| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Elizabeth D English | Q57061306 |
| P2093 | author name string | J P Boyle | |
| Y Adomako-Ankomah | |||
| P2860 | cites work | Comparative genomics of the apicomplexan parasites Toxoplasma gondii and Neospora caninum: Coccidia differing in host range and transmission strategy | Q21090491 |
| Determinants of GBP recruitment to Toxoplasma gondii vacuoles and the parasitic factors that control it | Q27321401 | ||
| The polymorphic pseudokinase ROP5 controls virulence in Toxoplasma gondii by regulating the active kinase ROP18 | Q27341809 | ||
| A Conserved Non-canonical Motif in the Pseudoactive Site of the ROP5 Pseudokinase Domain Mediates Its Effect on Toxoplasma Virulence | Q27670588 | ||
| Phosphorylation of mouse immunity-related GTPase (IRG) resistance proteins is an evasion strategy for virulent Toxoplasma gondii | Q28476607 | ||
| A Toxoplasma gondii pseudokinase inhibits host IRG resistance proteins | Q28481222 | ||
| Fatal outbreak of human toxoplasmosis along the Maroni River: epidemiological, clinical, and parasitological aspects | Q29353941 | ||
| Globalization and the population structure of Toxoplasma gondii | Q30355588 | ||
| Redescription of Neospora caninum and its differentiation from related coccidia. | Q31084246 | ||
| Redescription of Hammondia hammondi and its differentiation from Toxoplasma gondii | Q33194144 | ||
| The opportunistic pathogen Toxoplasma gondii deploys a diverse legion of invasion and survival proteins | Q33218406 | ||
| ROP18 is a rhoptry kinase controlling the intracellular proliferation of Toxoplasma gondii | Q33274196 | ||
| A single polymorphic amino acid on Toxoplasma gondii kinase ROP16 determines the direct and strain-specific activation of Stat3. | Q33591077 | ||
| GRA25 is a novel virulence factor of Toxoplasma gondii and influences the host immune response | Q33602978 | ||
| Communication between Toxoplasma gondii and its host: impact on parasite growth, development, immune evasion, and virulence | Q33606893 | ||
| Efficient gene disruption in diverse strains of Toxoplasma gondii using CRISPR/CAS9. | Q33648073 | ||
| ROP18 is a key factor responsible for virulence difference between Toxoplasma gondii and Neospora caninum | Q33753887 | ||
| The Toxoplasma pseudokinase ROP5 forms complexes with ROP18 and ROP17 kinases that synergize to control acute virulence in mice | Q33861156 | ||
| Generation of a restriction fragment length polymorphism linkage map for Toxoplasma gondii | Q33960170 | ||
| In the absence of endogenous gamma interferon, mice acutely infected with Neospora caninum succumb to a lethal immune response characterized by inactivation of peritoneal macrophages | Q33999302 | ||
| Toxoplasma gondii rhoptry kinase ROP16 activates STAT3 and STAT6 resulting in cytokine inhibition and arginase-1-dependent growth control | Q34023014 | ||
| Lytic cycle of Toxoplasma gondii | Q34023676 | ||
| Strain-dependent host transcriptional responses to Toxoplasma infection are largely conserved in mammalian and avian hosts | Q34056304 | ||
| Toxoplasma rhoptry protein 16 (ROP16) subverts host function by direct tyrosine phosphorylation of STAT6. | Q34121309 | ||
| Infected dendritic cells facilitate systemic dissemination and transplacental passage of the obligate intracellular parasite Neospora caninum in mice | Q34189342 | ||
| Importance of nonenteric protozoan infections in immunocompromised people. | Q34189873 | ||
| Selective and strain-specific NFAT4 activation by the Toxoplasma gondii polymorphic dense granule protein GRA6. | Q34230563 | ||
| The Toxoplasma pseudokinase ROP5 is an allosteric inhibitor of the immunity-related GTPases | Q34283543 | ||
| The rhoptry proteins ROP18 and ROP5 mediate Toxoplasma gondii evasion of the murine, but not the human, interferon-gamma response. | Q34325516 | ||
| Hammondia hammondi, an avirulent relative of Toxoplasma gondii, has functional orthologs of known T. gondii virulence genes | Q34339536 | ||
