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Virulence Effectors of Pathogenic Mycoplasmas
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1521-4141(2002012)32:12<3337::aid-immu3337>3.0.co;2-iopenalex-snapshot
Differential recognition of structural details of bacterial lipopeptides by toll-like receptors
inferredcites →https://doi.org/10.1002/1521-4141(200212)32:12<3337::aid-immu3337>3.0.co;2-#openalex-snapshot
Differential recognition of structural details of bacterial lipopeptides by toll-like receptors
inferredcites →https://doi.org/10.1002/1529-0131(200005)43:5<1165::aid-anr27>3.0.co;2-hopenalex-snapshot
Hyaluronan oligosaccharides perturb cartilage matrix homeostasis and induce chondrocytic chondrolysis
inferredcites →https://doi.org/10.1002/eji.200324511openalex-snapshot
The Toll‐like receptor ligand MALP‐2 stimulates dendritic cell maturation and modulates proteasome composition and activity
inferredcites →https://doi.org/10.1006/bbrc.2000.2282openalex-snapshot
Induction of Leukemia Cell Differentiation and Apoptosis by Recombinant P48, a Modulin Derived from Mycoplasma fermentans
inferredcites →https://doi.org/10.1007/978-3-0348-8757-1_11openalex-snapshot
Aggressive and defensive roles for chitinases
inferredcites →https://doi.org/10.1007/bf00198458openalex-snapshot
Molecular characterization of the cfb gene encoding group B streptococcal CAMP-factor
inferredcites →https://doi.org/10.1007/s00253-014-6185-6openalex-snapshot
Mycoplasma gallisepticum MGA_0676 is a membrane-associated cytotoxic nuclease with a staphylococcal nuclease region essential for nuclear translocation and apoptosis induction in chicken cells
inferredcites →https://doi.org/10.1007/s00430-006-0027-9openalex-snapshot
Direct stimulatory effects of the TLR2/6 ligand bacterial lipopeptide MALP-2 on neutrophil granulocytes
inferredcites →https://doi.org/10.1016/0006-291x(80)91186-9openalex-snapshot
Mycoplasma pneumoniae: A prokaryote which consumes oxygen and generates superoxide but which lacks superoxide dismutase
inferredcites →https://doi.org/10.1016/0008-8749(83)90029-1openalex-snapshot
Induction of macrophage-mediated cytolysis of neoplastic cells by mycoplasmas
inferredcites →https://doi.org/10.1016/0197-1859(88)90041-6openalex-snapshot
Mycoplasma arthritidis mitogen: A potential new pathway of T-cell activation
inferredcites →https://doi.org/10.1016/0378-1097(92)90143-copenalex-snapshot
Urea-hydrolysis-dependent citrulline synthesis by Ureaplasma urealyticum
inferredcites →https://doi.org/10.1016/0378-1097(94)90256-9openalex-snapshot
Association of the CAMP phenomenon in Actinobacillus pleuropneumoniae with the RTX toxins ApxI, ApxII and ApxIII
inferredcites →https://doi.org/10.1016/j.bbrc.2008.02.079openalex-snapshot
Mycoplasma fermentans glycolipid-antigen as a pathogen of rheumatoid arthritis
inferredcites →https://doi.org/10.1016/j.biocel.2012.04.019openalex-snapshot
Killing me softly – Suicidal erythrocyte death
inferredcites →https://doi.org/10.1016/j.jmb.2010.04.030openalex-snapshot
Crystal Structure of the Mycoplasma arthritidis-Derived Mitogen in Apo Form Reveals a 3D Domain-Swapped Dimer
inferredcites →https://doi.org/10.1016/j.jprot.2018.08.018openalex-snapshot
Differential secretome profiling of a swine tracheal cell line infected with mycoplasmas of the swine respiratory tract
inferredcites →https://doi.org/10.1016/j.jri.2006.02.003openalex-snapshot
Macrophage-activating lipopeptide-2 induces cyclooxygenase-2 and prostaglandin E2 via toll-like receptor 2 in human placental trophoblast cells
