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Physiology of Batrachochytrium dendrobatidis, a Chytrid Pathogen of Amphibians
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf02451752openalex-snapshot
Attraction and attachment of zoospores of the parasitic chytridRozella allomycis in response to host-dependent factors
inferredcites →https://doi.org/10.1016/s0006-3207(00)00132-4openalex-snapshot
Evidence of a chytrid fungus infection involved in the decline of the common midwife toad (Alytes obstetricans) in protected areas of central Spain
inferredcites →https://doi.org/10.1017/s0953756296003085openalex-snapshot
Orientated zoospore attachment and cyst germination in Catenaria anguillulae, a facultative endoparasite of nematodes
inferredcites →https://doi.org/10.1046/j.1523-1739.1998.96359.xopenalex-snapshot
Decline of a Tropical Montane Amphibian Fauna
inferredcites →https://doi.org/10.1046/j.1523-1739.1999.97185.xopenalex-snapshot
Mass Mortality and Population Declines of Anurans at an Upland Site in Western Panama
inferredcites →https://doi.org/10.1073/pnas.95.15.9031openalex-snapshot
Chytridiomycosis causes amphibian mortality associated with population declines in the rain forests of Australia and Central America
inferredcites →https://doi.org/10.1128/aem.53.8.1819-1821.1987openalex-snapshot
Phototaxis in the Marine Fungus Rhizophydium littoreum
inferredcites →https://doi.org/10.1139/b69-139openalex-snapshot
Studies on Rhizophydium and Phlyctochytrium (Chytridiales). I. Comparative morphology
inferredcites →https://doi.org/10.1139/b70-068openalex-snapshot
Phlyctochytrium reinboldtae (Chytridiales): morphology and physiology
inferredcites →https://doi.org/10.1139/b70-330openalex-snapshot
Phlyctochytrium arcticum n. sp. (Chytridiales); morphology and physiology
inferredcites →https://doi.org/10.1139/m94-017openalex-snapshot
Some characteristics of extracellular proteases produced by members of the Chytridiales and the Spizellomycetales (Chytridiomycetes)
inferredcites →https://doi.org/10.1177/104063879901100219openalex-snapshot
Cutaneous Chytridiomycosis in Poison Dart Frogs ( Dendrobates spp.) and White's Tree Frogs ( Litoria Caerulea )
inferredcites →https://doi.org/10.2307/3761366openalex-snapshot
Batrachochytrium Dendrobatidis gen. et sp. nov., a Chytrid Pathogenic to Amphibians
inferredcites →https://doi.org/10.2307/3807702openalex-snapshot
Zoosporic Fungi in Teaching and Research
inferredcites →https://doi.org/10.3201/eid0506.990601openalex-snapshot
Emerging Infectious Diseases and Amphibian Population Declines
inferredcites →https://doi.org/10.7589/0090-3558-37.1.1openalex-snapshot
EXPERIMENTAL TRANSMISSION OF CUTANEOUS CHYTRIDIOMYCOSIS IN DENDROBATID FROGS
inferredcites →https://doi.org/10.7589/0090-3558-38.1.206openalex-snapshot
Chytridiomycosis in Native Arizona Frogs
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4795486openalex-extracted
Understanding and Predicting Disease Dynamics for an Endangered Amphibian Using Long-Term Surveys of Wild and Translocated Frogs
inferred← citeshttps://doi.org/10.1002/aah.10231openalex-snapshot
Chytridiomycosis in a colony of hellbenders Cryptobranchus alleganiensis
inferred← citeshttps://doi.org/10.1002/eap.1699openalex-snapshot
Host–pathogen metapopulation dynamics suggest high elevation refugia for boreal toads
inferred← citeshttps://doi.org/10.1002/eap.3085openalex-snapshot
Differential recruitment drives pathogen‐mediated competition between species in an amphibian chytridiomycosis system
inferred← citeshttps://doi.org/10.1002/ece3.1271openalex-snapshot
Host‐specific thermal profiles affect fitness of a widespread pathogen
inferred← citeshttps://doi.org/10.1002/ece3.2665openalex-snapshot
Islands within an island: Population genetic structure of the endemic Sardinian newt,Euproctus platycephalus
inferred← citeshttps://doi.org/10.1002/ece3.3309openalex-snapshot
Prevalence and genetic diversity of Batrachochytrium dendrobatidis in Central African island and continental amphibian communities
inferred← citeshttps://doi.org/10.1002/ece3.334openalex-snapshot
Temperature alters reproductive life history patterns in Batrachochytrium dendrobatidis, a lethal pathogen associated with the global loss of amphibians
inferred← citeshttps://doi.org/10.1002/ece3.3468openalex-snapshot
Rapid extirpation of a North American frog coincides with an increase in fungal pathogen prevalence: Historical analysis and implications for reintroduction
