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1 5 897 polymorphic markers within A. hypogaea germplasm.
2 ucing agronomically desirable WSMV-resistant germplasm.
3 infoin and their characterization in diverse germplasm.
4 s of environmental adaptation in the sampled germplasm.
5 of novel allelic variation using wild barley germplasm.
6 solidation of control and ownership of plant germplasm.
7 complex multi-NLR loci from uncharacterized germplasm.
8 nes for other marked trait intervals in this germplasm.
9 ic salinity-induced growth responses in rice germplasm.
10 gree, to some extent, with the origin of the germplasm.
11 for a mutual improvement between the sets of germplasm.
12 ld mandarins were part of the early breeding germplasm.
13 raits that can be improved with S. pennellii germplasm.
14 ortant to the development of resistant maize germplasm.
15 p molecular markers to select phenolics-rich germplasm.
16 and for the maintenance of accurately named germplasm.
17 shape varies significantly in the cultivated germplasm.
18 the existence of suppressors of OVATE in the germplasm.
19 lation of favorable alleles in today's elite germplasm.
20 ndosperm as a potential source of RH mapping germplasm.
21 n cultivars, embodying the majority of Greek germplasm.
22 olic mutants, human disease studies and crop germplasm.
23 terminant of awn suppression in global wheat germplasm.
24 athogens that must be excluded from valuable germplasm.
25 conserved haplotype in the yellow endosperm germplasm.
26 has not yet resulted in commercially viable germplasm.
27 ance resources have been discovered in wheat germplasm.
28 ations of marker alleles across very diverse germplasm.
29 and callus growth rate of high type II maize germplasm.
30 analyses revealed that Rf8 is rare in maize germplasm.
31 the way geneticists utilize wild and exotic germplasm.
32 tion allowing direct transformation of elite germplasm.
33 lerated integration of resistance into elite germplasm.
34 d, due to a large performance gap with elite germplasm.
35 been investigated due to the absence of such germplasm.
36 us making this variety a potential source of germplasm.
37 est for introgression in susceptible sorghum germplasm.
38 he accessions and cultivars in rice breeding germplasm.
39 h, and Mexican teosintes as well as in maize germplasm.
40 erlies seed mass variation in global sorghum germplasm.
41 SG profiles that are observed across Stevia germplasm.
42 hed genic SSRs (eSSRs) generated on the same germplasm.
43 artificial selection and be retained in crop germplasm.
44 mazzard), landrace and bred sweet cherry germplasm.
45 C, but not with catechin content, in diverse germplasm.
46 lines in a new diversity panel of 159 wheat germplasm.
47 ngo, representing Indian and Southeast Asian germplasm.
48 te metabolic engineering of chemically elite germplasm.
49 d availability of genetic variation in wheat germplasm.
50 genetic differences between local and exotic germplasms.
51 conducted in four distinct groups of soybean germplasm: 26 accessions of the wild ancestor of soybean
52 m provides an immortal collection of diverse germplasm, a high-density single-nucleotide polymorphism
53 ies were performed using a population of 214 germplasm accessions and 31,914 SNPs from the SoySNP50K
55 promoter and transcripts from various citrus germplasm accessions established a tight correlation bet
56 of total) taxa associated with 63 crops, no germplasm accessions exist, and a further 257 (23.9%) ar
57 biotic variables are partitioned across rice germplasm accessions may be key to identifying potential
64 yphyletic distribution of the kabuli form in germplasm, an absence of nested variation within the bHL
66 onstructed in crop species, and their inbred germplasm and associated phenotypic and genotypic data s
67 r cost effective and efficient management of germplasm and better stewarding of these valuable resour
69 ion of the fruit shape alleles in the tomato germplasm and evaluated their contribution to morphology
70 from a very small base of temperate japonica germplasm and having a relatively brief breeding history
71 f the genetic diversity in cultivated coffee germplasm and in wild populations growing in the center
72 ed trait architecture consistency in African germplasm and investigated further evidence for the dome
73 study focused on South American and African germplasm and investigated the genetic architecture of h
74 iting the allelic diversity within available germplasm and leveraging the knowledge of the mechanisms
75 ruit ionome indicated the major influence of germplasm and other locational factors on the acquisitio
76 results suggest that admixture shaped olive germplasm and perhaps also local domestication events.