inferredcites →https://doi.org/10.1016/j.micinf.2008.09.010openalex-snapshot
Crucial cytokine interactions in nitric oxide production induced by Mycoplasma arthritidis superantigen
inferredcites →https://doi.org/10.1016/j.micpath.2008.02.002openalex-snapshot
Genetic variation in sialidase and linkage to N-acetylneuraminate catabolism in Mycoplasma synoviae
inferredcites →https://doi.org/10.1016/j.mimet.2010.09.008openalex-snapshot
Mutagenesis of Propionibacterium acnes and analysis of two CAMP factor knock-out mutants
inferredcites →https://doi.org/10.1016/j.vetmic.2004.02.005openalex-snapshot
Differential clustering of Mycoplasma mycoides subsp. mycoides SC strains by PCR–REA of the bgl locus
inferredcites →https://doi.org/10.1016/j.vetmic.2006.10.009openalex-snapshot
Role of sialidase in Mycoplasma alligatoris-induced pulmonary fibroblast apoptosis
inferredcites →https://doi.org/10.1016/j.vetmic.2009.01.009openalex-snapshot
Secreted sialidase activity of canine mycoplasmas
inferredcites →https://doi.org/10.1016/j.vetmic.2011.05.031openalex-snapshot
The central role of lipoproteins in the pathogenesis of mycoplasmoses
inferredcites →https://doi.org/10.1016/j.vetmic.2011.08.026openalex-snapshot
Demonstration of neuraminidase activity in Mycoplasma neurolyticum and of neuraminidase proteins in three canine Mycoplasma species
inferredcites →https://doi.org/10.1016/j.vetmic.2018.08.001openalex-snapshot
Metabolite profiling of Mycoplasma gallisepticum mutants, combined with bioinformatic analysis, can reveal the likely functions of virulence-associated genes
inferredcites →https://doi.org/10.1016/s0005-2760(97)00088-xopenalex-snapshot
Structure of a novel phosphocholine-containing aminoglycoglycerolipid of Mycoplasma fermentans
inferredcites →https://doi.org/10.1016/s0006-8993(98)00573-3openalex-snapshot
Mycoplasma fermentans glycolipid triggers inflammatory response in rat astrocytes
inferredcites →https://doi.org/10.1016/s0021-9258(20)30105-8openalex-snapshot
Structure of a novel phosphocholine-containing glycoglycerolipid from Mycoplasma fermentans
inferredcites →https://doi.org/10.1016/s0022-1759(97)00135-xopenalex-snapshot
Detection of serum antibodies against phosphocholine-containing aminoglycoglycerolipid specific to Mycoplasma fermentans in HIV-1 infected individuals
inferredcites →https://doi.org/10.1016/s0041-0101(01)00163-5openalex-snapshot
Clostridial hydrolytic enzymes degrading extracellular components
inferredcites →https://doi.org/10.1016/s0140-6736(13)62115-7openalex-snapshot
Fatal hyperammonaemia caused by Mycoplasma hominis
inferredcites →https://doi.org/10.1016/s0140-6736(85)91554-5openalex-snapshot
TRANSIENT IDIOPATHIC HYPERAMMONAEMIA IN ADULTS
inferredcites →https://doi.org/10.1016/s0174-3031(83)80125-5openalex-snapshot
Studies of polyarthritis caused by mycoplasma arthritidis in rats III. Histopathological findings
inferredcites →https://doi.org/10.1016/s0378-1135(99)00170-4openalex-snapshot
Identification of the copper-zinc superoxide dismutase activity in Mycoplasma hyopneumoniae
inferredcites →https://doi.org/10.1016/s1286-4579(00)00312-9openalex-snapshot
Bacterial ureases in infectious diseases
inferredcites →https://doi.org/10.1016/s1286-4579(02)01610-6openalex-snapshot
Structural–functional relationship of pathogen-associated molecular patterns: lessons from BCG cell wall skeleton and mycoplasma lipoprotein M161Ag
inferredcites →https://doi.org/10.1016/s1286-4579(02)01622-2openalex-snapshot
Choline-containing lipids in mycoplasmas
inferredcites →https://doi.org/10.1016/s1357-2725(01)00164-9openalex-snapshot
