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1 p molecular markers to select phenolics-rich germplasm.
2 and for the maintenance of accurately named germplasm.
3 shape varies significantly in the cultivated germplasm.
4 the existence of suppressors of OVATE in the germplasm.
5 lation of favorable alleles in today's elite germplasm.
6 ndosperm as a potential source of RH mapping germplasm.
7 olic mutants, human disease studies and crop germplasm.
8 athogens that must be excluded from valuable germplasm.
9 conserved haplotype in the yellow endosperm germplasm.
10 has not yet resulted in commercially viable germplasm.
11 ations of marker alleles across very diverse germplasm.
12 and callus growth rate of high type II maize germplasm.
13 analyses revealed that Rf8 is rare in maize germplasm.
14 the way geneticists utilize wild and exotic germplasm.
15 tion allowing direct transformation of elite germplasm.
16 ucing agronomically desirable WSMV-resistant germplasm.
17 infoin and their characterization in diverse germplasm.
18 s of environmental adaptation in the sampled germplasm.
19 of novel allelic variation using wild barley germplasm.
20 solidation of control and ownership of plant germplasm.
21 complex multi-NLR loci from uncharacterized germplasm.
22 nes for other marked trait intervals in this germplasm.
23 5 897 polymorphic markers within A. hypogaea germplasm.
24 ic salinity-induced growth responses in rice germplasm.
25 gree, to some extent, with the origin of the germplasm.
26 for a mutual improvement between the sets of germplasm.
27 ld mandarins were part of the early breeding germplasm.
28 raits that can be improved with S. pennellii germplasm.
29 ortant to the development of resistant maize germplasm.
30 genetic differences between local and exotic germplasms.
31 conducted in four distinct groups of soybean germplasm: 26 accessions of the wild ancestor of soybean
32 m provides an immortal collection of diverse germplasm, a high-density single-nucleotide polymorphism
33 ies were performed using a population of 214 germplasm accessions and 31,914 SNPs from the SoySNP50K
35 of total) taxa associated with 63 crops, no germplasm accessions exist, and a further 257 (23.9%) ar
36 biotic variables are partitioned across rice germplasm accessions may be key to identifying potential
39 yphyletic distribution of the kabuli form in germplasm, an absence of nested variation within the bHL
40 ion of the fruit shape alleles in the tomato germplasm and evaluated their contribution to morphology
41 from a very small base of temperate japonica germplasm and having a relatively brief breeding history
42 results suggest that admixture shaped olive germplasm and perhaps also local domestication events.
43 ok policy, (5) keeping track of ownership of germplasm and plant genetic resources, and (6) promoting
44 alleles at a single locus in cultivated rice germplasm and provide evidence that amplification in wil
46 de sequence polymorphisms including alleles, germplasms and phenotypes, Gene Ontology annotations, ge
47 rth's surface, a potential source of ancient germplasm, and a laboratory for the study of rates of mi
48 ximately 800 Mbp), diploid genetics, diverse germplasm, and colinearity with other C4 grass genomes.
49 d after domestication and spread among maize germplasm, and the ZmWAK kinase domain underwent functio
50 p) relative to most other grasses, a diverse germplasm, and utility for comparative genomics with ric
52 f genetic variation between local and exotic germplasms as revealed by missing and unique alleles.
54 3 triploids and 7 tetraploids, in the Active Germplasm Bank, at Embrapa Cassava & Fruits, to evaluate
57 p in the clonal multiplication of elite tree germplasm, because the ability to form roots declines ra
58 asymmetrically localizing the protein to the germplasm before cleavage and subsequently degrading res
59 asm pool, while PH207 is a founder of Iodent germplasm, both of which have contributed substantially
60 ated with early flowering in global chickpea germplasm but was not widely distributed, indicating tha
61 between processing, fresh-market and vintage germplasm by using an F(st)-outlier method based on the
62 ering we demonstrated that shape categories, germplasm classes, and the shape genes were nonrandomly
63 geographical and ecological information for germplasm-collecting missions, as well as for the preser
64 he structure of genetic diversity in a plant germplasm collection is significantly influenced by its
65 ation by providing a framework for efficient germplasm collection management and guidance for future
66 orphological traits in a diverse C. baccatum germplasm collection spanning the species distribution.
67 was carried out on the USDA-ARS C. baccatum germplasm collection using data from GIS, morphological
69 genome, high-quality reference genome, large germplasm collection, and selfing nature make it an exce
70 ts adaptation to harsh environments, diverse germplasm collection, and value for comparing the genome
71 cultivars and rootstocks, originating from a germplasm collection, has been developed and validated.
72 genetic and biochemical diversity of a large germplasm collection, representing 80% of maize genetic
73 an lines were selected from the USDA-Soybean Germplasm Collection, were grown in Stoneville, MS for b
75 etic diversity within the local and regional germplasm collections can enhance the overall effectiven
76 The ability to access alleles from unadapted germplasm collections is a long-standing problem for gen
77 the most informative genotypes in sequenced germplasm collections to facilitate experiments for quan
78 ity, all traits available in most major crop germplasm collections, increases in productivity (7%) ar
79 ers to assess and enhance diversity in their germplasm collections, to introgress valuable traits fro
83 diversity of the apricot (Prunus armeniaca) germplasm containing resistance to PPV, next-generation
86 ces and their application to the analysis of germplasm currently in use in West African breeding prog
88 noid content, advantage was taken of a maize germplasm diversity collection that exhibits genetic and
89 cassava varieties that are representative of germplasm diversity within the crop, and in 212 individu
91 the efficiency of stevia evaluation through germplasm enhancement and agronomic improvement programs
94 genetic resources for salt tolerance in rice germplasm exist but are underutilized due to the difficu
95 reases our understanding of the domesticated germplasm, facilitating translation of acquired knowledg
96 nt varieties conserved in a national ex situ germplasm field collection in Finland, North Europe.
