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In vitro culture systems for the study of apicomplexan parasites in farm animals
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/expr.1993.1024openalex-snapshot
Cryptosporidium parvum: Culture in MDCK Cells
inferredcites →https://doi.org/10.1006/expr.1994.1039openalex-snapshot
Experimental Induction of Bradyzoite-Specific Antigen Expression and Cyst Formation by the RH Strain of Toxoplasma gondii in Vitro
inferredcites →https://doi.org/10.1006/expr.1998.4292openalex-snapshot
Theileria annulata:The Expression of Two Novel Macroschizont Antigens on the Surface of Infected Mononuclear Cells Differs duringin VitroAttenuation of a Virulent Cell Line
inferredcites →https://doi.org/10.1006/expr.2001.4655openalex-snapshot
Babesia bovis: Culture of Laboratory-Adapted Parasite Lines and Clinical Isolates in a Chemically Defined Medium
inferredcites →https://doi.org/10.1006/jmbi.2001.4730openalex-snapshot
Differential expression of two plant-like enolases with distinct enzymatic and antigenic properties during stage conversion of the protozoan parasite Toxoplasma gondii
inferredcites →https://doi.org/10.1007/bf00934377openalex-snapshot
Cytological and immunological responses toBabesia divergens in different hosts: Ox, gerbil, man
inferredcites →https://doi.org/10.1007/s00436-001-0531-1openalex-snapshot
Development of Eimeria bovis in vitro: suitability of several bovine, human and porcine endothelial cell lines, bovine fetal gastrointestinal, Madin–Darby bovine kidney (MDBK) and African green monkey kidney (VERO) cells
inferredcites →https://doi.org/10.1007/s00436-003-0846-1openalex-snapshot
Comparative development of Eimeria tenella (Apicomplexa) in host cells in vitro
inferredcites →https://doi.org/10.1007/s00436-005-1396-5openalex-snapshot
Phylogenetic relationships of Sarcocystis neurona of horses and opossums to other cyst-forming coccidia deduced from SSU rRNA gene sequences
inferredcites →https://doi.org/10.1007/s00436-008-1075-4openalex-snapshot
The differential protein expression profiles and immunogenicity of tachyzoites and bradyzoites of in vitro cultured Neospora caninum
inferredcites →https://doi.org/10.1007/s00436-008-1192-0openalex-snapshot
Reporter gene expression in cell culture stages and oocysts of Eimeria nieschulzi (Coccidia, Apicomplexa)
inferredcites →https://doi.org/10.1007/s00436-010-1899-6openalex-snapshot
Toxoplasma gondii: determinants of tachyzoite to bradyzoite conversion
inferredcites →https://doi.org/10.1007/s004360050431openalex-snapshot
Redescription of Babesia equi Laveran, 1901 as Theileria equi Mehlhorn, Schein 1998
inferredcites →https://doi.org/10.1007/s004360050568openalex-snapshot
Continuous in vitro cultivation of Babesia caballi in serum-free medium
inferredcites →https://doi.org/10.1007/s11626-007-9034-4openalex-snapshot
Establishment and characterization of a primary canine duodenal epithelial cell culture
inferredcites →https://doi.org/10.1007/s12639-011-0034-7openalex-snapshot
Control of poultry coccidiosis: changing trends
inferredcites →https://doi.org/10.1016/0020-7519(88)90118-xopenalex-snapshot
Effects of PH, buffers and medium-storage on the growth of Babesia bovis in vitro
inferredcites →https://doi.org/10.1016/0020-7519(95)00068-dopenalex-snapshot
Current research on Sarcocystis species of domestic animals
inferredcites →https://doi.org/10.1016/0022-1759(91)90122-vopenalex-snapshot
A flow cytometric method for assessing viability of intraerythrocytic hemoparasites