inferred← citeshttps://doi.org/10.1002/ece3.3616openalex-snapshot
Design‐ and model‐based recommendations for detecting and quantifying an amphibian pathogen in environmental samples
inferred← citeshttps://doi.org/10.1002/ece3.369openalex-snapshot
Higher temperature variability increases the impact of B atrachochytrium dendrobatidis and shifts interspecific interactions in tadpole mesocosms
inferred← citeshttps://doi.org/10.1002/ece3.5098openalex-snapshot
Infection with Batrachochytrium dendrobatidis is common in tropical lowland habitats: Implications for amphibian conservation
inferred← citeshttps://doi.org/10.1002/ece3.777openalex-snapshot
Daphnia predation on the amphibian chytrid fungus and its impacts on disease risk in tadpoles
inferred← citeshttps://doi.org/10.1002/ece3.7779openalex-snapshot
Exposure to a fungal pathogen increases the critical thermal minimum of two frog species
inferred← citeshttps://doi.org/10.1002/ece3.8379openalex-snapshot
Predicting the growth of the amphibian chytrid fungus in varying temperature environments
inferred← citeshttps://doi.org/10.1002/ece3.8798openalex-snapshot
Widespread occurrence of Batrachochytrium dendrobatidis in Ontario, Canada, and predicted habitat suitability for the emerging Batrachochytrium salamandrivorans
inferred← citeshttps://doi.org/10.1002/ece3.9123openalex-snapshot
Age structure of amphibian populations with endemic chytridiomycosis, across climatic regions with markedly different infection risk
inferred← citeshttps://doi.org/10.1002/ecs2.1740openalex-snapshot
Extreme drought, host density, sex, and bullfrogs influence fungal pathogen infection in a declining lotic amphibian
inferred← citeshttps://doi.org/10.1002/ecs2.2892openalex-snapshot
Effects of latitudinal, seasonal, and daily temperature variations on chytrid fungal infections in a North American frog
inferred← citeshttps://doi.org/10.1002/ecy.3759openalex-snapshot
Once a reservoir, always a reservoir? Seasonality affects the pathogen maintenance potential of amphibian hosts
inferred← citeshttps://doi.org/10.1002/edn3.283openalex-snapshot
Tracking the prevalence of a fungal pathogen, Batrachochytrium dendrobatidis (chytrid fungus), using environmental DNA
inferred← citeshttps://doi.org/10.1002/etc.2707openalex-snapshot
The effects of the amphibian chytrid fungus, insecticide exposure, and temperature on larval anuran development and survival
inferred← citeshttps://doi.org/10.1002/etc.5885openalex-snapshot
Glutathione-Mediated Metal Tolerance in an Amphibian Chytrid Fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1002/jez.1945openalex-snapshot
Cardiac adaptations of bullfrog tadpoles in response to chytrid infection
inferred← citeshttps://doi.org/10.1002/jez.2581openalex-snapshot
Does the thermal mismatch hypothesis predict disease outcomes in different morphs of a terrestrial salamander?
inferred← citeshttps://doi.org/10.1007/13836_2019_69openalex-snapshot
Population Genomics and Wildlife Adaptation in the Face of Climate Change
inferred← citeshttps://doi.org/10.1007/978-3-030-45367-1_7openalex-snapshot
Management of Landscapes for Established Invasive Species
inferred← citeshttps://doi.org/10.1007/978-3-319-56928-4_8openalex-snapshot
Effects of Climate Change on Wildlife in the Northern Rockies
inferred← citeshttps://doi.org/10.1007/978-3-319-65909-1_3openalex-snapshot
Colonization of Parasites and Vectors
inferred← citeshttps://doi.org/10.1007/978-3-642-55318-9_6openalex-snapshot
6 Chytridiomycota, Monoblepharidomycota, and Neocallimastigomycota
inferred← citeshttps://doi.org/10.1007/pl00021734openalex-snapshot
Experimental Exposures of Boreal Toads (Bufo boreas) to a Pathogenic Chytrid Fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1007/s00027-026-01287-2openalex-snapshot
Drivers of aquatic zoosporic parasites in natural and artificial environments
inferred← citeshttps://doi.org/10.1007/s00244-011-9744-1openalex-snapshot
The Impact of Pesticides on the Pathogen Batrachochytrium dendrobatidis Independent of Potential Hosts
inferred← citeshttps://doi.org/10.1007/s00248-021-01897-3openalex-snapshot
Habitat Disturbance Linked with Host Microbiome Dispersion and Bd Dynamics in Temperate Amphibians
inferred← citeshttps://doi.org/10.1007/s00265-008-0655-8openalex-snapshot
Ancient behaviors of larval amphibians in response to an emerging fungal pathogen, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1007/s00265-021-03057-6openalex-snapshot
