapshot
Interleukin-22 in human inflammatory diseases and viral infections
inferred← citeshttps://doi.org/10.1016/j.bbadis.2021.166171openalex-snapshot
IL-22 ameliorated cardiomyocyte apoptosis in cardiac ischemia/reperfusion injury by blocking mitochondrial membrane potential decrease, inhibiting ROS and cytochrome C
inferred← citeshttps://doi.org/10.1016/j.bbagen.2011.02.002openalex-snapshot
TH17 cells in asthma and inflammation
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.11.182openalex-snapshot
Interactions among the components of the interleukin-10 receptor complex
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.06.032openalex-snapshot
N-3 polyunsaturated fatty acid-enriched lipid emulsion improves Paneth cell function via the IL-22/Stat3 pathway in a mouse model of total parenteral nutrition
inferred← citeshttps://doi.org/10.1016/j.bbrc.2017.10.045openalex-snapshot
Interleukin-22 attenuates double-stranded RNA-induced upregulation of PD-L1 in airway epithelial cells via a STAT3-dependent mechanism
inferred← citeshttps://doi.org/10.1016/j.biochi.2017.05.002openalex-snapshot
Characterization of linear mimetic peptides of Interleukin-22 from dissection of protein interfaces
inferred← citeshttps://doi.org/10.1016/j.bionps.2022.100055openalex-snapshot
Innate lymphoid cells in depression: Current status and perspectives
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2024.108467openalex-snapshot
Implications of glycosylation for the development of selected cytokines and their derivatives for medical use
inferred← citeshttps://doi.org/10.1016/j.cellsig.2019.109388openalex-snapshot
IL-18/IL-18BP and IL-22/IL-22BP: Two interrelated couples with therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.108777openalex-snapshot
Optic nerve regeneration screen identifies multiple genes restricting adult neural repair
inferred← citeshttps://doi.org/10.1016/j.coi.2003.09.006openalex-snapshot
Cytokines and autoimmunity: redundancy defines their complex nature
inferred← citeshttps://doi.org/10.1016/j.coph.2009.04.008openalex-snapshot
Anti-inflammatory and pro-inflammatory roles of TGF-β, IL-10, and IL-22 in immunity and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.cyto.2009.07.005openalex-snapshot
Th17 cytokines and host-pathogen interactions at the mucosa: Dichotomies of help and harm
inferred← citeshttps://doi.org/10.1016/j.cyto.2011.03.015openalex-snapshot
Cloning, expression analysis and bioactivity studies of rainbow trout (Oncorhynchus mykiss) interleukin-22
inferred← citeshttps://doi.org/10.1016/j.cyto.2011.07.022openalex-snapshot
Hepatoprotective effects of IL-22 on fulminant hepatic failure induced by d-galactosamine and lipopolysaccharide in mice
inferred← citeshttps://doi.org/10.1016/j.cyto.2012.03.024openalex-snapshot
The promotional effect of IL-22 on mineralization activity of periodontal ligament cells
inferred← citeshttps://doi.org/10.1016/j.cyto.2012.08.005openalex-snapshot
Molecular characterization and immunological roles of avian IL-22 and its soluble receptor IL-22 binding protein
inferred← citeshttps://doi.org/10.1016/j.cyto.2014.09.007openalex-snapshot
IL-22, cell regeneration and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.cyto.2015.02.002openalex-snapshot
The role and modulation of CCR6+ Th17 cell populations in rheumatoid arthritis
inferred← citeshttps://doi.org/10.1016/j.cyto.2016.08.023openalex-snapshot
Role of Interleukin-22 in chronic liver injury
inferred← citeshttps://doi.org/10.1016/j.cyto.2018.01.008openalex-snapshot
Could the inhibition of IL-17 or IL-18 be a potential therapeutic opportunity for gastric cancer?
