On the public citation graph

Cancer-associated toll-like receptor modulation and insinuation in infection susceptibility: association or coincidence?

https://doi.org/10.1093/annonc/mdw053
0 signed · 216 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.02/ijaai.9199openalex-snapshot
Variant Toll-like receptor4 (Asp299Gly and Thr399Ile alleles) and Toll-like receptor2 (Arg753Gln and Arg677Trp alleles) in colorectal cancer.
inferredcites →https://doi.org/10.1001/archinte.162.9.1028openalex-snapshot
Relevance of Mutations in the TLR4 Receptor in Patients With Gram-Negative Septic Shock
inferredcites →https://doi.org/10.1001/archpedi.1984.02140460007005openalex-snapshot
Staphylococcus epidermidis Septicemia in Children With Leukemia and Lymphoma
inferredcites →https://doi.org/10.1001/jama.2013.4350openalex-snapshot
Identification of Genetic Loci Associated With Helicobacter pylori Serologic Status
inferredcites →https://doi.org/10.1001/jama.285.1.47openalex-snapshot
Serotypes of Chlamydia trachomatis and Risk for Development of Cervical Squamous Cell Carcinoma
inferredcites →https://doi.org/10.1002/eji.200939669openalex-snapshot
TLR2‐independent induction and regulation of chronic intestinal inflammation
inferredcites →https://doi.org/10.1002/eji.200940232openalex-snapshot
Does TLR2 regulate intestinal inflammation?
inferredcites →https://doi.org/10.1002/ijc.21731openalex-snapshot
The global health burden of infection‐associated cancers in the year 2002
inferredcites →https://doi.org/10.1002/ijc.23826openalex-snapshot
Genetic variation in the toll‐like receptor gene cluster (TLR10‐TLR1‐TLR6) and prostate cancer risk
inferredcites →https://doi.org/10.1002/ijc.26143openalex-snapshot
The toll‐like receptor 2 (TLR2) ‐196 to ‐174 del/ins polymorphism affects viral loads and susceptibility to hepatocellular carcinoma in chronic hepatitis C
inferredcites →https://doi.org/10.1002/ijc.26314openalex-snapshot
Toll‐like receptor genes and their association with colon and rectal cancer development and prognosis
inferredcites →https://doi.org/10.1002/jmv.23271openalex-snapshot
Toll‐like receptor 3 polymorphism and its association with hepatitis B virus infection in Saudi Arabian patients
inferredcites →https://doi.org/10.1002/lt.22327openalex-snapshot
Toll-like receptor 2 polymorphism and gram-positive bacterial infections after liver transplantation
inferredcites →https://doi.org/10.1002/mc.20325openalex-snapshot
Increased toll‐like receptor 9 expression in cervical neoplasia
inferredcites →https://doi.org/10.1002/path.2264openalex-snapshot
The role of TLR activation in inflammation
inferredcites →https://doi.org/10.1002/pros.21115openalex-snapshot
Expression of toll‐like receptor‐9 is increased in poorly differentiated prostate tumors
inferredcites →https://doi.org/10.1002/pros.21423openalex-snapshot
Genetic variation in the toll‐like receptor 4 and prostate cancer incidence and mortality
inferredcites →https://doi.org/10.1007/978-1-60327-411-1_1openalex-snapshot
SNPs: Impact on Gene Function and Phenotype
inferredcites →https://doi.org/10.1007/978-3-319-04220-6openalex-snapshot
Infectious Complications in Cancer Patients
inferredcites →https://doi.org/10.1007/978-3-319-04220-6_2openalex-snapshot
Epidemiology of Infections in Cancer Patients
inferredcites →https://doi.org/10.1007/978-3-540-72167-3_1openalex-snapshot
Toll-Like Receptors (TLRs) and Their Ligands
inferredcites →https://doi.org/10.1007/s00345-011-0690-3openalex-snapshot
Sequence variants of toll-like receptor 4 (TLR4) and the risk of prostate cancer in Korean men
inferredcites →https://doi.org/10.1007/s00405-006-0215-7openalex-snapshot
Assessment of expression of toll-like receptors 2, 3 and 4 in laryngeal carcinoma
inferredcites →https://doi.org/10.1007/s10549-012-2234-yopenalex-snapshot
Association of common genetic variants with breast cancer risk and clinicopathological characteristics in a Chinese population
inferredcites →https://doi.org/10.1007/s10620-012-2460-5openalex-snapshot
Profiles of Gene Polymorphisms in Cytokines and Toll-Like Receptors with Higher Risk for Gastric Cancer
inferredcites →https://doi.org/10.1007/s11033-008-9338-9openalex-snapshot
Increased expression of Toll-like receptors 4 and 9 in human lung cancer
inferredcites →https://doi.org/10.1007/s11033-009-9620-5openalex-snapshot
Toll-like receptor 9 agonists up-regulates the expression of cyclooxygenase-2 via activation of NF-κB in prostate cancer cells
inferredcites →https://doi.org/10.1007/s11033-010-0607-zopenalex-snapshot
Evaluation of Toll-like receptors 3 (c.1377C/T) and 9 (G2848A) gene polymorphisms in cervical cancer susceptibility
inferredcites →https://doi.org/10.1007/s11033-012-1556-5openalex-snapshot
Association of Toll-like receptor (TLR) 2, 3 and 9 genes polymorphism with prostate cancer risk in North Indian population
inferredcites →https://doi.org/10.1007/s11033-012-1695-8openalex-snapshot
Involvement of toll-like receptor 9 polymorphism in cervical cancer development
inferredcites →https://doi.org/10.1016/0002-9343(86)90510-3openalex-snapshot
Infection in cancer patients: A continuing association
