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1 hpf is confined to the lens, cerebellum, and pronephric duct.
2  also required for ciliogenesis in zebrafish pronephric duct.
3 otic vesicle and shorter motile cilia in the pronephric ducts.
4 bules, whereas zSMCTe mRNA is more distal in pronephric ducts.
5 s such as the brain, olfactory placodes, and pronephric ducts.
6 zebrafish embryos, bnc2 was expressed in the pronephric duct and cloaca, analogs of the mammalian low
7 on of vasculogenesis and concomitant loss of pronephric duct and somitic tissue.
8 ective zebrafish had too few motile cilia in pronephric ducts and in Kupffer's vesicle.
9 and disrupted ciliogenesis in the developing pronephric ducts and otic vesicles.
10 ecreased ciliary length in the spinal canal, pronephric ducts, and Kupffer's vesicle.
11  alpha 6 is also expressed in the elongating pronephric duct as well as a subset of the rhombencephal
12 ral tube, retina, notochord, somites, heart, pronephric ducts, branchial arches, and jaw muscles in e
13 topic podocyte-specific marker expression in pronephric duct cells correlates with loss of expression
14 ufficient to direct pathfinding of migrating pronephric duct cells in axolotl embryos by: (1) demonst
15  kidney development with highly disorganized pronephric duct cilia.
16 efects of the pronephric tubules but not the pronephric ducts, consistent with the tubular atrophy ob
17 asolateral membrane protein targeting in the pronephric duct epithelial cells is also severely affect
18                                These include pronephric duct extension, "gill bulge" formation, and e
19 ereas constitutively active CaMK-II restores pronephric duct formation in pkd2 morphants.
20 are incorporated into an integrated model of pronephric duct guidance consistent with all present evi
21                   The role of this matrix in pronephric duct guidance was assayed by presenting matri
22 e basal bodies in multiciliated cells of the pronephric duct in ift mutants were disorganized, with a
23 sited on microcarriers directly to migrating pronephric ducts in situ.
24 he epidermis overlying the migrating axolotl pronephric duct is known to participate in duct guidance
25                We have previously shown that pronephric duct is specified somewhat later, at stage 14
26 ds its effect to head, heart, pronephros and pronephric duct mesoderm inducing early blood and endoth
27 ucts caused a corresponding reorientation of pronephric duct migration.
28 pidermally deposited matrix from reorienting pronephric duct migration.
29  were detected and localized here, inhibited pronephric duct migration.
30 s, which give rise to the inner ear; and the pronephric ducts of the kidney.
31 -II-deficient zebrafish embryos fail to form pronephric ducts properly, and exhibit anterior cysts an
32 ies that recognize the pronephric tubules or pronephric duct to explore the induction of the embryoni
33 tion of F-actin and Na(+)/K(+)-ATPase in the pronephric ducts was disturbed.
34                            Interestingly the pronephric duct, which develops from the ventroposterior
35 tion occurs after the differentiation of the pronephric duct with both the glomeruli and tubules bein
36 lacodes with defective morphology as well as pronephric ducts with increased polyglutamylation.