inferredcites →https://doi.org/10.1016/b978-0-12-391429-3.00007-1openalex-snapshot
Cryptic Parasite Revealed
inferredcites →https://doi.org/10.1016/j.cveq.2014.08.012openalex-snapshot
Equine Protozoal Myeloencephalitis
inferredcites →https://doi.org/10.1016/j.exppara.2007.10.015openalex-snapshot
Phylogenetic analysis of Cystoisospora species at the rRNA ITS1 locus and development of a PCR-RFLP assay
inferredcites →https://doi.org/10.1016/j.exppara.2008.05.003openalex-snapshot
Plasmodium falciparum: Development of a transgenic line for screening antimalarials using firefly luciferase as the reporter
inferredcites →https://doi.org/10.1016/j.ijpara.2003.12.009openalex-snapshot
Toxoplasma gondii: the model apicomplexan
inferredcites →https://doi.org/10.1016/j.ijpara.2004.04.001openalex-snapshot
Complete development of Cryptosporidium parvum in host cell-free culture
inferredcites →https://doi.org/10.1016/j.ijpara.2004.07.001openalex-snapshot
Intergenic regions in the rhoptry associated protein-1 (rap-1) locus promote exogenous gene expression in Babesia bovis
inferredcites →https://doi.org/10.1016/j.ijpara.2006.02.022openalex-snapshot
Characterization and gene expression of Babesia bovis elongation factor-1α☆
inferredcites →https://doi.org/10.1016/j.ijpara.2008.05.012openalex-snapshot
Simple and sensitive antimalarial drug screening in vitro and in vivo using transgenic luciferase expressing Plasmodium berghei parasites
inferredcites →https://doi.org/10.1016/j.ijpara.2008.06.013openalex-snapshot
Stable transfection of Eimeria tenella: Constitutive expression of the YFP-YFP molecule throughout the life cycle
inferredcites →https://doi.org/10.1016/j.ijpara.2008.08.006openalex-snapshot
Stable expression of a GFP-BSD fusion protein in Babesia bovis merozoites
inferredcites →https://doi.org/10.1016/j.ijpara.2009.02.011openalex-snapshot
Development of forward genetics in Toxoplasma gondii
inferredcites →https://doi.org/10.1016/j.ijpara.2011.08.001openalex-snapshot
Evolution of Cryptosporidium in vitro culture
inferredcites →https://doi.org/10.1016/j.ijpara.2012.02.005openalex-snapshot
Phylogeny and evolution of the Piroplasmida as inferred from 18S rRNA sequences
inferredcites →https://doi.org/10.1016/j.ijpddr.2012.03.001openalex-snapshot
Di-cationic arylimidamides act against Neospora caninum tachyzoites by interference in membrane structure and nucleolar integrity and are active against challenge infection in mice
inferredcites →https://doi.org/10.1016/j.mcp.2011.11.001openalex-snapshot
Labeling surface epitopes to identify Cryptosporidium life stages using a scanning electron microscopy-based immunogold approach
inferredcites →https://doi.org/10.1016/j.meegid.2011.08.006openalex-snapshot
Molecular pathology, taxonomy and epidemiology of Besnoitia species (Protozoa: Sarcocystidae)
inferredcites →https://doi.org/10.1016/j.micinf.2004.02.016openalex-snapshot
Complete development of Cryptosporidium parvum in rabbit chondrocytes (VELI cells)
inferredcites →https://doi.org/10.1016/j.molbiopara.2004.05.007openalex-snapshot
Fluorescent protein tagging in Toxoplasma gondii: identification of a novel inner membrane complex component conserved among Apicomplexa
inferredcites →https://doi.org/10.1016/j.molbiopara.2005.08.011openalex-snapshot
A novel rhoptry protein in Toxoplasma gondii bradyzoites and merozoites
inferredcites →https://doi.org/10.1016/j.molbiopara.2006.06.003openalex-snapshot
Molecular genetic transfection of the coccidian parasite Sarcocystis neurona
inferredcites →https://doi.org/10.1016/j.molbiopara.2008.06.006openalex-snapshot
