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1 ason drought due to competitive release from Avena.
2 l timing and relative densities of the grass Avena barbata and forb Erodium botrys, parameterise a de
3 solated AMF from roots, we (13)CO(2)-labeled Avena barbata for 6 wk and measured the C Rhizophagus in
4                        The slender wild oat (Avena barbata) was widely studied in California using al
5 riticum aestivum), and tetraploid wild oats (Avena barbata) were compared following starch gel electr
6 aradices transported water to the host plant Avena barbata, wild oat.
7 domesticated oat species, Avena strigosa and Avena barbata.
8 nd SOM chemistry over three growth stages of Avena barbata.
9                                              Avena coleoptile sections were preincubated in either fu
10                                    The genus Avena consists of approximately 30 wild and cultivated o
11 omplex reticulate evolution have occurred in Avena, exemplifying the long-term persistence of tetrapl
12 os, performs the same role in the grass weed Avena fatua (common wild oat).
13 roteins peak during endosperm development of Avena fatua (wild oat) and are later degraded.
14                                          The Avena fatua (wild oat) homologue of VIVIPAROUS 1 (AfVP1)
15               In this study, inbred lines of Avena fatua were used to analyse the influence of genoty
16 bacterial networks associated with wild oat (Avena fatua) over two seasons in greenhouse microcosms.
17 yet the broader genetic diversity within the Avena gene pool remains underexplored and underexploited
18                        This resource for the Avena genus will help to leverage knowledge from other c
19 na longiglumis, AA, 2n = 14) and tetraploid (Avena insularis, CCDD, 2n = 4x = 28) progenitors.
20 plastid DNA fragments from 109 accessions of Avena L.
21 . sativa and close relatives of its diploid (Avena longiglumis, AA, 2n = 14) and tetraploid (Avena in
22 e present in highly purified preparations of Avena mitochondria was photoreversibly modulated by red/
23 e recording of starch grains attributable to Avena (oat) caryopses expands our information about the
24 ness-feeding (large foraging on few species, Avena or Cytisus: field, bordering both macchia and fall
25 ations, and/or reproductive barriers amongst Avena populations caused by differential chromosome stru
26         The light-oxygen-voltage domain 2 of Avena sativa (AsLOV2) undergoes a dramatic conformationa
27                   In developing endosperm of Avena sativa (cultivated oat), AV1, AV10 and Z1 mRNAs re
28                           Victoria blight of Avena sativa (oat) is caused by the fungus Cochliobolus
29  mutagenized population of LOV2 derived from Avena sativa (oat) phot1 were screened for variants that
30  blue light photoreceptor phototropin 1 from Avena sativa (oat).
31 f the uidA gene of Escherichia coli, in both Avena sativa and Arabidopsis thaliana.
32 omprising the AsLOV2 photoreceptor domain of Avena sativa fused to a Cre variant carrying destabilizi
33 of T1 plants of the cultivated hexaploid oat Avena sativa L. cotransformed by microprojectile bombard
34 ynthase from etioplasts from dark-grown oat (Avena sativa L. cv Garry) seedlings using traditional co
35     We solubilized 90% of the FCBP from oat (Avena sativa L. cv Victory) root PM in an active form wi
36       Pulvini of excised segments from oats (Avena sativa L. cv Victory) were treated unilaterally wi
37 ro in plasma membrane preparations from oat (Avena sativa L.) aleurone and from leaves and stems of w
38             The evolution of cultivated oat (Avena sativa L.) and its close relatives was inferred to
39       We have developed from crosses of oat (Avena sativa L.) and maize (Zea mays L.) 50 fertile line
40                                        Oats (Avena sativa L.) are a healthy food, being high in dieta
41 somes present in plants with a complete oat (Avena sativa L.) chromosome complement provides a unique
42 and in vivo protein phosphorylations in oat (Avena sativa L.) coleoptile segments were analyzed by so
43 a mays L.) chromosome addition lines of oat (Avena sativa L.) from oat x maize crosses enables us to
44 , and 60 %) as abiotic stressors during oat (Avena sativa L.) germination using a 2-level factorial d
45                              Cultivated oat (Avena sativa L.) is an allohexaploid (AACCDD, 2n = 6x =
46                                         Oat (Avena sativa L.) is an important cereal grain with a uni
47 enome was investigated in 13 transgenic oat (Avena sativa L.) lines produced using microprojectile bo
48 nsgene loci in two unrelated transgenic oat (Avena sativa L.) lines transformed using microprojectile
49  cut from the peduncular-1 internode of oat (Avena sativa L.) shoots so as to contain the gravirespon
50  partitioning method from two different oat (Avena sativa L.) tissues, the root and coleoptile, was c
51 etiolated wheat (Triticum aestivum L.), oat (Avena sativa L.), barley (Hordeum vulgare L.), tobacco (
52 bombardment of allohexaploid cultivated oat (Avena sativa L.).
