scholarly article | Q13442814 |
P2093 | author name string | Fried M | |
Duffy PE | |||
P433 | issue | 5267 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Plasmodium falciparum | Q311383 |
P304 | page(s) | 1502-1504 | |
P577 | publication date | 1996-06-01 | |
P1433 | published in | Science | Q192864 |
P1476 | title | Adherence of Plasmodium falciparum to chondroitin sulfate A in the human placenta | |
P478 | volume | 272 |
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Q49431533 | A brief review on features of falciparum malaria during pregnancy |
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Q36737343 | A model of parity-dependent immunity to placental malaria. |
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Q34425614 | A novel histological grading scheme for placental malaria applied in areas of high and low malaria transmission |
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Q36933288 | A simple protocol for platelet-mediated clumping of Plasmodium falciparum-infected erythrocytes in a resource poor setting |
Q34360455 | A single member of the Plasmodium falciparum var multigene family determines cytoadhesion to the placental receptor chondroitin sulphate A. |
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Q36793324 | Abundance of megalin and Dab2 is reduced in syncytiotrophoblast during placental malaria, which may contribute to low birth weight |
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Q43643657 | An in vitro microassay to assess the ability of Plasmodium falciparum-infected erythrocytes to bind to the human syncytiotrophoblast |
Q33396980 | An upstream open reading frame controls translation of var2csa, a gene implicated in placental malaria |
Q24792921 | Analysis of IgG with specificity for variant surface antigens expressed by placental Plasmodium falciparum isolates |
Q47996636 | Analysis of adhesive domains from the A4VAR Plasmodium falciparum erythrocyte membrane protein-1 identifies a CD36 binding domain |
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Q36718654 | Anti-malarial IgG subclasses pattern and FcγRIIa (CD32) polymorphism among pregnancy-associated malaria in semi-immune Saudi women. |
Q24793948 | Antibodies from malaria-exposed pregnant women recognize trypsin resistant epitopes on the surface of Plasmodium falciparum-infected erythrocytes selected for adhesion to chondroitin sulphate A |
Q36374795 | Antibodies that inhibit Plasmodium falciparum adhesion to chondroitin sulfate A are associated with increased birth weight and the gestational age of newborns |
Q36576445 | Antibodies that inhibit binding of Plasmodium falciparum-infected erythrocytes to chondroitin sulfate A and to the C terminus of merozoite surface protein 1 correlate with reduced placental malaria in Cameroonian women |
Q36804761 | Antibodies to Escherichia coli-expressed C-terminal domains of Plasmodium falciparum variant surface antigen 2-chondroitin sulfate A (VAR2CSA) inhibit binding of CSA-adherent parasites to placental tissue |
Q33822296 | Antibodies to a full-length VAR2CSA immunogen are broadly strain-transcendent but do not cross-inhibit different placental-type parasite isolates |
Q37036128 | Antibodies to variant surface antigens of Plasmodium falciparum-infected erythrocytes and adhesion inhibitory antibodies are associated with placental malaria and have overlapping and distinct targets |
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Q24672872 | Antigenic variation in Plasmodium falciparum: gene organization and regulation of the var multigene family |
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Q36437968 | Chondroitin-4-sulfate impairs in vitro and in vivo cytoadherence of Plasmodium falciparum infected erythrocytes. |
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Q47831862 | Inflammatory reactions in placental blood of Plasmodium falciparum-infected women and high concentrations of soluble E-selectin and a circulating P. falciparum protein in the cord sera |
Q37201119 | Influence of human chorionic gonadotropin (hCG) on in vitro growth of Plasmodium falciparum |
Q34973764 | Inhibition of Plasmodium falciparum growth in vitro and adhesion to chondroitin-4-sulfate by the heparan sulfate mimetic PI-88 and other sulfated oligosaccharides. |
Q34005689 | Inhibition of adhesion of Plasmodium falciparum-infected erythrocytes by structurally defined hyaluronic acid dodecasaccharides |