inferred← citeshttps://doi.org/10.1016/j.cyto.2020.155264openalex-snapshot
Altered serum profile of the interleukin-22 system in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.cyto.2021.155749openalex-snapshot
The role of Th22 cells, from tissue repair to cancer progression
inferred← citeshttps://doi.org/10.1016/j.cyto.2023.156293openalex-snapshot
IL-22 as a target for therapeutic intervention: Current knowledge on its role in various diseases
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2003.10.001openalex-snapshot
The Class II cytokine receptor (CRF2) family: overview and patterns of receptor–ligand interactions
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2006.09.001openalex-snapshot
Interleukin-22: A novel T- and NK-cell derived cytokine that regulates the biology of tissue cells
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.04.002openalex-snapshot
IL-28A, IL-28B, and IL-29: Promising cytokines with type I interferon-like properties
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.08.001openalex-snapshot
IL-20: Biological functions mediated through two types of receptor complexes
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.08.002openalex-snapshot
Interleukin-22: A cytokine produced by T, NK and NKT cell subsets, with importance in the innate immune defense and tissue protection
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.08.003openalex-snapshot
Structural analysis of cytokines comprising the IL-10 family
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.09.002openalex-snapshot
Biology of interleukin-10
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2010.10.007openalex-snapshot
Distinct roles of IL-22 in human psoriasis and inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2012.07.002openalex-snapshot
Emerging role of interleukin-22 in autoimmune diseases
inferred← citeshttps://doi.org/10.1016/j.cytogfr.2014.04.005openalex-snapshot
The role of the IL-22/IL-22R1 axis in cancer
inferred← citeshttps://doi.org/10.1016/j.dci.2014.08.012openalex-snapshot
Molecular characterisation of four class 2 cytokine receptor family members in rainbow trout, Oncorhynchus mykiss
inferred← citeshttps://doi.org/10.1016/j.dci.2022.104525openalex-snapshot
Evolution of developmental and comparative immunology in poultry: The regulators and the regulated
inferred← citeshttps://doi.org/10.1016/j.dci.2023.104916openalex-snapshot
Interleukin-22 induces immune-related gene expression in the gills of Japanese medaka Oryzias latipes
inferred← citeshttps://doi.org/10.1016/j.det.2016.07.003openalex-snapshot
Interleukin-22 and Cyclosporine in Aggressive Cutaneous Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1016/j.febslet.2008.07.046openalex-snapshot
Crystal structure of the IL‐22/IL‐22R1 complex and its implications for the IL‐22 signaling mechanism
inferred← citeshttps://doi.org/10.1016/j.fsi.2022.10.051openalex-snapshot
Interleukin (IL)-22 in common carp (Cyprinus carpio L.): Immune modulation, antibacterial defense, and activation of the JAK-STAT signaling pathway
inferred← citeshttps://doi.org/10.1016/j.gdata.2015.11.014openalex-snapshot
IL-22 regulation of functional gene expression in salivary gland cells
inferred← citeshttps://doi.org/10.1016/j.gene.2009.08.018openalex-snapshot
Expression and regulation of IL-22 by bovine peripheral blood γ/δ T cells
inferred← citeshttps://doi.org/10.1016/j.gene.2014.06.066openalex-snapshot
Molecular cloning, expression and characterization of Pekin duck interferon-λ
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e27578openalex-snapshot
IL-22 promotes liver regeneration after portal vein ligation
inferred← citeshttps://doi.org/10.1016/j.humimm.2012.04.015openalex-snapshot
Elevated profiles of Th22 cells and correlations with Th17 cells in patients with immune thrombocytopenia
inferred← citeshttps://doi.org/10.1016/j.imlet.2019.07.001openalex-snapshot
The connection between the Th17 cell related cytokines and cancer stem cells in cancer: Novel therapeutic targets
inferred← citeshttps://doi.org/10.1016/j.immuni.2004.07.007openalex-snapshot
IL-22 Increases the Innate Immunity of Tissues
inferred← citeshttps://doi.org/10.1016/j.immuni.2007.07.023openalex-snapshot
Interleukin-22 but Not Interleukin-17 Provides Protection to Hepatocytes during Acute Liver Inflammation