inferredcites →https://doi.org/10.1016/j.arcmed.2008.04.008openalex-snapshot
Possible Association of Helicobacter pylori Infection with Laryngeal Cancer Risk: An Evidence-based Meta-analysis
inferredcites →https://doi.org/10.1016/j.bbcan.2012.05.005openalex-snapshot
Normal to cancer microbiome transformation and its implication in cancer diagnosis
inferredcites →https://doi.org/10.1016/j.bpg.2006.04.008openalex-snapshot
Gastric cancer: global pattern of the disease and an overview of environmental risk factors
inferredcites →https://doi.org/10.1016/j.breast.2012.04.001openalex-snapshot
Toll-like receptors gene polymorphisms may confer increased susceptibility to breast cancer development
inferredcites →https://doi.org/10.1016/j.ccell.2014.11.009openalex-snapshot
Microbially Driven TLR5-Dependent Signaling Governs Distal Malignant Progression through Tumor-Promoting Inflammation
inferredcites →https://doi.org/10.1016/j.ccr.2012.08.010openalex-snapshot
STAT3-Driven Upregulation of TLR2 Promotes Gastric Tumorigenesis Independent of Tumor Inflammation
inferredcites →https://doi.org/10.1016/j.cell.2004.07.002openalex-snapshot
Recognition of Commensal Microflora by Toll-Like Receptors Is Required for Intestinal Homeostasis
inferredcites →https://doi.org/10.1016/j.critrevonc.2013.06.011openalex-snapshot
Lung cancer in never smokers: Disease characteristics and risk factors
inferredcites →https://doi.org/10.1016/j.critrevonc.2014.10.008openalex-snapshot
Hepatitis C virus and lymphoma
inferredcites →https://doi.org/10.1016/j.dld.2012.03.020openalex-snapshot
Immunoproliferative small intestinal disease associated with Campylobacter jejuni
inferredcites →https://doi.org/10.1016/j.dld.2012.08.006openalex-snapshot
Functional polymorphisms of Toll-like receptors 2 and 4 alter the risk for colorectal carcinoma in Europeans
inferredcites →https://doi.org/10.1016/j.enzmictec.2013.06.001openalex-snapshot
Specific detection of inflamed cells using TLR1 antibody and its secondary antibody-conjugated nano-beads
inferredcites →https://doi.org/10.1016/j.humimm.2013.08.277openalex-snapshot
Total expression of HLA-G and TLR-9 in chronic lymphocytic leukemia patients
inferredcites →https://doi.org/10.1016/j.humimm.2014.06.001openalex-snapshot
Genetic polymorphisms in the Toll-like receptor signalling pathway in Helicobacter pylori infection and related gastric cancer
inferredcites →https://doi.org/10.1016/j.humpath.2012.06.015openalex-snapshot
Down-regulation of Toll-like receptor 7 expression in hepatitis-virus–related human hepatocellular carcinoma
inferredcites →https://doi.org/10.1016/j.ijmm.2005.02.009openalex-snapshot
Toll-like receptors TLR4, TLR5 and TLR9 on gastric carcinoma cells: An implication for interaction with Helicobacter pylori
inferredcites →https://doi.org/10.1016/j.medin.2013.08.006openalex-snapshot
TLR2–TLR4/CD14 polymorphisms and predisposition to severe invasive infections by Neisseria meningitidis and Streptococcus pneumoniae
inferredcites →https://doi.org/10.1016/j.preghy.2014.10.298openalex-snapshot
[292-POS]
inferredcites →https://doi.org/10.1016/j.smim.2003.10.003openalex-snapshot
TLR signaling pathways
inferredcites →https://doi.org/10.1016/j.smim.2006.12.002openalex-snapshot
Innate immune sensing of pathogens and danger signals by cell surface Toll-like receptors
inferredcites →https://doi.org/10.1016/j.str.2011.02.004openalex-snapshot
The Structural Biology of Toll-like Receptors
inferredcites →https://doi.org/10.1016/s0092-8674(00)80412-2openalex-snapshot
Innate Immunity: The Virtues of a Nonclonal System of Recognition
inferredcites →https://doi.org/10.1016/s0140-6736(13)62146-7openalex-snapshot
Ovarian cancer
inferredcites →https://doi.org/10.1016/s0378-1119(99)00098-0openalex-snapshot
TLR6: A novel member of an expanding Toll-like receptor family
inferredcites →https://doi.org/10.1016/s0959-8049(03)00625-7openalex-snapshot
Impact of vaccinations and infectious diseases on the risk of melanoma—evaluation of an EORTC case–control study
inferredcites →https://doi.org/10.1016/s1471-4906(03)00242-4openalex-snapshot
Leucine-rich repeats and pathogen recognition in Toll-like receptors
inferredcites →https://doi.org/10.1016/s1473-3099(05)01308-3openalex-snapshot
Single nucleotide polymorphisms of Toll-like receptors and susceptibility to infectious disease
inferredcites →https://doi.org/10.1038/gene.2013.22openalex-snapshot
Toll-like receptor-associated sequence variants and prostate cancer risk among men of African descent
inferredcites →https://doi.org/10.1038/gene.2013.34openalex-snapshot
A TLR6 polymorphism is associated with increased risk of Legionnaires’ disease
inferredcites →https://doi.org/10.1038/gene.2014.67openalex-snapshot
Polymorphisms of Toll-like receptors (TLR2 and TLR4) are associated with the risk of infectious complications in acute myeloid leukemia
inferredcites →https://doi.org/10.1038/jhg.2009.90openalex-snapshot
Polymorphisms and haplotypes in TLR9 and MYD88 are associated with the development of Hodgkin's lymphoma: a candidate–gene association study
inferredcites →https://doi.org/10.1038/jid.2012.288openalex-snapshot
TLR Signaling and DNA Repair: Are They Associated?