Social group size influences pathogen transmission in salamanders
inferred← citeshttps://doi.org/10.1007/s00441-010-1014-4openalex-snapshot
The contribution of skin antimicrobial peptides to the system of innate immunity in anurans
inferred← citeshttps://doi.org/10.1007/s00442-008-1026-xopenalex-snapshot
The influence of temperature and spatial distribution on the susceptibility of southern leopard frog eggs to disease
inferred← citeshttps://doi.org/10.1007/s00442-009-1440-8openalex-snapshot
Experimental examination of the effects of ultraviolet-B radiation in combination with other stressors on frog larvae
inferred← citeshttps://doi.org/10.1007/s00442-014-3157-6openalex-snapshot
Evidence of a salt refuge: chytrid infection loads are suppressed in hosts exposed to salt
inferred← citeshttps://doi.org/10.1007/s00442-014-3165-6openalex-snapshot
Trophic dynamics in an aquatic community: interactions among primary producers, grazers, and a pathogenic fungus
inferred← citeshttps://doi.org/10.1007/s00442-015-3422-3openalex-snapshot
Infection dynamics in frog populations with different histories of decline caused by a deadly disease
inferred← citeshttps://doi.org/10.1007/s00442-016-3607-4openalex-snapshot
Susceptibility to disease varies with ontogeny and immunocompetence in a threatened amphibian
inferred← citeshttps://doi.org/10.1007/s00442-017-3866-8openalex-snapshot
Diversity in growth patterns among strains of the lethal fungal pathogen Batrachochytrium dendrobatidis across extended thermal optima
inferred← citeshttps://doi.org/10.1007/s00442-018-4167-6openalex-snapshot
Beyond the swab: ecosystem sampling to understand the persistence of an amphibian pathogen
inferred← citeshttps://doi.org/10.1007/s00442-020-04646-4openalex-snapshot
Assessing amphibian disease risk across tropical streams while accounting for imperfect pathogen detection
inferred← citeshttps://doi.org/10.1007/s00792-010-0323-6openalex-snapshot
Can zoosporic true fungi grow or survive in extreme or stressful environments?
inferred← citeshttps://doi.org/10.1007/s10393-007-0136-yopenalex-snapshot
High Prevalence of Batrachochytrium dendrobatidis in Wild Populations of Lowland Leopard Frogs Rana yavapaiensis in Arizona
inferred← citeshttps://doi.org/10.1007/s10393-008-0154-4openalex-snapshot
Presence of the Chytrid Fungus Batrachochytrium dendrobatidis in Populations of the Critically Endangered Frog Mannophryne olmonae in Tobago, West Indies
inferred← citeshttps://doi.org/10.1007/s10393-008-0155-3openalex-snapshot
Chytridiomycosis Survey in Wild and Captive Mexican Amphibians
inferred← citeshttps://doi.org/10.1007/s10393-009-0230-4openalex-snapshot
Distribution and Pathogenicity of Batrachochytrium dendrobatidis in Boreal Toads from the Grand Teton Area of Western Wyoming
inferred← citeshttps://doi.org/10.1007/s10393-010-0278-1openalex-snapshot
How Does Chytrid Infection Vary Among Habitats? The Case of Litoria wilcoxii (Anura, Hylidae) in SE Queensland, Australia
inferred← citeshttps://doi.org/10.1007/s10393-010-0281-6openalex-snapshot
The Link Between Rapid Enigmatic Amphibian Decline and the Globally Emerging Chytrid Fungus
inferred← citeshttps://doi.org/10.1007/s10393-010-0292-3openalex-snapshot
Determining Causality and Controlling Disease is Based on Collaborative Research involving Multidisciplinary Approaches
inferred← citeshttps://doi.org/10.1007/s10393-010-0350-xopenalex-snapshot
Immmunological Clearance of Batrachochytrium dendrobatidis Infection at a Pathogen-optimal Temperature in the Hylid Frog Hypsiboas crepitans
inferred← citeshttps://doi.org/10.1007/s10393-011-0685-yopenalex-snapshot
First Record of Batrachochytrium dendrobatidis Infecting Four Frog Families from Peninsular Malaysia
inferred← citeshttps://doi.org/10.1007/s10393-011-0689-7openalex-snapshot
Motile Zoospores of Batrachochytrium dendrobatidis Move Away from Antifungal Metabolites Produced by Amphibian Skin Bacteria
inferred← citeshttps://doi.org/10.1007/s10393-012-0771-9openalex-snapshot
Bd on the Beach: High Prevalence of Batrachochytrium dendrobatidis in the Lowland Forests of Gorgona Island (Colombia, South America)
inferred← citeshttps://doi.org/10.1007/s10393-013-0831-9openalex-snapshot
Batrachochytrium dendrobatidis Infection and Lethal Chytridiomycosis in Caecilian Amphibians (Gymnophiona)
inferred← citeshttps://doi.org/10.1007/s10393-014-0967-2openalex-snapshot