inferred← citeshttps://doi.org/10.1016/j.immuni.2008.03.004openalex-snapshot
The Biological Functions of T Helper 17 Cell Effector Cytokines in Inflammation
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.03.020openalex-snapshot
IL-10 Family Cytokines IL-10 and IL-22: from Basic Science to Clinical Translation
inferred← citeshttps://doi.org/10.1016/j.immuni.2021.03.008openalex-snapshot
The tissue protective functions of interleukin-22 can be decoupled from pro-inflammatory actions through structure-based design
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.003openalex-snapshot
Full house: 12 receptors for 27 cytokines
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.005openalex-snapshot
Human interleukin-19 and its receptor: a potential role in the induction of Th2 responses
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.007openalex-snapshot
Expression patterns of IL-10 ligand and receptor gene families provide leads for biological characterization
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.008openalex-snapshot
Interleukin-22 activates STAT3 and induces IL-10 by colon epithelial cells
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.010openalex-snapshot
Temporal associations between interleukin 22 and the extracellular domains of IL-22R and IL-10R2
inferred← citeshttps://doi.org/10.1016/j.intimp.2004.01.016openalex-snapshot
IL-22, a Th1 cytokine that targets the pancreas and select other peripheral tissues
inferred← citeshttps://doi.org/10.1016/j.intimp.2016.08.012openalex-snapshot
IL-22 promoted CD3 + T cell infiltration by IL-22R induced STAT3 phosphorylation in murine acute graft versus host disease target organs after allogeneic bone marrow transplantation
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.106277openalex-snapshot
Effects of IL-22 on cardiovascular diseases
inferred← citeshttps://doi.org/10.1016/j.intimp.2025.114482openalex-snapshot
Brusatol ameliorates intestinal mucosal injury in ulcerative colitis via activating IL-22/STAT3 pathway
inferred← citeshttps://doi.org/10.1016/j.it.2010.06.004openalex-snapshot
IL-17 and IL-22: siblings, not twins
inferred← citeshttps://doi.org/10.1016/j.it.2025.10.009openalex-snapshot
Interleukin-22: the hub bridging gut homeostasis and metabolism
inferred← citeshttps://doi.org/10.1016/j.jaci.2010.11.050openalex-snapshot
Interleukins, from 1 to 37, and interferon-γ: Receptors, functions, and roles in diseases
inferred← citeshttps://doi.org/10.1016/j.jaci.2012.05.003openalex-snapshot
TH17 and TH22 cells: A confusion of antimicrobial response with tissue inflammation versus protection
inferred← citeshttps://doi.org/10.1016/j.jaci.2018.05.032openalex-snapshot
IL-22 promotes allergic airway inflammation in epicutaneously sensitized mice
inferred← citeshttps://doi.org/10.1016/j.jaci.2025.08.033openalex-snapshot
Neutralizing IL-22RA1 improves histologic and molecular alterations associated with atopic dermatitis pathogenesis
inferred← citeshttps://doi.org/10.1016/j.jbc.2021.101463openalex-snapshot
Interleukin-22 regulates B3GNT7 expression to induce fucosylation of glycoproteins in intestinal epithelial cells
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2020.10.017openalex-snapshot
PLANT PRODUCTION AND FUNCTIONAL CHARACTERIZATION OF CATFISH INTERLEUKIN 22 AS A NATURAL IMMUNE STIMULANT FOR AQUACULTURE
inferred← citeshttps://doi.org/10.1016/j.jhep.2010.03.004openalex-snapshot
Amelioration of high fat diet induced liver lipogenesis and hepatic steatosis by interleukin-22
inferred← citeshttps://doi.org/10.1016/j.jid.2021.04.016openalex-snapshot
A Targetable, Noncanonical Signal Transducer and Activator of Transcription 3 Activation Induced by the Y-Less Region of IL-22 Receptor Orchestrates Imiquimod-Induced Psoriasis-Like Dermatitis in Mice
inferred← citeshttps://doi.org/10.1016/j.jim.2013.01.002openalex-snapshot
Quantitative determination of human interleukin 22 (IL-22) in serum using Singulex-Erenna® Technology
inferred← citeshttps://doi.org/10.1016/j.jmb.2004.07.069openalex-snapshot
The IL-10R2 Binding Hot Spot on IL-22 is Located on the N-terminal Helix and is Dependent on N-linked Glycosylation
inferred← citeshttps://doi.org/10.1016/j.jmb.2008.07.046openalex-snapshot
