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Cultivation of fish ciliate parasites: Progress and prospects
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jez.b.21354openalex-snapshot
Alternative processing of scrambled genes generates protein diversity in the ciliate Chilodonella uncinata
inferredcites →https://doi.org/10.1007/978-1-4020-8239-9openalex-snapshot
The Ciliated Protozoa: Characterization, Classification, and Guide to the Literature
inferredcites →https://doi.org/10.1007/bf00014331openalex-snapshot
Taxonomie und �kologie einiger Ciliaten (Protozoa, Ciliophora) des Saprobiensystems. II. Familie Chilodonellidae
inferredcites →https://doi.org/10.1007/s00239-011-9468-xopenalex-snapshot
Heterogeneous Rates of Molecular Evolution Among Cryptic Species of the Ciliate Morphospecies Chilodonella uncinata
inferredcites →https://doi.org/10.1007/s00436-006-0451-1openalex-snapshot
Light and scanning electron microscopic study of Balantidium ctenopharyngodoni Chen, 1955 (Class: Litostomatea) from China
inferredcites →https://doi.org/10.1007/s00436-012-3234-xopenalex-snapshot
Studies on Trichodinid and Chilodonellid Ciliophorans (Protozoa: Ciliophora) in the Indian freshwater and estuarine fishes with description of Trichodinella sunderbanensis sp. nov. and Trichodina nandusi sp. nov.
inferredcites →https://doi.org/10.1007/s00436-020-06628-0openalex-snapshot
Multi-gene phylogeny of Tetrahymena refreshed with three new histophagous species invading freshwater planarians
inferredcites →https://doi.org/10.1007/s10295-004-0135-8openalex-snapshot
Factorial designs: an efficient approach to choosing the main factors influencing growth and hydrolase production by Tetrahymena thermophila
inferredcites →https://doi.org/10.1007/s12639-014-0617-1openalex-snapshot
First record of protozoan parasites, Tetrahymena rostrata and Callimastix equi from the edible oyster in Sundarbans region of West Bengal, India
inferredcites →https://doi.org/10.1007/s12639-017-0938-yopenalex-snapshot
An overall estimation of losses caused by diseases in the Brazilian fish farms
inferredcites →https://doi.org/10.1016/0035-9203(61)90019-0openalex-snapshot
Natural infection of tropical mosquitoes by ciliated protozoa of the genus Tetrahymena
inferredcites →https://doi.org/10.1016/0044-8486(87)90041-xopenalex-snapshot
Biology of Cryptocaryon irritans and strategies for its control
inferredcites →https://doi.org/10.1016/0047-6374(79)90005-8openalex-snapshot
Germinal aging in Tetrahymena thermophila
inferredcites →https://doi.org/10.1016/b978-0-12-385967-9.00002-5openalex-snapshot
The Life and Times of Tetrahymena
inferredcites →https://doi.org/10.1016/b978-0-123-48350-8.x5001-8openalex-snapshot
The Biochemistry and Physiology of Tetrahymena
inferredcites →https://doi.org/10.1016/j.aquaculture.2006.04.026openalex-snapshot
A standardized method to propagate Cryptocaryon irritans on a susceptible host pompano Trachinotus ovatus
inferredcites →https://doi.org/10.1016/j.aquaculture.2009.10.001openalex-snapshot
A technique for the preservation of Cryptocaryon irritans at low temperatures
inferredcites →https://doi.org/10.1016/j.aquaculture.2011.08.028openalex-snapshot
In vitro and in vivo efficacies of ionophores against Cryptocaryon irritans
inferredcites →https://doi.org/10.1016/j.aquaculture.2014.03.041openalex-snapshot
Enhanced susceptibility of hybrid tilapia to Flavobacterium columnare after parasitism by Ichthyophthirius multifiliis
inferredcites →https://doi.org/10.1016/j.aquaculture.2016.08.041openalex-snapshot
Mortality of Cryptocaryon irritans in sludge from a digester of a marine recirculating aquaculture system
inferredcites →https://doi.org/10.1016/j.aquaculture.2017.11.024openalex-snapshot
Effects of temperature and host species on the life cycle of Cryptocaryon irritans