inferredcites →https://doi.org/10.1038/nature01182openalex-snapshot
Essential role for TIRAP in activation of the signalling cascade shared by TLR2 and TLR4
inferredcites →https://doi.org/10.1038/nature01322openalex-snapshot
Inflammation and cancer
inferredcites →https://doi.org/10.1038/ni.1836openalex-snapshot
CD36 ligands promote sterile inflammation through assembly of a Toll-like receptor 4 and 6 heterodimer
inferredcites →https://doi.org/10.1038/ni.1863openalex-snapshot
The role of pattern-recognition receptors in innate immunity: update on Toll-like receptors
inferredcites →https://doi.org/10.1038/ni986openalex-snapshot
TRAM is specifically involved in the Toll-like receptor 4–mediated MyD88-independent signaling pathway
inferredcites →https://doi.org/10.1038/nrc2541openalex-snapshot
Toll-like receptors and cancer
inferredcites →https://doi.org/10.1038/nrc2857openalex-snapshot
Helicobacter pylori: gastric cancer and beyond
inferredcites →https://doi.org/10.1038/onc.2013.302openalex-snapshot
The Yin and Yang of Toll-like receptors in cancer
inferredcites →https://doi.org/10.1038/oncsis.2013.22openalex-snapshot
Suppression of radiation-induced DNA double-strand break repair by MyD88 is accompanied by apoptosis and crypt loss in mouse colon
inferredcites →https://doi.org/10.1038/sj.gene.6364337openalex-snapshot
Gene polymorphisms in Toll-like receptors, interleukin-10, and interleukin-10 receptor alpha and lymphoma risk
inferredcites →https://doi.org/10.1038/sj.onc.1210912openalex-snapshot
Polymorphisms in Toll-like receptor genes and risk of cancer
inferredcites →https://doi.org/10.1053/j.gastro.2008.04.022openalex-snapshot
Toll-Like Receptor 5 Engagement Modulates Tumor Development and Growth in a Mouse Xenograft Model of Human Colon Cancer
inferredcites →https://doi.org/10.1053/j.gastro.2014.08.033openalex-snapshot
Intestinal Epithelial Cell Toll-like Receptor 5 Regulates the Intestinal Microbiota to Prevent Low-Grade Inflammation and Metabolic Syndrome in Mice
inferredcites →https://doi.org/10.1053/j.seminoncol.2005.12.013openalex-snapshot
Infectious Complications of Chronic Lymphocytic Leukemia
inferredcites →https://doi.org/10.1056/nejm199405053301803openalex-snapshot
Helicobacter pylori Infection and Gastric Lymphoma
inferredcites →https://doi.org/10.1056/nejmoa001999openalex-snapshot
Helicobacter pylori Infection and the Development of Gastric Cancer
inferredcites →https://doi.org/10.1056/nejmoa012673openalex-snapshot
Toll-like Receptor 4 Polymorphisms and Atherogenesis
inferredcites →https://doi.org/10.1056/nejmoa031887openalex-snapshot
Immunoproliferative Small Intestinal Disease Associated with Campylobacter jejuni
inferredcites →https://doi.org/10.1083/jcb.200612056openalex-snapshot
The interaction between the ER membrane protein UNC93B and TLR3, 7, and 9 is crucial for TLR signaling
inferredcites →https://doi.org/10.1084/jem.20031220openalex-snapshot
A Common Dominant TLR5 Stop Codon Polymorphism Abolishes Flagellin Signaling and Is Associated with Susceptibility to Legionnaires' Disease
inferredcites →https://doi.org/10.1086/431990openalex-snapshot
The Importance of Toll-Like Receptor 2 Polymorphisms in Severe Infections
inferredcites →https://doi.org/10.1086/653607openalex-snapshot
Association of Toll‐Like Receptor 4 Asp299Gly and Thr399Ile Polymorphisms with Increased Infection Risk in Patients with Advanced HIV‐1 Infection
inferredcites →https://doi.org/10.1089/cbr.2012.1395openalex-snapshot
Associations Between the Four Toll-Like Receptor Polymorphisms and the Risk of Gastric Cancer: A Meta-Analysis
inferredcites →https://doi.org/10.1093/carcin/bgt110openalex-snapshot
Genetic ancestry modifies the association between genetic risk variants and breast cancer risk among Hispanic and non-Hispanic white women