| Proteomic analysis of rhoptry organelles reveals many novel constituents for host-parasite interactions in Toxoplasma gondii | Q34432069 | ||
| Severe acquired toxoplasmosis in immunocompetent adult patients in French Guiana. | Q34438816 | ||
| Dogs are definitive hosts of Neospora caninum | Q34475050 | ||
| Strain-specific activation of the NF-kappaB pathway by GRA15, a novel Toxoplasma gondii dense granule protein. | Q34501481 | ||
| A secreted serine-threonine kinase determines virulence in the eukaryotic pathogen Toxoplasma gondii | Q34591236 | ||
| Hammondia hammondi harbors functional orthologs of the host-modulating effectors GRA15 and ROP16 but is distinguished from Toxoplasma gondii by a unique transcriptional profile | Q34592579 | ||
| A history of studies that examine the interactions of Toxoplasma with its host cell: Emphasis on in vitro models | Q34610212 | ||
| Guanylate-binding protein 1 (Gbp1) contributes to cell-autonomous immunity against Toxoplasma gondii | Q34697891 | ||
| Just one cross appears capable of dramatically altering the population biology of a eukaryotic pathogen like Toxoplasma gondii | Q34772368 | ||
| Virulence differences in Toxoplasma mediated by amplification of a family of polymorphic pseudokinases | Q35034984 | ||
| Polymorphic family of injected pseudokinases is paramount in Toxoplasma virulence | Q35035005 | ||
| Toxoplasma gondii: Infection natural congenital in cattle and an experimental inoculation of gestating cows with oocysts | Q60668398 | ||
| Toxoplasmosis in a calf | Q66918054 | ||
| Neospora caninum (Apicomplexa) in an aborted equine fetus | Q68559875 | ||
| Neosporosis-like abortions in a herd of dairy cattle | Q69155072 | ||
| A Neospora-like protozoon found in an aborted bovine placenta | Q69390288 | ||
| Toxoplasma gondii-induced abortion in dairy goats | Q69491150 | ||
| Primary and reactivated toxoplasma infection in patients with cardiac transplants. Clinical spectrum and problems in diagnosis in a defined population | Q70261374 | ||
| Spleen and lymph node cell populations, in vitro cell proliferation and interferon-gamma production during the primary immune response to Toxoplasma gondii | Q70324564 | ||
| Repeat transplacental transfer of Toxoplasma gondii in dairy goats | Q70372884 | ||
| Neonatal Neospora caninum infection in dogs: isolation of the causative agent and experimental transmission | Q70415014 | ||
| Abortion associated with toxoplasmosis in sheep in Oregon | Q70686429 | ||
| Immune response of mice to ingested Toxoplasma gondii: a model of toxoplasma infection acquired by ingestion | Q71276726 | ||
| A survey of the incidence of Neospora caninum infection in aborted and stillborn bovine fetuses in England and Wales | Q71771109 | ||
| Toxoplasma gondii Comprises Three Clonal Lineages: Correlation of Parasite Genotype with Human Disease | Q71829835 | ||
| Interferon-gamma and interleukin-12 mediate protection to acute Neospora caninum infection in BALB/c mice | Q73296745 | ||
| Murine ileitis after intracellular parasite infection is controlled by TGF-beta-producing intraepithelial lymphocytes | Q73570988 | ||
| Prevalence of antibodies to Neospora caninum and Toxoplasma gondii in cattle and water buffaloes in southern Vietnam | Q74496093 | ||
| Acute toxoplasmosis leads to lethal overproduction of Th1 cytokines | Q74601866 | ||
| Prevalence of Neospora caninum and Toxoplasma gondii in sheep and dogs from Guarapuava farms, Paraná State, Brazil | Q79698861 | ||
| The induction of acute ileitis by a single microbial antigen of Toxoplasma gondii | Q80418731 | ||
| Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in ovine from São Paulo State, Brazil | Q80483248 | ||
| Prevalence of anti-Toxoplasma gondii and anti-Neospora caninum antibodies in goats slaughtered in the public slaughterhouse of Patos city, Paraíba State, Northeast region of Brazil | Q80812076 | ||