inferredcites →https://doi.org/10.1016/j.aquaculture.2017.11.026openalex-snapshot
Dormancy induced by a hypoxic environment in tomonts of Cryptocaryon irritans , a parasitic ciliate of marine teleosts
inferredcites →https://doi.org/10.1016/j.aquaculture.2019.734311openalex-snapshot
Characterization of the proteases in the parasitic stage of Cryptocaryon irritans, and in vitro and in vivo effects of protease inhibitors on cryptocaryoniasis
inferredcites →https://doi.org/10.1016/j.aquaculture.2021.736535openalex-snapshot
First record of facultative parasitism of Chilodonella uncinata based on goldfish (Carassius auratus) infection model
inferredcites →https://doi.org/10.1016/j.aquaculture.2021.737686openalex-snapshot
An infection mechanism of Balantidium ctenopharyngodoni, based on its prevalence and in vitro cultivation
inferredcites →https://doi.org/10.1016/j.cryobiol.2017.11.010openalex-snapshot
Protocol for cryopreservation of the turbot parasite Philasterides dicentrarchi (Ciliophora, Scuticociliatia)
inferredcites →https://doi.org/10.1016/j.ejop.2014.09.002openalex-snapshot
Free-living ciliates from epiphytic tank bromeliads in Mexico
inferredcites →https://doi.org/10.1016/j.gene.2003.08.003openalex-snapshot
Structure of the micronuclear α-tubulin gene in the phyllopharyngean ciliate Chilodonella uncinata : implications for the evolution of chromosomal processing
inferredcites →https://doi.org/10.1016/j.ijfoodmicro.2011.03.015openalex-snapshot
Occurrence and diversity of free-living protozoa on butterhead lettuce
inferredcites →https://doi.org/10.1016/j.jcpa.2013.08.005openalex-snapshot
Comparative Study of Infection with Tetrahymena of Different Ornamental Fish Species
inferredcites →https://doi.org/10.1016/j.mex.2020.101000openalex-snapshot
Stable and quantitative small-scale laboratory propagation of Cryptocaryon irritans
inferredcites →https://doi.org/10.1016/j.mimet.2009.07.022openalex-snapshot
In vitro culture and cryopreservation of Uronema marinum isolated from farmed New Zealand groper (Polyprion oxygeneios)
inferredcites →https://doi.org/10.1016/j.parint.2010.07.002openalex-snapshot
Phylogenetic consideration of two scuticociliate genera, Philasterides and Boveria (Protozoa, Ciliophora) based on 18 S rRNA gene sequences
inferredcites →https://doi.org/10.1016/j.parint.2012.08.002openalex-snapshot
Identification of scuticociliates (Pseudocohnilembus persalinus, P. longisetus, Uronema marinum and Miamiensis avidus) based on the cox1 sequence
inferredcites →https://doi.org/10.1016/j.vetpar.2010.10.011openalex-snapshot
Intraspecific variability in several isolates of Philasterides dicentrarchi (syn. Miamiensis avidus), a scuticociliate parasite of farmed turbot
inferredcites →https://doi.org/10.1016/j.vetpar.2012.07.030openalex-snapshot
First record of Chilodonella hexasticha (Ciliophora: Chilodonellidae) in Brazilian cultured fish: A morphological and pathological assessment
inferredcites →https://doi.org/10.1016/j.vetpar.2017.03.004openalex-snapshot
Evidence of multiple species of Chilodonella (Protozoa, Ciliophora) infecting Australian farmed freshwater fishes
inferredcites →https://doi.org/10.1016/j.vetpar.2018.10.009openalex-snapshot
Epidemiology and identification of two species of Chilodonella affecting farmed fishes in China
inferredcites →https://doi.org/10.1016/j.ympev.2008.09.017openalex-snapshot
Phylogenetic relationships within the genus Tetrahymena inferred from the cytochrome c oxidase subunit 1 and the small subunit ribosomal RNA genes
inferredcites →https://doi.org/10.1016/j.ympev.2015.02.017openalex-snapshot
Molecular genetic diversity and characterization of conjugation genes in the fish parasite Ichthyophthirius multifiliis
inferredcites →https://doi.org/10.1016/s0003-9365(11)80075-8openalex-snapshot
Morphology and Infraciliature of Some Cyrtophorid Ciliates (Protozoa, Ciliophora) from Freshwater and Soil