inferredcites →https://doi.org/10.1093/carcin/bgt249openalex-snapshot
Role of bacterial infections in pancreatic cancer
inferredcites →https://doi.org/10.1093/cid/ciq155openalex-snapshot
Single Nucleotide Polymorphisms in TLR9 Are Highly Associated with Susceptibility to Bacterial Meningitis in Children
inferredcites →https://doi.org/10.1093/infdis/jis698openalex-snapshot
Human Papillomavirus Infection and Laryngeal Cancer Risk: A Systematic Review and Meta-Analysis
inferredcites →https://doi.org/10.1093/infdis/jiu080openalex-snapshot
TLR1, TLR2, and TLR6 Gene Polymorphisms Are Associated With Increased Susceptibility to Complicated Skin and Skin Structure Infections
inferredcites →https://doi.org/10.1093/jnci/dji070openalex-snapshot
Sequence Variants in Toll-Like Receptor Gene Cluster (TLR6-TLR1-TLR10) and Prostate Cancer Risk
inferredcites →https://doi.org/10.1093/oxfordjournals.qjmed.a030140openalex-snapshot
Bacterial meningitis in patients with nasopharyngeal carcinoma
inferredcites →https://doi.org/10.1097/igc.0b013e31827a2003openalex-snapshot
Toll-Like Receptors 7, 8, and 9 Expression and Function in Primary Human Cervical Cancer Langerhans Cells
inferredcites →https://doi.org/10.1097/inf.0000000000000395openalex-snapshot
Toll-like Receptor 6 V327M Polymorphism Is Associated with an Increased Risk of Klebsiella pneumoniae Infection
inferredcites →https://doi.org/10.1097/ppo.0000000000000048openalex-snapshot
Microbiome, Inflammation, and Cancer
inferredcites →https://doi.org/10.1098/rspb.2013.0364openalex-snapshot
Polymorphisms at the innate immune receptorTLR2are associated withBorreliainfection in a wild rodent population
inferredcites →https://doi.org/10.1111/cei.12578openalex-snapshot
Single nucleotide polymorphisms of Toll-like receptors and susceptibility to infectious diseases
inferredcites →https://doi.org/10.1111/j.1349-7006.2010.01491.xopenalex-snapshot
Toll‐like receptor 9 expression in breast and ovarian cancer is associated with poorly differentiated tumors
inferredcites →https://doi.org/10.1111/j.1365-2249.1992.tb06965.xopenalex-snapshot
Predictors of infection in chronic lymphocytic leukaemia (CLL)
inferredcites →https://doi.org/10.1111/j.1365-2567.2005.02200.xopenalex-snapshot
Toll‐like receptors‐2, ‐3 and ‐4 expression patterns on human colon and their regulation by mucosal‐associated bacteria
inferredcites →https://doi.org/10.1111/j.1399-0004.2006.00651.xopenalex-snapshot
Microsatelite GT polymorphism in the toll‐like receptor 2 is associated with colorectal cancer
inferredcites →https://doi.org/10.1111/j.1525-1438.2007.01008.xopenalex-snapshot
Increased expression of Toll-like receptor 5 during progression of cervical neoplasia
inferredcites →https://doi.org/10.1111/jcmm.12055openalex-snapshot
Toll‐like receptors in prostate infection and cancer between bench and bedside
inferredcites →https://doi.org/10.1111/tid.12033openalex-snapshot
Association between a functional polymorphism in Toll‐like receptor 3 and chronic hepatitis C in liver transplant recipients
inferredcites →https://doi.org/10.1126/science.1071059openalex-snapshot
The Danger Model: A Renewed Sense of Self
inferredcites →https://doi.org/10.1126/science.1179721openalex-snapshot
Metabolic Syndrome and Altered Gut Microbiota in Mice Lacking Toll-Like Receptor 5
inferredcites →https://doi.org/10.1128/cmr.16.4.637-646.2003openalex-snapshot
Role of Toll-Like Receptors in Pathogen Recognition
inferredcites →https://doi.org/10.1128/cvi.00460-10openalex-snapshot
Toll-Like Receptor 4 Gene ( TLR4 ), but Not TLR2 , Polymorphisms Modify the Risk of Tonsillar Disease Due to Streptococcus pyogenes and Haemophilus influenzae
inferredcites →https://doi.org/10.1128/iai.00897-09openalex-snapshot