97 t improvement is proposed to provide a novel germplasm for blackgram production on marginal lands.
98 propriate approach for the identification of germplasm for breeding varieties with increased proporti
101 c switchgrass lines can be used as potential germplasm for improvement of lignocellulosic feedstocks
102 planting materials, and efforts to evaluate germplasm for resistance to witches' broom are described
104 sual morphology, it is an important donor of germplasm for the cultivated tomato Solanum lycopersicum
105 f information prevents exploitation of these germplasms for genetic improvement of new cultivars and
106 was no evidence that it is introgressed with germplasm from two other alien Ligustrum species present
107 tensified crop management involving improved germplasm, greater inputs of fertilizer, production of t
108 ng for the combination of beneficial loci in germplasm has improved yields in diverse environments th
109 re of FCR resistance within cultivated wheat germplasm has significantly limited breeding efforts to
110 sult of widespread adoption of improved crop germplasm have saved natural ecosystems from being conve
111 ioning of sequence variation in modern elite germplasm, highlighting regions vulnerable to genetic er
112 Genetic studies using diverse sour cherry germplasm identified non-functional S-haplotypes for whi
115 biotics, ZmTps21 exists as a useful gene for germplasm improvement programs targeting optimized bioti
118 ow possible to sequence large collections of germplasm in crops for detecting genome-scale genetic va
119 ight responses among a diverse collection of germplasm, including a phytochrome-deficient mutant elm1
120 tegrates quantitative trait loci, traits and germplasm information along with genomic variation data,
124 zation, development of plant "chromonomics," germplasm introgression, and marker-assisted breeding.
127 on of flowering time variation in global pea germplasm is controlled by HR, with a single, widespread
130 t to show genetic variations among different germplasms; large-scale genome comparisons among Oryza s
133 athways, genetic diversity, genes, proteins, germplasm, literature, ontologies and a fully-structured
134 in most cultivated tomatoes, arose in tomato germplasm long before domestication; (4) extant accessio
135 in challenging environments exist within the germplasm of crops, their wild relatives and species tha
137 k for quantifying the contribution of exotic germplasm or older improved varieties to the genetic bac
138 ome-wide association approach on two diverse germplasm panels followed by quantitative trait loci (QT
139 to represent the genetic diversity of maize germplasm, partial or nearly complete loss of the tandem
141 hagy mediated by the SEPA-1 protein depletes germplasm proteins from somatic cells during early devel
142 , trait loci, genetic maps, genes, taxonomy, germplasm, publications and communication resources for
146 s challenging due to the limited genomic and germplasm resources available for comprehensive analysis
148 e cycle, small (440-Mb) genome, and advanced germplasm resources make birch an attractive model for f
149 ion in genes and metabolic pathways with the germplasm resources needed to accelerate varietal develo
153 airwise comparisons between local and exotic germplasms showed that the temperate and some IITA lines
154 r with unique alleles identified within each germplasm, shows the potential for a mutual improvement
155 will be necessary to develop improved plant germplasm specifically tailored to serve as energy crops
156 erved in cold-stored tubers from wild potato germplasm stocks that are resistant to cold-induced swee
157 l genetic variation for CCS in diverse maize germplasm, suggest that CCS merits attention as a potent
158 he large genetic variation for CCFN in maize germplasm suggests that CCFN merits attention as a breed
161 ) was higher in tea products from the Kenyan germplasm than in those from the Japanese cultivars.
162 identified in early flowering grain sorghum germplasm that contain unique loss-of-function mutations
164 sistance genes have been identified in plant germplasm, there is no easy way to predict the quality o
166 enetic diversity and possible acquisition of germplasm through hybridisation is fundamental to unders
169 findings provide new genes, SSR markers, and germplasm to enhance the breeding of commercially cultiv
171 e temperate-tropical division of early maize germplasms to different agricultural environments was ar
172 c frequency differences observed between the germplasms, together with unique alleles identified with
175 underlying phenotypic variation from diverse germplasm, using a mutant phenotype as a "reporter." In
177 ivars that make up the pedigree of US runner germplasm were genotyped and used to identify genomic re
178 erate maize depends upon the use of tropical germplasm, which harbors a rich source of natural alleli
179 lly and temporally independent selections of germplasm with a non-brittle rachis were made during the
184 goal was to evaluate overall differences in germplasm with quality traits classified as sweet, sweet
185 e, there is potential application of the new germplasm with reduced detrimental glucosinolates and in
186 d 7 were identified in both RILs and diverse germplasm with resolutions of 3.2 cM or less for each of
187 limitation, a resistance phenotype in tomato germplasm with the Ty-1 gene, and functional properties
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