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1 uld continue to play a role in the future of phylogeography.
2 we introduce the lion as a model for African phylogeography.
3 pecific concordance between biogeography and phylogeography.
4 pecific concordance between biogeography and phylogeography.
5 hich they have arisen are important goals of phylogeography.
6 ent upon epidemiological potential and local phylogeography.
7 n, the pks15/1 genotype, and M. tuberculosis phylogeography.
8 argely concordant with the mitochondrial DNA phylogeography.
9 nd bathymetric distributions, and contrasted phylogeography among species.
10                                          The phylogeography analysis combined with serotype-specific
11 emains an important source of information on phylogeography and demographic history for cetaceans and
12  genomics approach to investigate its global phylogeography and domestication fingerprints using a co
13 numbers of samples to more accurately assess phylogeography and estimate divergence times.
14                        Here we elucidate the phylogeography and evolutionary history of isolates from
15  for patients with subtype D using molecular phylogeography and identify transmission clusters and an
16                                              Phylogeography and landscape genetics have arisen within
17 hlighted, and I end by advocating a union of phylogeography and landscape genetics under the more gen
18                                 Instead, the phylogeography and microsatellite diversity of the E3b1f
19 e an important tool for improved statistical phylogeography and more precise estimates of divergence
20 ons and assess the relationship between host phylogeography and parasite beta diversity.
21                              We investigated phylogeography and spatial genetic structure in an intro
22 ilarity among populations to be coupled with phylogeography and the distribution of genotypes within
23 n the blooming fields of landscape genetics, phylogeography, and evolutionary epidemiology.
24                                              Phylogeography, and its extensions into comparative phyl
25                       We employed a Bayesian phylogeography approach to characterize the emergence of
26                                 Homo sapiens phylogeography begins with the species' origin nearly 20
27  need of more study, particularly phylogeny, phylogeography, chemosensory ecology, and comparative be
28 ics is a younger field (coined in 2003) than phylogeography (coined in 1987), early studies by Dobzha
29                               Third, how can phylogeography contribute to our understanding of functi
30  is time for a paradigm shift in comparative phylogeography, especially given the limited utility of
31                        The new discipline of phylogeography examines the distribution of allele genea
32     Here, we provide examples of comparative phylogeography from (i) tropical seas that host the high
33                                              Phylogeography has benefited from analytical approaches
34               For three decades, comparative phylogeography has conceptually and methodologically rel
35                                              Phylogeography has provided important insights into popu
36 ography, and its extensions into comparative phylogeography, have their roots in the layering of gene
37 can be used to identify detailed patterns of phylogeography in any organism regardless of existing ge
38 ny new evolutionary insights, application of phylogeography in plants has been hampered by difficulty
39 the current scope of continental comparative phylogeography, including geographic, conceptual, tempor
40  of forces generating reticulate patterns in phylogeography, including introgression, contact zones,
41 general concordance between biogeography and phylogeography indicates that the population-level genet
42 hantavirus host distribution, evolution, and phylogeography is emerging.
43                                              Phylogeography is said to be the bridge between populati
44  Almost 30 y ago, the field of intraspecific phylogeography laid the foundation for spatially explici
45   The widespread adoption of RAD-Seq data in phylogeography means genealogical relationships previous
46 o be made when studying plant hybridization, phylogeography, molecular systematics and seed dispersal
47                                           As phylogeography moves into the era of next-generation seq
48 ncordance-discordance dichotomy, comparative phylogeography needs to emphasize the contribution of ta
49                           With a statistical phylogeography of 192 hemagglutinin and neuraminidase is
50                                  Comparative phylogeography of African savannah mammals shows a congr
51                                 Although the phylogeography of European mammals has been extensively
52                In addition, we described the phylogeography of EV-A71 throughout Southeast Asia, docu
53                          Our analyses of the phylogeography of frogs and small mammals indicate that
54          We assessed the breeding system and phylogeography of geographically divergent Lasaea popula
55  perspective of the virus alone, by way of a phylogeography of H5N1 genetic sequences.
56                             To determine the phylogeography of influenza virus in a single population
57                However, the distribution and phylogeography of MJNV in other regions of ROK remain un
58       We test these propositions by studying phylogeography of paper mulberry, a common East Asian tr
59                             In contrast, the phylogeography of PLVB reflects the highly mobile mounta
60                                              Phylogeography of the associated single nucleotide polym
61 pDNA) markers (PCR-RFLP, cpSSR) to study the phylogeography of the species with 293 individuals from
62                                          The phylogeography of these subspecies and their subclades w
63 ern Oceans, allow us to determine the global phylogeography of this species.
64  Ancestral state reconstructions in Bayesian phylogeography of virus pandemics have been improved by
65 chondrial genes to examine the intraspecific phylogeography of Western European samples of E. ephippi
66  structure varied with host population, host phylogeography or geographical distance.
67 genealogies may have limited applications in phylogeography or other approaches dependent on populati
68 articular, studies in conservation genetics, phylogeography, population genetics, species delimitatio
69 igration and mutation patterns, the field of phylogeography provides a valuable tool for improving th
70 s from palaeo-biome reconstruction (PBR) and phylogeography regarding range shift history of EBLF dur
71   With new methods and markers, the focus in phylogeography shifted to previously unrecognized geogra
72 ore the theme of reticulation in comparative phylogeography, speciation analysis, and phylogenomics,
73    An evolutionary trace of HA(1) across the phylogeography suggests a mechanism by which H5N1 is abl
74  to characterize the molecular evolution and phylogeography throughout 10 years of continued sampling
75 tion of phenotypic data extends the reach of phylogeography to explain the origin and maintenance of
76                   Here, we scale comparative phylogeography up to the hemisphere level and examine wh
77 otated corpus of journal articles related to phylogeography using integrated heuristics for location
78 s ago, the approach now known as comparative phylogeography was introduced in a landmark study of a c
79 ricella-zoster virus (VZV) phylogenetics and phylogeography when placed in the broad context of geolo
80                        By combining Bayesian phylogeography with landscape resistance models, we proj

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