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1 ive weight of PV + gizzard (proventriculum + gizzard).
2 s) and the thick muscular posterior chamber (gizzard).
3 on factor Sox9 is a marker for the posterior gizzard.
4 ension of Bmp4 and Wnt5a expression into the gizzard.
5 that Bmp4 and Wnt5a are not expressed in the gizzard.
6 nd midgut, but is not expressed in the early gizzard.
7 -autonomous event within the mesoderm of the gizzard.
8 egulation of the SMGA gene in the developing gizzard.
9 ein, Mr = 100,000, in lysates of adult avian gizzard.
10 -actin solutions containing filamin (chicken gizzard), a protein that bundles actin filaments.
11  probed with a monoclonal Ab against chicken gizzard actin; tissue- and stage-specific changes in act
12            We found that recombinant chicken gizzard alpha-calponin co-sediments with myosin rod and,
13 cripts are present at intermediate levels in gizzard and lung, and at low levels in kidney.
14 ate level of expression was also detected in gizzard and retina.
15 lls with Ret increased in the ganglia of the gizzard and small intestine.
16 n a slight increase in rigor tension in both gizzard and soleus muscles, but a decrease in psoas musc
17  and ecto-apyrase (ATPDase) in adult chicken gizzard and stomach by immunofluorescence and laser scan
18 ith relatively low expression in the gonads, gizzard and subcutaneous fat tissues of chickens.
19  telokin (5-20 microM), purified from turkey gizzard, and recombinant rabbit telokin, expressed in Es
20  (ir) was found in a network of cells in the gizzard at embryonic day (E)3.5.
21 red in some HNK-1 cells in the esophagus and gizzard at embryonic day (E)3.5.
22 nalyses, using nuclear extracts derived from gizzards at various stages in development, showed that t
23      Bmp4 is not expressed in the developing gizzard but is expressed in the rest of the gut includin
24 t treatment, full-length recombinant chicken gizzard CaD overexpressed in insect cells (High-FiveTM)
25 l and C-terminal deletion mutants of chicken-gizzard CaD revealed that the major myosin-binding site
26                      Unphosphorylated turkey gizzard caldesmon (3 microM) significantly reduced mean
27 tatic interactions to the effects of chicken gizzard calponin on the kinetics of actin polymerization
28                          Ectopic BMP4 in the gizzard caused a thinning of the muscularis.
29              Chronic exposure of the phasic (gizzard) cells to endothelin-1 prolonged the time to pea
30 om a single progenitor can populate both the gizzard (chicken stomach) and the small intestine early
31                                       In the gizzard coincident with the shift in expression from the
32 did not detect ecto-apyrase in immunolabeled gizzard cryosections.
33 the reconstituted Ac:Tm filament formed with gizzard-derived Tm, we discuss two possible mechanisms f
34 crease in SRF protein and mRNA levels during gizzard development by Western and Northern blot analyse
35 es for canonical signaling in the developing gizzard, duodenum, and large intestine in chick were tes
36            The sequence homology between the gizzard ecto-ATPase and CD39 was confirmed by Western bl
37 antibodies that recognize the 66 kDa chicken gizzard ecto-ATPase monomer strengthened the hypothesis
38  antibodies, both raised against the chicken gizzard ecto-ATPase, were evaluated for their ability to
39 hnic mesoderm resulted in the failure of the gizzard epithelium to form microvilli.
40 nic contracting aorta and phasic contracting gizzard exclusively express the leucine zipper positive
41        Early during development, the chicken gizzard expresses the splice-in MYPT isoform, and GTPgam
42                                  Proteolytic gizzard heavy meromyosin regulatory light chains were pa
43 ng of both beta beta and gamma gamma chicken gizzard homodimers.
44 23 splicing as the rat portal vein and avian gizzard implement the fast program of gene expression in
45 ls of the fast-phasic contractile phenotype (gizzard), in which the central alternative exon is skipp
46 om that observed in seeds obtained from dove gizzards, indicating that seed passage through cougar gu
47  of Bapx1 in the proventriculus results in a gizzard-like morphology and inhibits the normal proventr
48 he sFv recognizes a single 100-kD protein in gizzard lysates.
49 ve apyrase) in Western blots of both chicken gizzard membrane extracts and partially purified anion e
50           Viral misexpression of Sox9 in the gizzard mesoderm is sufficient to specify epithelium cha
51 noggin down-regulates Sox9 expression in the gizzard mesoderm.
52 he chick, Tcf4 is expressed in the posterior gizzard mesoderm.
53 k of differentiation of smooth muscle in the gizzard mesoderm.
54 s and a decrease in proliferation within the gizzard mesoderm.
55 roperties of permeabilized strips of chicken gizzard muscle in rigor and in the presence of MgADP.
56 directly resolved and visualized cardiac and gizzard muscle Tm on filamentous Ac in the position that
57                             The results with gizzard muscle were similar after thiophosphorylation of
58           Bapx1 (Nkx3.2) is expressed in the gizzard musculature but not in the proventriculus or mid
59 cally interact with the S2 domain in chicken gizzard myosin and nonmuscle myosin IIA (MYH-9) but exhi
60                                              Gizzard myosin regulatory light chain (RLC) was labeled
61                                      Chicken gizzard myosin regulatory light chain (RLC) was labeled
62          Regulatory light chain from chicken gizzard myosin was covalently modified with iodoacetamid
63 prepared by proteolytic digestion of chicken gizzard myosin with between 5 and 95% heavy chain cleava
64 steine mutants of the smooth muscle (chicken gizzard) myosin regulatory light chain and performing el
65 een actin, MgADP, and smooth muscle (chicken gizzard) myosin subfragment 1 (smS1).