Q33756774 | Inhibition of binding of malaria-infected erythrocytes by a tetradecasaccharide fraction from chondroitin sulfate A |
Q33883564 | Inhibition of chondroitin-4-sulfate-specific adhesion of Plasmodium falciparum-infected erythrocytes by sulfated polysaccharides |
Q35913659 | Inhibition of dendritic cell maturation by malaria is dose dependent and does not require Plasmodium falciparum erythrocyte membrane protein 1 |
Q33721891 | Insight into antigenic diversity of VAR2CSA-DBL5ε domain from multiple Plasmodium falciparum placental isolates |
Q57784964 | Integrated proteomics reveals apoptosis-related mechanisms associated with placental malaria |
Q39794107 | Intercellular adhesion molecule-1 and CD36 synergize to mediate adherence of Plasmodium falciparum-infected erythrocytes to cultured human microvascular endothelial cells |
Q47151593 | Interleukin-10 and soluble tumor necrosis factor receptor II are potential biomarkers of Plasmodium falciparum infections in pregnant women: a case-control study from Nanoro, Burkina Faso |
Q37521618 | Intermittent preventive sulfadoxine-pyrimethamine treatment of primigravidae reduces levels of plasma immunoglobulin G, which protects against pregnancy-associated Plasmodium falciparum malaria |
Q35652102 | Intermittent preventive treatment for malaria in pregnancy in Africa: what's new, what's needed? |
Q28486791 | Intermittent preventive treatment in pregnant women is associated with increased risk of severe malaria in their offspring |
Q35452357 | Intermittent treatment to prevent pregnancy malaria does not confer benefit in an area of widespread drug resistance |
Q27336415 | Intravital placenta imaging reveals microcirculatory dynamics impact on sequestration and phagocytosis of Plasmodium-infected erythrocytes |
Q26799717 | Investigating the Pathogenesis of Severe Malaria: A Multidisciplinary and Cross-Geographical Approach |
Q33900642 | Investigating the host binding signature on the Plasmodium falciparum PfEMP1 protein family |
Q33828414 | Iron overload in Plasmodium berghei-infected placenta as a pathogenesis mechanism of fetal death |
Q35677598 | Is chloroquine chemoprophylaxis still effective to prevent low birth weight? Results of a study in Benin |
Q35106301 | Lack of gender-specific antibody recognition of products from domains of a var gene implicated in pregnancy-associated Plasmodium falciparum malaria |
Q36510147 | Large screen approaches to identify novel malaria vaccine candidates |
Q34601747 | Levels of plasma immunoglobulin G with specificity against the cysteine-rich interdomain regions of a semiconserved Plasmodium falciparum erythrocyte membrane protein 1, VAR4, predict protection against malarial anemia and febrile episodes |
Q35541393 | Limited response of NK92 cells to Plasmodium falciparum-infected erythrocytes |
Q37734391 | Llama immunization with full-length VAR2CSA generates cross-reactive and inhibitory single-domain antibodies against the DBL1X domain |
Q34239984 | Longitudinal studies of Plasmodium falciparum malaria in pregnant women living in a rural Cameroonian village with high perennial transmission |
Q28080325 | Malaria Parasites: The Great Escape |
Q35678578 | Malaria and immunity during pregnancy and postpartum: a tale of two species |
Q35751895 | Malaria burden in pregnancy at mulago national referral hospital in kampala, Uganda |
Q37287631 | Malaria diagnostics in clinical trials |
Q36284603 | Malaria during Pregnancy |
Q37488243 | Malaria evolution in South Asia: knowledge for control and elimination |
Q33821137 | Malaria immunity in man and mosquito: insights into unsolved mysteries of a deadly infectious disease |
Q81266084 | Malaria in pregnancy |
Q47899839 | Malaria in pregnancy in rural Mozambique: the role of parity, submicroscopic and multiple Plasmodium falciparum infections |
Q36717621 | Malaria in pregnancy: pathogenesis and immunity |
Q36717642 | Malaria in pregnancy: priorities for research |
Q41990397 | Malaria in pregnancy: the relevance of animal models for vaccine development. |
Q47896646 | Malaria invades Yorkshire |
Q34999453 | Malaria pathogenesis: a jigsaw with an increasing number of pieces |
Q37333056 | Malaria's deadly grip: cytoadhesion of Plasmodium falciparum-infected erythrocytes |
Q47827320 | Malaria--variety is the price of life. |
Q92308280 | Malaria-Associated Factors among Pregnant Women in Guinea |
Q27485634 | Malaria: progress, perils, and prospects for eradication |
Q28661352 | Malarial parasite diversity in chimpanzees: the value of comparative approaches to ascertain the evolution of Plasmodium falciparum antigens |