Activation of Human and Chicken Toll-Like Receptors by Campylobacter spp
inferredcites →https://doi.org/10.1128/iai.00903-09openalex-snapshot
Helicobacter pylori Lipopolysaccharides Upregulate Toll-Like Receptor 4 Expression and Proliferation of Gastric Epithelial Cells via the MEK1/2-ERK1/2 Mitogen-Activated Protein Kinase Pathway
inferredcites →https://doi.org/10.1136/bjophthalmol-2014-305690openalex-snapshot
Toll-like receptor 3 activation drives the inflammatory response in oxygen-induced retinopathy in rats
inferredcites →https://doi.org/10.1136/gut.50.suppl_3.iii2openalex-snapshot
Host-pathogen interactions: the seduction of molecular cross talk
inferredcites →https://doi.org/10.1136/jmg.2004.021600openalex-snapshot
TLR4 and TNF-α polymorphisms are associated with an increased risk for severe sepsis following burn injury
inferredcites →https://doi.org/10.1146/annurev.immunol.20.083001.084359openalex-snapshot
Innate Immune Recognition
inferredcites →https://doi.org/10.1155/2012/785825openalex-snapshot
Toll-Like Receptor Transcriptome in the HPV-Positive Cervical Cancer Microenvironment
inferredcites →https://doi.org/10.1155/2014/357062openalex-snapshot
The Association of Toll-Like Receptor 4 Polymorphism with Hepatitis C Virus Infection in Saudi Arabian Patients
inferredcites →https://doi.org/10.1158/0008-5472.can-05-3948openalex-snapshot
TLR-4 Signaling Promotes Tumor Growth and Paclitaxel Chemoresistance in Ovarian Cancer
inferredcites →https://doi.org/10.1158/0008-5472.can-07-0560openalex-snapshot
Increased Susceptibility to Colitis-Associated Cancer of Mice Lacking TIR8 , an Inhibitory Member of the Interleukin-1 Receptor Family
inferredcites →https://doi.org/10.1158/0008-5472.can-13-1746openalex-snapshot
Functional TLR5 Genetic Variants Affect Human Colorectal Cancer Survival
inferredcites →https://doi.org/10.1158/1055-9965.epi-05-0874openalex-snapshot
Sequence Variants in Toll-Like Receptor 10 Are Associated with Nasopharyngeal Carcinoma Risk
inferredcites →https://doi.org/10.1158/1055-9965.epi-11-0702openalex-snapshot
Genetic Variants of Toll-Like Receptor 2 and 5, Helicobacter Pylori Infection, and Risk of Gastric Cancer and Its Precursors in a Chinese Population
inferredcites →https://doi.org/10.1158/1055-9965.epi-12-1129openalex-snapshot
Gene Variants in Angiogenesis and Lymphangiogenesis and Cutaneous Melanoma Progression
inferredcites →https://doi.org/10.1158/1055-9965.epi-13-0463openalex-snapshot
Breast Cancer Subtypes and Previously Established Genetic Risk Factors: A Bayesian Approach
inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-0274openalex-snapshot
Toll-like Receptor 3 Expressed by Melanoma Cells as a Target for Therapy?
inferredcites →https://doi.org/10.1158/1078-0432.ccr-07-4467openalex-snapshot
Helicobacter pyloriAugments Growth of Gastric Cancers via the Lipopolysaccharide-Toll-like Receptor 4 Pathway whereas Its Lipopolysaccharide Attenuates Antitumor Activities of Human Mononuclear Cells
inferredcites →https://doi.org/10.1158/1078-0432.ccr-13-1343openalex-snapshot
Colonization of the Human Gut by E. coli and Colorectal Cancer Risk
inferredcites →https://doi.org/10.1158/1535-7163.mct-12-1019openalex-snapshot
TLR4 Is a Novel Determinant of the Response to Paclitaxel in Breast Cancer
inferredcites →https://doi.org/10.1158/1940-6207.capr-08-0024openalex-snapshot
Understanding Microbe-Induced Cancers
inferredcites →https://doi.org/10.1177/0300060513483398openalex-snapshot
Toll-like receptor 9 ( TLR9 ) gene polymorphisms associated with increased susceptibility of human papillomavirus-16 infection in patients with cervical cancer
inferredcites →https://doi.org/10.11817/j.issn.1672-7347.2015.02.015openalex-snapshot
[Toll-like receptors and non-resolving inflammation-related cancer].
