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1  exclusively in the direction from radial to bilateral symmetry.
2 ng to primitive streak formation, generating bilateral symmetry.
3 ion and expansion are responsible for floral bilateral symmetry.
4 marks the transition from radial symmetry to bilateral symmetry.
5 cata (DIV) specify the development of floral bilateral symmetry.
6 ng in the node is not essential for breaking bilateral symmetry.
7 olar differentiation and failed to establish bilateral symmetry.
8 II HD-Zip gene activity results in a loss of bilateral symmetry.
9 pacities involve a robust ability to restore bilateral symmetry.
10 like form can evolve in the absence of overt bilateral symmetry.
11 r establishment of the apical-basal axis and bilateral symmetry.
12  be required for the establishment of floral bilateral symmetry.
13 of the body plan of a majority of animals is bilateral symmetry.
14 ilateria is credited partly to the origin of bilateral symmetry.
15 ae and polyps in Hydrozoa, including loss of bilateral symmetry.
16  sea anemone Nematostella vectensis, exhibit bilateral symmetry.
17 f first cleavage corresponds to the plane of bilateral symmetry.
18  emerges for multiple object categories with bilateral symmetry.
19 to build rachis and converts radial downy to bilateral symmetry.
20 without clear transitions between radial and bilateral symmetry.
21 egumes, characterized by flowers with strong bilateral symmetry, a derived condition within angiosper
22              These changes include a reduced bilateral symmetry, a rough leaf lamina, a reduced numbe
23 expressed family member, fail to progress to bilateral symmetry and do not accumulate the SHOOT MERIS
24  embryonic development, and is necessary for bilateral symmetry and dorso-ventral axis organization o
25 e development of embryonic pattern including bilateral symmetry and left-right asymmetry.
26 in the LONESOME HIGHWAY (LHW) gene eliminate bilateral symmetry and reduce the number of cells in the
27 ning system in potentially active control of bilateral symmetry and should motivate systematic search
28 gular relationships relative to the plane of bilateral symmetry and the dorsoventral axis of the larv
29 d stimuli, their whiskers moved with greater bilateral symmetry, and synchronous spiking and enhanced
30 uding the development of a body pattern with bilateral symmetry, and the development of tissues into
31 onic axis of the blastocyst and its plane of bilateral symmetry are normally orthogonal to the plane
32  the reproducible pattern of cell states and bilateral symmetry arise from temporal averaging.
33                      These data suggest that bilateral symmetry arose before the evolutionary split o
34 h rate and for the transition from radial to bilateral symmetry associated with initiation of cotyled
35 uating asymmetry (FA; random deviations from bilateral symmetry) between the right and left forewings
36 ed that during the transition from radial to bilateral symmetry, both openings evolved simultaneously
37 er than the unidirectional nodal flow during bilateral symmetry breaking in vertebrates and provide i
38 is restores NICD, anterior segmentation, and bilateral symmetry but does not rescue rostral/caudal id
39 dinates of the body axis in all animals with bilateral symmetry, but a detailed knowledge of their mo
40 rtebrate embryos define an anatomic plane of bilateral symmetry by establishing rudimentary anteropos
41                                              Bilateral symmetry defines much of the animal kingdom an
42 l to establish a distinct protoderm and lack bilateral symmetry, developing multiple cotyledonary pri
43 s ligand Trunk(3)-is critical for preserving bilateral symmetry during Drosophila body axis elongatio
44                                              Bilateral symmetry during vertebrate development is brok
45 the vertebrate body plan organization is its bilateral symmetry, evident at the level of vertebrae an
46 ght, we also present adjusted definitions of bilateral symmetry exhibited by this connectome.