Q48022331 | Matched Placental and Circulating Plasmodium falciparum Parasites are Genetically Homologous at the var2csa ID1-DBL2X Locus by Deep Sequencing |
Q38741552 | Maternal Microchimerism Predicts Increased Infection but Decreased Disease due to Plasmodium falciparum During Early Childhood |
Q24814453 | Maternal malaria and gravidity interact to modify infant susceptibility to malaria |
Q36492379 | Maternal peripheral blood level of IL-10 as a marker for inflammatory placental malaria |
Q64985715 | Maternal-Fetal Conflict During Infection: Lessons From a Mouse Model of Placental Malaria. |
Q61716953 | Maternally derived antibodies to Schizont Egress Antigen-1 and protection of infants from severe malaria |
Q35533138 | Microbial adherence to and invasion through proteoglycans |
Q37255276 | Microfluidic approaches to malaria pathogenesis |
Q27319921 | Microfluidic modeling of cell-cell interactions in malaria pathogenesis |
Q28071399 | Modeling cytoadhesion of Plasmodium falciparum-infected erythrocytes and leukocytes-common principles and distinctive features |
Q37702795 | Modulation of dendritic cell responses by parasites: a common strategy to survive |
Q64076612 | Molecular Principles of Intrauterine Growth Restriction in Plasmodium Falciparum Infection |
Q35868719 | Molecular aspects of Plasmodium falciparum Infection during pregnancy |
Q24550715 | Molecular aspects of severe malaria |
Q41739876 | Molecular basis for evasion of host immunity and pathogenesis in malaria |
Q34098784 | Molecular basis for the dichotomy in Plasmodium falciparum adhesion to CD36 and chondroitin sulfate A |
Q34279841 | Molecular basis of severe malaria |
Q28139047 | Molecular cloning and expression of chondroitin 4-sulfotransferase |
Q34190504 | Molecular mechanisms of Plasmodium falciparum placental adhesion. |
Q37018621 | Monitoring and evaluation of malaria in pregnancy - developing a rational basis for control |
Q47838974 | Motherhood and malaria |
Q36558721 | Multilaboratory approach to preclinical evaluation of vaccine immunogens for placental malaria |
Q39571758 | Multiple adhesive phenotypes linked to rosetting binding of erythrocytes in Plasmodium falciparum malaria |
Q40120062 | Multiplexing detection of IgG against Plasmodium falciparum pregnancy-specific antigens |
Q37002285 | Murine Model for Preclinical Studies of Var2CSA-Mediated Pathology Associated with Malaria in Pregnancy |
Q34602096 | Murine malaria infection induces fetal loss associated with accumulation of Plasmodium chabaudi AS-infected erythrocytes in the placenta |
Q37546441 | MyD88 signaling is directly involved in the development of murine placental malaria |
Q24535094 | N-linked oligosaccharides are required to produce and stabilize the active form of chondroitin 4-sulphotransferase-1 |
Q37689434 | NK Cells: Uncertain Allies against Malaria |
Q34614540 | NSR-seq transcriptional profiling enables identification of a gene signature of Plasmodium falciparum parasites infecting children |
Q35124285 | Natural hemozoin stimulates syncytiotrophoblast to secrete chemokines and recruit peripheral blood mononuclear cells |
Q36936271 | Natural selection of FLT1 alleles and their association with malaria resistance in utero |
Q34194564 | Neonatal and maternal immunological responses to conserved epitopes within the DBL-gamma3 chondroitin sulfate A-binding domain of Plasmodium falciparum erythrocyte membrane protein 1. |
Q36980850 | New approaches to pathogenesis of malaria in pregnancy. |
Q36330969 | New insights into acquisition, boosting, and longevity of immunity to malaria in pregnant women |
Q38353755 | New tools to identify var sequence tags and clone full-length genes using type-specific primers to Duffy binding-like domains |
Q35025223 | Nonimmune immunoglobulin binding and multiple adhesion characterize Plasmodium falciparum-infected erythrocytes of placental origin |
Q35165595 | Nonspecific immunoglobulin M binding and chondroitin sulfate A binding are linked phenotypes of Plasmodium falciparum isolates implicated in malaria during pregnancy |
Q34881813 | Novel Plasmodium falciparum malaria vaccines: evidence-based searching for variant surface antigens as candidates for vaccination against pregnancy-associated malaria |
Q36073865 | Nrf2-driven CD36 and HO-1 gene expression in circulating monocytes correlates with favourable clinical outcome in pregnancy-associated malaria |