Extremely Low Prevalence of Batrachochytrium dendrobatidis in Frog Populations from Neotropical Dry Forest of Costa Rica Supports the Existence of a Climatic Refuge from Disease
inferred← citeshttps://doi.org/10.1007/s10393-015-1010-yopenalex-snapshot
Variation in the Presence of Anti-Batrachochytrium dendrobatidis Bacteria of Amphibians Across Life Stages and Elevations in Ecuador
inferred← citeshttps://doi.org/10.1007/s10393-015-1035-2openalex-snapshot
American Bullfrogs (Lithobates catesbeianus) Resist Infection by Multiple Isolates of Batrachochytrium dendrobatidis, Including One Implicated in Wild Mass Mortality
inferred← citeshttps://doi.org/10.1007/s10393-016-1101-4openalex-snapshot
Prevalence and Seasonality of the Amphibian Chytrid Fungus Batrachochytrium dendrobatidis Along Widely Separated Longitudes Across the United States
inferred← citeshttps://doi.org/10.1007/s10393-016-1106-zopenalex-snapshot
Leaf Litter Inhibits Growth of an Amphibian Fungal Pathogen
inferred← citeshttps://doi.org/10.1007/s10393-017-1240-2openalex-snapshot
Batrachochytrium dendrobatidis and the Decline and Survival of the Relict Leopard Frog
inferred← citeshttps://doi.org/10.1007/s10393-017-1269-2openalex-snapshot
The Influence of Temperature on Chytridiomycosis In Vivo
inferred← citeshttps://doi.org/10.1007/s10393-017-1278-1openalex-snapshot
Batrachochytrium salamandrivorans and the Risk of a Second Amphibian Pandemic
inferred← citeshttps://doi.org/10.1007/s10393-018-1383-9openalex-snapshot
The Chytrid Fungus, Batrachochytrium dendrobatidis, is Widespread Among Cuban Amphibians
inferred← citeshttps://doi.org/10.1007/s10393-019-01414-6openalex-snapshot
Quantifying Batrachochytrium dendrobatidis and Batrachochytrium salamandrivorans Viability
inferred← citeshttps://doi.org/10.1007/s10393-019-01432-4openalex-snapshot
Pathogen Dynamics in an Invasive Frog Compared to Native Species
inferred← citeshttps://doi.org/10.1007/s10393-019-01446-yopenalex-snapshot
Population-Level Resistance to Chytridiomycosis is Life-Stage Dependent in an Imperiled Anuran
inferred← citeshttps://doi.org/10.1007/s10393-020-01501-zopenalex-snapshot
Differences in Fungal Disease Dynamics in Co-occurring Terrestrial and Aquatic Amphibians
inferred← citeshttps://doi.org/10.1007/s10393-021-01570-8openalex-snapshot
Three Pathogens Impact Terrestrial Frogs from a High-Elevation Tropical Hotspot
inferred← citeshttps://doi.org/10.1007/s10393-023-01668-1openalex-snapshot
Batrachochytrium dendrobatidis in the Arid and Thermally Extreme Sonoran Desert
inferred← citeshttps://doi.org/10.1007/s10393-025-01698-xopenalex-snapshot
Climatically Specialized Lineages of Batrachochytrium dendrobatidis, and its Likely Asian Origins
inferred← citeshttps://doi.org/10.1007/s10393-025-01734-wopenalex-snapshot
Ecophysiological Suitability of Batrachochytrium dendrobatidis in Mexico
inferred← citeshttps://doi.org/10.1007/s10452-019-09727-yopenalex-snapshot
Batrachochytrium dendrobatidis infection in amphibians from a high elevation habitat in the trans-Mexican volcanic belt
inferred← citeshttps://doi.org/10.1007/s10452-021-09869-yopenalex-snapshot
Effects of intrinsic and extrinsic factors on the prevalence of the fungus Batrachochytrium dendrobatidis (Chytridiomycota) in stream tadpoles in the Atlantic Forest domain
inferred← citeshttps://doi.org/10.1007/s10453-015-9374-6openalex-snapshot
Presence of amphibian chytrid fungus (Batrachochytrium dendrobatidis) in rainwater suggests aerial dispersal is possible
inferred← citeshttps://doi.org/10.1007/s10530-009-9577-2openalex-snapshot
Presence of Batrachochytrium dendrobatidis in feral populations of Xenopus laevis in Chile
inferred← citeshttps://doi.org/10.1007/s10530-017-1390-8openalex-snapshot
Unraveling the historical prevalence of the invasive chytrid fungus in the Bolivian Andes: implications in recent amphibian declines
inferred← citeshttps://doi.org/10.1007/s10530-019-02041-6openalex-snapshot
The invasive red swamp crayfish (Procambarus clarkii) increases infection of the amphibian chytrid fungus (Batrachochytrium dendrobatidis)
inferred← citeshttps://doi.org/10.1007/s10530-020-02218-4openalex-snapshot
Effects of invasive larval bullfrogs (Rana catesbeiana) on disease transmission, growth and survival in the larvae of native amphibians
inferred← citeshttps://doi.org/10.1007/s10530-025-03648-8openalex-snapshot
Is exposure to chytrid fungus and ranavirus higher in ponds invaded by American bullfrogs?