Restriction enzyme-mediated transfection improved transfection efficiency in vitro in Apicomplexan parasite Eimeria tenella
inferredcites →https://doi.org/10.1016/j.molbiopara.2008.07.006openalex-snapshot
A toolbox facilitating stable transfection of Eimeria species
inferredcites →https://doi.org/10.1016/j.molbiopara.2009.07.003openalex-snapshot
Transient transfection of Cryptosporidium parvum using green fluorescent protein (GFP) as a marker
inferredcites →https://doi.org/10.1016/j.molbiopara.2011.11.001openalex-snapshot
Stable expression of green fluorescent protein and targeted disruption of thioredoxin peroxidase-1 gene in Babesia bovis with the WR99210/dhfr selection system
inferredcites →https://doi.org/10.1016/j.molbiopara.2012.05.003openalex-snapshot
Acute and persistent infection by a transfected Mo7 strain of Babesia bovis
inferredcites →https://doi.org/10.1016/j.parint.2008.12.003openalex-snapshot
Thioureides of 2-(phenoxymethyl)benzoic acid 4-R substituted: A novel class of anti-parasitic compounds
inferredcites →https://doi.org/10.1016/j.parint.2012.01.010openalex-snapshot
Chimeric fluorescent reporter as a tool for generation of transgenic Eimeria (Apicomplexa, Coccidia) strains with stage specific reporter gene expression
inferredcites →https://doi.org/10.1016/j.pt.2006.08.001openalex-snapshot
What is Cryptosporidium? Reappraising its biology and phylogenetic affinities
inferredcites →https://doi.org/10.1016/j.pt.2009.06.006openalex-snapshot
Reporter genes facilitating discovery of drugs targeting protozoan parasites
inferredcites →https://doi.org/10.1016/j.pt.2011.12.003openalex-snapshot
Transgenic parasites accelerate drug discovery
inferredcites →https://doi.org/10.1016/j.vetpar.2006.01.042openalex-snapshot
Live vaccines against bovine babesiosis
inferredcites →https://doi.org/10.1016/j.vetpar.2008.02.025openalex-snapshot
Models for experimental infection of dogs fed with tissue from fetuses and neonatal cattle naturally infected with Neospora caninum
inferredcites →https://doi.org/10.1016/j.vetpar.2009.03.022openalex-snapshot
In vitro efficacy of nitro- and halogeno-thiazolide/thiadiazolide derivatives against Sarcocystis neurona
inferredcites →https://doi.org/10.1016/j.vetpar.2009.09.022openalex-snapshot
Transfection systems for Babesia bovis: A review of methods for the transient and stable expression of exogenous genes
inferredcites →https://doi.org/10.1016/j.vetpar.2010.08.013openalex-snapshot
Bovine besnoitiosis: Epidemiological and clinical aspects
inferredcites →https://doi.org/10.1016/j.vetpar.2010.10.047openalex-snapshot
Experimental infection of dogs (Canis familiaris) with sporulated oocysts of Neospora caninum
inferredcites →https://doi.org/10.1016/j.vetpar.2011.01.027openalex-snapshot
Exploring the life cycle of Besnoitia besnoiti—Experimental infection of putative definitive and intermediate host species
inferredcites →https://doi.org/10.1016/j.vetpar.2011.10.018openalex-snapshot
Effect of the diclazuril on Hsp90 in the second-generation merozoites of Eimeria tenella
inferredcites →https://doi.org/10.1016/j.vetpar.2012.03.049openalex-snapshot
Chick embryo tracheal organ: A new and effective in vitro culture model for Cryptosporidium baileyi
inferredcites →https://doi.org/10.1016/s0020-7519(00)00135-1openalex-snapshot
Epidemiology of Cryptosporidium: transmission, detection and identification
inferredcites →https://doi.org/10.1016/s0020-7519(00)00150-8openalex-snapshot
Cell: sporozoite interactions and invasion by apicomplexan parasites of the genus Eimeria