inferredcites →https://doi.org/10.1186/1471-2164-8-124openalex-snapshot
Comparative sequence analysis of leucine-rich repeats (LRRs) within vertebrate toll-like receptors
inferredcites →https://doi.org/10.1186/1471-2334-12-204openalex-snapshot
Bacterial brain abscess in patients with nasopharyngeal carcinoma following radiotherapy: microbiology, clinical features and therapeutic outcomes
inferredcites →https://doi.org/10.1186/1471-2334-14-238openalex-snapshot
Mycobacterial infection of breast prosthesis – a conservative treatment: a case report
inferredcites →https://doi.org/10.1186/1471-2407-10-665openalex-snapshot
Study of TLR3, TLR4 and TLR9 in breast carcinomas and their association with metastasis
inferredcites →https://doi.org/10.1186/1743-422x-9-270openalex-snapshot
Toll-like receptor 3 gene polymorphisms and severity of pandemic A/H1N1/2009 influenza in otherwise healthy children
inferredcites →https://doi.org/10.1186/1750-9378-7-8openalex-snapshot
Chlamydia psittaci in ocular adnexa MALT lymphoma: a possible role in lymphomagenesis and a different geographical distribution
inferredcites →https://doi.org/10.1186/s12881-014-0123-4openalex-snapshot
The association of polymorphisms of TLR4 and CD14genes with susceptibility to sepsis in a Chinese population
inferredcites →https://doi.org/10.1371/journal.pone.0005704openalex-snapshot
The Role of Toll-Like Receptor 2 in Inflammation and Fibrosis during Progressive Renal Injury
inferredcites →https://doi.org/10.1371/journal.pone.0024370openalex-snapshot
Association of Inherited Variation in Toll-Like Receptor Genes with Malignant Melanoma Susceptibility and Survival
inferredcites →https://doi.org/10.1371/journal.pone.0044176openalex-snapshot
TLR-4 Signalling Accelerates Colon Cancer Cell Adhesion via NF-κB Mediated Transcriptional Up-Regulation of Nox-1
inferredcites →https://doi.org/10.1371/journal.pone.0051434openalex-snapshot
Chronic Prostatic Infection and Inflammation by Propionibacterium acnes in a Rat Prostate Infection Model
inferredcites →https://doi.org/10.1371/journal.pone.0060327openalex-snapshot
The Role of TLR2, TLR4 and CD14 Genetic Polymorphisms in Gastric Carcinogenesis: A Case-Control Study and Meta-Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0060671openalex-snapshot
Characterization of the Toll-like Receptor Expression Profile in Human Multiple Myeloma Cells
inferredcites →https://doi.org/10.1371/journal.pone.0098239openalex-snapshot
Functional Effects of Toll-Like Receptor (TLR)3, 7, 9, RIG-I and MDA-5 Stimulation in Nasal Epithelial Cells
inferredcites →https://doi.org/10.1684/bdc.2014.2037openalex-snapshot
Involvement of Toll-like receptors in cervical cancer susceptibility among Tunisian women
inferredcites →https://doi.org/10.3109/10428194.2013.856426openalex-snapshot
Toll-like receptor 4 and 9 expression in B-chronic lymphocytic leukemia: relationship with infections, autoimmunity and disease progression
inferredcites →https://doi.org/10.3349/ymj.2014.55.2.428openalex-snapshot
Single Nucleotide Polymorphisms of Toll-Like Receptor 7 and Toll-Like Receptor 9 in Hepatitis C Virus Infection Patients from Central China
inferredcites →https://doi.org/10.3389/fimmu.2014.00367openalex-snapshot
Toll-Like Receptors and Cancer: MYD88 Mutation and Inflammation
inferredcites →https://doi.org/10.3389/fimmu.2014.00464openalex-snapshot
Toll-Like Receptors and Cancer, Particularly Oral Squamous Cell Carcinoma
inferredcites →https://doi.org/10.3390/ijms16010159openalex-snapshot
Upregulation of TLRs and IL-6 as a Marker in Human Colorectal Cancer
inferredcites →https://doi.org/10.3748/wjg.v17.i32.3745openalex-snapshot
Overexpression of TLR3, TLR4, TLR7 and TLR9 in esophageal squamous cell carcinoma
inferredcites →https://doi.org/10.3748/wjg.v2.i1.22openalex-snapshot
Bacterial infections in cirrhotic patients with hepatocellular carcinoma
inferredcites →https://doi.org/10.3748/wjg.v7.i2.266openalex-snapshot
Mycoplasma infections and different human carcinomas
inferredcites →https://doi.org/10.3892/etm.2015.2258openalex-snapshot
Expression of Toll-like receptors in the mucosa of patients with ulcerative colitis
inferredcites →https://doi.org/10.3892/ijmm.2011.656openalex-snapshot
Flagellin promotes the proliferation of gastric cancer cells via the Toll-like receptor 5
inferredcites →https://doi.org/10.3892/ijo.2012.1374openalex-snapshot
Expression profiles of Toll-like receptors in non-small cell lung cancer and idiopathic pulmonary fibrosis
inferredcites →https://doi.org/10.3892/ijo_00000730openalex-snapshot
Functional cell surface expression of Toll-like receptor 9 promotes cell proliferation and survival in human hepatocellular carcinomas
inferredcites →https://doi.org/10.4049/jimmunol.1201545openalex-snapshot
Differential Trafficking of TLR1 I602S Underlies Host Protection against Pathogenic Mycobacteria
inferredcites →https://doi.org/10.4049/jimmunol.178.10.6252openalex-snapshot
TLR2 Is Constitutively Expressed within the Kidney and Participates in Ischemic Renal Injury through Both MyD88-Dependent and -Independent Pathways