inferredcites →https://doi.org/10.1016/s0020-7519(96)00162-2openalex-snapshot
Epizootiology of protozoans in farmed salmonids at northern latitudes
inferredcites →https://doi.org/10.1016/s0044-8486(01)00529-4openalex-snapshot
In vitro assessment of the antiparasitic effect of caprylic acid against several fish parasites
inferredcites →https://doi.org/10.1016/s0044-8486(03)00114-5openalex-snapshot
Differences between short- and long-term cultures of Uronema marinum (Ciliophora: Scuticociliatida) in chemiluminescence inhibitory activity, antioxidative enzyme and protease activity
inferredcites →https://doi.org/10.1016/s0065-308x(05)59003-1openalex-snapshot
Ichthyophthirius multifiliis Fouquet and Ichthyophthiriosis in Freshwater Teleosts
inferredcites →https://doi.org/10.1016/s0932-4739(11)80097-0openalex-snapshot
Philasterides dicentrarchi, n. sp., (ciliophora, scuticociliatida), a histophagous opportunistic parasite of Dicentrarchus labrax (Linnaeus, 1758), a reared marine fish
inferredcites →https://doi.org/10.1017/s0031182000018333openalex-snapshot
Comparative studies on holotrichous ciliates in theColpidium-Glaucoma-Leucophrys-Tetrahymenagroup
inferredcites →https://doi.org/10.1017/s0031182005009534openalex-snapshot
Ultrastructure and phylogeny ofPhilasterides dicentrarchi(Ciliophora, Scuticociliatia) from farmed turbot in NW Spain
inferredcites →https://doi.org/10.1017/s0031182017000749openalex-snapshot
New data on flatfish scuticociliatosis reveal thatMiamiensis avidusandPhilasterides dicentrarchiare different species
inferredcites →https://doi.org/10.1038/sj.jim.7000013openalex-snapshot
Modeling Tetrahymena thermophila growth and protease production
inferredcites →https://doi.org/10.1046/j.1439-0426.2001.00279.xopenalex-snapshot
Temperature- and salinity-dependent development of a Nordic strain of Ichthyophthirius multifiliis from rainbow trout
inferredcites →https://doi.org/10.1046/j.1444-2906.2000.00164.xopenalex-snapshot
Experimental infections of a ciliate Tetrahymena pyriformis on ornamental fishes
inferredcites →https://doi.org/10.1093/gbe/evw099openalex-snapshot
Nuclear Architecture and Patterns of Molecular Evolution Are Correlated in the CiliateChilodonella uncinata
inferredcites →https://doi.org/10.1098/rstb.1983.0027openalex-snapshot
Tetrahymena dimorpha sp.nov. (Hymenostomatida: Tetrahymenidae), a new ciliate parasite of Simuliidae (Diptera) with potential as a model for the study of ciliate morphogenesis
inferredcites →https://doi.org/10.1098/rstb.1985.0102openalex-snapshot
A Paradigm for the study of insect-ciliate Relationships: Tetrahymena sialidos sp. nov. (Hymenostomatida: Tetrahymenidae), Parasite of Larval Sialis Lutaria (Linn.) (Megaloptera: Sialidae)
inferredcites →https://doi.org/10.1099/0022-1317-81-1-143openalex-snapshot
Growth of infectious salmon anaemia virus in CHSE-214 cells and evidence for phenotypic differences between virus strains
inferredcites →https://doi.org/10.1099/ijs.0.64865-0openalex-snapshot
Barcoding ciliates: a comprehensive study of 75 isolates of the genus Tetrahymena
inferredcites →https://doi.org/10.1101/pdb.prot4472openalex-snapshot
Long-Term Storage of UnfrozenTetrahymenaCultures in Soybean Medium
inferredcites →https://doi.org/10.1111/are.14087openalex-snapshot
A massive Chilodonella hexasticha infestation associated with yellowtail tetra Astyanax lacustris mortality in aquaculture: Identification and pathology
inferredcites →https://doi.org/10.1111/j.1095-8649.1973.tb04466.xopenalex-snapshot
Ichthyophthirius multifiliis (Fouquet) in the mirror carp, Cyprinus carpio L.
inferredcites →https://doi.org/10.1111/j.1365-2761.1978.tb00015.xopenalex-snapshot
Intestinal lesions in grasscarpCtenopharyngodon idella(Valenciennes) infected withBalantidium ctenopharyngodonisChen.