inferredcites →https://doi.org/10.1016/s0020-7519(01)00212-0openalex-snapshot
Complete development and long-term maintenance of Cryptosporidium parvum human and cattle genotypes in cell culture
inferredcites →https://doi.org/10.1016/s0020-7519(01)00230-2openalex-snapshot
Dogs shed Neospora caninum oocysts after ingestion of naturally infected bovine placenta but not after ingestion of colostrum spiked with Neospora caninum tachyzoites
inferredcites →https://doi.org/10.1016/s0020-7519(02)00126-1openalex-snapshot
Exogenous nitric oxide triggers Neospora caninum tachyzoite-to-bradyzoite stage conversion in murine epidermal keratinocyte cell cultures
inferredcites →https://doi.org/10.1016/s0020-7519(02)00199-6openalex-snapshot
Successful in vitro cultivation of Cryptosporidium andersoni: evidence for the existence of novel extracellular stages in the life cycle and implications for the classification of Cryptosporidium
inferredcites →https://doi.org/10.1016/s0020-7519(99)00031-4openalex-snapshot
Enzyme immunoassay detection of Cryptosporidium parvum inhibition by sinefungin in sporozoite infected HCT-8 enterocytic cells
inferredcites →https://doi.org/10.1016/s0020-7519(99)00121-6openalex-snapshot
A structural study of the Neospora caninum oocyst
inferredcites →https://doi.org/10.1016/s0020-7519(99)00130-7openalex-snapshot
The in vitro development of Neospora caninum bradyzoites
inferredcites →https://doi.org/10.1016/s0021-9975(05)80075-1openalex-snapshot
Interferon gamma inhibits the intracellular multiplication of Neospora caninum, as shown by incorporation of 3H uracil
inferredcites →https://doi.org/10.1016/s0065-308x(08)60230-4openalex-snapshot
Immunity and Vaccine Development in the Bovine Theilerioses
inferredcites →https://doi.org/10.1016/s0065-308x(08)60241-9openalex-snapshot
The Host-Parasite Relationship in Neosporosis
inferredcites →https://doi.org/10.1016/s0166-6851(01)00238-9openalex-snapshot
Transient transfection of Theileria annulata
inferredcites →https://doi.org/10.1016/s0166-6851(98)00128-5openalex-snapshot
Transient expression of β-galactosidase in differentiating sporozoites of Eimeria tenella
inferredcites →https://doi.org/10.1016/s0304-4017(00)00279-xopenalex-snapshot
Neospora hughesi: experimental infections in mice, gerbils, and dogs
inferredcites →https://doi.org/10.1016/s0304-4017(00)00280-6openalex-snapshot
Determination of the activity of ponazuril against Sarcocystis neurona in cell cultures
inferredcites →https://doi.org/10.1016/s0304-4017(00)00384-8openalex-snapshot
A review of Sarcocystis neurona and equine protozoal myeloencephalitis (EPM)
inferredcites →https://doi.org/10.1016/s0304-4017(00)00391-5openalex-snapshot
In vitro culture and synchronous release of Sarcocystis neurona merozoites from host cells
inferredcites →https://doi.org/10.1016/s0304-4017(00)00402-7openalex-snapshot
Sarcocystis neurona and Sarcocystis falcatula: monitoring of schizogony in cell culture using fluorescent nuclear labeling
inferredcites →https://doi.org/10.1016/s0304-4017(00)00418-0openalex-snapshot
Initiation of a Sarcocystis neurona expressed sequence tag (EST) sequencing project: a preliminary report
inferredcites →https://doi.org/10.1016/s0304-4017(99)00019-9openalex-snapshot
Infectivity of feline enteroepithelial stages of Toxoplasma gondii isolated by Percoll-density gradient centrifugation
inferredcites →https://doi.org/10.1016/s0749-0739(17)30257-2openalex-snapshot
Equine Protozoal Myeloencephalitis
inferredcites →https://doi.org/10.1016/s0968-0896(03)00330-4openalex-snapshot