inferred← citeshttps://doi.org/10.1007/s10531-011-0066-4openalex-snapshot
Species-level correlates of susceptibility to the pathogenic amphibian fungus Batrachochytrium dendrobatidis in the United States
inferred← citeshttps://doi.org/10.1007/s10531-017-1468-8openalex-snapshot
The anurofauna of a vanishing savanna: the case of the Brazilian Cerrado
inferred← citeshttps://doi.org/10.1007/s10531-019-01734-7openalex-snapshot
Persistence through tough times: fixed and shifting refuges in threatened species conservation
inferred← citeshttps://doi.org/10.1007/s10531-021-02224-5openalex-snapshot
Modelling the amphibian chytrid fungus spread by connectivity analysis: towards a national monitoring network in Italy
inferred← citeshttps://doi.org/10.1007/s10750-010-0270-3openalex-snapshot
Potential distribution of Batrachochytrium dendrobatidis in Argentina: implications in amphibian conservation
inferred← citeshttps://doi.org/10.1007/s10750-017-3367-0openalex-snapshot
Stream tadpoles present high prevalence but low infection loads of Batrachochytrium dendrobatidis (Chytridiomycota)
inferred← citeshttps://doi.org/10.1007/s10750-020-04339-2openalex-snapshot
High temporal and individual variation in the prevalence and intensity of chytrid infection in the southernmost Leaf Frog of the genus Pithecopus (Anura, Phyllomedusidae)
inferred← citeshttps://doi.org/10.1007/s11046-008-9135-yopenalex-snapshot
Growth Characteristics and Enzyme Activity in Batrachochytrium dendrobatidis Isolates
inferred← citeshttps://doi.org/10.1007/s11259-024-10449-2openalex-snapshot
Spontaneous reoccurrence of Batrachochytrium dendrobatidis infections in Australian green tree frogs (Litoria caerulea) following apparently successful heat therapy: Case report
inferred← citeshttps://doi.org/10.1007/s12237-014-9847-9openalex-snapshot
Warming Reduces Pathogen Pressure on a Climate-Vulnerable Seagrass Species
inferred← citeshttps://doi.org/10.1007/s13225-018-0413-9openalex-snapshot
The world’s ten most feared fungi
inferred← citeshttps://doi.org/10.1007/s41745-021-00227-3openalex-snapshot
Chytridiomycosis in Asian Amphibians, a Global Resource for Batrachochytrium dendrobatidis (Bd) Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-384890-1.00004-2openalex-snapshot
Epidemiology and Evolution of Fungal Pathogens in Plants and Animals
inferred← citeshttps://doi.org/10.1016/b978-0-12-799942-5.00004-4openalex-snapshot
Epidemiology and Evolution of Fungal Pathogens in Plants and Animals
inferred← citeshttps://doi.org/10.1016/b978-0-12-821139-7.00145-8openalex-snapshot
The Decline of Australian Heath Frogs and Summary of Current Threats
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2016.07.035openalex-snapshot
Chytrid Batrachochytrium dendrobatidis fungal infection in freshwater prawn, Macrobrachium rosenbergii (de Man) - A new report
inferred← citeshttps://doi.org/10.1016/j.bbamem.2009.03.008openalex-snapshot
The role of amphibian antimicrobial peptides in protection of amphibians from pathogens linked to global amphibian declines
inferred← citeshttps://doi.org/10.1016/j.biocon.2008.03.011openalex-snapshot
Distribution and environmental limitations of an amphibian pathogen in the Rocky Mountains, USA
inferred← citeshttps://doi.org/10.1016/j.biocon.2008.04.014openalex-snapshot
Decline and extirpation of an endangered Panamanian stream frog population (Craugastor punctariolus) due to an outbreak of chytridiomycosis
inferred← citeshttps://doi.org/10.1016/j.biocon.2009.02.007openalex-snapshot
Magnitude of the US trade in amphibians and presence of Batrachochytrium dendrobatidis and ranavirus infection in imported North American bullfrogs (Rana catesbeiana)
inferred← citeshttps://doi.org/10.1016/j.biocon.2011.03.018openalex-snapshot
Disease dynamics vary spatially and temporally in a North American amphibian
inferred← citeshttps://doi.org/10.1016/j.biocon.2011.08.008openalex-snapshot
Factors related to the distribution and prevalence of the fungal pathogen Batrachochytrium dendrobatidis in Rana cascadae and other amphibians in the Klamath Mountains
inferred← citeshttps://doi.org/10.1016/j.biocon.2012.09.013openalex-snapshot
Disease in a dynamic landscape: Host behavior and wildfire reduce amphibian chytrid infection
inferred← citeshttps://doi.org/10.1016/j.biocon.2012.11.023openalex-snapshot
High prevalence of infection in tadpoles increases vulnerability to fungal pathogen in high-Andean amphibians
inferred← citeshttps://doi.org/10.1016/j.biocon.2014.11.032openalex-snapshot
Low impact of chytridiomycosis on frog recruitment enables persistence in refuges despite high adult mortality
inferred← citeshttps://doi.org/10.1016/j.biocon.2014.12.007openalex-snapshot
A century of Batrachochytrium dendrobatidis in Illinois amphibians (1888–1989)
inferred← citeshttps://doi.org/10.1016/j.biocon.2015.08.039openalex-snapshot
Reconstructing historical and contemporary disease dynamics: A case study using the California slender salamander
inferred← citeshttps://doi.org/10.1016/j.biocon.2016.12.010openalex-snapshot
After the epidemic: Ongoing declines, stabilizations and recoveries in amphibians afflicted by chytridiomycosis
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.032openalex-snapshot
Living with the enemy: Facilitating amphibian coexistence with disease
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.108247openalex-snapshot
Title: Recruitment is key to understanding amphibian’s different population-level responses to chytrid fungus infection
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.108373openalex-snapshot
Contrasting demographic responses of toad populations to regionally synchronous pathogen (Batrachochytrium dendrobatidis) dynamics