Q37470684 | Oncofetal Chondroitin Sulfate Glycosaminoglycans Are Key Players in Integrin Signaling and Tumor Cell Motility. |
Q37271796 | Optimizing expression of the pregnancy malaria vaccine candidate, VAR2CSA in Pichia pastoris |
Q36640619 | Overproduction, purification and crystallization of a chondroitin sulfate A-binding DBL domain from a Plasmodium falciparum var2csa-encoded PfEMP1 protein |
Q89595553 | PRIMVAC vaccine adjuvanted with Alhydrogel or GLA-SE to prevent placental malaria: a first-in-human, randomised, double-blind, placebo-controlled study |
Q60947070 | Parasite Recognition and Signaling Mechanisms in Innate Immune Responses to Malaria |
Q34292107 | Parasite adhesion and immune evasion in placental malaria. |
Q38182100 | Parasite dissemination and the pathogenesis of toxoplasmosis |
Q47727463 | Parasites and pregnancy |
Q35692279 | Parasitologic Assessment of Two-Dose and Monthly Intermittent Preventive Treatment of Malaria during Pregnancy with Sulphadoxine-Pyrimethamine (IPTP-SP) in Lagos, Nigeria |
Q34740303 | Parity and placental infection affect antibody responses against Plasmodium falciparum during pregnancy |
Q35609294 | Parity-dependent recognition of DBL1X-3X suggests an important role of the VAR2CSA high-affinity CSA-binding region in the development of the humoral response against placental malaria |
Q35693520 | Pathogens and the placental fortress |
Q35637028 | Performance of a histidine-rich protein 2 rapid diagnostic test, Paracheck Pf®, for detection of malaria infections in Ugandan pregnant women |
Q38282573 | Perioperative considerations of the patient with malaria |
Q34484783 | Persistence of Plasmodium falciparum parasites in infected pregnant Mozambican women after delivery |
Q43179011 | Phenotypes of Plasmodium falciparum from the peripheral blood of pregnant women |
Q92632114 | Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA |
Q35025427 | Physical linkage to drug resistance genes results in conservation of var genes among West Pacific Plasmodium falciparum isolates |
Q55354236 | Placenta-specific drug delivery by trophoblast-targeted nanoparticles in mice. |
Q27973758 | Placental Sequestration of Plasmodium falciparum Malaria Parasites Is Mediated by the Interaction Between VAR2CSA and Chondroitin Sulfate A on Syndecan-1 |
Q44424266 | Placental malaria and the relationship to pregnancy outcome at Gushegu District Hospital, Northern Ghana |
Q33716582 | Placental malaria diminishes development of antibody responses to Plasmodium falciparum epitopes in infants residing in an area of western Kenya where P. falciparum is endemic |
Q34034060 | Placental malaria induces variant-specific antibodies of the cytophilic subtypes immunoglobulin G1 (IgG1) and IgG3 that correlate with adhesion inhibitory activity |
Q33738991 | Placental malaria is associated with reduced early life weight development of affected children independent of low birth weight |
Q91996104 | Placental malaria vaccine candidate antigen VAR2CSA displays atypical domain architecture in some Plasmodium falciparum strains |
Q42483373 | Placental pathology in malaria: a histological, immunohistochemical, and quantitative study |
Q33526296 | Plasma levels of apolipoprotein A1 in malaria-exposed primigravidae are associated with severe anemia |
Q92528198 | Plasmodium asexual growth and sexual development in the haematopoietic niche of the host |
Q35812804 | Plasmodium chabaudi AS induces pregnancy loss in association with systemic pro-inflammatory immune responses in A/J and C57BL/6 mice |
Q35206903 | Plasmodium falciparum adhesion in the placenta |
Q36555167 | Plasmodium falciparum domain mediating adhesion to chondroitin sulfate A: a receptor for human placental infection. |
Q36980841 | Plasmodium falciparum during pregnancy: a puzzling parasite tissue adhesion tropism |
Q33700519 | Plasmodium falciparum erythrocyte membrane protein 1 diversity in seven genomes--divide and conquer |
Q34853037 | Plasmodium falciparum expressing domain cassette 5 type PfEMP1 (DC5-PfEMP1) bind PECAM1. |
Q91722797 | Plasmodium falciparum infection dysregulates placental autophagy |
Q43924333 | Plasmodium falciparum infection early in pregnancy has profound consequences for foetal growth |
Q47675155 | Plasmodium falciparum infection of the placenta affects newborn immune responses |
Q30940547 | Plasmodium falciparum infection significantly impairs placental cytokine profile in HIV infected Cameroonian women |
