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1 ffected its gene flow, genetic structure and phylogeography.
2  climate, are a pioneer model in Pleistocene phylogeography.
3  is known about its population structure and phylogeography.
4 d helping to establish the species' baseline phylogeography.
5                   This issue is pervasive in phylogeography.
6 us work into a comprehensive model of Mammut phylogeography.
7 uld continue to play a role in the future of phylogeography.
8 we introduce the lion as a model for African phylogeography.
9 pecific concordance between biogeography and phylogeography.
10 pecific concordance between biogeography and phylogeography.
11 hich they have arisen are important goals of phylogeography.
12 ent upon epidemiological potential and local phylogeography.
13 n, the pks15/1 genotype, and M. tuberculosis phylogeography.
14 argely concordant with the mitochondrial DNA phylogeography.
15 nd bathymetric distributions, and contrasted phylogeography among species.
16                                          The phylogeography analysis combined with serotype-specific
17 ding understanding adaptation, biodiversity, phylogeography and co-evolution.
18 emains an important source of information on phylogeography and demographic history for cetaceans and
19  genomics approach to investigate its global phylogeography and domestication fingerprints using a co
20 numbers of samples to more accurately assess phylogeography and estimate divergence times.
21                        Here we elucidate the phylogeography and evolutionary history of isolates from
22  somatic mutations in this cancer record its phylogeography and evolutionary history.
23 's GenBank for downstream analysis including phylogeography and genomic epidemiology.
24  for patients with subtype D using molecular phylogeography and identify transmission clusters and an
25                                              Phylogeography and landscape genetics have arisen within
26 hlighted, and I end by advocating a union of phylogeography and landscape genetics under the more gen
27                                 Instead, the phylogeography and microsatellite diversity of the E3b1f
28 e an important tool for improved statistical phylogeography and more precise estimates of divergence
29 vides the first description of elephant bird phylogeography and offers insight into the ecology and e
30 ons and assess the relationship between host phylogeography and parasite beta diversity.
31  unprecedented insight into L. monocytogenes phylogeography and population dynamics and highlights th
32          But despite their ubiquity, leopard phylogeography and population history have not yet been
33 ve genomics to assess the genetic diversity, phylogeography and potential origins of B. pseudomallei
34 agged viral genomes using spatially-explicit phylogeography and simulating virus dispersal, we find t
35                              We investigated phylogeography and spatial genetic structure in an intro
36 ilarity among populations to be coupled with phylogeography and the distribution of genotypes within
37                  Combining molecular dating, phylogeography, and comparative genomic analyses of a la
38 n the blooming fields of landscape genetics, phylogeography, and evolutionary epidemiology.
39                                              Phylogeography, and its extensions into comparative phyl
40                       We employed a Bayesian phylogeography approach to characterize the emergence of
41 resent-day patterns of genetic diversity and phylogeography are influenced by various factors, with h
42                                 Homo sapiens phylogeography begins with the species' origin nearly 20
43 spread as a Brownian motion (Brownian Motion Phylogeography, BMP) in continuous space and time, akin
44 d DNA, whose use in comparative genomics and phylogeography can shed light on the emergence and evolu
45  need of more study, particularly phylogeny, phylogeography, chemosensory ecology, and comparative be
46 ics is a younger field (coined in 2003) than phylogeography (coined in 1987), early studies by Dobzha
47                               Third, how can phylogeography contribute to our understanding of functi
48  Whole-genome sequencing (WGS) combined with phylogeography enables us to track the dissemination of
49  is time for a paradigm shift in comparative phylogeography, especially given the limited utility of
50 gh mitochondrial DNA has been widely used in phylogeography, evidence has emerged that factors such a
51                        The new discipline of phylogeography examines the distribution of allele genea
52     Here, we provide examples of comparative phylogeography from (i) tropical seas that host the high
53  and reconstruct spatial tumor evolution, or phylogeography, from SRT data.
54 ther areas, from wing pattern development to phylogeography, from toxicology to epigenetics.
55 y complementary approaches in phylogenetics, phylogeography, genomics, ecology, paleobotany, populati
56                                              Phylogeography has benefited from analytical approaches
57               For three decades, comparative phylogeography has conceptually and methodologically rel
58                                              Phylogeography has provided important insights into popu
59 ography, and its extensions into comparative phylogeography, have their roots in the layering of gene
60 can be used to identify detailed patterns of phylogeography in any organism regardless of existing ge
61 sides of the prostate, forming a bifurcating phylogeography in both genetic and physical space.