inferredcites →https://doi.org/10.1111/j.1365-2761.1979.tb00152.xopenalex-snapshot
Chilodonella hexasticha (Kiernik, 1909) (Protozoa, Ciliata) from North American warmwater fish
inferredcites →https://doi.org/10.1111/j.1365-2761.1980.tb00400.xopenalex-snapshot
Studies on the morphology of Uronema marinum Dujardin (Ciliatea: Uronematidae) with a description of the histopathology of the infection in marine fishes
inferredcites →https://doi.org/10.1111/j.1365-2761.1993.tb00867.xopenalex-snapshot
Cryptocaryon irritans Brown, 1951 (Ichthyophthiriidae): the ultrastructure of the somatic cortex throughout the life cycle
inferredcites →https://doi.org/10.1111/j.1365-2761.1993.tb00877.xopenalex-snapshot
Ichthyophthirius multifiliis: axenic isolation and short‐term maintenance in selected monophasic media
inferredcites →https://doi.org/10.1111/j.1365-2761.2005.00658.xopenalex-snapshot
Environmental and physiological conditions affecting Tetrahymena sp. infection in guppies, Poecilia reticulata Peters
inferredcites →https://doi.org/10.1111/j.1365-2761.2007.00876.xopenalex-snapshot
Vaccination of turbot, Psetta maxima (L.), against the protozoan parasite Philasterides dicentrarchi: effects on antibody production and protection
inferredcites →https://doi.org/10.1111/j.1365-2761.2009.01062.xopenalex-snapshot
Tetrahymena sp. infection in guppies, Poecilia reticulata Peters: parasite characterization and pathology of infected fish
inferredcites →https://doi.org/10.1111/j.1365-2761.2009.01089.xopenalex-snapshot
Antigenic differences of the scuticociliate Miamiensis avidus from Japan
inferredcites →https://doi.org/10.1111/j.1439-0450.2004.00756.xopenalex-snapshot
Role of Ichthyophthirius multifiliis in the Infection of Aeromonas hydrophila
inferredcites →https://doi.org/10.1111/j.1550-7408.1958.tb02552.xopenalex-snapshot
Experimental Infections of Various Animals with Strains of the Genus Tetrahymena*
inferredcites →https://doi.org/10.1111/j.1550-7408.1964.tb01766.xopenalex-snapshot
Miamiensis avidus n. g., n. sp., a Marine Facultative Parasite in the Ciliate Order Hymenostomatida*
inferredcites →https://doi.org/10.1111/j.1550-7408.1972.tb03519.xopenalex-snapshot
The Cultivation of Symbiote‐free Marine Ciliates in Axenic Medium
inferredcites →https://doi.org/10.1111/j.1550-7408.1975.tb05849.xopenalex-snapshot
The Life Cycle of the Histophagous Ciliate Tetrahymena corlissi Thompson, 1955*
inferredcites →https://doi.org/10.1111/j.1550-7408.1980.tb04270.xopenalex-snapshot
Long‐Term Maintenance of Tetrahymena Spp.
