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1 es of ultrafiltration-based excretory organs are patterned by a conserved set of developmental genes,
6 pport the respiratory lamellae of the gills, are patterned by a shh-expressing gill arch epithelial r
9 study, we demonstrate that the early nephron is patterned by a gradient in beta-catenin activity alon
10 e dorsoventral axis of the Drosophila embryo is patterned by a gradient of bone morphogenetic protein
11 e results suggest that the C. elegans embryo is patterned by a juxtaposition of distinct lineage-spec
13 is supported by a spiracular cartilage that is patterned by a shh-expressing epithelial signalling c
14 animal groups, the secondary embryonic axis is patterned by a small group of cells, often called an
15 idence suggests that the Drosophila ectoderm is patterned by a spatial gradient of bone morphogenetic
17 into why the frequency and distance of moves is patterned by age, birth cohort, racial/ethnic identit
18 psis, de novo organogenesis of lateral roots is patterned by an oscillatory mechanism called the root
19 e we present evidence that the P compartment is patterned by another morphogen, Wingless, which is in
25 tes of PVD neurons in Caenorhabditis elegans are patterned by distinct pathways downstream of the DMA
26 f inorganic NCs deposited on a substrate can be patterned by e-beam lithography, altering the structu
34 indicate that bristle type and pigmentation are patterned by hh at widely different times in pupal d
36 hese cells, which we have termed endoblasts, are patterned by homothorax (Hth) and undergo asymmetric
38 uctures starts with an epithelial sheet that is patterned by inductive cues that control the spatiote
41 atively quiescent during the next hour as it is patterned by maternal inductive signals and zygotic g
42 e posterior end of the follicular epithelium is patterned by midline (MID) and its paralog H15, the D
43 second set, the dorso-ventral muscles, DVMs is patterned by mono-nucleate founder cells (FCs) that a
45 ions to the mammalian forebrain are known to be patterned by neural activity, but it remains unknown
46 ventral axis of the Drosophila visual cortex is patterned by nonautonomous signals expressed at its d
47 dorsal longitudinal (flight) muscles, DLMs, is patterned by persistent larval scaffolds; the second
49 f an "aromatic face" on the helix, which can be patterned by positioning aromatic residues with three
50 hermore, the accuracy of teacher expectation was patterned by pupil socioeconomic background but not
53 Evidence is presented that the developing MG is patterned by sequential Ephrin/FGF/MAPK and Delta/Not
54 ral structures in the central nervous system are patterned by signals emanating from the underlying m
58 d floorplate cells, and ventral neural cells are patterned by the activities of Hh-regulated transcri
60 Terminal regions of the Drosophila embryo are patterned by the localized activation of the mitogen
62 show that all three axes of cuttlefish limbs are patterned by the same signaling networks that act in
63 la indicates that the larval and adult forms are patterned by the same underlying sets of development
65 The anterior region of the Drosophila embryo is patterned by the concentration gradient of the homeod
67 rminant of yield potential in many crops and is patterned by the organization and developmental fate
70 ignalling, and in consequence cell division, is patterned by the specification of a second cell type
71 -of-concept demonstrations, quinone surfaces were patterned by the delivery of the oxidant cerric amm
73 lk and surface defects in nematic fluids can be patterned by tuning the topology of colloidal particl
74 inside microchannels, surface free energies were patterned by use of self-assembled monolayers (SAMs