scholarly article | Q13442814 |
P2093 | author name string | S D Wright | |
D G Russell | |||
P2860 | cites work | Three distinct antigens associated with human T-lymphocyte-mediated cytolysis: LFA-1, LFA-2, and LFA-3 | Q24628750 |
Adhesion-promoting receptors on human macrophages recognize Escherichia coli by binding to lipopolysaccharide | Q28646196 | ||
The Leishmania receptor for macrophages is a lipid-containing glycoconjugate | Q33930909 | ||
Molecular cloning of the major surface antigen of leishmania | Q34175378 | ||
Arg-Gly-Asp: a versatile cell recognition signal | Q34382464 | ||
C3bi receptor (complement receptor type 3) recognizes a region of complement protein C3 containing the sequence Arg-Gly-Asp | Q34609354 | ||
Monoclonal antibody affinity purification of a Leishmania membrane glycoprotein and its inhibition of leishmania-macrophage binding | Q35584110 | ||
Receptors for C3b and C3bi promote phagocytosis but not the release of toxic oxygen from human phagocytes | Q36348349 | ||
Macrophage complement and lectin-like receptors bind Leishmania in the absence of serum. | Q36350361 | ||
Interferon-gamma depresses binding of ligand by C3b and C3bi receptors on cultured human monocytes, an effect reversed by fibronectin | Q36351807 | ||
Role of the adherence-promoting receptors, CR3, LFA-1, and p150,95, in binding of Histoplasma capsulatum by human macrophages | Q36352376 | ||
Leishmania promastigotes are recognized by the macrophage receptor for advanced glycosylation endproducts | Q36352407 | ||
Macrophage type 3 complement receptors mediate serum-independent binding of Leishmania donovani. Detection of macrophage-derived complement on the parasite surface by immunoelectron microscopy | Q36352962 | ||
Metacyclogenesis is a major determinant of Leishmania promastigote virulence and attenuation | Q37008099 | ||
Identification of the C3bi receptor of human monocytes and macrophages by using monoclonal antibodies | Q37349469 | ||
Leishmania and Trypanosoma surface glycoproteins have a common glycophospholipid membrane anchor | Q37394868 | ||
Variants of the cell recognition site of fibronectin that retain attachment-promoting activity | Q37569976 | ||
The involvement of the major surface glycoprotein (gp63) of Leishmania promastigotes in attachment to macrophages | Q38351081 | ||
Cell surface receptors for extracellular matrix molecules | Q39160059 | ||
Cultivation and in vitro cloning or procyclic culture forms of Trypanosoma brucei in a semi-defined medium. Short communication | Q39295878 | ||
Parasite antigens, their role in protection, diagnosis and escape: the leishmaniases | Q39834819 | ||
Fusion of Host Cell Secondary Lysosomes with the Parasitophorous Vacuoles ofLeishmania mexicana-inlected Macrophages | Q39963493 | ||
Generation of superoxide anion and chemiluminescence by human monocytes during phagocytosis and on contact with surface-bound immunoglobulin G | Q39990763 | ||
Tumor-promoting phorbol esters stimulate C3b and C3b' receptor-mediated phagocytosis in cultured human monocytes | Q42012431 | ||
Production of monoclonal antibodies to group A erythrocytes, HLA and other human cell surface antigens-new tools for genetic analysis | Q42802250 | ||
The major surface protein of Leishmania promastigotes is a fibronectin-like molecule | Q42804658 | ||
Fibronectin receptor of human macrophages recognizes the sequence Arg-Gly-Asp-Ser | Q42937517 | ||
Characterization of a novel differentiation antigen complex recognize by a monoclonal antibody (A-1A5): unique activation-specific molecular forms on stimulated T cells | Q44415393 | ||
The generation of infective stage Leishmania major promastigotes is associated with the cell-surface expression and release of a developmentally regulated glycolipid | Q45221580 | ||
Cell-sized, supported artificial membranes (pseudocytes): response of precursor cytotoxic T lymphocytes to class I MHC proteins. | Q52136216 | ||
Identification of an infective stage of Leishmania promastigotes. | Q52524667 | ||
Identification and purification of membrane and soluble forms of the major surface protein of Leishmania promastigotes. | Q54424461 | ||
The third component of complement (C3) is responsible for the intracellular survival of Leishmania major | Q59096916 | ||
Multiplication of a human parasite (Leishmania donovani) in phagolysosomes of hamster macrophages in vitro | Q67775834 | ||
The mouse macrophage receptor for C3bi (CR3) is a major mechanism in the phagocytosis of Leishmania promastigotes | Q67918535 | ||