inferredcites →https://doi.org/10.1111/j.1550-7408.1985.tb03055.xopenalex-snapshot
Ichthyophthirius multifiliis (Ciliophora) Invasion of Gill Epithelium1
inferredcites →https://doi.org/10.1111/j.1550-7408.1986.tb05625.xopenalex-snapshot
Ichthyophthirius multifiliis (Ciliophora) Development in Gill Epithelium1
inferredcites →https://doi.org/10.1111/j.1550-7408.1991.tb04802.xopenalex-snapshot
Tetrahymena Thermophila: Growth In Synthetic Nutrient Medium In the Presence and Absence of Glucose
inferredcites →https://doi.org/10.1111/j.1550-7408.1995.tb05897.xopenalex-snapshot
A Simple, Efficient Technique for Freezing Tetrahymena thermophila
inferredcites →https://doi.org/10.1111/j.1550-7408.1999.tb04571.xopenalex-snapshot
Interface‐Mediated Death of Unconditioned Tetrahymena Cells: Effect of the Medium Composition
inferredcites →https://doi.org/10.1111/j.1550-7408.2001.tb00322.xopenalex-snapshot
The I‐antigens of Ichthyophthirius multifiliis are GPI‐Anchored Proteins
inferredcites →https://doi.org/10.1111/j.1574-6968.2012.02518.xopenalex-snapshot
Ichthyophthirius multifiliis as a potential vector of Edwardsiella ictaluri in channel catfish
inferredcites →https://doi.org/10.1111/j.1748-5827.1984.tb03424.xopenalex-snapshot
An outbreak of white spot disease (Ichthyophthirius multifiliis) in young fingerling rainbow trout (Salmo gairdneri Richardson)
inferredcites →https://doi.org/10.1111/j.1749-7345.2011.00479.xopenalex-snapshot
Effects of Water pH and Hardness on Infection of Silver Catfish, Rhamdia quelen, Fingerlings by Ichthyophthirius multifiliis
inferredcites →https://doi.org/10.1111/jeu.12109openalex-snapshot
Characterization of the Life Cycle and Heteromeric Nature of the Macronucleus of the Ciliate Chilodonella uncinata Using Fluorescence Microscopy
inferredcites →https://doi.org/10.1111/jeu.12214openalex-snapshot
Some but not All Tetrahymena Species Destroy Monolayer Cultures of Cells from a Wide Range of Tissues and Species
inferredcites →https://doi.org/10.1111/jeu.12642openalex-snapshot
Barcodes Reveal 48 New Species of Tetrahymena , Dexiostoma , and Glaucoma : Phylogeny, Ecology, and Biogeography of New and Established Species
inferredcites →https://doi.org/10.1111/jeu.12791openalex-snapshot
Identification of Intracellular Bacteria in the CiliateBalantidium ctenopharyngodoni(Ciliophora, Litostomatea)
inferredcites →https://doi.org/10.1111/jfd.12204openalex-snapshot
Controlled infection of P oecilia reticulata P eters (guppy) with T etrahymena by immersion and intraperitoneal injection
inferredcites →https://doi.org/10.1111/jfd.12523openalex-snapshot
Current status of parasitic ciliates Chilodonella spp. (Phyllopharyngea: Chilodonellidae) in freshwater fish aquaculture
inferredcites →https://doi.org/10.1128/aem.00850-09openalex-snapshot
Endosymbiotic Bacteria in the Parasitic Ciliate Ichthyophthirius multifiliis
inferredcites →https://doi.org/10.1128/aem.02421-10openalex-snapshot
Preferential Feeding by the Ciliates Chilodonella and Tetrahymena spp. and Effects of These Protozoa on Bacterial Biofilm Structure and Composition
inferredcites →https://doi.org/10.1128/cmr.15.3.327-328.2002openalex-snapshot
Culture of Protozoan Parasites
inferredcites →https://doi.org/10.1139/z85-367openalex-snapshot
Studies on Chilodonella cyprini and C. hexasticha (Protozoa, Ciliata) by scanning electron microscopy
inferredcites →https://doi.org/10.1163/1570756041445182openalex-snapshot
First Record of Chilodonella hexasticha (Kiernik, 1909) Kahl, 1931 (Ciliophora: Chilodonellidae) infesting a freshwater fish Nandus nandus (Hamilton) from Gangetic West Bengal, India
inferredcites →https://doi.org/10.1186/1471-2148-1-5openalex-snapshot
Parallel evolution of histophagy in ciliates of the genus Tetrahymena
inferredcites →https://doi.org/10.1186/1472-6750-6-19openalex-snapshot
Secretion of functional human enzymes by Tetrahymena thermophila
inferredcites →https://doi.org/10.1186/1743-422x-2-75openalex-snapshot