77 ok policy, (5) keeping track of ownership of germplasm and plant genetic resources, and (6) promoting
78 undation for large-scale characterization of germplasm and population genomics, and a resource for tr
79 alleles at a single locus in cultivated rice germplasm and provide evidence that amplification in wil
80 th commercial varieties clustered with India germplasms and demonstrating allelic admixture, and indi
82 de sequence polymorphisms including alleles, germplasms and phenotypes, Gene Ontology annotations, ge
83 rth's surface, a potential source of ancient germplasm, and a laboratory for the study of rates of mi
84 ximately 800 Mbp), diploid genetics, diverse germplasm, and colinearity with other C4 grass genomes.
85 identified for qP-FF4.1 in the sweet cherry germplasm, and the "soft" alleles were dominant over the
86 d after domestication and spread among maize germplasm, and the ZmWAK kinase domain underwent functio
87 me some of the most well-characterized maize germplasm, and their de novo assemblies were recently ma
88 p) relative to most other grasses, a diverse germplasm, and utility for comparative genomics with ric
90 f genetic variation between local and exotic germplasms as revealed by missing and unique alleles.
94 ollection of genomic DNA (gDNA) samples from germplasm bank, and two gDNA samples from historical her
95 3 triploids and 7 tetraploids, in the Active Germplasm Bank, at Embrapa Cassava & Fruits, to evaluate
96 e provide a brief introduction to macroalgal germplasm banking and its application to conservation, i
97 ine preservation of marine algal species via germplasm banking with an overview of the technical adva
100 worldwide necessitating a broadening of the germplasm base required to source and incorporate novel
102 d the discrimination of different jack fruit germplasm based on their geographical origin in India.
103 p in the clonal multiplication of elite tree germplasm, because the ability to form roots declines ra
104 asymmetrically localizing the protein to the germplasm before cleavage and subsequently degrading res
105 asm pool, while PH207 is a founder of Iodent germplasm, both of which have contributed substantially
107 ated with early flowering in global chickpea germplasm but was not widely distributed, indicating tha
108 between processing, fresh-market and vintage germplasm by using an F(st)-outlier method based on the
110 ering we demonstrated that shape categories, germplasm classes, and the shape genes were nonrandomly
111 geographical and ecological information for germplasm-collecting missions, as well as for the preser
112 he structure of genetic diversity in a plant germplasm collection is significantly influenced by its
113 ation by providing a framework for efficient germplasm collection management and guidance for future
114 rtain the magnitude of variability in a core germplasm collection of diverse origin and predict pearl
115 e bioaccessibility of phenolics in a diverse germplasm collection representing cultivated highbush bl
117 orphological traits in a diverse C. baccatum germplasm collection spanning the species distribution.
118 was carried out on the USDA-ARS C. baccatum germplasm collection using data from GIS, morphological
120 total of 265 tomato accessions from the USDA germplasm collection were evaluated at the seedling stag
121 ity panel derived from the Ecofibre Cannabis germplasm collection, an extreme-phenotype genome-wide a
122 ybrids shows a narrow genetic base in the US germplasm collection, and points to the importance of co
123 genome, high-quality reference genome, large germplasm collection, and selfing nature make it an exce
124 ts adaptation to harsh environments, diverse germplasm collection, and value for comparing the genome
125 cultivars and rootstocks, originating from a germplasm collection, has been developed and validated.
