about
What can aquatic gastropods tell us about phenotypic plasticity? A review and meta-analysis.Development and disease: how susceptibility to an emerging pathogen changes through anuran development.Widespread occurrence of ranavirus in pond-breeding amphibian populations.Ecology and pathology of amphibian ranaviruses.Species diversity reduces parasite infection through cross-generational effects on host abundance.Parasite diversity and coinfection determine pathogen infection success and host fitness.Host and parasite diversity jointly control disease risk in complex communities.The contribution of phenotypic plasticity to the evolution of insecticide tolerance in amphibian populations.Effects of clothianidin on aquatic communities: Evaluating the impacts of lethal and sublethal exposure to neonicotinoids.Cutaneous Microbial Community Variation across Populations of Eastern Hellbenders (Cryptobranchus alleganiensis alleganiensis).Reciprocal effects of pesticides and pathogens on amphibian hosts: The importance of exposure order and timing.Trends in Ranavirus Prevalence Among Plethodontid Salamanders in the Great Smoky Mountains National Park.A Severe Ranavirus Outbreak in Captive, Wild-Caught Box Turtles.The benefits of coinfection: trematodes alter disease outcomes associated with virus infection.Immediate and lag effects of pesticide exposure on parasite resistance in larval amphibians.Mosquitoes as a Potential Vector of Ranavirus Transmission in Terrestrial Turtles.Anuran susceptibilities to ranaviruses: role of species identity, exposure route, and a novel virus isolate.Heterogeneous hosts: how variation in host size, behaviour and immunity affects parasite aggregation.Widespread co-occurrence of virulent pathogens within California amphibian communities.Evolved pesticide tolerance influences susceptibility to parasites in amphibians.Evolved pesticide tolerance in amphibians: Predicting mechanisms based on pesticide novelty and mode of action.Phylogenetic patterns of trait and trait plasticity evolution: Insights from amphibian embryos.Of poisons and parasites-the defensive role of tetrodotoxin against infections in newts.Phylogeny, life history, and ecology contribute to differences in amphibian susceptibility to ranaviruses.Experimental exposure of Helisoma trivolvis and Biomphalaria glabrata (Gastropoda) to Ribeiroia ondatrae (Trematoda).Parasitism in a community context: trait-mediated interactions with competition and predation.Population-specific toxicity of six insecticides to the trematode Echinoparyphium sp.Effects of Emerging Infectious Diseases on Amphibians: A Review of Experimental StudiesReliability of non-lethal surveillance methods for detecting ranavirus infectionDoes timing matter? How priority effects influence the outcome of parasite interactions within hostsChronic Per-/Polyfluoroalkyl Substance Exposure Under Environmentally Relevant Conditions Delays Development in Northern Leopard Frog (Rana pipiens) LarvaeHealthy but smaller herds: Predators reduce pathogen transmission in an amphibian assemblagePerfluoroalkyl Substances Increase Susceptibility of Northern Leopard Frog Tadpoles to Trematode Infection
P50
Q27323160-01498855-83A9-4DC0-B480-17B779E886F5Q31027385-9194A1BB-56AF-4B7C-A899-1041A5110A6CQ34029846-E23CC673-1FB6-4AFA-BD61-C3CFE8C34E8CQ34094579-E7527B71-AD78-4012-837D-EE244D2FCE59Q34225281-267024B5-8E92-4FA3-837F-192CA2CA82B7Q34276872-EC3C9702-1270-4974-A9FE-CE84504EF8B8Q35003123-224276AF-3328-4200-8037-84475AEA17B1Q35777242-C068A53B-0ADC-415C-BD56-3B4DBA37B9A3Q36320061-554F1E74-B494-437E-BB21-BA46692ACCDCQ38645735-71191570-EEA6-457B-BD01-0D161C949259Q39112717-37F0645B-99B4-4814-A176-5D64F4D70DFFQ39500517-46AA1F16-630D-48A4-9742-54332AF3BD87Q40098539-94CF595E-2CBC-4B6D-9ECE-6168CB0226CCQ40286065-CDEAF12A-7F82-4068-882A-85CBB75DDFE7Q40377625-A1B0414D-7C58-4984-9B0C-6EDCE278EB9DQ41742634-78D15B6D-AEC4-46A2-A261-638E72C7FDFEQ45376703-B05D2DD8-7DC8-4710-9E41-9CD3B6C049A0Q46104503-6D55B99E-67CF-49DC-BB7D-1D752638C461Q46113331-BF8B13B0-0DB9-4460-8B67-13F9AE5C333EQ46194832-29AA292F-0DCC-4F07-B2FB-5248122EB0FFQ46705269-42E7D3BB-F4D4-4276-9A03-C41CC6F9FB4EQ48220440-ABA42D18-45E5-4570-84A0-C63288A86408Q51151406-A25619A8-DD57-4AE5-86D6-B0EF6DDBA7CAQ51170960-69DB4752-2C7F-4D0C-B2A0-B88F39A95E94Q51595656-D6BAA880-8C65-48E0-842D-F9B866335E5BQ51623189-B380DA6F-82D0-4C22-8E04-40CF6377F908Q52844512-F2219F62-8AA3-4E85-8482-A8D5DCD9206BQ56794617-3748BEBE-F6A8-4F36-9663-684FE8343344Q60632799-C9496F2D-6F9C-4438-ABBE-0A9D9FFE0486Q61856477-24598E6D-E792-4CE5-A845-8325D7ADE97DQ89772557-B1B6DF97-60EC-40EB-8B50-BC697F2900B5Q92598805-9901D362-D1A6-4186-9541-C52087AE9E19Q93033494-56EC6440-12CB-4378-A964-33E3E408D4F2
P50
description
onderzoeker
@nl
researcher
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հետազոտող
@hy
name
Jason T Hoverman
@ast
Jason T Hoverman
@en
Jason T Hoverman
@es
Jason T Hoverman
@nl
Jason T Hoverman
@sl
type
label
Jason T Hoverman
@ast
Jason T Hoverman
@en
Jason T Hoverman
@es
Jason T Hoverman
@nl
Jason T Hoverman
@sl
prefLabel
Jason T Hoverman
@ast
Jason T Hoverman
@en
Jason T Hoverman
@es
Jason T Hoverman
@nl
Jason T Hoverman
@sl
P1053
D-1756-2013
P106
P2798
P31
P3829
P496
0000-0002-4002-2728