1 In
semi-intact animals, stimulating the same neurons also p
2 ncies during crawling-like motor patterns in
semi-intact animals.
3 Manipulation of the
semi-intact cell assay is used to distinguish freely dif
4 Moreover,
semi-intact cell membranes containing elevated levels of
5 s or depletion of p115 from a VSVtsO45 based
semi-intact cell transport assay inhibited transport.
6 lute requirement for ATP, and occurs in both
semi-intact cells and on purified lysosomes, suggesting
7 sion, overall ER to Golgi transport in yeast
semi-intact cells depends on COPII proteins (components
8 urified Epstein-Barr virus deubiquitylase to
semi-intact cells indeed initiates dislocation of a stal
9 By exposing
semi-intact cells to buffers of variable Ca(2+) concentr
10 A) transport to the cell surface in infected
semi-intact cells.
11 e A23187 and in streptolysin-O-permeabilized
semi-intact cells.
12 dependent localization of Golgi complexes in
semi-intact Chinese hamster ovary cells.
13 dependent localization of Golgi complexes in
semi-intact Chinese hamster ovary cells.
14 dependent localization of Golgi complexes in
semi-intact CHO cells.
15 Using a
semi-intact epithelial preparation we examined the Ca(2+
16 In patch-clamp studies of hair cells in a
semi-intact epithelial preparation, we observed a variet
17 of two basolateral and one apical marker in
semi-intact fibroblasts (3T3), pituitary (GH3), and epit
18 We assessed this possibility across
semi-intact heart preparations in two separate analyses.
19 rge properties, and synaptic pharmacology in
semi-intact in vitro preparations of larval Xenopus laev
20 ements of neurotransmission within intact or
semi-intact neuronal networks.
21 clustering potently inhibited secretion from
semi-intact PC12 cells.
22 corded from neurons of the swim circuit in a
semi-intact preparation and found that the vibrotactile
23 vioral sensitization and dishabituation in a
semi-intact preparation of the Aplysia siphon-withdrawal
24 A
semi-intact preparation of the chick basilar papilla was
25 Here, we used a
semi-intact preparation to test whether differential cla
26 In a
semi-intact preparation, stimulation of the PT elicited
27 e oscillatory responses of hair cells in the
semi-intact preparation.
28 gle DSI elicits beating of the foot cilia in
semi-intact preparations and crawling in intact animal t
29 Finally, we elicit motor programs in
semi-intact preparations and show that during radula ope
30 Using
semi-intact preparations of Xenopus laevis tadpoles, we
31 urons, we have used whole-cell recordings in
semi-intact preparations to characterize Rohon-Beard cel
32 Free-moving animals and
semi-intact preparations were used to test whether NO is
33 In
semi-intact preparations, blockade of this region with 6
34 When B51 is depolarized in
semi-intact preparations, radula closing/retractions are
35 We also show, using intact and
semi-intact preparations, that steroids hierarchically m
36 Second, using
semi-intact preparations, we found that tail shock (TS)
37 cellular recordings from the siphon nerve in
semi-intact preparations.
38 , which initiated retrograde contractions in
semi-intact preparations.
39 rminals, to monitor heart beat in intact and
semi-intact preparations.
40 n the isolated central nervous system and in
semi-intact preparations.
41 In
semi-intact SOAT1-/SOAT2-CHO cells prepared by a treatme
42 This
semi-intact somatosensory preparation enables recording
43 reflexive shortening itself, as measured in
semi-intact specimens.
44 approach to measure exocytosis in vitro from
semi-intact synaptosomes, we establish that the Ca2+-dep
45 Using
semi-intact tissue culture cells, we performed a polysom
46 terns during locomotive contraction waves in
semi-intact wild-type and mutant larval preparations.
47 ite the different GVS electrode placement in
semi-intact X. laevis preparations and humans and the mo
48 induced import of FBPase into the vacuole in
semi-intact yeast cells using radiolabeled FBPase, an AT