inferredcites →https://doi.org/10.4049/jimmunol.179.5.3119openalex-snapshot
Damping Excessive Inflammation and Tissue Damage in Mycobacterium tuberculosis Infection by Toll IL-1 Receptor 8/Single Ig IL-1-Related Receptor, a Negative Regulator of IL-1/TLR Signaling
inferredcites →https://doi.org/10.4049/jimmunol.179.5.3171openalex-snapshot
Association of TLR4 Polymorphisms with Symptomatic Respiratory Syncytial Virus Infection in High-Risk Infants and Young Children
inferredcites →https://doi.org/10.4081/hmr.v1i5.265openalex-snapshot
Immunoproliferative small intestinal disease associated with Campylobacter jejuni
inferredcites →https://doi.org/10.4161/cc.23406openalex-snapshot
TLR2 enhances ovarian cancer stem cell self-renewal and promotes tumor repair and recurrence
inferredcites →https://doi.org/10.7150/ijbs.6.675openalex-snapshot
The application of Toll like receptors for cancer therapy
inferredcites →https://doi.org/10.7150/ijms.8428openalex-snapshot
The Expression of Toll-like Receptor 8 and Its Relationship with VEGF and Bcl-2 in Cervical Cancer
inferredcites →https://doi.org/10.7150/jca.2.136openalex-snapshot
Medulloblastoma and Brucellosis - Molecular Evidence of Brucella sp in Association with Central Nervous System Cancer
inferredcites →https://doi.org/10.7326/0003-4819-96-1-47openalex-snapshot
Biphasic Pattern of Bacterial Infection in Multiple Myeloma

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3990791openalex-extracted
In Vitro Conditioning of Antigen-Reactive CD8 + T Cells with Toll-Like Receptor Agonists Enhances Their Expansion In Vivo in an Adoptive Transfer Mouse Model
inferred← citeshttps://doi.org/10.1002/advs.202509456openalex-snapshot
Transfer Learning and Permutation‐Invariance Improving Predicting Genome‐Wide, Cell‐Specific and Directional Interventions Effects of Complex Systems
inferred← citeshttps://doi.org/10.1002/ijc.31660openalex-snapshot
Genetic variant of IRAK2 in the toll‐like receptor signaling pathway and survival of non‐small cell lung cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-32316-5_29openalex-snapshot
Cancer Biology and Carcinogenesis: Fundamental Biological Processes and How They Are Deranged in Oral Cancer
inferred← citeshttps://doi.org/10.1007/978-94-024-1084-6_1openalex-snapshot
Introduction—The Biology and Pathology of Squamous Cell Carcinomata in the Head and Neck
inferred← citeshttps://doi.org/10.1007/978-981-33-6699-2_9openalex-snapshot
The Role of Toll-Like Receptor (TLR) Polymorphisms in Urinary Bladder Cancer
inferred← citeshttps://doi.org/10.1007/s00520-024-08752-4openalex-snapshot
Updated perspectives on the contribution of the microbiome to the pathogenesis of mucositis using the MASCC/ISOO framework
inferred← citeshttps://doi.org/10.1007/s12094-021-02690-xopenalex-snapshot
Microbiota and cancer: current understanding and mechanistic implications
inferred← citeshttps://doi.org/10.1016/b978-0-12-819265-8.00047-4openalex-snapshot
The Gut Microbiome and Cancer: A Comprehensive Review of Melanoma, Lung, Head and Neck and Gastrointestinal Tumors
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2017.06.003openalex-snapshot
Toll-like receptor 2 rs4696480 polymorphism and risk of oral cancer and oral potentially malignant disorder
inferred← citeshttps://doi.org/10.1016/j.bbcan.2023.188989openalex-snapshot
Microbial influence on triggering and treatment of host cancer: An intestinal barrier perspective
inferred← citeshttps://doi.org/10.1016/j.bbcan.2024.189229openalex-snapshot
Implication of Toll-Like Receptors in growth and management of health and diseases: Special focus as a promising druggable target to Prostate Cancer
inferred← citeshttps://doi.org/10.1016/j.canlet.2017.11.036openalex-snapshot
Interplay between the lung microbiome and lung cancer
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2019.102841openalex-snapshot
Gut microbiome and response to checkpoint inhibitors in non-small cell lung cancer—A review
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2024.104262openalex-snapshot
Microbiomes in pancreatic cancer can be an accomplice or a weapon
inferred← citeshttps://doi.org/10.1016/j.phrs.2020.105017openalex-snapshot
Promising targets based on pattern recognition receptors for cancer immunotherapy
inferred← citeshttps://doi.org/10.1080/2314808x.2025.2492432openalex-snapshot
Short-term stimulation of mouse CD8 + T cells in vitro with the TLR9 agonist CpG enhances their antigen-specific expansion in vivo after administration of the TLR3 agonist Poly(I:C)
inferred← citeshttps://doi.org/10.1093/ckj/sfad110openalex-snapshot
Influenza vaccination is associated with lower risk of renal cell carcinoma among chronic kidney disease patients: a population-based cohort study
inferred← citeshttps://doi.org/10.1097/in9.0000000000000050openalex-snapshot
Impact of gut microbiota and its metabolites on immunometabolism in colorectal cancer
inferred← citeshttps://doi.org/10.1097/io9.0000000000000148openalex-snapshot