inferred← citeshttps://doi.org/10.1016/j.biocon.2020.108521openalex-snapshot
Synergistic effects of warming and disease linked to high mortality in cool-adapted terrestrial frogs
inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109246openalex-snapshot
Fungal disease cluster in tropical terrestrial frogs predicted by low rainfall
inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109247openalex-snapshot
Livestock grazing, climatic variation, and breeding phenology jointly shape disease dynamics and survival in a wild amphibian
inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109300openalex-snapshot
Occurrence of Batrachochytrium dendrobatidis within and between species: A review of influential variables as identified from field studies
inferred← citeshttps://doi.org/10.1016/j.biocon.2021.109391openalex-snapshot
Chytrid infection dynamics in frog populations from climatically disparate regions
inferred← citeshttps://doi.org/10.1016/j.bioflm.2019.100009openalex-snapshot
Characteristics of monolayer formation in vitro by the chytrid Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1016/j.cbpa.2012.02.018openalex-snapshot
Urinary corticosterone metabolites and chytridiomycosis disease prevalence in a free-living population of male Stony Creek frogs (Litoria wilcoxii)
inferred← citeshttps://doi.org/10.1016/j.cbpa.2016.09.019openalex-snapshot
Does physiological response to disease incur cost to reproductive ecology in a sexually dichromatic amphibian species?
inferred← citeshttps://doi.org/10.1016/j.cimid.2013.07.002openalex-snapshot
Bacterial flora on Cascades frogs in the Klamath mountains of California
inferred← citeshttps://doi.org/10.1016/j.cub.2022.04.006openalex-snapshot
Amphibian mucus triggers a developmental transition in the frog-killing chytrid fungus
inferred← citeshttps://doi.org/10.1016/j.cvex.2013.05.009openalex-snapshot
Pathogenesis, Diagnosis, and Treatment of Amphibian Chytridiomycosis
inferred← citeshttps://doi.org/10.1016/j.dci.2004.11.004openalex-snapshot
Antimicrobial peptide defenses against chytridiomycosis, an emerging infectious disease of amphibian populations
inferred← citeshttps://doi.org/10.1016/j.dci.2005.10.005openalex-snapshot
Antimicrobial peptide defenses of the mountain yellow-legged frog (Rana muscosa)
inferred← citeshttps://doi.org/10.1016/j.dci.2016.07.002openalex-snapshot
Amphibian immunity–stress, disease, and climate change
inferred← citeshttps://doi.org/10.1016/j.dci.2017.05.022openalex-snapshot
Evolutionary dynamics of an expressed MHC class IIβ locus in the Ranidae (Anura) uncovered by genome walking and high-throughput amplicon sequencing
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2015.09.015openalex-snapshot
A model for the interaction of frog population dynamics with Batrachochytrium dendrobatidis, Janthinobacterium lividum and temperature and its implication for chytridiomycosis management
inferred← citeshttps://doi.org/10.1016/j.envres.2008.09.001openalex-snapshot
Effect of road deicing salt on the susceptibility of amphibian embryos to infection by water molds
inferred← citeshttps://doi.org/10.1016/j.fbr.2008.02.001openalex-snapshot
The ecology of chytrids in aquatic ecosystems: roles in food web dynamics
inferred← citeshttps://doi.org/10.1016/j.fgb.2012.07.002openalex-snapshot
Batrachochytrium dendrobatidis zoospore secretions rapidly disturb intercellular junctions in frog skin
inferred← citeshttps://doi.org/10.1016/j.foreco.2009.06.043openalex-snapshot
Thermal characteristics of amphibian microhabitats in a fire-disturbed landscape
inferred← citeshttps://doi.org/10.1016/j.funbio.2012.10.005openalex-snapshot
Immune evasion or avoidance: Fungal skin infection linked to reduced defence peptides in Australian green-eyed treefrogs, Litoria serrata
inferred← citeshttps://doi.org/10.1016/j.funbio.2013.05.002openalex-snapshot
A novel subtilisin-like serine protease of Batrachochytrium dendrobatidis is induced by thyroid hormone and degrades antimicrobial peptides
inferred← citeshttps://doi.org/10.1016/j.funbio.2019.10.008openalex-snapshot
Gene expression varies within and between enzootic and epizootic lineages of Batrachochytrium dendrobatidis (Bd) in the Americas
inferred← citeshttps://doi.org/10.1016/j.funeco.2008.12.002openalex-snapshot
Structure and function of fungal zoospores: ecological implications
inferred← citeshttps://doi.org/10.1016/j.funeco.2009.11.004openalex-snapshot
A correlation between chytrid abundance and ecological integrity in New Jersey pine barrens waters
inferred← citeshttps://doi.org/10.1016/j.funeco.2014.04.001openalex-snapshot
Multiple zoosporic parasites pose a significant threat to amphibian populations
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.007openalex-snapshot
History and recent progress on chytridiomycosis in amphibians
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.09.014openalex-snapshot
Local phenotypic variation in amphibian-killing fungus predicts infection dynamics
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.12.001openalex-snapshot
Genetic characterization of chytrids isolated from larval amphibians collected in central and east Texas
inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100995openalex-snapshot
Biotic and abiotic determinants of Batrachochytrium dendrobatidis infections in amphibians of the Brazilian Atlantic Forest
inferred← citeshttps://doi.org/10.1016/j.gecco.2015.07.003openalex-snapshot
The demography of Atelopus decline: Harlequin frog survival and abundance in central Panama prior to and during a disease outbreak
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2013.04.002openalex-snapshot
Do invasive cane toads affect the parasite burdens of native Australian frogs?
