ライフサイエンスコーパス: bilateral symmetry

1 ng to primitive streak formation, generating bilateral symmetry.

2 marks the transition from radial symmetry to bilateral symmetry.

3 cata (DIV) specify the development of floral bilateral symmetry.

4 ng in the node is not essential for breaking bilateral symmetry.

5 olar differentiation and failed to establish bilateral symmetry.

6 II HD-Zip gene activity results in a loss of bilateral symmetry.

7 pacities involve a robust ability to restore bilateral symmetry.

8 like form can evolve in the absence of overt bilateral symmetry.

9 r establishment of the apical-basal axis and bilateral symmetry.

10 be required for the establishment of floral bilateral symmetry.

11 of the body plan of a majority of animals is bilateral symmetry.

12 ilateria is credited partly to the origin of bilateral symmetry.

13 sea anemone Nematostella vectensis, exhibit bilateral symmetry.

14 f first cleavage corresponds to the plane of bilateral symmetry.

15 exclusively in the direction from radial to bilateral symmetry.

16 egumes, characterized by flowers with strong bilateral symmetry, a derived condition within angiosper

17 These changes include a reduced bilateral symmetry, a rough leaf lamina, a reduced numbe

18 expressed family member, fail to progress to bilateral symmetry and do not accumulate the SHOOT MERIS

19 embryonic development, and is necessary for bilateral symmetry and dorso-ventral axis organization o

20 e development of embryonic pattern including bilateral symmetry and left-right asymmetry.

21 in the LONESOME HIGHWAY (LHW) gene eliminate bilateral symmetry and reduce the number of cells in the

22 gular relationships relative to the plane of bilateral symmetry and the dorsoventral axis of the larv

23 uding the development of a body pattern with bilateral symmetry, and the development of tissues into

24 onic axis of the blastocyst and its plane of bilateral symmetry are normally orthogonal to the plane

25 These data suggest that bilateral symmetry arose before the evolutionary split o

26 h rate and for the transition from radial to bilateral symmetry associated with initiation of cotyled

27 ed that during the transition from radial to bilateral symmetry, both openings evolved simultaneously

28 er than the unidirectional nodal flow during bilateral symmetry breaking in vertebrates and provide i

29 is restores NICD, anterior segmentation, and bilateral symmetry but does not rescue rostral/caudal id

30 dinates of the body axis in all animals with bilateral symmetry, but a detailed knowledge of their mo

31 rtebrate embryos define an anatomic plane of bilateral symmetry by establishing rudimentary anteropos

32 l to establish a distinct protoderm and lack bilateral symmetry, developing multiple cotyledonary pri

33 Bilateral symmetry during vertebrate development is brok

34 the vertebrate body plan organization is its bilateral symmetry, evident at the level of vertebrae an

35 Echinoderms have either radial or bilateral symmetry, hemichordates include bilateral ente

36 p mutant background mitigates the defects in bilateral symmetry, implying that the two gene families

37 The first obvious sign of bilateral symmetry in mammalian and avian embryos is the

38 neuronal morphology, which reveal remarkable bilateral symmetry in myelinated reticulospinal and late

39 mbryos suggest a defect in the transition to bilateral symmetry in the apical embryo domain, further

40 t cleavage furrow with regard to the axes of bilateral symmetry in the gastrula and pluteus larva.

41 fter two transverse divisions that establish bilateral symmetry in the trunk.

42 Bilateral symmetry is a striking feature of the vertebra

43 Breaking bilateral symmetry is critical for vertebrate morphogene

44 ryo development, the breaking of the initial bilateral symmetry is translated into asymmetric gene ex

45 ed by which the vertebrate midline, and thus bilateral symmetry, is established and maintained by ant

46 lfactory receptor neuron projection patterns-bilateral symmetry, local clustering, and local variabil

47 In nervous systems with bilateral symmetry, many neurons project axons across th

48 ematostella uses homologous genes to achieve bilateral symmetry: Multiple Hox genes are expressed in

49 trategy based upon a comparative decrease in bilateral symmetry of cytochrome oxidase (COX) histochem

50 ticular, the interior of one dark band shows bilateral symmetry of parallel lineaments and pit comple

51 he distribution of polar bodies, the axis of bilateral symmetry of the early blastocysts is normally

52 answered the interesting question of how the bilateral symmetry of the embryo is initially broken to

53 The plane of bilateral symmetry of the larva begins to be set up betw

54 rs an invariant relationship to the plane of bilateral symmetry of the larval body.

55 It follows that, in normal development, bilateral symmetry of the mouse blastocyst anticipates t

56 der is a physical mechanism that ensures the bilateral symmetry of the spinal column.

57 owth must be dynamically regulated to ensure bilateral symmetry of the spinal column.

58 d would seem to require that rats adjust the bilateral symmetry of whisker movements in response to h

59 acting in the molecular control of embryonic bilateral symmetry.Retinoic acid (RA) regulates the main

60 rb ridge organization-->creation of rachis-->bilateral symmetry sequence.

61 al meristem, and in severe cases, eliminates bilateral symmetry; these phenotypes implicate these thr

62 mechanism that controls the transition from bilateral symmetry to LR asymmetry in vertebrates.

63 over from one group to the other, disrupting bilateral symmetry, whereas such mixing was never observ

64 hese results are consistent with approximate bilateral symmetry, with the Co to 3-fluorophthalate dis