Q37036123 | Plasmodium falciparum isolates from infected pregnant women and children are associated with distinct adhesive and antigenic properties |
Q34602087 | Plasmodium falciparum parasites expressing pregnancy-specific variant surface antigens adhere strongly to the choriocarcinoma cell line BeWo |
Q46949604 | Plasmodium falciparum persists in the placenta after three days' treatment with quinine |
Q37464100 | Plasmodium falciparum picks (on) EPCR. |
Q33946646 | Plasmodium falciparum population dynamics in a cohort of pregnant women in Senegal |
Q30042320 | Plasmodium falciparum proteins involved in cytoadherence of infected erythrocytes to chemokine CX3CL1 |
Q34003113 | Plasmodium falciparum rosette formation is uncommon in isolates from pregnant women |
Q33325481 | Plasmodium falciparum transcriptome analysis reveals pregnancy malaria associated gene expression |
Q33301011 | Plasmodium falciparum uses gC1qR/HABP1/p32 as a receptor to bind to vascular endothelium and for platelet-mediated clumping. |
Q41676911 | Plasmodium falciparum-infected erythrocyte adhesion to the type 3 repeat domain of thrombospondin-1 is mediated by a modified band 3 protein |
Q35098438 | Plasmodium falciparum-infected erythrocytes adhere both in the intervillous space and on the villous surface of human placenta by binding to the low-sulfated chondroitin sulfate proteoglycan receptor |
Q37354879 | Plasmodium falciparum: Assessment of parasite-infected red blood cell binding to placental chondroitin proteoglycan and bovine tracheal chondroitin sulfate A. |
Q47905916 | Plasmodium falciparum: PCR detection and genotyping of isolates from peripheral, placental, and cord blood of pregnant Malawian women and their infants |
Q61332555 | Plasmodium falciparum: Pathogenesis, polymorphism and the infected red cell surface |
Q38861772 | Plasmodium falciparum: analysis of transcribed var gene sequences in natural isolates from the Brazilian Amazon region |
Q36980846 | Plasmodium in the placenta: parasites, parity, protection, prevention and possibly preeclampsia |
Q37188081 | Plasmodium in the postgenomic era: new insights into the molecular cell biology of malaria parasites. |
Q36155071 | Plasmodium vivax VIR Proteins Are Targets of Naturally-Acquired Antibody and T Cell Immune Responses to Malaria in Pregnant Women |
Q31056451 | Plasmodium vivax adherence to placental glycosaminoglycans |
Q77157550 | Plasmodium-falciparum-infected erythrocytes adhere to immortalized human bone marrow endothelial cells |
Q34105789 | Platelet-mediated clumping of Plasmodium falciparum-infected erythrocytes is a common adhesive phenotype and is associated with severe malaria |
Q33908405 | Platelets alter gene expression profile in human brain endothelial cells in an in vitro model of cerebral malaria |
Q34988334 | Positive selection of Plasmodium falciparum parasites with multiple var2csa-type PfEMP1 genes during the course of infection in pregnant women |
Q38691920 | Pre-clinical and clinical development of the first placental malaria vaccine |
Q26827604 | Pregnancy and infection |
Q27005799 | Pregnancy and susceptibility to infectious diseases |
Q33319580 | Pregnancy outcome and placenta pathology in Plasmodium berghei ANKA infected mice reproduce the pathogenesis of severe malaria in pregnant women |
Q33963392 | Pregnancy-associated malaria and malaria in infants: an old problem with present consequences |
Q36399361 | Pregnancy-associated malaria and the prospects for syndrome-specific antimalaria vaccines |
Q92666131 | Pregnancy-specific malarial immunity and risk of malaria in pregnancy and adverse birth outcomes: a systematic review |
Q34993578 | Pregnant women are a reservoir of malaria transmission in Blantyre, Malawi |
Q37172842 | Prevalence and risk of Plasmodium falciparum and P. vivax malaria among pregnant women living in the hypoendemic communities of the Peruvian Amazon |
Q36088608 | Prevalence of Malaria and Anemia among Pregnant Women Attending a Traditional Birth Home in Benin City, Nigeria |
Q44270197 | Prevalence, risk factors and effects of placental malaria in the UMTH, Maiduguri, North-eastern, Nigeria: a cross-sectional study |
Q35738477 | Prospects and Pitfalls of Pregnancy-Associated Malaria Vaccination Based on the Natural Immune Response to Plasmodium falciparum VAR2CSA-Expressing Parasites |
Q36253322 | Proteoglycans in host-pathogen interactions: molecular mechanisms and therapeutic implications |