A lipoprotein family from Mycoplasma fermentans confers host immune activation through Toll-like receptor 2
inferredcites →https://doi.org/10.1023/a:1026706732081openalex-snapshot
Biochemical Characterization of Mycoplasma bovirhinis, Mycoplasma dispar and Recent Bovine Isolates of Mycoplasma canis
inferredcites →https://doi.org/10.1038/210963a0openalex-snapshot
Methaemoglobin Formation by Mycoplasma gallisepticum: the Role of Hydrogen Peroxide
inferredcites →https://doi.org/10.1038/jid.1952.36openalex-snapshot
The Occurrence of a Pleuropneumonia-Like Organism in Fuso-Spirillary Infections of the Human Genital Mucosa
inferredcites →https://doi.org/10.1038/nsmb1187openalex-snapshot
Identification and structural basis of binding to host lung glycogen by streptococcal virulence factors
inferredcites →https://doi.org/10.1038/nsmb1193openalex-snapshot
Crystal structure of a complete ternary complex of TCR, superantigen and peptide-MHC
inferredcites →https://doi.org/10.1038/sj.cdd.4400380openalex-snapshot
Mycoplasma nucleases able to induce internucleosomal DNA degradation in cultured cells possess many characteristics of eukaryotic apoptotic nucleases
inferredcites →https://doi.org/10.1042/bj3190919openalex-snapshot
cDNA and genomic cloning and expression of the P48 monocytic differentiation/activation factor, a Mycoplasma fermentans gene product
inferredcites →https://doi.org/10.1074/jbc.273.20.12407openalex-snapshot
Structural and Functional Properties of Complement-activating Protein M161Ag, a Mycoplasma fermentans Gene Product That Induces Cytokine Production by Human Monocytes
inferredcites →https://doi.org/10.1078/0171-2985-00234openalex-snapshot
Synthetic mycoplasma-derived lipopeptide MALP-2 induces maturation and function of dendritic cells
inferredcites →https://doi.org/10.1093/clinids/17.supplement_1.s163openalex-snapshot
Immunomodulation In Vivo by the Mycoplasma arthritidis Superantigen, MAM
inferredcites →https://doi.org/10.1093/clinids/17.supplement_1.s283openalex-snapshot
Fatal Systemic Infections of Nonhuman Primates by Mycoplasma fermentans (Incognitus Strain)
inferredcites →https://doi.org/10.1093/clinids/17.supplement_1.s289openalex-snapshot
Cytopathogenicity of Mycoplasma fermentans (Including Strain Incognitus)
inferredcites →https://doi.org/10.1093/gbe/evu033openalex-snapshot
Molecular Evolution of the Substrate Utilization Strategies and Putative Virulence Factors in Mosquito-Associated Spiroplasma Species
inferredcites →https://doi.org/10.1093/infdis/jir557openalex-snapshot
Synthesis and Distribution of CARDS Toxin During Mycoplasma pneumoniae Infection in a Murine Model
inferredcites →https://doi.org/10.1093/nar/24.22.4420openalex-snapshot
Complete Sequence Analysis of the Genome of the Bacterium Mycoplasma Pneumoniae
inferredcites →https://doi.org/10.1093/nar/gku976openalex-snapshot
Transcriptome analysis reveals novel regulatory mechanisms in a genome-reduced bacterium
inferredcites →https://doi.org/10.1093/rheumatology/40.12.1355openalex-snapshot
The prevalence of Mycoplasma fermentans in patients with inflammatory arthritides
inferredcites →https://doi.org/10.1097/00006454-198611010-00024openalex-snapshot
Energy production in Ureaplasma urealyticum
inferredcites →https://doi.org/10.1099/00221287-131-4-817openalex-snapshot
Reaction Components Influencing CAMP Factor Induced Lysis
inferredcites →https://doi.org/10.1099/00221287-135-2-315openalex-snapshot
The Urease of Ureaplasma urealyticum
inferredcites →https://doi.org/10.1099/00222615-34-4-219openalex-snapshot
Oxygen uptake and H2O2 production by fermentative Mycoplasma spp.