Synthesis and evaluation of a series of 1,4-Diarylbutadienes for anticoccidial activity
inferredcites →https://doi.org/10.1016/s1471-4922(02)02248-1openalex-snapshot
Toxoplasma gondii tachyzoite–bradyzoite interconversion
inferredcites →https://doi.org/10.1017/s0031182007002417openalex-snapshot
In vitro efficacy of nitro- and bromo-thiazolyl-salicylamide compounds (thiazolides) against Besnoitia besnoiti infection in Vero cells
inferredcites →https://doi.org/10.1017/s0031182008004599openalex-snapshot
NcGRA2as a molecular target to assess the parasiticidal activity of toltrazuril againstNeospora caninum
inferredcites →https://doi.org/10.1017/s003118200900585xopenalex-snapshot
The evolution of the knowledge of cat and dog coccidia
inferredcites →https://doi.org/10.1017/s0031182009990588openalex-snapshot
Endogenous and exogenous transplacental transmission of Neospora caninum – how the route of transmission impacts on epidemiology and control of disease
inferredcites →https://doi.org/10.1017/s0031182009990837openalex-snapshot
Morphological characterization ofCryptosporidium parvumlife-cycle stages in anin vitromodel system
inferredcites →https://doi.org/10.1017/s0031182010000685openalex-snapshot
Morphological changes and viability ofCryptosporidium parvumsporozoites after excystation in cell-free culture media
inferredcites →https://doi.org/10.1017/s0031182010001666openalex-snapshot
Genetic manipulation of Neospora caninum to express the bradyzoite-specific protein NcSAG4 in tachyzoites
inferredcites →https://doi.org/10.1017/s0031182011000114openalex-snapshot
In vitroeffects of arylimidamides againstBesnoitia besnoitiinfection in Vero cells
inferredcites →https://doi.org/10.1017/s0031182011000217openalex-snapshot
Cryptosporidiumcell culture infectivity assay design
inferredcites →https://doi.org/10.1017/s0031182011001776openalex-snapshot
The adaptive potential of a survival artist: characterization of thein vitrointeractions ofToxoplasma gondiitachyzoites with di-cationic compounds in human fibroblast cell cultures
inferredcites →https://doi.org/10.1017/s0031182097008937openalex-snapshot
Continuous in vitro culture of Babesia divergens in a serum-free medium
inferredcites →https://doi.org/10.1017/s003118209800376xopenalex-snapshot
Development of Sarcocystis falcatula in cell cultures demonstrates that it is different from Sarcocystis neurona
inferredcites →https://doi.org/10.1017/s1431927604040930openalex-snapshot
Tissue Culture and Explant Approaches to Studying and VisualizingNeospora caninumand Its Interactions with the Host Cell
inferredcites →https://doi.org/10.1038/nature07935openalex-snapshot
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
inferredcites →https://doi.org/10.1093/jac/dkp363openalex-snapshot
Stable expression of Escherichia coli -glucuronidase A (GusA) in Giardia lamblia: application to high-throughput drug susceptibility testing
inferredcites →https://doi.org/10.1093/jac/dkq522openalex-snapshot
In vitro assessment of anticryptosporidial efficacy and cytotoxicity of adenosine analogues using a SYBR Green real-time PCR method
inferredcites →https://doi.org/10.1093/nar/gkg072openalex-snapshot
ToxoDB: accessing the Toxoplasma gondii genome
inferredcites →https://doi.org/10.1111/j.1365-3024.2011.01301.xopenalex-snapshot
Genomics and population biology of Cryptosporidium species
inferredcites →https://doi.org/10.1111/j.1472-765x.2006.02101.xopenalex-snapshot
In vitro development of Cryptosporidium parvum in serum-free media