Q58831352 | Purification and characterization of fetal bovine serum beta-N-acetyl-D-galactosaminyltransferase and beta-D-glucuronyltransferase involved in chondroitin sulfate biosynthesis |
Q92523390 | Quantification of malaria antigens PfHRP2 and pLDH by quantitative suspension array technology in whole blood, dried blood spot and plasma |
Q44825165 | Quantitative computer image analysis of chondroitin sulfate A expression in placentas infected with Plasmodium falciparum |
Q33769097 | Rapid acquisition of isolate-specific antibodies to chondroitin sulfate A-adherent plasmodium falciparum isolates in Ghanaian primigravidae |
Q97070164 | Rapid activation of distinct members of multigene families in Plasmodium spp |
Q30381400 | Real-time measurement of Plasmodium falciparum-infected erythrocyte cytoadhesion with a quartz crystal microbalance. |
Q56355140 | Recent advances in the molecular epidemiology of clinical malaria |
Q40859266 | Recombinant human thrombomodulin(csa+): a tool for analyzing Plasmodium falciparum adhesion to chondroitin-4-sulfate |
Q33450639 | Recrudescent Plasmodium berghei from pregnant mice displays enhanced binding to the placenta and induces protection in multigravida |
Q35679569 | Reduced CD36-dependent tissue sequestration of Plasmodium-infected erythrocytes is detrimental to malaria parasite growth in vivo |
Q33990390 | Reduced prevalence of placental malaria in primiparae with blood group O |
Q34633270 | Reduced risk for placental malaria in iron deficient women |
Q37248735 | Regulatory T cells and the immune pathogenesis of prenatal infection |
Q37116542 | Relationship between human immunodeficiency virus type 1 coinfection, anemia, and levels and function of antibodies to variant surface antigens in pregnancy-associated malaria |
Q33952181 | Relevant assay to study the adhesion of Plasmodium falciparum-infected erythrocytes to the placental epithelium |
Q36284299 | Reliability of rapid diagnostic tests in diagnosing pregnancy-associated malaria in north-eastern Tanzania. |
Q36713881 | Role of chondroitin-4-sulfate in pregnancy-associated malaria |
Q46453882 | Rosetting in Plasmodium falciparum: a cytoadherence phenotype with multiple actors |
Q34675111 | Rosetting in Plasmodium vivax: a cytoadhesion phenotype associated with anaemia |
Q92910897 | Rosetting revisited: a critical look at the evidence for host erythrocyte receptors in Plasmodium falciparum rosetting |
Q33835894 | Safety and benefits of antenatal oral iron supplementation in low-income countries: a review |
Q89619474 | Screening and surveillance of multiple solid tumours using plasma placental-like chondroitin sulfate A (pl-CSA) |
Q34132871 | Selective accumulation of mature asexual stages of Plasmodium falciparum-infected erythrocytes in the placenta |
Q34162904 | Sequence polymorphism, segmental recombination and toggling amino acid residues within the DBL3X domain of the VAR2CSA placental malaria antigen |
Q29396069 | Sequestration and Tissue Accumulation of Human Malaria Parasites: Can We Learn Anything from Rodent Models of Malaria? |
Q35666823 | Sequestration: causes and consequences |
Q29614923 | Severe falciparum malaria. World Health Organization, Communicable Diseases Cluster |
Q36574313 | Shared themes of antigenic variation and virulence in bacterial, protozoal, and fungal infections. |
Q34111618 | Short-chain aliphatic polysulfonates inhibit the entry of Plasmodium into red blood cells |
Q44148115 | Short-range attractiveness of pregnant women to Anopheles gambiae mosquitoes |
Q37442983 | Simultaneous transcription of duplicated var2csa gene copies in individual Plasmodium falciparum parasites |
Q36097316 | Six genes are preferentially transcribed by the circulating and sequestered forms of Plasmodium falciparum parasites that infect pregnant women |
Q37721429 | Small variant surface antigens and Plasmodium evasion of immunity |
Q34221892 | Specific antibody responses against membrane proteins of erythrocytes infected by Plasmodium falciparum of individuals briefly exposed to malaria |
Q33842019 | Specific receptor usage in Plasmodium falciparum cytoadherence is associated with disease outcome |
Q91971710 | Sticking for a Cause: The Falciparum Malaria Parasites Cytoadherence Paradigm |
Q47857297 | Sticky sugars attract malaria to the fetus |
Q33691325 | Strain-transcendent immune response to recombinant Var2CSA DBL5-ε domain block P. falciparum adhesion to placenta-derived BeWo cells under flow conditions |
Q93006668 | Stringent Selection of Knobby Plasmodium falciparum-Infected Erythrocytes during Cytoadhesion at Febrile Temperature |
