コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 are significant contributors to the oceanic 'gene pool'.
2 that reshuffled the ancestral Tibeto-Burman gene pool.
3 r a genetic continuity model in the maternal gene pool.
4 counts for 50.6% of the Tibetan Y-chromosome gene pool.
5 injection of a biased set of genes into the gene pool.
6 ion for salt tolerance within the cultivated gene pool.
7 rise a significant fraction of Earth's phage gene pool.
8 roteins that could be produced from a finite gene pool.
9 cies I to identify the conserved chromosomal gene pool.
10 c resources already available for the Andean gene pool.
11 urrently characterized avian influenza virus gene pool.
12 ed breeds, each of which represents a closed gene pool.
13 in the remaining 352 members of the variable gene pool.
14 ad a considerable influence on the Icelandic gene pool.
15 Neanderthals) have contributed to the modern gene pool.
16 gnized allelic isoforms present in the human gene pool.
17 VSG) genes and are thought to expand the VSG gene pool.
18 ent an ancestral mutation within the Italian gene pool.
19 populations through the sharing of a common gene pool.
20 among the founders of the domestic dromedary gene pool.
21 wer LGD load than typical genes in the human gene pool.
22 ahmaputra valley as the source of the indica gene pool.
23 ts small size and low frequency in the wheat gene pool.
24 icial rare genetic variation from the future gene pool.
25 laining the formation of the modern Armenian gene pool.
26 ld best be practised within each common bean gene pool.
27 selectively eliminate the mutation from the gene pool.
28 contributed to the formation of the Na-Dene gene pool.
29 ng Middle American gene pool from the Andean gene pool.
30 manner consistent with a dynamic horizontal gene pool.
31 al structure was observed in the C. baccatum gene pool.
32 the chromosomal background and the flexible gene pool.
33 e detrimental to the integrity of the native gene pool.
34 p between Basmati varieties and the Japonica gene pool.
35 quency in the West African than the European gene pool.
36 aladaptive alleles into the modern sunflower gene pool.
37 ate the split of the Mesoamerican and Andean gene pools.
38 t of the Mesoamerican and Andean P. vulgaris gene pools.
39 lf was too rapid to be manifested in the moa gene pools.
40 important for the enrichment of African tea gene pools.
41 domestication alleles between divergent rice gene pools.
42 ically reduce genetic diversity within elite gene pools.
44 ly facilitate characterization of the global gene pool accessible to individual bacterial species.
45 n with clonal groups emphasize the extensive gene pool and frequent horizontal DNA transfer events th
47 similarities to the early European Neolithic gene pool and modern-day Sardinians, as well as a geneti
48 omly selected from 184 soybean seed specific gene pool and their expressions were quantified using qu
49 y-wide access to the plasmid-borne accessory gene pool and thus potentiating future evolvability.
50 y mouse are derived from a limited ancestral gene pool and thus QTL detected in multiple crosses are
51 ing groups/clades of organisms with distinct gene pools and genomic properties, which may confer dist
52 ility to invade and proliferate in microbial gene pools and like symbionts when they coevolve with th
53 omo lineages contributed to the modern human gene pool, and more importantly, whether such contributi
54 Yangtze valley as the source of the japonica gene pool, and populations in Indochina and the Brahmapu
55 this range, the species is divided into two gene pools (Andean and Middle American) along a latitudi
57 ority of the Lingayat and Vokkaliga paternal gene pools are composed of four Y-chromosomal haplogroup
58 individuals emerged from the same ancestral gene pool as early farmers in other parts of Europe, sug
59 thic central Anatolians belonged to the same gene pool as the first Neolithic migrants spreading into
60 manner, accompanied by gradual separation of gene pools as evidenced by increased habitat specificity
62 of the age (1.2-1.4 million yr) of the maize gene pool based on te1 is roughly consistent with previo
64 estication and intense selection within each gene pool by breeders; association mapping would best be
65 e relative contributions to the Mestizo FRDA gene pool by Native American and European genes were 76-
66 iphtheriae clinical isolates for their pilin gene pool by PCR and for the expression of the respectiv
67 parity between responding genes in different gene pools confirms recent evidence that surprisingly la
69 ese findings support the idea that H. pylori gene pools differ regionally and emphasize the potential
70 estimate the degree and patterns of spatial gene pool differentiation, and their possible causes.
71 It is estimated that the two current wild gene pools diverged from a common ancestor approximately
73 ntains the FV Leiden mutation in the general gene pool due to a survival advantage of VL+/- in severe
75 ral agreement on the origins of the European gene pool, even though Europe has been more thoroughly i
77 utation that rose to prominence in the human gene pool faster than expected under neutral evolution.
