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1 responding to rotation around three distinct body axes.
2 nding on their positions with respect to the body axes.
3 velopment is the establishment of the future body axes.
4 udding animals establish and maintain linked body axes.
5  animals with linked but completely opposite body axes.
6 sential for the development of the embryonic body axes.
7 ng the anterior-posterior and dorsal-ventral body axes.
8 rient diverse structures with respect to the body axes.
9 low resulting from rotation around different body axes.
10 bit precise orientations with respect to the body axes.
11  simultaneous recordings along the different body axes.
12 mining how such polarity is aligned with the body axes.
13 orthogonal dorsoventral and anterioposterior body axes.
14 d then aggregate to form the germ layers and body axes.
15 ture is highly polarized with respect to the body axes.
16  important signaling pathways to pattern the body axes.
17 ttern of pre-existing tissues, such as along body axes.
18 me, or limbs, across tissue compartments and body axes.
19 egration of positional information along the body axes.
20  coordinated patterning of tissues along the body axes.
21 ential for proper establishment of the major body axes.
22  dorsal-ventral and anterior-posterior (A-P) body axes, although the molecular mechanism underlying p
23 crosstalk between developmentally programmed body axes and environmentally influenced growth vectors.
24 involves cell fate decisions that define the body axes and establish pools of progenitor cells.
25 unagi/Y14 is required to establish the major body axes and for the localization of primordial germ ce
26 indicate that pbx promotes pole formation of body axes and formation of regenerative progenitors for
27 als play important roles in establishing the body axes and germ layers in the vertebrate embryo.
28 t developing hemichordates retain the larval body axes and major larval tissues after metamorphosis i
29 ormal head/brain development, curved/twisted body axes and no circulating blood cells, and died by 72
30 imal pole, following which we detected major body axes and tissues corresponding to all three germ la
31 le cell-to-oocyte signal to define the major body axes and to localize components necessary for deter
32                               The Drosophila body axes are established in the oocyte during oogenesis
33 ed by proper cell polarity in the developing body axes are fundamental to the elongation of the notoc
34  transduce that polarity to organismal scale body axes are poorly understood outside of select model
35 that control their alignment relative to the body axes are unknown.
36  pole, which is key to forming the embryonic body axes as well as the germline in most vertebrates.
37  (MTOC) relative to the cell nucleus and the body axes, as a marker of cell polarity.
38 ventral mesoderm, induce extensive secondary body axes, block mesoderm induction by BMP4 and directly
39 er168 to alanine resulted in embryos lacking body axes, demonstrating that Ser168 is essential to axi
40 xplain regional specification of tissues and body axes during animal development.
41                      The ectopic and primary body axes form side-by-side conjoined twins, with the se
42 g in the regeneration and maintenance of the body axes have been uncovered, among other regulatory fa
43 sing antisense morpholinos (MOs) led to bent body axes, hydrocephalus and oedema.
44                                 The two main body axes in Drosophila become polarised as a result of
45 rfamily, play a key role in establishing the body axes in many vertebrates, but their role in teleost
46 ed by the mother to the embryo determine the body axes in most animals.
47 ord coordinates the development of all three body axes in the vertebrate body plan.
48 archical model of pattern integration across body axes in which DV patterning is central by producing
49       The ability of CKI to induce secondary body axes in Xenopus embryos was reduced by the B56 regu
50                           Defining the three body axes is a central event of vertebrate morphogenesis
51 al orientation of hair cells relative to the body axes is established through an interaction between
52                  Patterning along developing body axes is regulated by gradients of transcription fac
53                       To establish the major body axes, late Drosophila oocytes localize determinants
54 ining transcription factors that pattern the body axes of animal embryos.
55 n between antennal position and the relative body axes of dancer and follower bees.
56                                          The body axes of Drosophila are established during oogenesis
57 tial domains along the anteroposterior (A/P) body axes of many organisms.
58 ly leading to the establishment of the major body axes of the animal.
59               The establishment of the major body axes of the Drosophila egg and future embryo requir
60 nterior-posterior (A-P) and left-right (L-R) body axes of the vertebrate embryo.
61 , but our data suggest the pathway regulates body axes patterning in planarians.
62 t, and molecules involved in determining the body axes provide a coordinate system for subsequent pat
63 nto distinct territories and act to organize body axes, regulate growth, maintain stem cell niches, o
64 s a wide range of developmental events, from body axes specification in insects to cardiac developmen
65                               The organismal body axes that are formed during embryogenesis are intim
66 quires regional specification along multiple body axes, the proliferation and differentiation of prog
67 euronal and immune cells co-operate in brain-body axes to orchestrate metabolism and obesity.
68 t body shapes across the animal kingdom, the body axes, which are arguably the most fundamental featu