Q27657099 | Structural Comparison of Two CSPG-Binding DBL Domains from the VAR2CSA Protein Important in Malaria during Pregnancy |
Q36078717 | Structural and functional insight into how the Plasmodium falciparum VAR2CSA protein mediates binding to chondroitin sulfate A in placental malaria. |
Q38300914 | Structural basis for binding of Plasmodium falciparum erythrocyte membrane protein 1 to chondroitin sulfate and placental tissue and the influence of protein polymorphisms on binding specificity |
Q38307897 | Structural basis for the adherence of Plasmodium falciparum-infected erythrocytes to chondroitin 4-sulfate and design of novel photoactivable reagents for the identification of parasite adhesive proteins |
Q33320197 | Structural insight into epitopes in the pregnancy-associated malaria protein VAR2CSA |
Q37791592 | Structural insights into chondroitin sulfate binding in pregnancy-associated malaria |
Q47871941 | Structural requirements for the adherence of Plasmodium falciparum-infected erythrocytes to chondroitin sulfate proteoglycans of human placenta |
Q36139430 | Structure of the DBL3X-DBL4ε region of the VAR2CSA placental malaria vaccine candidate: insight into DBL domain interactions |
Q27653526 | Structure of the DBL3x domain of pregnancy-associated malaria protein VAR2CSA complexed with chondroitin sulfate A |
Q34674872 | Structure-function-immunogenicity studies of PfEMP1 domain DBL2βPF11_0521, a malaria parasite ligand for ICAM-1. |
Q24804747 | Sub-grouping of Plasmodium falciparum 3D7 var genes based on sequence analysis of coding and non-coding regions |
Q39257195 | Submicroscopic Plasmodium falciparum infections in pregnancy in Ghana |
Q37678948 | Submicroscopic infection of placenta by Plasmodium produces Th1/Th2 cytokine imbalance, inflammation and hypoxia in women from north-west Colombia |
Q50047198 | Submicroscopic placental infection by non-falciparum Plasmodium spp |
Q34944523 | Sulfotransferases and sulfated oligosaccharides |
Q34161839 | Surface antigens of Plasmodium falciparum-infected erythrocytes as immune targets and malaria vaccine candidates |
Q36261056 | Syncytiotrophoblast Functions and Fetal Growth Restriction during Placental Malaria: Updates and Implication for Future Interventions |
Q50094534 | Targeted delivery of doxorubicin by CSA-binding nanoparticles for choriocarcinoma treatment. |
Q30042328 | Targeted disruption of a ring-infected erythrocyte surface antigen (RESA)-like export protein gene in Plasmodium falciparum confers stable chondroitin 4-sulfate cytoadherence capacity |
Q36683860 | Targeting Human Cancer by a Glycosaminoglycan Binding Malaria Protein |
Q47389892 | Targeting a DBL3gamma domain of the Plasmodium falciparum erythrocyte membrane protein 1 to the surface of Saccharomyces cerevisiae. |
Q34482493 | Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony |
Q47926260 | The 3D7var5.2 (var COMMON) type var gene family is commonly expressed in non-placental Plasmodium falciparum malaria |
Q36888570 | The Cryptosporidium parvum C-Type Lectin CpClec Mediates Infection of Intestinal Epithelial Cells via Interactions with Sulfated Proteoglycans |
Q34461507 | The Malaria in Pregnancy Library: a bibliometric review. |
Q60305299 | The Rough Guide to Monocytes in Malaria Infection |
Q27650818 | The Structure of a Chondroitin Sulfate-binding Domain Important in Placental Malaria |
Q36339851 | The adhesion of Plasmodium falciparum-infected erythrocytes to chondroitin sulfate A is mediated by P. falciparum erythrocyte membrane protein 1. |
Q39698908 | The case for PfEMP1-based vaccines to protect pregnant women against Plasmodium falciparum malaria |
Q34170375 | The chondroitin sulfate A-binding site of the VAR2CSA protein involves multiple N-terminal domains |
Q35033540 | The conserved clag multigene family of malaria parasites: essential roles in host-pathogen interaction |
Q33578805 | The effect of malaria and intestinal helminth coinfection on birth outcomes in Kumasi, Ghana |
Q47923663 | The effect of placental malaria infection on cord blood and maternal immunoregulatory responses at birth |
Q80393538 | The effect of substitution of the N-acetyl groups of N-acetylgalactosamine residues in chondroitin sulfate on its degradation by chondroitinase ABC |
Q35162525 | The epidemiology and consequences of maternal malaria: a review of immunological basis |
Q38666558 | The immunological balance between host and parasite in malaria |