126 genetic and biochemical diversity of a large germplasm collection, representing 80% of maize genetic
127 an lines were selected from the USDA-Soybean Germplasm Collection, were grown in Stoneville, MS for b
130 This study shows that evaluation of large germplasm collections across north-south geographic clin
131 screening the extensive genetic diversity in germplasm collections and enabling maximal recombination
132 date the genetic and phenotypic diversity of germplasm collections and populations and, yet, biochemi
133 ic diversity of HIPM and DIPM genes in Malus germplasm collections and used a candidate gene-based as
134 etic diversity within the local and regional germplasm collections can enhance the overall effectiven
135 d genebank management and the utilization of germplasm collections for linking natural variation to h
136 The ability to access alleles from unadapted germplasm collections is a long-standing problem for gen
137 the most informative genotypes in sequenced germplasm collections to facilitate experiments for quan
138 ity, all traits available in most major crop germplasm collections, increases in productivity (7%) ar
139 ers to assess and enhance diversity in their germplasm collections, to introgress valuable traits fro
144 This has implications for the scales of germplasm conservation and exploitation of sources of re
145 c gene or chromosome regions and identifying germplasm conserving allelic diversity missing in curren
146 diversity of the apricot (Prunus armeniaca) germplasm containing resistance to PPV, next-generation
149 ces and their application to the analysis of germplasm currently in use in West African breeding prog
151 genetic diversity in Portuguese common bean germplasm, details on its metabolomics profiles are stil
152 noid content, advantage was taken of a maize germplasm diversity collection that exhibits genetic and
153 cassava varieties that are representative of germplasm diversity within the crop, and in 212 individu
156 the efficiency of stevia evaluation through germplasm enhancement and agronomic improvement programs
157 and SNPs are widely used in genetic mapping, germplasm evaluation and marker assisted selection.
160 genetic resources for salt tolerance in rice germplasm exist but are underutilized due to the difficu
161 reases our understanding of the domesticated germplasm, facilitating translation of acquired knowledg
162 nt varieties conserved in a national ex situ germplasm field collection in Finland, North Europe.
163 t improvement is proposed to provide a novel germplasm for blackgram production on marginal lands.
165 propriate approach for the identification of germplasm for breeding varieties with increased proporti
168 c switchgrass lines can be used as potential germplasm for improvement of lignocellulosic feedstocks
169 ction (MASS) targeted towards widening peach germplasm for maturity, particularly early maturity.
170 planting materials, and efforts to evaluate germplasm for resistance to witches' broom are described
174 sual morphology, it is an important donor of germplasm for the cultivated tomato Solanum lycopersicum
177 f information prevents exploitation of these germplasms for genetic improvement of new cultivars and
179 was no evidence that it is introgressed with germplasm from two other alien Ligustrum species present
180 tensified crop management involving improved germplasm, greater inputs of fertilizer, production of t
182 ng for the combination of beneficial loci in germplasm has improved yields in diverse environments th
183 re of FCR resistance within cultivated wheat germplasm has significantly limited breeding efforts to
184 sult of widespread adoption of improved crop germplasm have saved natural ecosystems from being conve
185 ioning of sequence variation in modern elite germplasm, highlighting regions vulnerable to genetic er
186 Genetic studies using diverse sour cherry germplasm identified non-functional S-haplotypes for whi
188 es with 68 representative japonica or indica germplasms identified rice Lysine-Histidine-type Transpo
191 biotics, ZmTps21 exists as a useful gene for germplasm improvement programs targeting optimized bioti
194 ages secured a tripling of rice output, with germplasm improvements providing benefits beyond US$4.3
197 ow possible to sequence large collections of germplasm in crops for detecting genome-scale genetic va
198 ight responses among a diverse collection of germplasm, including a phytochrome-deficient mutant elm1
199 tegrates quantitative trait loci, traits and germplasm information along with genomic variation data,
201 ipal Component Analysis (PCA) stratified the germplasm into five clusters (Mississippi-River, West No
204 zation, development of plant "chromonomics," germplasm introgression, and marker-assisted breeding.