62                        Here we assess global phylogeography in Maurolicus, the Pearlsides, an ecologi
63  the feasibility and relevance of predictive phylogeography in monitoring epidemics in time and space
64 ny new evolutionary insights, application of phylogeography in plants has been hampered by difficulty
65 table questions of molecular systematics and phylogeography in slowly evolving groups of ancient fish
66                CalicoST reconstructs a tumor phylogeography in three-dimensional space for two patien
67 the current scope of continental comparative phylogeography, including geographic, conceptual, tempor
68  of forces generating reticulate patterns in phylogeography, including introgression, contact zones,
69 general concordance between biogeography and phylogeography indicates that the population-level genet
70 hantavirus host distribution, evolution, and phylogeography is emerging.
71                                              Phylogeography is said to be the bridge between populati
72  Almost 30 y ago, the field of intraspecific phylogeography laid the foundation for spatially explici
73   The widespread adoption of RAD-Seq data in phylogeography means genealogical relationships previous
74 o be made when studying plant hybridization, phylogeography, molecular systematics and seed dispersal
75                                           As phylogeography moves into the era of next-generation seq
76 ncordance-discordance dichotomy, comparative phylogeography needs to emphasize the contribution of ta
77                                 The parallel phylogeographies of rare, yet widely distributed HV*(xH,
78                           With a statistical phylogeography of 192 hemagglutinin and neuraminidase is
79                                  Comparative phylogeography of African savannah mammals shows a congr
80             To this end, we investigated the phylogeography of both clinical and aquatic toxigenic V.
81 of the world's countries and showed that the phylogeography of crAssphage is locally clustered within
82                                 Although the phylogeography of European mammals has been extensively
83                In addition, we described the phylogeography of EV-A71 throughout Southeast Asia, docu
84                          Our analyses of the phylogeography of frogs and small mammals indicate that
85          We assessed the breeding system and phylogeography of geographically divergent Lasaea popula
86  perspective of the virus alone, by way of a phylogeography of H5N1 genetic sequences.
87                             To determine the phylogeography of influenza virus in a single population
88                However, the distribution and phylogeography of MJNV in other regions of ROK remain un
89                    Here we assess the global phylogeography of neustonic daphniids.
90       We test these propositions by studying phylogeography of paper mulberry, a common East Asian tr
91                             In contrast, the phylogeography of PLVB reflects the highly mobile mounta
92                                Inferring the phylogeography of species with large distributions helps
93                                              Phylogeography of the associated single nucleotide polym
94 pDNA) markers (PCR-RFLP, cpSSR) to study the phylogeography of the species with 293 individuals from
95                                          The phylogeography of these subspecies and their subclades w
96 ion for future analyses of the diversity and phylogeography of this globally important genetic sub-gr
97 ern Oceans, allow us to determine the global phylogeography of this species.
98  Ancestral state reconstructions in Bayesian phylogeography of virus pandemics have been improved by
99 chondrial genes to examine the intraspecific phylogeography of Western European samples of E. ephippi
100  structure varied with host population, host phylogeography or geographical distance.
101 genealogies may have limited applications in phylogeography or other approaches dependent on populati
102    In fact, existing probabilistic models in phylogeography or spatial population genetics generally
103 cally distinct, a rare example of a class II phylogeography pattern.
104 articular, studies in conservation genetics, phylogeography, population genetics, species delimitatio
105 igration and mutation patterns, the field of phylogeography provides a valuable tool for improving th
106                                  Statistical phylogeography provides useful tools to characterize and
107 s from palaeo-biome reconstruction (PBR) and phylogeography regarding range shift history of EBLF dur
108   With new methods and markers, the focus in phylogeography shifted to previously unrecognized geogra
109 ore the theme of reticulation in comparative phylogeography, speciation analysis, and phylogenomics,
110    An evolutionary trace of HA(1) across the phylogeography suggests a mechanism by which H5N1 is abl
111                                              Phylogeography suggests importation of dengue-2 into Ken
112  to characterize the molecular evolution and phylogeography throughout 10 years of continued sampling
113 tion of phenotypic data extends the reach of phylogeography to explain the origin and maintenance of
114                                      We used phylogeography to reconstruct the geospatial viral migra
115                   Here, we scale comparative phylogeography up to the hemisphere level and examine wh
116 otated corpus of journal articles related to phylogeography using integrated heuristics for location
117 s ago, the approach now known as comparative phylogeography was introduced in a landmark study of a c
118 ricella-zoster virus (VZV) phylogenetics and phylogeography when placed in the broad context of geolo
119                        By combining Bayesian phylogeography with landscape resistance models, we proj
120                A popular model in continuous phylogeography-with location data provided in the form o

 
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