inferredcites →https://doi.org/10.1099/mic.0.030643-0openalex-snapshot
A peroxiredoxin from Mycoplasma hyopneumoniae with a possible role in H2O2 detoxification
inferredcites →https://doi.org/10.1099/mic.0.051839-0openalex-snapshot
Bacterial chitinases and chitin-binding proteins as virulence factors
inferredcites →https://doi.org/10.1099/mic.0.25742-0openalex-snapshot
Characterization of a chromosomal region of Mycoplasma sp. bovine group 7 strain PG50 encoding a glycerol transport locus (gtsABC)
inferredcites →https://doi.org/10.1111/j.1462-5822.2010.01513.xopenalex-snapshot
Mycoplasma pneumoniae Mpn133 is a cytotoxic nuclease with a glutamic acid-, lysine- and serine-rich region essential for binding and internalization but not enzymatic activity
inferredcites →https://doi.org/10.1111/j.1462-5822.2010.01540.xopenalex-snapshot
Novel interactions of a microbial superantigen with TLR2 and TLR4 differentially regulate IL-17 and Th17-associated cytokines
inferredcites →https://doi.org/10.1111/j.1472-765x.1996.tb01153.xopenalex-snapshot
Cholesterol oxidase from Rhodococcus equi is likely the major factor involved in the cooperative lytic process (CAMP reaction) with Listeria monocytogenes
inferredcites →https://doi.org/10.1111/j.1749-6632.1967.tb27648.xopenalex-snapshot
MYCOPLASMA PNEUMONIAE: HYDROGEN PEROXIDE SECRETION AND ITS POSSIBLE ROLE IN VIRULENCE*
inferredcites →https://doi.org/10.1126/scisignal.262pe14openalex-snapshot
Bacterial FIC Proteins AMP Up Infection
inferredcites →https://doi.org/10.1126/scitranslmed.aaa8419openalex-snapshot
Disseminated Ureaplasma infection as a cause of fatal hyperammonemia in humans
inferredcites →https://doi.org/10.1128/aac.39.10.2187openalex-snapshot
Growth inhibition of Ureaplasma urealyticum by the proton pump inhibitor lansoprazole: direct attribution to inhibition by lansoprazole of urease activity and urea-induced ATP synthesis in U. urealyticum
inferredcites →https://doi.org/10.1128/cvi.00132-10openalex-snapshot
Identification of Mycoplasma mycoides subsp. mycoides Small Colony Genes Coding for T-Cell Antigens
inferredcites →https://doi.org/10.1128/genomea.00348-13openalex-snapshot
Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle
inferredcites →https://doi.org/10.1128/iai.00154-10openalex-snapshot
Identification of Lipoprotein MslA as a Neoteric Virulence Factor ofMycoplasma gallisepticum
inferredcites →https://doi.org/10.1128/iai.01212-12openalex-snapshot
Implication of Glycerol and Phospholipid Transporters in Mycoplasma pneumoniae Growth and Virulence
inferredcites →https://doi.org/10.1128/iai.02208-14openalex-snapshot
Hydrogen Peroxide Production from Glycerol Metabolism Is Dispensable for Virulence of Mycoplasma gallisepticum in the Tracheas of Chickens
inferredcites →https://doi.org/10.1128/iai.13.3.915-925.1976openalex-snapshot
Growth and effects of ureaplasmas (T mycoplasmas) in bovine oviductal organ cultures
inferredcites →https://doi.org/10.1128/iai.15.3.995-996.1977openalex-snapshot
Ureaplasmal epithelial lesions related to ammonia
inferredcites →https://doi.org/10.1128/iai.18.2.310-317.1977openalex-snapshot
Lymphocyte activation by various Mycoplasma strains and species
inferredcites →https://doi.org/10.1128/iai.18.2.393-399.1977openalex-snapshot
Mycoplasma-dependent activation of normal lymphocytes: mitogenic potential of mycoplasmas for mouse lymphocytes
inferredcites →https://doi.org/10.1128/iai.3.1.80-86.1971openalex-snapshot
Effect of Medium on H 2 O 2 Levels and Peroxidase-Like Activity by Mycoplasma pneumoniae
inferredcites →https://doi.org/10.1128/iai.30.2.353-361.1980openalex-snapshot