| HUMAN TOXOPLASMOSIS: OCCURRENCE IN INFANTS AS AN ENCEPHALOMYELITIS VERIFICATION BY TRANSMISSION TO ANIMALS | Q80891678 | ||
| Seroprevalence of Toxoplasma gondii and Neospora caninum in dairy goats from Romania | Q83002070 | ||
| Histopathology of the reproductive system of male sheep experimentally infected with Toxoplasma gondii | Q83346950 | ||
| Seroprevalence of Toxoplasma gondii and Neospora caninum infection in dairy cows in subtropical southern China | Q84420606 | ||
| Experimental infection by Toxoplasma gondii using contaminated semen containing different doses of tachyzoites in sheep | Q40363898 | ||
| A Hammondia-like parasite from the European fox (Vulpes vulpes) forms biologically viable tissue cysts in cell culture. | Q40659332 | ||
| Experimental toxoplasmosis in calves and pregnant cows. | Q40864111 | ||
| Cross-immunity between Hammondia and Toxoplasma infections in mice and hamsters | Q40907815 | ||
| Experimental neosporosis in pregnant ewes and their offspring | Q40921821 | ||
| Hammondia hammondi cysts in cell cultures | Q41292848 | ||
| Abortions, fetal death, and stillbirths in pregnant pygmy goats inoculated with tachyzoites of Neospora caninum. | Q41307483 | ||
| Sexual transmission of Toxoplasma gondii in sheep | Q42276185 | ||
| Isolated, spontaneous Toxoplasma abortion in a young sow | Q42969593 | ||
| Neospora caninum (Apicomplexa) in a stillborn goat | Q43208709 | ||
| Isolation of Toxoplasma gondii from a Naturally Infected Beef Cow | Q43208804 | ||
| Neospora caninum-like protozoon associated with fatal myelitis in newborn calves | Q43209417 | ||
| Neospora caninum (Protozoa: apicomplexa) infections in mice | Q43209672 | ||
| Toxoplasma gondii-induced abortion in sheep | Q43209917 | ||
| Hammondia hammondi: A new coccidium of cats producing cysts in muscle of other mammals | Q43827285 | ||
| Differential induction of TLR3-dependent innate immune signaling by closely related parasite species | Q35088720 | ||
| ATF6beta is a host cellular target of the Toxoplasma gondii virulence factor ROP18. | Q35102296 | ||
| Toxoplasma effector MAF1 mediates recruitment of host mitochondria and impacts the host response | Q35159661 | ||
| Efficient genome engineering of Toxoplasma gondii using CRISPR/Cas9. | Q35196266 | ||
| Toxoplasma gondii effectors are master regulators of the inflammatory response | Q35434828 | ||
| A monomorphic haplotype of chromosome Ia is associated with widespread success in clonal and nonclonal populations of Toxoplasma gondii | Q35547974 | ||
| Toxoplasma gondii targets a protein phosphatase 2C to the nuclei of infected host cells. | Q35641036 | ||
| A single chromosome unexpectedly links highly divergent isolates of Toxoplasma gondii. | Q35652335 | ||
| Toxoplasma and Plasmodium protein kinases: roles in invasion and host cell remodelling | Q36191387 | ||
| Newly recognized fatal protozoan disease of dogs | Q36453577 | ||
| Role of NK cells and gamma interferon in transplacental passage of Toxoplasma gondii in a mouse model of primary infection | Q36576126 | ||
| High rate of transplacental infection and transmission of Neospora caninum following experimental challenge of cattle at day 210 of gestation | Q36597151 | ||
| Tissue distribution of Neospora caninum in experimentally infected cattle | Q36606763 | ||
| Hammondia hammondi gen. nov., sp.nov., from domestic cats, a new coccidian related to Toxoplasma and Sarcocystis | Q36738279 | ||
| Oral oocyst-induced mouse model of toxoplasmosis: effect of infection with Toxoplasma gondii strains of different genotypes, dose, and mouse strains (transgenic, out-bred, in-bred) on pathogenesis and mortality | Q36931850 | ||
| Kiss and spit: the dual roles of Toxoplasma rhoptries | Q37024471 | ||
| Toxoplasma co-opts host gene expression by injection of a polymorphic kinase homologue | Q37087502 | ||
| Polymorphic secreted kinases are key virulence factors in toxoplasmosis | Q37105671 | ||
