戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 is inserted into the skin, and a more distal rachis.
2  parallel barbs branch from the sides of the rachis.
3 iption, but not in the equally proliferative rachis.
4 ion, leading to the fusion and creation of a rachis.
5 ges toward the source and created an ectopic rachis.
6 pidermis hair cells of the lemma, glume, and rachis.
7 ed to a common pool of cytoplasm, termed the rachis.
8  still produce significant concentrations in rachis.
9 n pool of cytoplasm, which we term the proto-rachis.
10 homologous with the ventral groove of modern rachises.
11 e identified the causal mutations in Brittle Rachis 1 (TtBtr1) genes controlling shattering, a key do
12 ssessed barbules when they fused to form the rachis [19].
13 CAP-1 depletion require contractility of the rachis actomyosin corset.
14           Extracts of acai seed and of grape rachis alone or in combination with alpha-tocopherol wer
15 mation and barb fusion, and noggin enhancing rachis and barb branching.
16 ferentiated cortex and medullary pith of the rachis and barb rami.
17 rphogenesis of the ventral components of the rachis and barb rami.
18 of pinnate feathers, which clearly feature a rachis and barbs, on a small, non-avian dromaeosaur from
19 works as a key hub of Wnt signaling to build rachis and converts radial downy to bilateral symmetry.
20 c ring progressively moves towards the proto-rachis and eventually integrates with it.
21 e shown in the NILs and include thinner leaf rachises and stems, twisted leaf rachises, increased ser
22 ue ventrally concave and dorsoventrally thin rachis, and a dorsal groove (sometimes pigmented) that w
23 with actomyosin structures in the cortex and rachis, and its depletion or overexpression led to sever
24 s similar, with higher expression in leaves, rachises, and flowers and lower transcript levels in roo
25 d myosin or Rho kinase demonstrated that the rachis architecture defects associated with CAP-1 deplet
26                                Variations in rachis, barb and barbule morphology result in other feat
27 vidence that centralspindlin function at the rachis bridge involves ZEN-4 action on the microtubules
28 ally at 40 mM showed less weight loss (35%), rachis browning (30%) and decay incident (63%) compared
29 gana, with distinctive variation in leaf and rachis characters, exhibits three centers of geographic
30 lter MP concentrations in Cabernet Sauvignon rachis compared to own-rooted varieties, but whether Shi
31 incision experiments revealed an increase in rachis contractility.
32 ed by feather inclusions including a partial rachis-dominated feather.
33 e") with lithic, two-dimensionally preserved rachis-dominated feathers, first recognized in the Jehol
34 an elongate central pair of fully pennaceous rachis-dominated plumes, constituting a new tail plumage
35 ntify as the "medial stripe" visible in many rachis-dominated rectrices of Mesozoic birds.
36               MPs are readily extracted from rachis during fermentation, producing Shiraz wines with
37 ity not dependent on concentration for grape rachis extracts and a concentration-dependent prooxidati
38                          Acai seed and grape rachis extracts served as good sources of procyanidins a
39 ant potential of AhJ33 fruit waste (rind and rachis) extracts from three different extraction methods
40 pact of chemotherapeutic agents, whereas the rachis (feather axis) remains unperturbed.
41 f xylem anatomical traits of leaf pinnae and rachises for 20 cycad species.
42 le in feather branching, with BMP4 promoting rachis formation and barb fusion, and noggin enhancing r
43                                              Rachis fragility, glume shape, and glume tenacity mimick
44 ted traits such as glume shape and tenacity, rachis fragility, spike length, plant height, and spike
45 es disconnect prematurely from the defective rachis, generating embryos of varying sizes.
46 elical barb ridge organization-->creation of rachis-->bilateral symmetry sequence.
47 lusion trials, which significantly increased rachis IBMP concentrations.
48 unolocalisation studies in leaves, stems and rachis in plants at flowering showed GS protein to be pr
49 hinner leaf rachises and stems, twisted leaf rachises, increased serrations of the leaflets, and dram
50 e to three single-flowered spikelets at each rachis internode.
51  two lateral spikelets) are produced at each rachis internode.
52 uted to changes in canopy coverage impacting rachis light exposure.
53  tissues, including seedlings, inflorescence rachis, mature leaves, and flowers.
54           Nanocellulose obtained from banana rachis (NCBR) was loaded (through simple impregnation) w
55 e an inchworm, and twine around and grab the rachis of a flower based on their geometry.
56  3-sec-butyl-2-methoxypyrazine (SBMP) in the rachis of Shiraz bunches sampled during multiple vintage
57 were also found in the epidermis of the leaf rachis of stp mutants.
58 gest that the concave ventral surface of the rachis of these Cretaceous feathers is not homologous wi
59                              Analysis of the rachises of their primary feathers shows that the rachis
60 ne," converting the brittle floral axis (the rachis) of the wild-type into a tough, non-brittle form
61  of flexible blades attached to a transverse rachis on the trunk segments; these blades probably func
62 ific adventitious shoot development from the rachis or rachillae of the leaves.
63 e, with leaflets arranged in succession on a rachis, or palmate, with leaflets clustered together at
64  leaf margins, shortened petioles, increased rachises, petioles acquiring motor organ characteristics
65 eristems on leaves, and by the conversion of rachis-petiolule junctions into "axillary" positions whe
66 pithelial cells became permanent structures (rachis, ramus, barbules).
67 cant decrease (p < 0.01) in Fusarium-damaged rachis rate, Fusarium-diseased kernel rate and DON conte
68 1 resulted in dwarf plants with petioles and rachises reduced in length, and the epidermal cells gain
69                               The nonbrittle rachis, resulting in a seed head which does not shatter
70 verse traits, including increased cob width, rachis segment length, and cupule width.
71                                  In general, rachis showed higher antioxidant capacity than pomace ex
72 ons that gave rise to types with non-fragile rachises, soft glumes, and free-threshing seed.
73 ous histodifferentiation of the barb rami or rachis suggests that these feathers could have been form
74 arogyasri Community Health Insurance Scheme (RACHIS) that provides access to free tertiary care for m
75 g oogenesis to maintain the structure of the rachis, the central core of cytoplasm that connects the
76                            For both rind and rachis, the maceration technique yielded extracts with t
77     It was defective in infectious growth in rachis tissues and spreading in wheat heads.
78 4600 which is upregulated in wheat spike and rachis tissues during FHB infection.
79 spreading and mainly grew intercellularly in rachis tissues.
80  is important for infectious growth in wheat rachis tissues.
81 ells connect to a shared cytoplasm core (the rachis) via intercellular bridges.
82 t selections of germplasm with a non-brittle rachis were made during the domestication of barley by f
83 ses of their primary feathers shows that the rachises were much thinner and weaker than those of mode
84                  Only if the primary feather rachises were solid in cross-section (the strongest stru
85 ical similarities (e.g., proportionally wide rachis with a "medial stripe") with lithic, two-dimensio
86       Many feathers exhibit a short, slender rachis with alternating barbs and a uniform series of co
87 pike) comprises a multi-noded central stalk (rachis) with tri-partite clusters of uni-floretted spike