ライフサイエンスコーパス: rachis

1 iption, but not in the equally proliferative rachis.

2 ion, leading to the fusion and creation of a rachis.

3 ges toward the source and created an ectopic rachis.

4 pidermis hair cells of the lemma, glume, and rachis.

5 e identified the causal mutations in Brittle Rachis 1 (TtBtr1) genes controlling shattering, a key do

6 ssessed barbules when they fused to form the rachis [19].

7 Extracts of acai seed and of grape rachis alone or in combination with alpha-tocopherol wer

8 mation and barb fusion, and noggin enhancing rachis and barb branching.

9 of pinnate feathers, which clearly feature a rachis and barbs, on a small, non-avian dromaeosaur from

10 e shown in the NILs and include thinner leaf rachises and stems, twisted leaf rachises, increased ser

11 s similar, with higher expression in leaves, rachises, and flowers and lower transcript levels in roo

12 vidence that centralspindlin function at the rachis bridge involves ZEN-4 action on the microtubules

13 gana, with distinctive variation in leaf and rachis characters, exhibits three centers of geographic

14 ity not dependent on concentration for grape rachis extracts and a concentration-dependent prooxidati

15 Acai seed and grape rachis extracts served as good sources of procyanidins a

16 ant potential of AhJ33 fruit waste (rind and rachis) extracts from three different extraction methods

17 pact of chemotherapeutic agents, whereas the rachis (feather axis) remains unperturbed.

18 le in feather branching, with BMP4 promoting rachis formation and barb fusion, and noggin enhancing r

19 Rachis fragility, glume shape, and glume tenacity mimick

20 ted traits such as glume shape and tenacity, rachis fragility, spike length, plant height, and spike

21 es disconnect prematurely from the defective rachis, generating embryos of varying sizes.

22 elical barb ridge organization-->creation of rachis-->bilateral symmetry sequence.

23 unolocalisation studies in leaves, stems and rachis in plants at flowering showed GS protein to be pr

24 hinner leaf rachises and stems, twisted leaf rachises, increased serrations of the leaflets, and dram

25 e to three single-flowered spikelets at each rachis internode.

26 two lateral spikelets) are produced at each rachis internode.

27 tissues, including seedlings, inflorescence rachis, mature leaves, and flowers.

28 were also found in the epidermis of the leaf rachis of stp mutants.

29 Analysis of the rachises of their primary feathers shows that the rachis

30 ne," converting the brittle floral axis (the rachis) of the wild-type into a tough, non-brittle form

31 of flexible blades attached to a transverse rachis on the trunk segments; these blades probably func

32 ific adventitious shoot development from the rachis or rachillae of the leaves.

33 e, with leaflets arranged in succession on a rachis, or palmate, with leaflets clustered together at

34 leaf margins, shortened petioles, increased rachises, petioles acquiring motor organ characteristics

35 eristems on leaves, and by the conversion of rachis-petiolule junctions into "axillary" positions whe

36 pithelial cells became permanent structures (rachis, ramus, barbules).

37 1 resulted in dwarf plants with petioles and rachises reduced in length, and the epidermal cells gain

38 The nonbrittle rachis, resulting in a seed head which does not shatter

39 verse traits, including increased cob width, rachis segment length, and cupule width.

40 In general, rachis showed higher antioxidant capacity than pomace ex

41 ons that gave rise to types with non-fragile rachises, soft glumes, and free-threshing seed.

42 arogyasri Community Health Insurance Scheme (RACHIS) that provides access to free tertiary care for m

43 g oogenesis to maintain the structure of the rachis, the central core of cytoplasm that connects the

44 For both rind and rachis, the maceration technique yielded extracts with t

45 ells connect to a shared cytoplasm core (the rachis) via intercellular bridges.

46 t selections of germplasm with a non-brittle rachis were made during the domestication of barley by f

47 ses of their primary feathers shows that the rachises were much thinner and weaker than those of mode

48 Only if the primary feather rachises were solid in cross-section (the strongest stru

49 Many feathers exhibit a short, slender rachis with alternating barbs and a uniform series of co

50 pike) comprises a multi-noded central stalk (rachis) with tri-partite clusters of uni-floretted spike