| Materno-fetal Toxoplasma gondii infection: critical review of available diagnostic methods. | Q37119599 | ||
| Severe acquired toxoplasmosis caused by wild cycle of Toxoplasma gondii, French Guiana | Q37164712 | ||
| A Toxoplasma dense granule protein, GRA24, modulates the early immune response to infection by promoting a direct and sustained host p38 MAPK activation. | Q37194952 | ||
| Experimental infection with a low virulence isolate of Neospora caninum at 70 days gestation in cattle did not result in foetopathy | Q37246826 | ||
| Reciprocal virulence and resistance polymorphism in the relationship between Toxoplasma gondii and the house mouse | Q37262073 | ||
| Toxoplasma gondii, "new" genotypes and virulence | Q37278534 | ||
| Differential locus expansion distinguishes Toxoplasmatinae species and closely related strains of Toxoplasma gondii | Q37631484 | ||
| Toxoplasma gondii prevalence in farm animals in the United States | Q38064203 | ||
| Seroprevalence of antibodies to Neospora caninum and Toxoplasma gondii in water buffaloes (Bubalus bubalis) from Egypt | Q38978806 | ||
| Neospora caninum is associated with abortion in Algerian cattle | Q39021601 | ||
| The extent of parasite-associated necrosis in the placenta and foetal tissues of cattle following Neospora caninum infection in early and late gestation correlates with foetal death. | Q39023059 | ||
| Neospora caninum in cattle: experimental infection with oocysts can result in exogenous transplacental infection, but not endogenous transplacental infection in the subsequent pregnancy | Q39231233 | ||
| Acute phase toxoplasma abortions in sheep. | Q39331566 | ||
| Transplacental transmission in cattle: is Toxoplasma gondii less potent than Neospora caninum? | Q39591901 | ||
| Experimental Hammondia hammondi Infection in Monkeys | Q39601801 | ||
| A helical membrane-binding domain targets the Toxoplasma ROP2 family to the parasitophorous vacuole | Q39812575 | ||
| Fatal Toxoplasma gondii Dissemination in a Heart Transplant Recipient: Description of a Case | Q40263480 | ||
| Development of lesions and tissue distribution of parasite in lambs orally infected with sporulated oocysts of Toxoplasma gondii. | Q40329839 | ||
| Toxoplasmosis and neosporosis among beef cattle slaughtered for food in Western Thailand. | Q43875260 | ||
| Toxoplasma gondii in cats: fecal stages identified as coccidian oocysts | Q44047126 | ||
| Toxoplasma-induced abortion in dairy goats. | Q44139987 | ||
| Studies on the role of interleukin-12 in acute murine toxoplasmosis | Q44321828 | ||
| Prevalence of Toxoplasma gondii and Neospora caninum infections in sheep from Federal District, central region of Brazil | Q44375480 | ||
| Pathogenic characterization in mice of Neospora caninum isolates obtained from asymptomatic calves | Q44460553 | ||
| Toxoplasma gondii: inconsistent dissemination patterns following oral infection in mice. | Q44517620 | ||
| Seroprevalence of Toxoplasma gondii and Neospora caninum infections in goats in Poland. | Q44709962 | ||
| Interferon-gamma: the major mediator of resistance against Toxoplasma gondii | Q45128276 | ||
| Virulent strains of Toxoplasma gondii comprise a single clonal lineage | Q46105888 | ||
| Detection of Neospora sp. from infected bovine tissues by PCR and probe hybridization | Q46275068 | ||
| Experimental vaginal infection of goats with semen contaminated with the "CPG" strain of Toxoplasma gondii. | Q46326606 | ||
| Oocysts of Neospora caninum, Hammondia heydorni, Toxoplasma gondii and Hammondia hammondi in faeces collected from dogs in Germany. | Q46730415 | ||
| Recent expansion of Toxoplasma through enhanced oral transmission | Q47411368 | ||
| The pathogenesis of experimental neosporosis in pregnant sheep | Q47889692 | ||
| Antigenic similarity between Hammondia hammondi and Toxoplasma gondii tachyzoites | Q47913610 | ||