Effective immunization against cutaneous leishmaniasis with defined membrane antigens reconstituted into liposomes | Q68091096 | ||
Single-step separation of red blood cells. Granulocytes and mononuclear leukocytes on discontinuous density gradients of Ficoll-Hypaque | Q68821605 | ||
The macrophage-attachment glycoprotein gp63 is the predominant C3-acceptor site on Leishmania mexicana promastigotes | Q68943287 | ||
Structure of the lipid moiety of the Leishmania donovani lipophosphoglycan | Q69139484 | ||
Structure of the major carbohydrate fragment of the Leishmania donovani lipophosphoglycan | Q69464707 | ||
Infectivity of Leishmania braziliensis promastigotes is dependent on the increasing expression of a 65,000-dalton surface antigen | Q69665263 | ||
Evidence that arginyl-glycyl-aspartate peptides and fibrinogen gamma chain peptides share a common binding site on platelets | Q69725156 | ||
p150/95, Third member of the LFA-1/CR3 polypeptide family identified by anti-Leu M5 monoclonal antibody | Q69949918 | ||
Formation of the functional alternative pathway of complement by human monocytes in vitro as demonstrated by phagocytosis of agarose beads | Q70022461 | ||
Modulation of macrophage mannosyl-specific receptors by cultivation on immobilized zymosan. Effects on superoxide-anion release and phagocytosis | Q70153680 | ||
A study of the differential respiratory burst activity elicited by promastigotes and amastigotes of Leishmania donovani in murine resident peritoneal macrophages | Q70646526 | ||
Attachment of plasma membrane vesicles of human macrophages to Leishmania tropica promastigotes | Q71043356 | ||
Leishmania donovani-macrophage binding mediated by surface glycoproteins/antigens: Characterization in vitro by a radioisotopic assay | Q71050409 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 279-292 | |
P577 | publication date | 1988-07-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | Complement receptor type 3 (CR3) binds to an Arg-Gly-Asp-containing region of the major surface glycoprotein, gp63, of Leishmania promastigotes | |
P478 | volume | 168 |
Q37230330 | A comprehensive analysis of LACK (Leishmania homologue of receptors for activated C kinase) in the context of Visceral Leishmaniasis |
Q42637823 | A gp63 based vaccine candidate against Visceral Leishmaniasis |
Q40697853 | A molecular basis for integrin alphaMbeta 2 ligand binding promiscuity |
Q46679368 | Analysis of immune responses in dogs with canine visceral leishmaniasis before, and after, drug treatment. |
Q38749527 | Analysis of the cellular parameters of the immune responses contributing to resistance and susceptibility of mice to infection with the intracellular parasite, Leishmania major |
Q35091251 | Antibodies raised against synthetic peptides from the Arg-Gly-Asp-containing region of the Leishmania surface protein gp63 cross-react with human C3 and interfere with gp63-mediated binding to macrophages. |
Q33607690 | Antigen-coated latex particles as a model system for probing monocyte responses in leprosy |
Q35104130 | Binding of Mycobacterium avium-Mycobacterium intracellulare to human leukocytes. |
Q35545045 | Binding of the 68-kilodalton protein of Mycobacterium avium to alpha(v)beta3 on human monocyte-derived macrophages enhances complement receptor type 3 expression. |
Q68508704 | Biochemical evidence of the antigenic cell surface heterogeneity of Leishmania mexicana |
Q40069852 | Bordetella pertussis adenylate cyclase toxin (ACT) induces cyclooxygenase-2 (COX-2) in murine macrophages and is facilitated by ACT interaction with CD11b/CD18 (Mac-1). |
Q36363899 | Bordetella pertussis filamentous hemagglutinin interacts with a leukocyte signal transduction complex and stimulates bacterial adherence to monocyte CR3 (CD11b/CD18). |
Q28646185 | CR3 (CD11b/CD18) expresses one binding site for Arg-Gly-Asp-containing peptides and a second site for bacterial lipopolysaccharide |
Q40594287 | Cell adhesion molecules in inflammation and immunity: relevance to periodontal diseases |
Q37891077 | Characterization of kinetics and target proteins for binding of human complement component C3 to the surface-exposed outer membrane of Chlamydia trachomatis serovar L2. |
Q30786486 | Cloning and characterization of a gene encoding an immunoglobulin-binding receptor on the cell surface of some members of the family Trypanosomatidae |
Q37055410 | Common themes in microbial pathogenicity |