78 i accounting for 52.2 % of the captive panda gene pool, followed by Minshan with 21.5 %, Qinling with
79 as hurricanes likely help to homogenize the gene pool for all Caribbean marine species susceptible t
81 e show that two haplotypes entered the maize gene pool from its wild progenitor, teosinte, and that o
84 l divergence, subsequent bottlenecks in each gene pool, gene pool-specific domestication and intense
85 Thus, our findings show that a pan-domain gene pool has facilitated environmental adaptation in th
88 recombination between distinct sweet potato gene pools, have reshuffled the crop's initial genetic b
89 or permafrost as a depository for an ancient gene pool, i.e., preexisting life, which hypothetically
90 c and functional variability of the HSV-1 TK gene pool in paired trigeminal ganglia (TG) of 5 immunoc
91 y play a critical role in shaping the mobile gene pool in these organisms, yet complex mobile element
94 he idea of using wild or currently unadapted gene pools in rice to enhance breeding efforts to secure
96 for an Indian contribution to the Australian gene pool is contradictory; most studies of autosomal ma
100 sequilibrium (LD) in samples of the parental gene pools is moderate and should respond to sampling sc
101 r odd features of the island's Y-chromosomal gene pool, is best explained as the genetic impact of a
103 mechanistic insights, a meta-data "knowledge gene pool" (KGP) is first constructed from multiple data
104 ted that 1-4% of the non-Sub-Saharan African gene pool may be Neanderthal derived, while 6-8% of the
105 erthal derived, while 6-8% of the Melanesian gene pool may be the product of admixture between the De
108 an-American and Caucasian-American H. pylori gene pools may bear on our understanding of H. pylori tr
113 is thought to have caused revolutions in the gene pool of many species, most evidently in microbial c
114 legacy remains as sedimentary layers in the gene pool of modern Europeans, and our understanding of
115 significant contribution to the contemporary gene pool of NEAS, and the Sino-Tibetan expansion has le
116 ja Sieb. and Zucc., which represents a large gene pool of potentially agronomically valuable traits.
117 onservation efforts aimed at maintaining the gene pool of the current population or establishing new
120 lts support the hypothesis that the paternal gene pools of Jewish communities from Europe, North Afri
121 equencing of two diploids from the ancestral gene pools of quinoa, which enables the identification o
126 gy (GO) terms for enrichment among candidate gene pools, performs multiple hypothesis testing adjustm
128 ivated olives clustered into three different gene pools (Q1, Q2 and Q3), corresponding loosely to the
129 fter the introduction of PCV7, the accessory gene pool re-expanded mainly by genes already circulatin
130 he Andes of southern Peru, possess a diverse gene pool representing more than 100 tuber-bearing relat
132 nce of spatial patterns of nuclear and mtDNA gene pools results from a phylogeographic background and
135 evels and patterns of variation in different gene pools, shed light on relationships of allelic diver
136 omprehensive analyses of the global Bacillus gene pool showed that only an asymmetric region around t
137 that secondary symbionts form a "horizontal gene pool" shuttling adaptive genes among host lineages
138 e, subsequent bottlenecks in each gene pool, gene pool-specific domestication and intense selection w
139 an cultivars from the Andean or Mesoamerican gene pool that contain the dominant allele share the sam
140 ean mutant FRDA genes in the Native American gene pool that existed prior to contact with Europeans.
141 ondary symbiont community forms a horizontal gene pool that influences the adaptation and distributio
142 cal gene-exchange networks by tapping into a gene pool that is adaptive towards local, continuously c
143 both on determinants acquired from a mobile gene pool that is likely available to clinical and agric
144 of gene frequency, i.e. the 'success' in the gene pool that is supposed to be attributable to the 'se
146 ottleneck during the formation of the Andean gene pool that predates the domestication, which was sug
147 lecting introgression between the respective gene pools that may have occurred hundreds of years ago.
149 frica has played in shaping the modern human gene pool through at least two--not one--major expansion
150 ansgenes) and perhaps by other native exotic gene pools through comparative analyses of plants' biolo
152 est that single mTECs shift through distinct gene pools, thus scanning a sizeable fraction of the ove
153 s of four different segments of the landrace gene pool to each inbred group's gene pool were estimate
155 of a mutant allele that enter a population's gene pool together due to replication from a premeiotic
156 e pools will soon be complemented by another gene pool (transgenes) and perhaps by other native exoti
158 cs, characterize their genetic potential (or gene pool) using metagenomics, and describe their ongoin
159 ts suggest that the composition of H. pylori gene pools varies geographically and that other as-yet-u
160 y had more recently entered the H.influenzae gene pool via horizontal gene transfer from other specie
164 th internal genes from the chicken H9N2/H7N9 gene pool, was responsible for at least five human H5N6
165 cally differentiated Mesoamerican and Andean gene pools, we confirmed 2 independent domestications fr
166 he landrace gene pool to each inbred group's gene pool were estimated using a novel likelihood-based
167 re generated in a plasmid vector, and mutant gene pools were transformed into N. gonorrhoeae to selec
168 d with roughly 65.4% of the average European gene pool, which clinally diminishes with distance from
169 ure LD caused by occurrence of more than one gene pool, which would downwardly bias Ne and (2) reduct
171 barriers of sexual reproduction, the native gene pools will soon be complemented by another gene poo
172 etric gene flow was detected between the two gene pools with a larger number of migrants entering Mid
174 nd japonica) arose from genetically distinct gene pools within a common wild ancestor, Oryza rufipogo
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。