inferredcites →https://doi.org/10.1111/j.1550-7408.1984.tb04306.xopenalex-snapshot
Complete Development of Isospora suis of Swine in Chicken Embryos1
inferredcites →https://doi.org/10.1111/j.1550-7408.1995.tb01556.xopenalex-snapshot
A Cell Culture System for Study of the Development of Toxoplasma gondii Bradyzoites
inferredcites →https://doi.org/10.1111/j.1550-7408.1997.tb05669.xopenalex-snapshot
In Vitro Cultivation of the Vascular Phase of Sarcocystis singaporensis
inferredcites →https://doi.org/10.1111/j.1550-7408.1997.tb05963.xopenalex-snapshot
Sexual and Asexual Development of Cryptosporidium parvum in Five Oocyst– or Sporozoite‐Infected Human Enterocytic Cell Lines
inferredcites →https://doi.org/10.1111/j.1749-6632.2000.tb05286.xopenalex-snapshot
Culture‐Derived Parasites in Vaccination of Cattle against Tick‐Borne Diseases
inferredcites →https://doi.org/10.1111/j.1863-2378.2009.01276.xopenalex-snapshot
A Brief History and Overview ofToxoplasma gondii
inferredcites →https://doi.org/10.1126/science.168.3935.1104openalex-snapshot
Sarcocystis : Development in Cultured Avian and Mammalian Cells
inferredcites →https://doi.org/10.1126/science.175.4017.65openalex-snapshot
Gametogony of Sarcocystis sp. in Cell Culture
inferredcites →https://doi.org/10.1126/science.7355284openalex-snapshot
Babesia bovis : Continuous Cultivation in a Microaerophilous Stationary Phase Culture
inferredcites →https://doi.org/10.1128/aac.01236-07openalex-snapshot
Host Cells Participate in the In Vitro Effects of Novel Diamidine Analogues against Tachyzoites of the Intracellular Apicomplexan ParasitesNeospora caninumandToxoplasma gondii
inferredcites →https://doi.org/10.1128/aac.41.9.1849openalex-snapshot
Use of Toxoplasma gondii expressing beta-galactosidase for colorimetric assessment of drug activity in vitro
inferredcites →https://doi.org/10.1128/aac.42.4.818openalex-snapshot
In Vitro Evaluation of Drug Susceptibilities of Babesia divergens Isolates
inferredcites →https://doi.org/10.1128/aac.47.1.309-316.2003openalex-snapshot
High-Throughput Growth Assay forToxoplasma gondiiUsing Yellow Fluorescent Protein
inferredcites →https://doi.org/10.1128/aac.47.2.800-803.2003openalex-snapshot
Growth-Inhibitory Effects of Artesunate, Pyrimethamine, and Pamaquine againstBabesia equiandBabesia caballiin In Vitro Cultures
inferredcites →https://doi.org/10.1128/aac.49.9.3715-3723.2005openalex-snapshot
In Vitro Efficacies of Nitazoxanide and Other Thiazolides against Neospora caninum Tachyzoites Reveal Antiparasitic Activity Independent of the Nitro Group
inferredcites →https://doi.org/10.1128/cdli.6.5.765-767.1999openalex-snapshot
Serological Evidence of Human Infection with the ProtozoanNeospora caninum
inferredcites →https://doi.org/10.1128/cmr.05013-11openalex-snapshot
Epidemiology of and Diagnostic Strategies for Toxoplasmosis
inferredcites →https://doi.org/10.1128/cmr.15.3.365-373.2002openalex-snapshot
Cultivation ofBabesiaandBabesia-Like Blood Parasites: Agents of an Emerging Zoonotic Disease
inferredcites →https://doi.org/10.1128/cmr.17.4.894-902.2004openalex-snapshot
Sarcocystis spp. in Human Infections
inferredcites →https://doi.org/10.1128/iai.64.1.349-354.1996openalex-snapshot
Complete development of Cryptosporidium parvum in bovine fallopian tube epithelial cells
inferredcites →https://doi.org/10.1128/iai.72.1.576-583.2004openalex-snapshot
In Vitro Induction of Neospora caninum Bradyzoites in Vero Cells Reveals Differential Antigen Expression, Localization, and Host-Cell Recognition of Tachyzoites and Bradyzoites
