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1 tants for the Wnt/PCP core component Vangl2 (Trilobite).
2 r observations of healed lesions observed in trilobites.
3 ic surroundings associated with the Cambrian trilobites.
4 as unusual among Cambrian taxa or only early trilobites.
5 s been previously suggested only for certain trilobites.
6 n the pronounced Cambrian diversification of trilobites.
7 tructural plan proposed for the eyes of some trilobites.
8 nd are among the closest extant relatives of trilobites.
10 ptical system, as in the calcified lenses of trilobite and ostracod arthropods, other parts of the vi
11 iled in the trunk of exceptionally preserved trilobites and their close relatives, and is suggestive
12 ed non-biomineralized compound eyes of a non-trilobite arthropod Cindarella eucalla from the lower Ca
15 mation of Morocco, making this the first non-trilobite Cambrian euarthropod known from North Africa.
16 plexity already seen in the fossils of early trilobites, Darwin was at a loss to explain why there we
18 e basal region of epithelial cells in knypek;trilobite double mutant embryos shows that polarization
20 at the deficiency of adaxial cells in knypek;trilobite double mutants is due to impaired C&E movement
22 ovician are related to clade size: Surviving trilobite families show higher genus diversity than exti
23 stratigraphic distribution of all Ordovician trilobite families, based on a comprehensive taxonomic d
29 is in wild-type zebrafish and in the mutants trilobite(m209) (tri), knypek(m119) (kny), and kny;tri,
30 lectronic character of this hybrid class of "trilobite" molecules is dominated by degenerate Rydberg
32 y, blocking cell division leads to rescue of trilobite neural tube morphogenesis despite persistent d
33 trulation mutant knypek, indicating that the trilobite neuron phenotype does not arise nonspecificall
35 meric organization of the digestive tract in trilobites provides further support to this new interpre
36 w data set up a testable model for revealing trilobite segmentation and provide fresh insights into t
37 and extent of morphological variation in 982 trilobite species are greatest early in the evolution of
38 anonical Wnt signaling components Knypek and Trilobite strongly impairs C&E gastrulation movements.
40 We compared our comprehensive database of trilobites to the equivalent portion of J. J. Sepkoski J
42 We show here that mutations in zebrafish trilobite (tri) that affect gastrulation-associated cell
43 we show that pk1 interacts genetically with trilobite (tri)/strabismus to mediate the caudally direc
44 y well-preserved articulated specimen of the trilobite Trimerocephalus from the Late Devonian of the
45 , of the segmental units that constitute the trilobite trunk and their associated exoskeletal element
46 of the Paleozoic Evolutionary Fauna; hence, trilobites were active participants in the great Ordovic
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