Toll-like receptor-8 mRNA expression as a predictor of enterocolitis in hirschsprung disease: a cross-sectional study
inferred← citeshttps://doi.org/10.1128/mbio.02843-20openalex-snapshot
Pseudomonas aeruginosa Stimulates Inflammation and Enhances Kaposi’s Sarcoma Herpesvirus-Induced Cell Proliferation and Cellular Transformation through both Lipopolysaccharide and Flagellin
inferred← citeshttps://doi.org/10.1155/2016/5715719openalex-snapshot
Immunosuppression Induced by Chronic Inflammation and the Progression to Oral Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1155/2022/4436646openalex-snapshot
Comprehensive Bioinformatics Analysis of Toll‐Like Receptors (TLRs) in Pan‐Cancer
inferred← citeshttps://doi.org/10.1158/2326-6066.cir-19-0510openalex-snapshot
Previous Infection Positively Correlates to the Tumor Incidence Rate of Patients with Cancer
inferred← citeshttps://doi.org/10.1186/s40364-022-00436-7openalex-snapshot
Targeting toll-like receptor 7/8 for immunotherapy: recent advances and prospectives
inferred← citeshttps://doi.org/10.1186/s40364-023-00463-yopenalex-snapshot
Neutrophil extracellular traps primed intercellular communication in cancer progression as a promising therapeutic target
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1193120/v1openalex-snapshot
Integrin Alpha L as an Immune-Related Biomarker Correlated with the Prognosis and Effect of Immunotherapy in Gliomas
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1236618/v1openalex-snapshot
In vitro conditioning of antigen-reactive CD8+ T cells with toll-like receptor agonists enhances their expansion in vivo in an adoptive transfer mouse model
inferred← citeshttps://doi.org/10.2147/jir.s344321openalex-snapshot
Oral-Intestinal Microbiota in Colorectal Cancer: Inflammation and Immunosuppression
inferred← citeshttps://doi.org/10.21873/anticanres.15762openalex-snapshot
The Role of Toll-like Receptors in Esophageal Cancer
inferred← citeshttps://doi.org/10.2217/fmb-2021-0072openalex-snapshot
Biological Roles of Toll-Like Receptors and Gut Microbiota In Colorectal Cancer
inferred← citeshttps://doi.org/10.2478/cipms-2020-0020openalex-snapshot
The role of toll-like receptor 9 (TLR9) in Epstein-Barr virus-associated gastric cancer
inferred← citeshttps://doi.org/10.31146/1682-8658-ecg-162-2-68-74openalex-snapshot
Genetic and psychological prerequisites for development of refractory variant of irritable bowel syndrome
inferred← citeshttps://doi.org/10.3389/fcell.2020.00503openalex-snapshot
Characterization of lncRNA-Perturbed TLR-Signaling Network Identifies Novel lncRNA Prognostic Biomarkers in Colorectal Cancer
inferred← citeshttps://doi.org/10.3389/fcimb.2024.1348279openalex-snapshot
Dysbiosis of the gut microbiota and its effect on α-synuclein and prion protein misfolding: consequences for neurodegeneration
inferred← citeshttps://doi.org/10.3389/fimmu.2022.1049340openalex-snapshot
Toll-like receptor-targeted anti-tumor therapies: Advances and challenges
inferred← citeshttps://doi.org/10.3389/fimmu.2023.1177604openalex-snapshot
Effect of NETs/COX-2 pathway on immune microenvironment and metastasis in gastric cancer
inferred← citeshttps://doi.org/10.3389/fmolb.2021.751842openalex-snapshot
Development and Validation of Ten-RNA Binding Protein Signature Predicts Overall Survival in Osteosarcoma
inferred← citeshttps://doi.org/10.3389/fonc.2023.1206482openalex-snapshot
Differential gene expression of immunity and inflammation genes in colorectal cancer using targeted RNA sequencing
inferred← citeshttps://doi.org/10.3389/ijph.2023.1605370openalex-snapshot
Effect of Annual Influenza Vaccination on the Risk of Lung Cancer Among Patients With Hypertension: A Population-Based Cohort Study in Taiwan
inferred← citeshttps://doi.org/10.3390/cancers13174269openalex-snapshot
The Role of Bacteria in KSHV Infection and KSHV-Induced Cancers
inferred← citeshttps://doi.org/10.3390/cancers8100087openalex-snapshot
Novel Immunotherapeutic Approaches for Head and Neck Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.3390/cells11193137openalex-snapshot
The Toll-like Receptor 4 Polymorphism Asp299Gly Is Associated with an Increased Risk of Ovarian Cancer
inferred← citeshttps://doi.org/10.3390/microorganisms10071405openalex-snapshot
Nasal Microbiota, Olfactory Health, Neurological Disorders and Aging—A Review
inferred← citeshttps://doi.org/10.4014/jmb.1703.03068openalex-snapshot
Lipoteichoic Acid Isolated from Staphylococcus aureus Induces Both Epithelial-Mesenchymal Transition and Wound Healing in HaCaT Cells
inferred← citeshttps://doi.org/10.4103/sjg.sjg_424_23openalex-snapshot
Prediction of the survival status and tumor microenvironment in colorectal cancer through genotyping analysis based on toll-like receptors
inferred← citeshttps://doi.org/10.51643/22562915.372openalex-snapshot
Cáncer gástrico: historia de la enfermedad y factores de riesgo
inferred← citeshttps://doi.org/10.70389/pji.100008openalex-snapshot
Combinatorial Toll-like Receptor Agonists: Advancing Immune Modulation for Global Health Challenges
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.