Effective sizes of macroparasite populations: a conceptual model.
about
Nematode endoparasites do not codiversify with their stick insect hostsNon-invasive sampling of schistosomes from humans requires correcting for family structure.Large bottleneck size in Cauliflower Mosaic Virus populations during host plant colonization.The origin and phylogeography of dog rabies virus.The population structure of Glossina palpalis gambiensis from island and continental locations in Coastal Guinea.Transmission of Schistosoma japonicum in marshland and hilly regions of China: parasite population genetic and sibship structure.Applying evolutionary genetics to schistosome epidemiology.Heterozygote deficiencies in parasite populations: an evaluation of interrelated hypotheses in the raccoon tick, Ixodes texanus.Molecular approaches to trematode systematics: 'best practice' and implications for future study.Spatial dynamics and genetics of infectious diseases on heterogeneous landscapes.Intra- and interspecific genetic diversity of New Zealand hairworms (Nematomorpha).Species mtDNA genetic diversity explained by infrapopulation size in a host-symbiont system.Temporal sampling helps unravel the genetic structure of naturally occurring populations of a phytoparasitic nematode. 1. Insights from the estimation of effective population sizesA phylogenetic test of the Red Queen Hypothesis: outcrossing and parasitism in the Nematode phylum.Testing local-scale panmixia provides insights into the cryptic ecology, evolution, and epidemiology of metazoan animal parasites.Influence of life history traits on the population genetic structure of parasitic helminths: a minireview.Role of parasite transmission in promoting inbreeding: II. Pedigree reconstruction reveals sib-transmission and consequent kin-mating.Intestinal schistosomiasis in chimpanzees on Ngamba Island, Uganda: observations on liver fibrosis, schistosome genetic diversity and praziquantel treatment.Role of parasite transmission in promoting inbreeding: I. Infection intensities drive individual parasite selfing rates.Inequalities in body size among mermithid nematodes parasitizing earwigs.Inbreeding in stochastic subdivided mating systems: the genetic consequences of host spatial structure, aggregated transmission dynamics and life history characteristics in parasite populations.Genetic Drift, Not Life History or RNAi, Determine Long-Term Evolution of Transposable Elements.An anomaly against a current paradigm--extremely low rates of individual fecundity variability of the Gordian worm (Nematomorpha: Gordiida).Evidence of cryptic speciation in mesostigmatid mites from South Africa.Causes of intraspecific variation in body size among trematode metacercariae.Apparent high recombination rates in clonal parasitic organisms due to inappropriate sampling design.Copulation order, density cues and variance in fertilization success in a cestode.Biogeography and host-related factors trump parasite life history: limited congruence among the genetic structures of specific ectoparasitic lice and their rodent hosts.Prevalence of infection as a predictor of multiple genotype infection frequency in parasites with multiple-host life cycle.
P2860
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P2860
Effective sizes of macroparasite populations: a conceptual model.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
Effective sizes of macroparasite populations: a conceptual model.
@ast
Effective sizes of macroparasite populations: a conceptual model.
@en
type
label
Effective sizes of macroparasite populations: a conceptual model.
@ast
Effective sizes of macroparasite populations: a conceptual model.
@en
prefLabel
Effective sizes of macroparasite populations: a conceptual model.
@ast
Effective sizes of macroparasite populations: a conceptual model.
@en
P356
P1476
Effective sizes of macroparasite populations: a conceptual model.
@en
P2093
Charles D Criscione
Michael S Blouin
P304
P356
10.1016/J.PT.2005.03.002
P577
2005-05-01T00:00:00Z