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1 spectrin mutants was in morphogenesis of the invaginated apical domain, although basolateral defects
2 and gill slits, structures which form where invaginated atrial siphon ectoderm apposes pharyngeal en
3 air collections caused by separation of the invaginated bronchus from the recipient bronchus were se
5 at assembly process progresses toward deeply invaginated buds, focally synthesized phosphoinositides
7 ggest that some G protein is associated with invaginated caveolae, but most of the protein resides in
8 , to a collar-like arrangement around partly invaginated CCSs with actin filament barbed ends abuttin
11 ase dynamin catalyzes the scission of deeply invaginated clathrin-coated pits at the plasma membrane,
12 in self-assembles around the necks of deeply invaginated coated pits at the plasma membrane and catal
15 o 0.02 mN/m, and at the substratum, membrane invaginated, creating transient vacuole-like dilations.
17 uck behind the nucleus, the center of the IS invaginated dramatically to approach the centrosome.
18 Caveolae are related domains that become invaginated due to the presence of the structural protei
19 ammalian Dynamins causes the accumulation of invaginated endocytic pits at synapses, sometimes also o
23 e invading parasite and the host cell as the invaginated host plasma membrane is forced inward by the
26 ssion electron microscopy showed spirochetes invaginated into the host cell membrane with resultant e
28 y of spectrin into tetramers is required for invaginated membrane system maturation and proplatelet e
29 hrough its participation in the formation of invaginated membranes and in the maintenance of proplate
30 C induces some vesicles to form multidomain, invaginated morphologies that differ from the typical tw
31 hallus), which grows from apical cells in an invaginated "notch." The genetic mechanisms regulating l
32 Distinctive features included extensively invaginated nuclei and well-developed Golgi apparati; Fo
33 motoneurons measuring 15 x 5 microns with an invaginated nucleus were also present in both subdivisio
34 nin-immunoreactive population, containing an invaginated nucleus, synapses with nerve fibers, and a s
35 serotonin-immunoreactive taste cells have an invaginated nucleus, synaptic contacts with nerve fibers
36 tility, model epithelia smoothly deform into invaginated or evaginated shapes similar to those observ
37 ccurs inside numerous virus-induced vesicles invaginated or otherwise elaborated from a continuous, o
39 rane-connected cisternae, in contrast to the invaginated pits that accumulate in shi(ts1) mutants.
42 1Delta abp1Delta double-mutant cells exhibit invaginated plasma membranes and impaired endocytosis, f
44 s associated with RNA replication from small invaginated spherules to large, karmellae-like, multilay
45 clathrin-coated pits are frozen at a deeply invaginated state, that is, cells that lack dynamin (fib
49 has remained under debate because the small, invaginated synaptic cleft has precluded measurement.
51 ad 1) vesiculated, spine-like processes that invaginated type I cells and 2) other, elongate processe
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