Q40270382 | Comparison of receptors required for entry of Leishmania major amastigotes into macrophages |
Q39098197 | Complement C3 is required for the progression of cutaneous lesions and neutrophil attraction in Leishmania major infection |
Q37769810 | Complement and periodontitis. |
Q34581686 | Complement component C1q enhances invasion of human mononuclear phagocytes and fibroblasts by Trypanosoma cruzi trypomastigotes |
Q33656648 | Complement receptor type three (CD11b/CD18) of human polymorphonuclear leukocytes recognizes fibrinogen |
Q36002260 | Consequences of microbial attachment: directing host cell functions with adhesins |
Q41300889 | Defence against the immune barrage: helminth survival strategies |
Q43906929 | Delineation of the key amino acids involved in neutrophil inhibitory factor binding to the I-domain supports a mosaic model for the capacity of integrin alphaMbeta 2 to recognize multiple ligands |
Q42696487 | Differences in human macrophage receptor usage, lysosomal fusion kinetics and survival between logarithmic and metacyclic Leishmania infantum chagasi promastigotes |
Q47854421 | Differentially expressed Leishmania major gp63 genes encode cell surface leishmanolysin with distinct signals for glycosylphosphatidylinositol attachment. |
Q34002959 | Episomal expression of specific sense and antisense mRNAs in Leishmania amazonensis: modulation of gp63 level in promastigotes and their infection of macrophages in vitro |
Q38963317 | Expression of LPG and GP63 by different developmental stages of Leishmania major in the sandfly Phlebotomus papatasi |
Q37038952 | Extrachromosomal genetic complementation of surface metalloproteinase (gp63)-deficient Leishmania increases their binding to macrophages |
Q37229935 | FML vaccine against canine visceral leishmaniasis: from second-generation to synthetic vaccine |
Q72104053 | Further Studies on Guinea Pig Z‐1 Antigen That Is Involved in Phagocytosis of Zymosan by Macrophages: Cell Type Distribution of the Antigen and Cross‐Reactivity of Anti‐Z‐1 with Human CR3 |
Q36531011 | Generation of signals activating neutrophil functions by leukocyte integrins: LFA-1 and gp150/95, but not CR3, are able to stimulate the respiratory burst of human neutrophils |
Q71823340 | Identification of a fibronectin-like molecule on Eimeria tenella |
Q36223757 | Identification of an Arg-Gly-Asp (RGD) cell adhesion site in human immunodeficiency virus type 1 transactivation protein, tat |
Q35010045 | Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increase |
Q56449802 | In vitro cytocidal effects on Trypanosoma brucei and inhibition of Leishmania major GP63 by peptidomimetic metalloprotease inhibitors |
Q67662039 | Induction of cell-associated interleukin 1 through stimulation of the adhesion-promoting proteins LFA-1 (CD11a/CD18) and CR3 (CD11b/CD18) of human monocytes |
Q37137144 | Influence of parasite encoded inhibitors of serine peptidases in early infection of macrophages with Leishmania major |
Q38004492 | Innate immune activation and subversion of Mammalian functions by leishmania lipophosphoglycan. |
Q33756963 | Integrin signalling in neutrophils and macrophages |
Q34001707 | Interaction of Leishmania gp63 with cellular receptors for fibronectin |
Q46060080 | Involvement of the GP63 protease in infection of Trichomonas vaginalis |
Q57080131 | Involvement of β1 integrins in the binding and entry ofTrypanosoma cruzi into human macrophages |
Q35823997 | Kistrin, an integrin antagonist, blocks endocytosis of fibrinogen into guinea pig megakaryocyte and platelet alpha-granules |
Q41623601 | Leishmania phagolysosome: drug trafficking and protein sorting across the compartment |
Q36530759 | Leishmania promastigotes require opsonic complement to bind to the human leukocyte integrin Mac-1 (CD11b/CD18) |
Q36726750 | Leishmania vaccines: progress and problems. |
Q35228369 | Leishmaniasis epidemiology: all down to the DNA |
Q37592810 | Leukocyte adhesion molecules deficiency: its structural basis, pathophysiology and implications for modulating the inflammatory response |
Q38296713 | Leukocyte adhesion proteins: their role in neutrophil function. |
Q35377451 | Lipophosphoglycan blocks attachment of Leishmania major amastigotes to macrophages. |
Q38759213 | Mammalian cell adhesion functions and cellular penetration of enteropathogenic Yersinia species |
Q27010243 | Mechanisms of cellular invasion by intracellular parasites |
Q38749505 | Molecular basis of host-parasite relationship: towards the definition of protective antigens |