inferredcites →https://doi.org/10.1128/iai.73.2.1023-1033.2005openalex-snapshot
Sarcocystis neuronaMerozoites Express a Family of Immunogenic Surface Antigens That Are Orthologues of theToxoplasma gondiiSurface Antigens (SAGs) and SAG-Related Sequences
inferredcites →https://doi.org/10.1146/annurev.micro.53.1.1openalex-snapshot
Transformation of Leukocytes byTheileria parvaandT. annulata
inferredcites →https://doi.org/10.1371/journal.pone.0029998openalex-snapshot
Transcriptomic Analysis of Toxoplasma Development Reveals Many Novel Functions and Structures Specific to Sporozoites and Oocysts
inferredcites →https://doi.org/10.1371/journal.ppat.0030148openalex-snapshot
Genome Sequence of Babesia bovis and Comparative Analysis of Apicomplexan Hemoprotozoa
inferredcites →https://doi.org/10.1371/journal.ppat.1002567openalex-snapshot
Comparative Genomics of the Apicomplexan Parasites Toxoplasma gondii and Neospora caninum: Coccidia Differing in Host Range and Transmission Strategy
inferredcites →https://doi.org/10.1590/s0074-02762007005000071openalex-snapshot
More productive in vitro culture of Cryptosporidium parvum for better study of the intra- and extracellular phases
inferredcites →https://doi.org/10.1590/s0074-02762009000600007openalex-snapshot
Primary culture of intestinal epithelial cells as a potential model for Toxoplasma gondii enteric cycle studies
inferredcites →https://doi.org/10.1645/0022-3395(2000)086[0671:ivcoso]2.0.co;2openalex-snapshot
IN VITRO CULTIVATION OF SCHIZONTS OF SARCOCYSTIS SPEERI Dubey and Lindsay, 1999
inferredcites →https://doi.org/10.1645/ge-1273.1openalex-snapshot
Primary Culture of Skeletal Muscle Cells as a Model for Studies of Toxoplasma gondii Cystogenesis
inferredcites →https://doi.org/10.1645/ge-1412.1openalex-snapshot
Transfected Eimeria tenella Could Complete Its Endogenous Development In Vitro
inferredcites →https://doi.org/10.1645/ge-1812.1openalex-snapshot
Infection of Primary Canine Duodenal Epithelial Cell Cultures with Neospora caninum
inferredcites →https://doi.org/10.1645/ge-1951.1openalex-snapshot
Development and Ultrastructure of Cystoisospora canis Nemeséri, 1959 (syn. Isospora canis) Monozoic Cysts in Two Noncanine Cell Lines
inferredcites →https://doi.org/10.1645/ge-3298openalex-snapshot
COMPARATIVE ANALYSIS OF STRESS AGENTS IN A SIMPLIFIED IN VITRO SYSTEM OF NEOSPORA CANINUM BRADYZOITE PRODUCTION
inferredcites →https://doi.org/10.1645/ge-379ropenalex-snapshot
DIFFERENTIAL EFFECTS OF INTERFERON-γ AND TUMOR NECROSIS FACTOR-α ON TOXOPLASMA GONDII PROLIFERATION IN ORGANOTYPIC RAT BRAIN SLICE CULTURES
inferredcites →https://doi.org/10.1645/ge-661r.1openalex-snapshot
Failure to Propagate Cryptosporidium spp. in Cell-Free Culture
inferredcites →https://doi.org/10.2307/3283317openalex-snapshot
Incorporation of [ 3 H]Hypoxanthine by Short-Term Cultured Theileria sergenti and Its Inhibition by Drugs
inferredcites →https://doi.org/10.2307/3283752openalex-snapshot
Babesia equi Erythrocytic Stage Continuously Cultured in an Enriched Medium
inferredcites →https://doi.org/10.2307/3284741openalex-snapshot
Complete Development of the Porcine Coccidium Isospora suis Biester, 1934 in Cell Cultures
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Lack of Serologic Evidence ofNeospora caninumin Humans, England
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Additional file 1 of In vivo and in vitro models show unexpected degrees of virulence among Toxoplasma gondii type II and III isolates from sheep
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