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2019.12.005openalex-snapshot
Chiggers (Acariformes: Trombiculoidea) do not increase rates of infection by Batrachochytrium dendrobatidis fungus in the endemic Dwarf Mexican Treefrog Tlalocohyla smithii (Anura: Hylidae)
inferred← citeshttps://doi.org/10.1016/j.meegid.2012.07.024openalex-snapshot
Hybrid advantage in skin peptide immune defenses of water frogs (Pelophylax esculentus) at risk from emerging pathogens
inferred← citeshttps://doi.org/10.1016/j.micinf.2010.09.015openalex-snapshot
Interactions between Batrachochytrium dendrobatidis and its amphibian hosts: a review of pathogenesis and immunity
inferred← citeshttps://doi.org/10.1016/j.mimet.2012.04.021openalex-snapshot
Magnetic capture hybridization of Batrachochytrium dendrobatidis genomic DNA
inferred← citeshttps://doi.org/10.1016/j.mimet.2016.05.019openalex-snapshot
A fast and reliable procedure for spore collection from anaerobic fungi: Application for RNA uptake and long-term storage of isolates
inferred← citeshttps://doi.org/10.1016/j.mycres.2006.10.009openalex-snapshot
Preservation of Chytridiomycota in culture collections
inferred← citeshttps://doi.org/10.1016/j.rmb.2015.07.007openalex-snapshot
First record of Batrachochytrium dendrobatidis infecting threatened populations of Tandilean Red-belly toad (Melanophryniscus aff. montevidensis) in Argentina
inferred← citeshttps://doi.org/10.1016/j.rmb.2016.01.020openalex-snapshot
Temperature treatments boost subclinical infections of Batrachochytrium dendrobatidis in a Mexican salamander (Pseudoeurycea leprosa)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.12.006openalex-snapshot
People, pollution and pathogens – Global change impacts in mountain freshwater ecosystems
inferred← citeshttps://doi.org/10.1016/j.tree.2009.07.011openalex-snapshot
The ecology and impact of chytridiomycosis: an emerging disease of amphibians
inferred← citeshttps://doi.org/10.1016/j.ygcen.2019.113269openalex-snapshot
Relationships between glucocorticoids and infection with Batrachochytrium dendrobatidis in three amphibian species
inferred← citeshttps://doi.org/10.1017/s0953756204002163openalex-snapshot
The growth response of some Chytridiomycota to temperatures commonly observed in the soil
inferred← citeshttps://doi.org/10.1021/acs.est.6b06055openalex-snapshot
Effect of Simultaneous Amphibian Exposure to Pesticides and an Emerging Fungal Pathogen,Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1038/ismej.2009.27openalex-snapshot
Skin microbes on frogs prevent morbidity and mortality caused by a lethal skin fungus
inferred← citeshttps://doi.org/10.1038/laban1009-329openalex-snapshot
A novel system for individually housing bullfrogs
inferred← citeshttps://doi.org/10.1038/nature04246openalex-snapshot
Widespread amphibian extinctions from epidemic disease driven by global warming
inferred← citeshttps://doi.org/10.1038/ncomms15048openalex-snapshot
Chytrid fungus infection in zebrafish demonstrates that the pathogen can parasitize non-amphibian vertebrate hosts
inferred← citeshttps://doi.org/10.1038/s41396-019-0388-xopenalex-snapshot
Integrating the role of antifungal bacteria into skin symbiotic communities of three Neotropical frog species
inferred← citeshttps://doi.org/10.1038/s41586-024-07582-yopenalex-snapshot
Hotspot shelters stimulate frog resistance to chytridiomycosis
inferred← citeshttps://doi.org/10.1038/s41598-017-05798-9openalex-snapshot
Antifungal treatment of wild amphibian populations caused a transient reduction in the prevalence of the fungal pathogen, Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1038/s41598-017-09950-3openalex-snapshot
Infection increases vulnerability to climate change via effects on host thermal tolerance
inferred← citeshttps://doi.org/10.1038/s41598-018-24472-2openalex-snapshot
Development and worldwide use of non-lethal, and minimal population-level impact, protocols for the isolation of amphibian chytrid fungi
inferred← citeshttps://doi.org/10.1038/s41598-018-35874-7openalex-snapshot
Interaction between temperature and sublethal infection with the amphibian chytrid fungus impacts a susceptible frog species
inferred← citeshttps://doi.org/10.1038/s42003-023-05600-9openalex-snapshot
Linking microbiome and stress hormone responses in wild tropical treefrogs across continuous and fragmented forests