IL-22R, IL-10R2, and IL-22BP Binding Sites Are Topologically Juxtaposed on Adjacent and Overlapping Surfaces of IL-22
inferred← citeshttps://doi.org/10.1016/j.molimm.2014.07.006openalex-snapshot
Molecular cloning, expression analysis and functional characterization of interleukin-22 in So-iny mullet, Liza haematocheila
inferred← citeshttps://doi.org/10.1016/j.molimm.2024.06.010openalex-snapshot
Endogenous IL-22 contributes to the pathogenesis of salivary gland dysfunction in the non-obese diabetic model of Sjögren’s syndrome
inferred← citeshttps://doi.org/10.1016/j.pan.2018.02.014openalex-snapshot
Diverse effects of interleukin-22 on pancreatic diseases
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2004.12.002openalex-snapshot
Evolution of the Class 2 cytokines and receptors, and discovery of new friends and relatives
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2005.11.005openalex-snapshot
mda-7/IL-24: Multifunctional cancer-specific apoptosis-inducing cytokine
inferred← citeshttps://doi.org/10.1016/j.rgmx.2016.02.002openalex-snapshot
Polimorfismos genéticos de interleucina-22 en pacientes con colitis ulcerosa
inferred← citeshttps://doi.org/10.1016/j.rgmxen.2016.02.006openalex-snapshot
Genetic polymorphisms of interleukin-22 in patients with ulcerative colitis
inferred← citeshttps://doi.org/10.1016/j.smim.2007.10.016openalex-snapshot
Targeting the development and effector functions of TH17 cells
inferred← citeshttps://doi.org/10.1016/j.smim.2017.09.006openalex-snapshot
Microbiome, inflammation and colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.str.2008.06.005openalex-snapshot
Structure of IL-22 Bound to Its High-Affinity IL-22R1 Chain
inferred← citeshttps://doi.org/10.1016/j.str.2010.02.009openalex-snapshot
Structure and Mechanism of Receptor Sharing by the IL-10R2 Common Chain
inferred← citeshttps://doi.org/10.1016/j.trsl.2019.10.004openalex-snapshot
Molecular signature of interleukin-22 in colon carcinoma cells and organoid models
inferred← citeshttps://doi.org/10.1016/j.vaccine.2016.02.021openalex-snapshot
Protective role of Th17 cells in pulmonary infection
inferred← citeshttps://doi.org/10.1016/j.virol.2010.02.022openalex-snapshot
Lambda and alpha interferons inhibit hepatitis B virus replication through a common molecular mechanism but with different in vivo activities
inferred← citeshttps://doi.org/10.1016/s0065-2423(03)37005-2openalex-snapshot
Clinical applications of cytokine assays
inferred← citeshttps://doi.org/10.1016/s0065-3233(04)68006-5openalex-snapshot
Structural Analysis of IL-10 and Type I Interferon Family Members and their Complexes with Receptor
inferred← citeshttps://doi.org/10.1016/s0083-6729(06)74003-1openalex-snapshot
Structural Studies of the Interleukin‐19 Subfamily of Cytokines
inferred← citeshttps://doi.org/10.1016/s0083-6729(06)74004-3openalex-snapshot
Interleukin‐22 and Its Crystal Structure
inferred← citeshttps://doi.org/10.1016/s0083-6729(06)74007-9openalex-snapshot
Interleukins and STAT Signaling
inferred← citeshttps://doi.org/10.1016/s0092-8674(02)00701-8openalex-snapshot
Cytokine Signaling in 2002
inferred← citeshttps://doi.org/10.1016/s0165-2427(02)00082-xopenalex-snapshot
New technologies for studying immune regulation in ruminants
inferred← citeshttps://doi.org/10.1016/s0338-9898(00)80226-7openalex-snapshot
Cytokines : Physiologie et implications diagnostiques et thérapeutiques
inferred← citeshttps://doi.org/10.1016/s0378-1119(02)00398-0openalex-snapshot
Signaling through the JAK/STAT pathway, recent advances and future challenges
inferred← citeshttps://doi.org/10.1016/s0960-9822(01)00312-8openalex-snapshot
Cytokines: IL-20 — a new effector in skin inflammation
inferred← citeshttps://doi.org/10.1016/s0969-2126(02)00797-9openalex-snapshot
Crystal Structure of Recombinant Human Interleukin-22
inferred← citeshttps://doi.org/10.1016/s1074-7613(01)00169-8openalex-snapshot
Crystal Structure of the IL-10/IL-10R1 Complex Reveals a Shared Receptor Binding Site
inferred← citeshttps://doi.org/10.1016/s1359-6101(00)00027-7openalex-snapshot
The virus battles: IFN induction of the antiviral state and mechanisms of viral evasion
inferred← citeshttps://doi.org/10.1016/s1359-6101(02)00012-6openalex-snapshot
The family of IL-10-related cytokines and their receptors: related, but to what extent?
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