53 e been recovered via embryo rescue from oat (Avena sativa L., 2n = 6x = 42) x maize (Zea mays L., 2n
54  addition lines of hexaploid cultivated oat (Avena sativa L., 2n = 6x = 42), where maize chromosomes
55 n, Zea Mays L.-soybean, Glycine max L.-oats, Avena sativa L.-CC with cattle grazing); natural ecosyst
56 ed the effects of more than 100 mutations in Avena sativa light-oxygen-voltage domain 2, a model prot
57 he inhibitory domains to the light-sensitive Avena sativa light-oxygen-voltage-sensing (LOV) 2-photot
58 to capture the light-induced dimerization of Avena sativa LOV2.
59 hetic interaction between the LOV2 domain of Avena sativa phototropin 1 (AsLOV2) and an engineered PD
60 cial photoswitch based on the LOV2 domain of Avena sativa phototropin 1 (AsLOV2).
61 n the naturally photoactive LOV2 domain from Avena sativa phototropin 1 and the Escherichia coli trp
62 t a conserved glutamine residue [Q513 in the Avena sativa phototropin 1 LOV2 (AsLOV2) domain] switche
63             In the C-terminal LOV2 domain of Avena sativa phototropin 1, formation of this bond trigg
64 combinant C450A mutant of the LOV2 domain of Avena sativa phototropin was reconstituted with universa
65 ting myosin VI by fusing the light-sensitive Avena sativa phototropin1 LOV2 domain to a peptide from
66 ochemical and functional characterization of Avena sativa phytochrome A (AsphyA) as a potential prote
67 tions, we singly inoculated and coinoculated Avena sativa with two virus species, barley yellow dwarf
68 us victoriae causes Victoria blight of oats (Avena sativa) and is pathogenic due to its production of
69 cereale], and their wild relatives) and oat (Avena sativa) and its wild relatives.
70 sion profiles for multiple cultivars of oat (Avena sativa) and wheat with and without cold treatment.
71 ulgare), wheat (Triticum aestivum), and oat (Avena sativa) are anchored by a set of curated correspon
72 sis heat shock protein 21 (HSP21) mRNA, oat (Avena sativa) globulin, wheat (Triticum aestivum) germin
73                                         Oat (Avena sativa) is a nutritionally important cereal crop t
74                                        Oat, (Avena sativa) is an excellent source of mixed linkage be
75                                        Oat- (Avena sativa) maize (Zea mays) chromosome additions are
76 eletion and alanine-scanning mutants of oat (Avena sativa) phyA in transgenic tobacco (Nicotiana taba
77 InsP(3)) in the gravitropic response of oat (Avena sativa) shoot pulvini.
78  a feasible strategy to develop low-oil oat (Avena sativa) varieties, which aligns with specific proc
79 c tissues from rye (Secale cereale) and oat (Avena sativa) were studied in an isothermal calorimeter
80 ey (Hordeum vulgare), maize (Zea mays), oat (Avena sativa), and wheat (Triticum aestivum); but the di
81 stivum), barley (Hordeum vulgare), and oats (Avena sativa), predominate in the northern temperate zon
82 dual maize (Zea mays) centromeres using oat (Avena sativa)-maize chromosome addition lines.
83 olation from protoplasts of Petunia and oat (Avena sativa).
84 tro with recombinant phytochrome A from oat (Avena sativa).
85 l dynamics along single growing plant roots (Avena sativa).
86  additions to the haploid complement of oat (Avena sativa, 2n = 6x = 42) among F(1) plants generated
87 mydomonas reinhardtii and the LOV2 domain of Avena sativa, both before and after the photoreaction, t
88 he light-oxygen-voltage 2 (LOV2) domain from Avena sativa.
89 )) chromosomes to be investigated in an oat (Avena sativa; C(3)) genetic background.
90 The crown ages of two infrageneric lineages (Avena sect.
91          Ventricosa Baum ex Romero-Zarco and Avena sect.
92                                        Oats (Avena spp) synthesize antimicrobial triterpenoids (avena
93                                        Oats (Avena spp.) make root-derived antimicrobial triterpenes
94                                        Oats (Avena spp.) produce antimicrobial compounds, avenacins,
95 liths, and isolated cells from awns of oats (Avena sterilis).
96 ent of two other undomesticated oat species, Avena strigosa and Avena barbata.
97  and 40 cm sward height) on mixed black oat (Avena strigosa) and Italian ryegrass (Lolium multiflorum
98 seedlings of wheat (Triticum aestivum), oat (Avena strigosa), rice (Oryza sativa), sorghum (Sorghum b
99 t at low levels in the roots of diploid oat (Avena strigosa).
100                                              Avena) were estimated to be in the early to middle Mioce