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1 ell to produce a ventral cue embedded in the vitelline membrane.
2 astic plates representing the blastoderm and vitelline membrane.
3 d growth of disulfide linked networks in the vitelline membrane.
4 derivatives are gradually released from the vitelline membrane and become localized within distinct
5 is involved in coordinating assembly of the vitelline membrane and is required for functional proper
6 r anti-adhesive quality as the ovomucin from vitelline membrane, and that this anti-adhesive property
9 n, is essential for the morphogenesis of the vitelline membrane as sV23 protein null mutants lay flac
10 ive targets of Pipe, this work points to the vitelline membrane as the source of signals that generat
11 os were transiently dissociated within their vitelline membranes at different time points prior to th
12 ruptions during the initial synthesis of the vitelline membrane by somatic follicle cells surrounding
14 ase autoactivation temporally coincides with vitelline membrane cross-linking and can be triggered in
15 onal regulation (cup, orb, bru1, me31B), and vitelline membrane formation (fs(1)N, fs(1)M3, clos).
23 vatives are generated in the oocyte proximal vitelline membrane layer, they are differentially distri
26 in each row of cells drives adhesion to the vitelline membrane mediated by integrins, apical spreadi
27 ential role in aligning molecules within the vitelline membrane network, much like hydrophobic domain
32 e other cell differentiation events, such as vitelline membrane protein expression, that lead to the
34 rmal uptake into the oocyte of sV17, a major vitelline membrane protein, and defects in non-disulfide
36 These mutations also block cross-linking of vitelline membrane proteins that normally occurs upon eg
37 ermost layer of the Drosophila eggshell, the vitelline membrane, provides structural support and posi
38 ence of mechanosensitivity is not due to the vitelline membrane, rapid MG channel adaptation or tensi
40 Nudel protease function produce eggs having vitelline membranes that are abnormally permeable to the
41 sts of three major proteinaceous layers: the vitelline membrane, the inner chorionic layer, and the o
43 t abundant proprotein, is cleaved within the vitelline membrane to three mature derivatives in a deve
44 that additional structural components of the vitelline membrane undergo Pipe-dependent sulfation.
45 lies between the embryonic membrane and the vitelline membrane (VM), the inner layer of the eggshell