inferred← citeshttps://doi.org/10.1038/srep01515openalex-snapshot
Hot bodies protect amphibians against chytrid infection in nature
inferred← citeshttps://doi.org/10.1038/srep08037openalex-snapshot
Treatment of urodelans based on temperature dependent infection dynamics of Batrachochytrium salamandrivorans
inferred← citeshttps://doi.org/10.1038/srep13472openalex-snapshot
Natural disturbance reduces disease risk in endangered rainforest frog populations
inferred← citeshttps://doi.org/10.1038/srep30772openalex-snapshot
Dynamics and genetics of a disease-driven species decline to near extinction: lessons for conservation
inferred← citeshttps://doi.org/10.1053/j.jepm.2015.06.013openalex-snapshot
Chytridiomycosis in Amphibians
inferred← citeshttps://doi.org/10.1071/ma05085openalex-snapshot
Amphibian disease and declines: Chytridiomycosis
inferred← citeshttps://doi.org/10.1071/wr14097openalex-snapshot
Low humidity is a failed treatment option for chytridiomycosis in the critically endangered southern corroboree frog
inferred← citeshttps://doi.org/10.1071/wr15223openalex-snapshot
The role of non-declining amphibian species as alternative hosts for Batrachochytrium dendrobatidis in an amphibian community
inferred← citeshttps://doi.org/10.1071/wr16145openalex-snapshot
Assessing host response to disease treatment: how chytrid-susceptible frogs react to increased water salinity
inferred← citeshttps://doi.org/10.1071/wr23126openalex-snapshot
High chytrid prevalence and infection intensities in tadpoles of Mixophyes fleayi
inferred← citeshttps://doi.org/10.1073/pnas.0804173105openalex-snapshot
Global gene expression profiles for life stages of the deadly amphibian pathogen Batrachochytrium dendrobatidis
inferred← citeshttps://doi.org/10.1073/pnas.0806368105openalex-snapshot
Evaluating the links between climate, disease spread, and amphibian declines
inferred← citeshttps://doi.org/10.1073/pnas.0912886107openalex-snapshot
Enzootic and epizootic dynamics of the chytrid fungal pathogen of amphibians
inferred← citeshttps://doi.org/10.1073/pnas.1014497108openalex-snapshot
Tropical amphibian populations experience higher disease risk in natural habitats
inferred← citeshttps://doi.org/10.1079/cabicompendium.109124openalex-snapshot
Batrachochytrium dendrobatidis (Bd)
inferred← citeshttps://doi.org/10.1080/01650521.2016.1163857openalex-snapshot
Crossing the threshold: an amphibian assemblage highly infected with Batrachochytrium dendrobatidis in the southern Brazilian Atlantic forest
inferred← citeshttps://doi.org/10.1080/15627020.2011.11407483openalex-snapshot
Seasonal Pattern of Chytridiomycosis in Common River Frog (Amietia angolensis) Tadpoles in the South African Grassland Biome
inferred← citeshttps://doi.org/10.1080/17513751003777515openalex-snapshot
Stability and permanence in gender- and stage-structured models for the boreal toad
inferred← citeshttps://doi.org/10.1093/conphys/coab074openalex-snapshot
Applied ecoimmunology: using immunological tools to improve conservation efforts in a changing world
inferred← citeshttps://doi.org/10.1093/conphys/coaf037openalex-snapshot
Skin pH and buffering ability vary between two co-occurring semi-aquatic frog species
inferred← citeshttps://doi.org/10.1093/conphys/cot022openalex-snapshot
Using physiology to understand climate-driven changes in disease and their implications for conservation
inferred← citeshttps://doi.org/10.1093/conphys/cou012openalex-snapshot
First line of defence: the role of sloughing in the regulation of cutaneous microbes in frogs
inferred← citeshttps://doi.org/10.1093/conphys/cow077openalex-snapshot
Environmental and physiological correlates of the severity of clinical signs of snake fungal disease in a population of pigmy rattlesnakes,Sistrurus miliarius
inferred← citeshttps://doi.org/10.1093/femsec/fiaa168openalex-snapshot
Columbia spotted frogs (Rana luteiventris) have characteristic skin microbiota that may be shaped by cutaneous skin peptides and the environment
inferred← citeshttps://doi.org/10.1093/icb/icr095openalex-snapshot
Amphibian Immune Defenses against Chytridiomycosis: Impacts of Changing Environments
inferred← citeshttps://doi.org/10.1093/ismejo/wrae189openalex-snapshot
Biofilms inactivate the free-living stage of Batrachochytrium dendrobatidis, the most destructive pathogen for vertebrate diversity
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