Q82544502 | Molecular cloning and characterization of cDNA encoding CD11b of cattle |
Q46019384 | Molecular cloning, characterization and gene expression of the full length cDNA encoding the porcine CD11b(αM) and chromosomal localization of the porcine CD11a(αL)-CD11b(αM)-CD11b(αD) gene cluster. |
Q40641469 | Molecular mimicry. |
Q32062538 | Molecular, cellular and functional characterizations of a novel ICAM-like molecule of the immunoglobulin superfamily from Leishmania mexicana amazonensis |
Q38952696 | Monoclonal antibodies that recognize distinct epitopes of the macrophage type three complement receptor differ in their ability to inhibit binding of Leishmania promastigotes harvested at different phases of their growth cycle. |
Q38991040 | More than complementing Tolls: complement-Toll-like receptor synergy and crosstalk in innate immunity and inflammation |
Q67728143 | Mutagenesis of the Arg-Gly-Asp triplet in human complement component C3 does not abolish binding of iC3b to the leukocyte integrin complement receptor type III (CR3, CD11b/CD18) |
Q35732468 | Non-parasite-specific cytokine responses may influence disease outcome following infection. |
Q34007906 | Nonopsonic phagocytosis of zymosan and Mycobacterium kansasii by CR3 (CD11b/CD18) involves distinct molecular determinants and is or is not coupled with NADPH oxidase activation |
Q52657150 | Optimizing Tumor Microenvironment for Cancer Immunotherapy: β-Glucan-Based Nanoparticles. |
Q38936511 | Pathobiology of neutrophil-epithelial interactions |
Q34325331 | Pathogenic trickery: deception of host cell processes |
Q34249094 | Phagocytosis of leprosy bacilli is mediated by complement receptors CR1 and CR3 on human monocytes and complement component C3 in serum |
Q42712047 | Pharmacological Tools to Activate Microglia and their Possible use to Study Neural Network Patho-physiology. |
Q39672031 | Role of beta-D-galactofuranose in Leishmania major macrophage invasion |
Q70229220 | Secondary structure of the promastigote surface protease of Leishmania |
Q28290074 | Strategies of obligate intracellular parasites for evading host defences |
Q44240438 | Studies on the attachment of Leishmania flagella to sand fly midgut epithelium |
Q36985810 | Study of Leishmania major-infected macrophages by use of lipophosphoglycan-specific monoclonal antibodies |
Q37113561 | Subversion of innate immunity by periodontopathic bacteria via exploitation of complement receptor-3 |
Q46161784 | Surface coat remodeling during differentiation of Trypanosoma brucei |
Q28594369 | The Abl and Arg kinases mediate distinct modes of phagocytosis and are required for maximal Leishmania infection |
Q36383058 | The I domain is a major recognition site on the leukocyte integrin Mac-1 (CD11b/CD18) for four distinct adhesion ligands. |
Q40630924 | The Src kinases Hck, Fgr and Lyn activate Arg to facilitate IgG-mediated phagocytosis and Leishmania infection. |
Q33751497 | The alphaMbeta2 integrin and its role in neutrophil function |
Q36351071 | The distinct leukocyte integrins of mouse spleen dendritic cells as identified with new hamster monoclonal antibodies |
Q36356275 | The human mannose-binding protein functions as an opsonin |
Q38318002 | The invasin protein of Yersinia spp. provides co-stimulatory activity to human T cells through interaction with beta 1 integrins |
Q57962408 | The leukocyte integrins |
Q41752302 | The major surface glycoprotein (GP63) is present in both life stages of Leishmania |
Q50054197 | The role of LPD-nanoparticles containing recombinant major surface glycoprotein of Leishmania (rgp63) in protection against leishmaniasis in murine model |
Q37855061 | The role of the type 3 complement receptor in the induced recruitment of myelomonocytic cells to inflammatory sites in the mouse |
Q33688574 | Therapeutic intervention with complement and beta-glucan in cancer |
Q39997561 | Transcriptional inhibition of interleukin-12 promoter activity in Leishmania spp.-infected macrophages |
Q48323102 | Treatment with anti-CR3 antibodies ED7 and ED8 suppresses experimental allergic encephalomyelitis in Lewis rats |
Q37191380 | Trypanosoma cruzi GP63 proteins undergo stage-specific differential posttranslational modification and are important for host cell infection |
Q34351885 | Yersinia enterocolitica invasin: a primary role in the initiation of infection |
Q36045498 | gp63 homologues in Trypanosoma cruzi: surface antigens with metalloprotease activity and a possible role in host cell infection. |
Search more.