Q41918908 | The impact of insecticide-treated bednets on malaria and anaemia in pregnancy in Kassena-Nankana district, Ghana: a randomized controlled trial |
Q24644343 | The impact of malaria parasitism: from corpuscles to communities |
Q26799240 | The influence of host genetics on erythrocytes and malaria infection: is there therapeutic potential? |
Q43708209 | The low sulfated chondroitin sulfate proteoglycans of human placenta have sulfate group-clustered domains that can efficiently bind Plasmodium falciparum-infected erythrocytes |
Q34470655 | The malaria-infected red blood cell: structural and functional changes |
Q29615020 | The pathogenic basis of malaria |
Q58732770 | The prevalence of submicroscopic Plasmodium falciparum gametocyte carriage and multiplicity of infection in children, pregnant women and adults in a low malaria transmission area in Southern Ghana |
Q26862567 | The role of PfEMP1 adhesion domain classification in Plasmodium falciparum pathogenesis research |
Q33849067 | The role of Plasmodium falciparum var genes in malaria in pregnancy. |
Q34541105 | The structural basis for CD36 binding by the malaria parasite |
Q38290142 | The structural motif in chondroitin sulfate for adhesion of Plasmodium falciparum-infected erythrocytes comprises disaccharide units of 4-O-sulfated and non-sulfated N-acetylgalactosamine linked to glucuronic acid |
Q74235566 | The surface antigen SAG3 mediates the attachment of Toxoplasma gondii to cell-surface proteoglycans |
Q37909178 | Thrombomodulin and its role in inflammation. |
Q33619319 | Towards the rational design of a candidate vaccine against pregnancy associated malaria: conserved sequences of the DBL6epsilon domain of VAR2CSA. |
Q34975870 | Transcribed var genes associated with placental malaria in Malawian women. |
Q30828703 | Transcription of multiple var genes by individual, trophozoite-stage Plasmodium falciparum cells expressing a chondroitin sulphate A binding phenotype |
Q35838605 | Transcription of var genes other than var2csa in Plasmodium falciparum parasites infecting Mozambican pregnant women |
Q39546704 | Treating malaria in pregnancy in developing countries: priorities in clinical research and drug development |
Q48036116 | Treatment and prevention of malaria in pregnancy: opportunities and challenges. |
Q38287355 | Two DBLgamma subtypes are commonly expressed by placental isolates of Plasmodium falciparum |
Q37554737 | Usefulness of a biomarker to identify placental dysfunction in the context of malaria |
Q40670564 | VAR2CSA Domain-Specific Analysis of Naturally Acquired Functional Antibodies to Plasmodium falciparum Placental Malaria |
Q90186732 | VAR2CSA Serology to Detect Plasmodium falciparum Transmission Patterns in Pregnancy |
Q34706475 | VAR2CSA and protective immunity against pregnancy-associated Plasmodium falciparum malaria. |
Q46608178 | VAR2CSA domains expressed in Escherichia coli induce cross-reactive antibodies to native protein |
Q34921119 | VAR2CSA signatures of high Plasmodium falciparum parasitemia in the placenta |
Q37742181 | Var gene expression and human Plasmodium pathogenesis |
Q36478198 | Var transcription profiling of Plasmodium falciparum 3D7: assignment of cytoadherent phenotypes to dominant transcripts |
Q36891434 | Var2CSA DBL6-epsilon domain expressed in HEK293 induces limited cross-reactive and blocking antibodies to CSA binding parasites. |
Q28744428 | Var2CSA minimal CSA binding region is located within the N-terminal region |
Q37285731 | Variable var transition rates underlie antigenic variation in malaria |
Q27972539 | Variant antigens of Plasmodium falciparum encoded by the var multigenic family are multifunctional macromolecules |
Q47232540 | Variant surface antigen-specific IgG and protection against clinical consequences of pregnancy-associated Plasmodium falciparum malaria |
Q39365658 | Variant surface antigens of Plasmodium falciparum and their roles in severe malaria |
Q37191299 | Variant-specific immunity to Plasmodium berghei in pregnant mice |
Q33879876 | Virulence of malaria is associated with differential expression of Plasmodium falciparum var gene subgroups in a case-control study |
Q37246673 | What really happens to dendritic cells during malaria? |
Q44168891 | Wheat germ cell-free technology for accelerating the malaria vaccine research |
Q37426820 | World Malaria Day 2009: what malaria knows about the immune system that immunologists still do not. |
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