207 on of flowering time variation in global pea germplasm is controlled by HR, with a single, widespread
211 t to show genetic variations among different germplasms; large-scale genome comparisons among Oryza s
213 multiple disease resistant (MDR) watermelon germplasm lines have been developed by the USDA in Charl
215 athways, genetic diversity, genes, proteins, germplasm, literature, ontologies and a fully-structured
216 in most cultivated tomatoes, arose in tomato germplasm long before domestication; (4) extant accessio
218 in challenging environments exist within the germplasm of crops, their wild relatives and species tha
220 he sharing and inconsistent documentation of germplasm often results in unintentionally duplicated co
221 are frequently found in current elite barley germplasm; one is probably the product of mutation breed
222 k for quantifying the contribution of exotic germplasm or older improved varieties to the genetic bac
223 o propose an ideal genotypic, phenotypic and germplasm 'package' that multi-parent populations should
225 ome-wide association approach on two diverse germplasm panels followed by quantitative trait loci (QT
226 to represent the genetic diversity of maize germplasm, partial or nearly complete loss of the tandem
228 rt to characterize the primary and secondary germplasm pools for quinoa, we report the complete mitoc
229 novel SHELL alleles in noncommercial African germplasm populations from the Malaysian Palm Oil Board.
231 ic diversity captured by the National Animal Germplasm Program and explores genetic structure and dif
232 hagy mediated by the SEPA-1 protein depletes germplasm proteins from somatic cells during early devel
233 antitative trait locus discovered in Chinese germplasm, provides the most stable and the largest effe
234 , trait loci, genetic maps, genes, taxonomy, germplasm, publications and communication resources for
239 servation and exploitation of European peach germplasm resources and, ultimately, as a true heritage
241 s challenging due to the limited genomic and germplasm resources available for comprehensive analysis
243 e cycle, small (440-Mb) genome, and advanced germplasm resources make birch an attractive model for f
244 ion in genes and metabolic pathways with the germplasm resources needed to accelerate varietal develo
250 airwise comparisons between local and exotic germplasms showed that the temperate and some IITA lines
251 r with unique alleles identified within each germplasm, shows the potential for a mutual improvement
253 gume of Indo-African continents with diverse germplasm sources demonstrating alternating mechanisms d
254 will be necessary to develop improved plant germplasm specifically tailored to serve as energy crops
255 erved in cold-stored tubers from wild potato germplasm stocks that are resistant to cold-induced swee
257 l genetic variation for CCS in diverse maize germplasm, suggest that CCS merits attention as a potent
258 he large genetic variation for CCFN in maize germplasm suggests that CCFN merits attention as a breed
261 ) was higher in tea products from the Kenyan germplasm than in those from the Japanese cultivars.
263 identified in early flowering grain sorghum germplasm that contain unique loss-of-function mutations
265 n of 2742 modern cassava landraces and elite germplasm, the legacy of a 1930s era breeding to combat
266 sistance genes have been identified in plant germplasm, there is no easy way to predict the quality o
268 enetic diversity and possible acquisition of germplasm through hybridisation is fundamental to unders
271 findings provide new genes, SSR markers, and germplasm to enhance the breeding of commercially cultiv
273 e temperate-tropical division of early maize germplasms to different agricultural environments was ar
274 c frequency differences observed between the germplasms, together with unique alleles identified with
277 t is imperative to characterize the breeding germplasms using standard phenomic and genomic character
278 underlying phenotypic variation from diverse germplasm, using a mutant phenotype as a "reporter." In
280 understanding of genomic controls underlying germplasm variations for this trait in Indian mustard.
283 ivars that make up the pedigree of US runner germplasm were genotyped and used to identify genomic re
284 ncipal component and cluster analysis, sumac germplasms were categorized into three groups: i.e., gro
285 ng region were not observed in diverse wheat germplasm whereas a nearby polymorphism was highly predi
286 erm cells would provide a reserve of monarch germplasm, which could be utilized in the event of popul
287 erate maize depends upon the use of tropical germplasm, which harbors a rich source of natural alleli
289 lly and temporally independent selections of germplasm with a non-brittle rachis were made during the
294 nowledge can be used to develop agricultural germplasm with more predictable vernalization responses
296 goal was to evaluate overall differences in germplasm with quality traits classified as sweet, sweet
297 e, there is potential application of the new germplasm with reduced detrimental glucosinolates and in
298 d 7 were identified in both RILs and diverse germplasm with resolutions of 3.2 cM or less for each of
299 limitation, a resistance phenotype in tomato germplasm with the Ty-1 gene, and functional properties
300 ening the genetic base of commercial alfalfa germplasm with these valuable genetic variations can be