Interaction of Mycoplasma gallisepticum with sialyl glycoproteins
inferredcites →https://doi.org/10.1128/iai.59.3.1170-1171.1991openalex-snapshot
Virulence of ureaplasmal urease for mice
inferredcites →https://doi.org/10.1128/iai.60.1.56-62.1992openalex-snapshot
A neutral glycoprotease of Pasteurella haemolytica A1 specifically cleaves O-sialoglycoproteins
inferredcites →https://doi.org/10.1128/iai.62.9.3793-3800.1994openalex-snapshot
A 48-kilodalton Mycoplasma fermentans membrane protein induces cytokine secretion by human monocytes
inferredcites →https://doi.org/10.1128/iai.65.6.2000-2005.1997openalex-snapshot
Functional analysis of Mycoplasma arthritidis-derived mitogen interactions with class II molecules
inferredcites →https://doi.org/10.1128/iai.72.3.1657-1665.2004openalex-snapshot
Relationship between Structures and Biological Activities of Mycoplasmal Diacylated Lipopeptides and Their Recognition by Toll-Like Receptors 2 and 6
inferredcites →https://doi.org/10.1128/iai.74.1.40-48.2006openalex-snapshot
Role of Hyaluronidase in Subcutaneous Spread and Growth of Group A Streptococcus
inferredcites →https://doi.org/10.1128/jb.00664-12openalex-snapshot
Genome Annotation of Five Mycoplasma canis Strains
inferredcites →https://doi.org/10.1128/jb.175.11.3253-3258.1993openalex-snapshot
Hydrolysis of urea by Ureaplasma urealyticum generates a transmembrane potential with resultant ATP synthesis
inferredcites →https://doi.org/10.1128/jb.187.19.6824-6831.2005openalex-snapshot
A Metabolic Enzyme as a Primary Virulence Factor of Mycoplasma mycoides subsp. mycoides Small Colony
inferredcites →https://doi.org/10.1128/jb.43.2.211-228.1942openalex-snapshot
Observations on Some Biological Characteristics of Organisms of the Pleuropneumonia Group
inferredcites →https://doi.org/10.1128/jb.89.3.813-818.1965openalex-snapshot
Hemolysin of Mycoplasma pneumoniae
inferredcites →https://doi.org/10.1128/jb.95.4.1425-1430.1968openalex-snapshot
Relation of Catalase to Substrate Utilization by Mycoplasma pneumoniae
inferredcites →https://doi.org/10.1128/jb.98.3.1036-1040.1969openalex-snapshot
Relationship of Hydrogen Peroxide Production by Mycoplasma pulmonis to Virulence for Catalase-deficient Mice
inferredcites →https://doi.org/10.1128/mbio.01497-14openalex-snapshot
Annexin A2 Mediates Mycoplasma pneumoniae Community-Acquired Respiratory Distress Syndrome Toxin Binding to Eukaryotic Cells
inferredcites →https://doi.org/10.1128/mbio.02186-14openalex-snapshot
ADP-Ribosylation of NLRP3 by Mycoplasma pneumoniae CARDS Toxin Regulates Inflammasome Activity
inferredcites →https://doi.org/10.1128/mmbr.62.4.1094-1156.1998openalex-snapshot
Molecular Biology and Pathogenicity of Mycoplasmas
inferredcites →https://doi.org/10.1136/ard.30.3.316openalex-snapshot
Reproducible polyarthritis in rats caused by Mycoplasma arthritidis.
inferredcites →https://doi.org/10.1136/ard.32.4.319openalex-snapshot
Mycoplasmas and bacteria in synovial fluid from patients with arthritis.
inferredcites →https://doi.org/10.1155/2012/640762openalex-snapshot
The Phospholipid Profile of Mycoplasmas
inferredcites →https://doi.org/10.1159/000329957openalex-snapshot
Hemotrophic Mycoplasmas Induce Programmed Cell Death in Red Blood Cells
inferredcites →https://doi.org/10.1159/000354322openalex-snapshot
Analysis of the Complete Genomes of Acholeplasma brassicae, A. palmae and A. laidlawii and Their Comparison to the Obligate Parasites from ‘Candidatus Phytoplasma'
inferredcites →https://doi.org/10.1177/09680519000060061001openalex-snapshot
MALP-2, a Mycoplasma lipopeptide with classical endotoxic properties: end of an era of LPS monopoly?