| Molecular and biological characterization of first isolates of Hammondia hammondi from cats from Ethiopia | Q48040242 | ||
| Repetitive abortion in Neospora-infected ewes | Q48199380 | ||
| Comparison of the biological characteristics of two isolates of Neospora caninum | Q48203183 | ||
| Characterisation of the first Australian isolate of Neospora caninum from cattle | Q48433059 | ||
| Neospora caninum: high susceptibility to the parasite in C57BL/10ScCr mice. | Q48454611 | ||
| Simultaneous depletion of CD4+ and CD8+ T lymphocytes is required to reactivate chronic infection with Toxoplasma gondii | Q48464908 | ||
| Outbreak of central-nervous-system toxoplasmosis in western Europe and North America | Q48662823 | ||
| Experimental infection of non-pregnant and pregnant sheep with Neospora caninum | Q48665095 | ||
| Occurrence of Neospora caninum and Toxoplasma gondii infections in ovine and caprine abortions. | Q48703379 | ||
| Neospora caninum: role for immune cytokines in host immunity | Q48811296 | ||
| Distribution of lesions in fetal brains following experimental infection of pregnant sheep with Toxoplasma gondii | Q48834740 | ||
| Fatal congenital Neospora caninum infection in a lamb | Q49116433 | ||
| Maternal infection with toxoplasma gondii in pregnancy and the risk of hearing loss in the offspring | Q50440055 | ||
| Chronic Neospora caninum infection and repeat abortion in dairy cows: a 3-year study. | Q50803633 | ||
| Serologic diagnosis of toxoplasmosis in experimentally infected pregnant goats and transplacentally infected kids. | Q50916246 | ||
| Toxoplasma gondii and Neospora caninum antibodies in sheep in the Czech Republic. | Q51669441 | ||
| Construction of a molecular karyotype for Toxoplasma gondii | Q54272649 | ||
| Detection of Toxoplasma gondii in the reproductive system of male goats | Q54406907 | ||
| Fetal death in cows experimentally infected with Neospora caninum at 110 days of gestation | Q57743080 | ||
| Evidence that primary infection of Charollais sheep with Toxoplasma gondii may not prevent foetal infection and abortion in subsequent lambings | Q58416874 | ||
| Gerbils ( Meriones unguiculatus ) are highly susceptible to oral infection with Neospora caninum oocysts | Q58708364 | ||
| Mouse Model for Central Nervous System Neospora caninum Infections | Q58708751 | ||
| P275 | copyright license | Creative Commons Attribution-NonCommercial 4.0 International | Q34179348 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Toxoplasma | Q9360606 |
| eukaryote | Q19088 | ||
| Toxoplasma gondii | Q131003 | ||
| toxoplasmosis | Q154878 | ||
| pathogenesis | Q372016 | ||
| P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
| P304 | page(s) | 127-140 | |
| P577 | publication date | 2015-03-01 | |
| P1433 | published in | Parasite Immunology | Q15751559 |
| P1476 | title | Secreted effectors in Toxoplasma gondii and related species: determinants of host range and pathogenesis? | |
| P478 | volume | 37 |
| Q91026493 | Annotating the 'hypothetical' in hypothetical proteins: In-silico analysis of uncharacterised proteins for the Apicomplexan parasite, Neospora caninum |
| Q26776334 | Flagellar membrane proteins in kinetoplastid parasites |
| Q58702723 | Genome Wide Identification of Mutational Hotspots in the Apicomplexan Parasite Neospora caninum and the Implications for Virulence |
| Q48277104 | Human Placental Syncytiotrophoblasts Restrict Toxoplasma gondii Attachment and Replication and Respond to Infection by Producing Immunomodulatory Chemokines |
| Q33847295 | IgG Avidity Test in Congenital Toxoplasmosis Diagnoses in Newborns |
| Q89516778 | Immediate Interferon Gamma Induction Determines Murine Host Compatibility Differences between Toxoplasma gondii and Neospora caninum |
| Q26747055 | Recent advances in understanding apicomplexan parasites |
| Q37499182 | Vacuolar protein sorting mechanisms in apicomplexan parasites |
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