Constitutive expression of Atlantic salmon Mx1 protein in CHSE-214 cells confers resistance to Infectious Salmon Anaemia virus
inferredcites →https://doi.org/10.1186/gb-2011-12-10-r100openalex-snapshot
Comparative genomics of the pathogenic ciliate Ichthyophthirius multifiliis, its free-living relatives and a host species provide insights into adoption of a parasitic lifestyle and prospects for disease control
inferredcites →https://doi.org/10.1371/journal.pgen.1009627openalex-snapshot
Tetrahymena meiosis: Simple yet ingenious
inferredcites →https://doi.org/10.14411/fp.2004.021openalex-snapshot
Histophagous scuticociliatids (Ciliophora) parasitizing turbot Scophthalmus maximus: morphology, in vitro culture and virulence
inferredcites →https://doi.org/10.1534/genetics.114.169748openalex-snapshot
Tetrahymenaas a Unicellular Model Eukaryote: Genetic and Genomic Tools
inferredcites →https://doi.org/10.1556/004.2016.021openalex-snapshot
Molecular genetic investigations on Balantidium ctenopharyngodoni Chen, 1955, a parasite of the grass carp (Ctenopharyngodon idella)
inferredcites →https://doi.org/10.1577/1548-8667(1992)004<0188:semapo>2.3.co;2openalex-snapshot
Scanning Electron Microscopy and Pathogenicity ofChilodonella piscicola(Ciliophora) on Juvenile Salmonids
inferredcites →https://doi.org/10.1577/1548-8667(1994)006<0197:lpocio>2.3.co;2openalex-snapshot
Laboratory Propagation ofCryptocaryon irritanson a Saltwater-AdaptedPoeciliaHybrid, the Black Molly
inferredcites →https://doi.org/10.1577/1548-8667(2000)012<0290:tedoim>2.0.co;2openalex-snapshot
The Early Development of Ichthyophthirius multifiliis in Channel Catfish in Vitro
inferredcites →https://doi.org/10.1645/0022-3395(2002)088[0041:ctoima]2.0.co;2openalex-snapshot
COMPARING TOLERANCE OF ICHTHYOPHTHIRIUS MULTIFILIIS AND TETRAHYMENA THERMOPHILA FOR NEW CRYOPRESERVATION METHODS
inferredcites →https://doi.org/10.2298/avb0601055nopenalex-snapshot
Occurrence of Chilodonella hexasticha (Ciliophora, Protista) on farmed rainbow trout (Oncorhynchus mykiss) throughout the season
inferredcites →https://doi.org/10.2307/1538562openalex-snapshot
NUCLEO-CYTOPLASMIC INTERACTION DURING CONJUGATION IN TETRAHYMENA
inferredcites →https://doi.org/10.2307/3225796openalex-snapshot
Tetrahymena rotunda n. sp. (Hymenostomatida: Tetrahymenidae), a Ciliate Parasite of the Hemolymph of Simulium (Diptera: Simuliidae)
inferredcites →https://doi.org/10.2307/3278995openalex-snapshot
A Disease of Freshwater Fishes Caused by Tetrahymena corlissi Thompson, 1955, and a Key for Identification of Holotrich Ciliates of Freshwater Fishes
inferredcites →https://doi.org/10.2307/3283760openalex-snapshot
A Standardized Method for the In vivo Maintenance of Cryptocaryon irritans (Ciliophora) Using the Grey Mullet Chelon labrosus as an Experimental Host
inferredcites →https://doi.org/10.2307/3284065openalex-snapshot
Sustained Growth of Ichthyophthirius multifiliis at Low Temperature in the Laboratory
inferredcites →https://doi.org/10.2307/3284114openalex-snapshot
Influence of Temperature and Host Species on the Development of Cryptocaryon irritans
inferredcites →https://doi.org/10.2460/javma.1995.207.11.1473openalex-snapshot
Parasitisms of catfish and other farm-raised food fish
inferredcites →https://doi.org/10.3147/jsfp.28.131openalex-snapshot
Isolation and in vitro Cultivation of an Unidentified Ciliate Causing Scuticociliatosis in Japanese Flounder (Paralichthys olivaceus).
inferredcites →https://doi.org/10.3147/jsfp.35.67openalex-snapshot
Tetrahymena Infection in Guppy, Poecilia reticulata.
inferredcites →https://doi.org/10.3147/jsfp.36.195openalex-snapshot
Some Biological Characteristics of Tetrahymena corlissi Isolated from Guppy in Thailand.
inferredcites →https://doi.org/10.3147/jsfp.36.231openalex-snapshot
Effects of High Temperature and Dissolved Oxygen Concentration on the Development of Cryptocaryon irritans (Ciliophora) with a Comment on the Autumn Outbreaks of Cryptocaryoniasis.