inferredcites →https://doi.org/10.1186/1297-9716-43-66openalex-snapshot
Mycoplasma haemocanis – the canine hemoplasma and its feline counterpart in the genomic era
inferredcites →https://doi.org/10.1186/1297-9716-44-6openalex-snapshot
Mycoplasma suis infection results endothelial cell damage and activation: new insight into the cell tropism and pathogenicity of hemotrophic mycoplasma
inferredcites →https://doi.org/10.1186/1756-0500-4-195openalex-snapshot
Retrospective survey for sialidase activity in Mycoplasma pneumoniae isolates from cases of community-acquired pneumonia
inferredcites →https://doi.org/10.1186/1756-0500-6-9openalex-snapshot
Animal model of Mycoplasma fermentans respiratory infection
inferredcites →https://doi.org/10.1371/journal.pgen.1003191openalex-snapshot
Comprehensive Methylome Characterization of Mycoplasma genitalium and Mycoplasma pneumoniae at Single-Base Resolution
inferredcites →https://doi.org/10.1371/journal.pone.0007562openalex-snapshot
Analysis of Pulmonary Inflammation and Function in the Mouse and Baboon after Exposure to Mycoplasma pneumoniae CARDS Toxin
inferredcites →https://doi.org/10.1371/journal.pone.0009006openalex-snapshot
Structure and Kinetic Investigation of Streptococcus pyogenes Family GH38 α-Mannosidase
inferredcites →https://doi.org/10.1371/journal.pone.0014797openalex-snapshot
Propionibacterium acnes CAMP Factor and Host Acid Sphingomyelinase Contribute to Bacterial Virulence: Potential Targets for Inflammatory Acne Treatment
inferredcites →https://doi.org/10.1371/journal.pone.0062706openalex-snapshot
Mycoplasma pneumoniae CARDS Toxin Is Internalized via Clathrin-Mediated Endocytosis
inferredcites →https://doi.org/10.1371/journal.pone.0089312openalex-snapshot
Metabolomic Analysis of Three Mollicute Species
inferredcites →https://doi.org/10.1371/journal.pone.0105188openalex-snapshot
Reduction of Hydrogen Peroxide Accumulation and Toxicity by a Catalase from Mycoplasma iowae
inferredcites →https://doi.org/10.1371/journal.pone.0110327openalex-snapshot
Unravelling the Transcriptome Profile of the Swine Respiratory Tract Mycoplasmas
inferredcites →https://doi.org/10.1371/journal.ppat.1002263openalex-snapshot
A Trigger Enzyme in Mycoplasma pneumoniae: Impact of the Glycerophosphodiesterase GlpQ on Virulence and Gene Expression
inferredcites →https://doi.org/10.1378/chest.11-0221openalex-snapshot
Persistence of Community-Acquired Respiratory Distress Syndrome Toxin-Producing Mycoplasma pneumoniae in Refractory Asthma
inferredcites →https://doi.org/10.1637/7806-120106-regr.1openalex-snapshot
Sialidase Activity in Mycoplasma Synoviae
inferredcites →https://doi.org/10.20944/preprints201809.0533.v1openalex-snapshot
Virulence Effectors of Pathogenic Mycoplasmas
inferredcites →https://doi.org/10.2460/ajvr.1972.33.12.2593openalex-snapshot
Detection of Hydrogen Peroxide in Mycoplasma Organisms Frequently Isolated from Domesticated Animals
inferredcites →https://doi.org/10.3109/03009746109165190openalex-snapshot
Mycoplasma Organisms in Synovial Fluid from Rheumatic Joints
inferredcites →https://doi.org/10.3109/rhe1.1961.7.issue-1-4.47openalex-snapshot
Mycoplasma Organisms in Synovial Fluid from Rheumatic Joints
inferredcites →https://doi.org/10.3181/00379727-131-34061openalex-snapshot
The Interrelationship of Virulence, Cytadsorption, and Peroxide Formation in Mycoplasma pneumoniae
inferredcites →https://doi.org/10.3389/fmicb.2010.00113openalex-snapshot
AMPylation: something old is new again
inferredcites →https://doi.org/10.3892/ijmm.3.3.291openalex-snapshot
M161Ag is a potent cytokine inducer with complement activating function (review).
inferredcites →https://doi.org/10.4049/jimmunol.137.5.1581openalex-snapshot
Stimulation of mouse lymphocytes by a mitogen derived from Mycoplasma arthritidis. V. A small basic protein from culture supernatants is a potent T cell mitogen.
inferredcites →https://doi.org/10.4049/jimmunol.162.7.4171openalex-snapshot
Induction and Regulation of Macrophage Metalloelastase by Hyaluronan Fragments in Mouse Macrophages
inferredcites →https://doi.org/10.4049/jimmunol.174.10.6308openalex-snapshot
The Mucosal Adjuvant Macrophage-Activating Lipopeptide-2 Directly Stimulates B Lymphocytes via the TLR2 without the Need of Accessory Cells
inferredcites →https://doi.org/10.7892/boris.22356openalex-snapshot
Beta-D-glucoside utilization by Mycoplasma mycoides subsp. mycoides SC: possible involvement in the control of cytotoxicity towards bovine lung cells
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1080/21505594.2021.1889813openalex-snapshot
Infection strategies of mycoplasmas: Unraveling the panoply of virulence factors
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