66                          Recombinant chicken gizzard MYPT1 (M130) was phosphorylated in vitro by a re
67 switch coincides with the development in the gizzard of a cGMP-resistant phenotype, i.e. inability to
68  measurements showed that cultured embryonic gizzard (phasic) cells developed force more rapidly (8 +
69  in the diets on the relative weight of PV + gizzard (proventriculum + gizzard).
70 change, we have measured distances between a gizzard regulatory light chain (Cys 108) and the active
71  to study the rotational dynamics of chicken gizzard regulatory light chain (RLC) bound to scallop ad
72                           Engineered chicken gizzard regulatory light chain (RLC), labeled with bisio
73                                              Gizzard regulatory light chain was labeled with a nitrox
74 terminal domain of caldesmon (CaD-4, chicken gizzard residues 597-756) bound to tropomyosin with grea
75 LC cys177 and RLC cys154; and ELC cys177 and gizzard RLC cys108.
76 s was extracted and replaced completely with gizzard RLC labeled specifically at Cys 108 with erythro
77 yzed a series of purified mutants of chicken gizzard smooth muscle CaD generated by internal deletion
78 ion and internal deletion mutants of chicken gizzard smooth muscle CaD were systematically designed u
79 yptophan residues (W659 and W692) in chicken gizzard smooth muscle caldesmon (CaD) are located within
80 gion between residues 598-756 of the chicken gizzard smooth muscle caldesmon (CaD) molecule.
81                       The ability of chicken gizzard smooth muscle caldesmon (CaD) to inhibit actomyo
82 es of C-terminal deletion mutants of chicken gizzard smooth muscle caldesmon (CaD) were made using a
83 activation, forced expression of MLC(17b) in gizzard smooth muscle cells decreased (p < 0.05) the rat
84 immunoelectron microscopy studies of chicken gizzard smooth muscle cells showed that in certain areas
85         Our findings suggest that in chicken gizzard smooth muscle cells, calponin may be an integral
86  transfected into cultured embryonic chicken gizzard smooth muscle cells.
87 single cultured chicken embryonic aortic and gizzard smooth muscle cells.
88 ntaining complexes were not present early in gizzard smooth muscle development, but appeared as devel
89 cto-ATPase enzyme, cross-linking the chicken gizzard smooth muscle ecto-ATPase with 3,3'-dithiobis(su
90 m chicken skeletal muscle myosin for that of gizzard smooth muscle heavy meromyosin (HMM) causes acti
91               Domain dynamics of the chicken gizzard smooth muscle myosin catalytic domain (heavy cha
92                 Fluorescently labeled turkey gizzard smooth muscle myosin was prepared by removal of
93 o mutants of a truncated fragment of chicken gizzard smooth muscle myosin, which includes the motor d
94 eplaced by either the tail domain of chicken gizzard smooth muscle or Acanthamoeba myosin II are 20 t
95 ty were examined in goose (GG) and duck (DG) gizzard smooth muscle stored at 5 degrees C.
96 rescently colocalizes with myosin in chicken gizzard smooth muscle, and interacts with two configurat
97 dividual folded myosin molecules from turkey gizzard smooth muscle, we show that they are more compac
98 ortant role in the postmortem proteolysis of gizzard smooth muscle.
99                 The ecto-ATPase from chicken gizzard (smooth muscle) was solubilized, and the 66-kDa
100 ession of the TIA and SR proteins in phasic (gizzard) smooth muscle around hatching coincided with th
101 urify with unphosphorylated SMM from chicken gizzard, suggesting that they are tightly bound.
102     Thus, purified talin head liberated from gizzard talin by calpain cleavage cosediments with F-act
103                       Recombinant and native gizzard telokins were phosphorylated, in vitro, by the c
104                                   In chicken gizzard, the ecto-ATPase was distributed in discrete clu
105 g visceral smooth muscle cells (SMCs) during gizzard tissue development.
106 phate) (ATPgammaS) phosphorylated only adult gizzard tissue, the only tissue that did not demonstrate
107 he ratio was approximately 23-37% of that in gizzard tissue.
108 ate filaments and dense bodies isolated from gizzard tissues.
109 e a horny beak (rhamphotheca) and a muscular gizzard to acquire and process food.
110 beta beta and gamma gamma species of chicken gizzard tropomyosin concludes that their unfolding trans
111 rted on these homodimeric species of chicken gizzard tropomyosin with a single interchain disulfide c
112 mally limited to the region of the posterior gizzard under the regulation of BMP signaling from the a
113  esophagus at E3.5 but did not appear in the gizzard until E4.5.
114 ession of an activated form of BMPR1b in the gizzard upregulates Sox9 expression, while the BMP antag
115 d bacterium called J1, isolated from chicken gizzard, was noted to produce a bacteriocin (BacJ1) that
116 activity in erythrocytes, platelets, and the gizzard, we hypothesized that calmodulin increases cross
117 e BMP receptors act similarly to BMP4 in the gizzard when ectopically expressed.
118 ough the primitive esophagus to colonize the gizzard where an extensive cellular network forms.
119 rms is also developmentally regulated in the gizzard, which switches from leucine zipper positive to

 
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