inferredcites →https://doi.org/10.3147/jsfp.39.175openalex-snapshot
Short Term In vitro Culture of Cryptocaryon irritans, a Protozoan Parasite of Marine Fishes
inferredcites →https://doi.org/10.3147/jsfp.55.38openalex-snapshot
Control of the Daily Rhythms by Photoperiods in Protomont Detachment and Theront Excystment of the Parasitic Ciliate Cryptocaryon irritans
inferredcites →https://doi.org/10.3354/dao001019openalex-snapshot
Aspects of the biology of Cryptocaryon irritans, and hyposalinity as a control measure in cultured gilthead sea bream Sparus aurata
inferredcites →https://doi.org/10.3354/dao002191openalex-snapshot
Cranial ulceration in Atlantic salmon Salmo salar associated with Tetrahymena sp.
inferredcites →https://doi.org/10.3354/dao01857openalex-snapshot
In vitro culture technique for Cryptocaryon irritans, a parasitic ciliate of marine teleosts
inferredcites →https://doi.org/10.3354/dao02017openalex-snapshot
Pathogenicity of Miamiensis avidus (syn. Philasterides dicentrarchi), Pseudocohnilembus persalinus, Pseudocohnilembus hargisi and Uronema marinum (Ciliophora, Scuticociliatida)
inferredcites →https://doi.org/10.3354/dao02116openalex-snapshot
Effect of hyposalinity on the infection and pathogenicity of Miamiensis avidus causing scuticociliatosis in olive flounder Paralichthys olivaceus
inferredcites →https://doi.org/10.3354/dao03188openalex-snapshot
Tetrahymena glochidiophila n. sp., a new species of Tetrahymena (Ciliophora) that causes mortality to glochidia larvae of freshwater mussels (Bivalvia)
inferredcites →https://doi.org/10.3354/dao042215openalex-snapshot
Prolonged in vitro cultivation of Ichthyophthirius multifiliis using an EPC cell line as substrate
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Parasitic infections in freshwater ornamental fish in Sri Lanka
inferredcites →https://doi.org/10.3354/dao073227openalex-snapshot
Miamiensis avidus (Ciliophora: Scuticociliatida) causes systemic infection of olive flounder Paralichthys olivaceus and is a senior synonym of Philasterides dicentrarchi
inferredcites →https://doi.org/10.3354/dao074049openalex-snapshot
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inferredcites →https://doi.org/10.3389/fcell.2021.807313openalex-snapshot
HAP2-Mediated Gamete Fusion: Lessons From the World of Unicellular Eukaryotes
inferredcites →https://doi.org/10.3389/fmars.2020.00400openalex-snapshot
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inferredcites →https://doi.org/10.3389/fmicb.2017.00189openalex-snapshot
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inferredcites →https://doi.org/10.3724/issn1000-3207-1955-2-123-kopenalex-snapshot
THE PROTOZOAN PARASITES FROM FOUR SPECLES OF CHINESE POND FISHES:CTENOPHARYNGODON IDELLUS,MYLOPHARYNGODON AETHIOPS,ARISTICHTHYS NOBILIS AND HYPOPHTHALMICHTHYS MOLITRIX Ⅰ.THE PROTOZOAN PARASITES OF CTENOPHARYNGODON IDELLUS
inferredcites →https://doi.org/10.4467/16890027ap.15.027.3541openalex-snapshot
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inferredcites →https://doi.org/10.52517/9781789181531openalex-snapshot
Fish Parasites: A Handbook of Protocols for their Isolation, Culture and Transmission
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1016/j.fsi.2024.109429openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fsi.2025.110679openalex-snapshot
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Asymmetrical interactions between Ulva prolifera with different health status and its epiphytic diatoms and ciliates
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A novel method for evaluating the efficacy of pharmaceuticals against the in vivo stage of Ichthyophthirius multifiliis in fish
inferred← citeshttps://doi.org/10.1016/j.protis.2023.125975openalex-snapshot
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Bioremediation of heavy metals using a novel species of ciliate Paramecium multimicronucleatum isolated from industrial wastewater
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Comparative genomics reveals details into the metabolism of peritrich ciliates (Ciliophora, Oligohymenophorea and Peritrichia)
inferred← citeshttps://doi.org/10.1111/jfd.13749openalex-snapshot
Comparison of droplet digital PCR and real‐time quantitative PCR for quantitative detection of the parasitic ciliate Ichthyophthirius multifiliis in the water environment
inferred← citeshttps://doi.org/10.1111/jfd.13881openalex-snapshot
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