47  importance of four floral character states (bilateral symmetry, fused corollas, horizontal orientati
48            Echinoderms have either radial or bilateral symmetry, hemichordates include bilateral ente
49                In many animal species with a bilateral symmetry, Hox genes are clustered either at on
50 p mutant background mitigates the defects in bilateral symmetry, implying that the two gene families
51 mic mechanism, which controls organ size and bilateral symmetry in a narrow developmental time window
52 conserved patterning networks that establish bilateral symmetry in early embryos,(1) but how this sym
53                         The establishment of bilateral symmetry in flowers depends on the precise reg
54 of MlCYC2A, contributing to the formation of bilateral symmetry in flowers, a key trait in angiosperm
55 reak, a transient embryonic structure, marks bilateral symmetry in mammalian and avian embryos and he
56                    The first obvious sign of bilateral symmetry in mammalian and avian embryos is the
57                              The breaking of bilateral symmetry in most vertebrates is critically dep
58 neuronal morphology, which reveal remarkable bilateral symmetry in myelinated reticulospinal and late
59        The developmental mechanisms ensuring bilateral symmetry in organ size are mostly unknown.
60                                  Significant bilateral symmetry in root morphology was noted.
61 R (TCP) protein family are known to regulate bilateral symmetry in single flowers.
62 mbryos suggest a defect in the transition to bilateral symmetry in the apical embryo domain, further
63 t cleavage furrow with regard to the axes of bilateral symmetry in the gastrula and pluteus larva.
64 fter two transverse divisions that establish bilateral symmetry in the trunk.
65 zation phenotype (tight seizure coupling and bilateral symmetry) in these mice, indicating that Kv7.2
66                                              Bilateral symmetry independently evolved at least 130 ti
67  fixed-speed treadmill walking ABSTRACT: The bilateral symmetry inherent in healthy human walking is
68                                              Bilateral symmetry is a striking feature of the vertebra
69                                     Breaking bilateral symmetry is critical for vertebrate morphogene
70                                              Bilateral symmetry is the predominant body plan in the a
71 ryo development, the breaking of the initial bilateral symmetry is translated into asymmetric gene ex
72 ed by which the vertebrate midline, and thus bilateral symmetry, is established and maintained by ant
73 lfactory receptor neuron projection patterns-bilateral symmetry, local clustering, and local variabil
74                      In nervous systems with bilateral symmetry, many neurons project axons across th
75 ematostella uses homologous genes to achieve bilateral symmetry: Multiple Hox genes are expressed in
76 stigate this problem via a case study on the bilateral symmetry of a larval Drosophila brain connecto
77 trategy based upon a comparative decrease in bilateral symmetry of cytochrome oxidase (COX) histochem
78 ticular, the interior of one dark band shows bilateral symmetry of parallel lineaments and pit comple
79 he distribution of polar bodies, the axis of bilateral symmetry of the early blastocysts is normally
80 answered the interesting question of how the bilateral symmetry of the embryo is initially broken to
81                                 The plane of bilateral symmetry of the larva begins to be set up betw
82 rs an invariant relationship to the plane of bilateral symmetry of the larval body.
83      It follows that, in normal development, bilateral symmetry of the mouse blastocyst anticipates t
84 der is a physical mechanism that ensures the bilateral symmetry of the spinal column.
85 owth must be dynamically regulated to ensure bilateral symmetry of the spinal column.
86 d would seem to require that rats adjust the bilateral symmetry of whisker movements in response to h
87  as a sister group to all other animals with bilateral symmetry or as an early diverging ambulacraria
88 acting in the molecular control of embryonic bilateral symmetry.Retinoic acid (RA) regulates the main
89 rb ridge organization-->creation of rachis-->bilateral symmetry sequence.
90 al meristem, and in severe cases, eliminates bilateral symmetry; these phenotypes implicate these thr
91  morphological interrelationships along with bilateral symmetry to increase diagnostic accuracy, clin
92  mechanism that controls the transition from bilateral symmetry to LR asymmetry in vertebrates.
93                     We translate notions of 'bilateral symmetry' to generative models of the network
94                   We found that flowers with bilateral symmetry usually have the capacity to reorient
95                                    Prominent bilateral symmetry was noticed for all features, and tau
96 over from one group to the other, disrupting bilateral symmetry, whereas such mixing was never observ
97 mans deploy motile cilia in the LRO to break bilateral symmetry, while reptiles, birds, even-toed mam
98 ough side bias existed, we found significant bilateral symmetry, with one side being functionally a m
99 hese results are consistent with approximate bilateral symmetry, with the Co to 3-fluorophthalate dis