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1 ssion in the dorsal ectoderm and mesoderm is metameric and requires a combination of Dpp and Wingless
2 d homologs in establishing and maintaining a metameric body plan may have arisen only once during ani
3                            The generation of metameric body plans is a key process in development.
4 e anterior sclerotome and differentiate into metameric dorsal root and sympathetic ganglia.
5  the segregation of sensory NCC progeny into metameric dorsal root ganglia (DRG).
6 egmental neural crest migration, but not for metameric dorsal root gangliogenesis.
7 les responsible for establishing the initial metameric expression of sloppy-paired-1 (slp1) in the Dr
8                                  The initial metameric expression of the Drosophila sloppy paired 1 (
9 f soluble ephrin-B1 results in a loss of the metameric migratory pattern and a disorganization of neu
10  and posterior sclerotome halves, disrupting metameric NCC streaming and DRG segmentation.
11 ene Ultrabithorax, whose derepression in two metameric neurons leads to self-righting defects.
12                                          The metameric organization of the digestive tract in trilobi
13                                          The metameric organization of the insect body plan is initia
14                                          The metameric organization of the vertebrate body plan is es
15                                          The metameric organization of the vertebrate hindbrain into
16                                          The metameric organization of the vertebrate trunk is a char
17  embryo, expression of connectin (con) in 11 metameric patches within the VM reveals VM subdivisions
18 nd sympathetic ganglia (SG), which form in a metameric pattern along the anterior-posterior axis of t
19 en-skipped is required for the initiation of metameric pattern in Drosophila.
20 , in Dll1-deficient mouse embryos, a primary metameric pattern is established in mesoderm, and cytodi
21 nesis, which is crucial for establishing the metameric pattern of axial tissues such as the vertebral
22      Similarly, in whole trunk explants, the metameric pattern of neural crest migration was disrupte
23 l types, which are arranged in a stereotyped metameric pattern.
24 er, amphioxus embryos express AmphiEn in non-metameric patterns - transiently in the embryonic ectode
25 nt and the steps and signals that generate a metameric peripheral nervous system, attempting to recon
26 an evolutionary inheritance either from some metameric protostome or from a more closely related deut
27 metameres in embryos of Drosophila and other metameric protostomes.
28 e rostral hindbrain, which is organized in a metameric series of rhombomere-derived (rd) territories,
29 he post-cranial axial skeleton consists of a metameric series of vertebral bodies and intervertebral
30 y accounting for these results proposes that metameric slp1 expression is achieved through the Runt-d
31 rae develop from the sclerotome layer of the metameric somites, and PNS neurons and glia differentiat
32 We developed a behavioral protocol that uses metameric stimuli to estimate the receptive field sizes
33  expressed along the anteroposterior axis as metameric stripes, each located in the posterior part of
34 ion of the paraxial mesoderm into repeating, metameric structures called somites.
35 rae and their associated muscles derive from metameric structures of mesodermal origin, the somites.
36 nt, the paraxial mesoderm is subdivided into metameric subunits called somites.
37 a segmented structure divided into repeating metameric units termed rhombomeres (r).
38 tterned along the anterior-posterior axis in metameric units, or somites, in a bilaterally symmetric
39 irst subdivision of the embryo into repeated metameric units.
40 ory paths and cell fates that generate these metameric vessels of the trunk.

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