ライフサイエンスコーパス: gizzard

1 s) and the thick muscular posterior chamber (gizzard).

2 on factor Sox9 is a marker for the posterior gizzard.

3 ension of Bmp4 and Wnt5a expression into the gizzard.

4 that Bmp4 and Wnt5a are not expressed in the gizzard.

5 nd midgut, but is not expressed in the early gizzard.

6 -autonomous event within the mesoderm of the gizzard.

7 egulation of the SMGA gene in the developing gizzard.

8 ein, Mr = 100,000, in lysates of adult avian gizzard.

9 -actin solutions containing filamin (chicken gizzard), a protein that bundles actin filaments.

10 probed with a monoclonal Ab against chicken gizzard actin; tissue- and stage-specific changes in act

11 We found that recombinant chicken gizzard alpha-calponin co-sediments with myosin rod and,

12 cripts are present at intermediate levels in gizzard and lung, and at low levels in kidney.

13 ate level of expression was also detected in gizzard and retina.

14 lls with Ret increased in the ganglia of the gizzard and small intestine.

15 n a slight increase in rigor tension in both gizzard and soleus muscles, but a decrease in psoas musc

16 and ecto-apyrase (ATPDase) in adult chicken gizzard and stomach by immunofluorescence and laser scan

17 ith relatively low expression in the gonads, gizzard and subcutaneous fat tissues of chickens.

18 telokin (5-20 microM), purified from turkey gizzard, and recombinant rabbit telokin, expressed in Es

19 (ir) was found in a network of cells in the gizzard at embryonic day (E)3.5.

20 red in some HNK-1 cells in the esophagus and gizzard at embryonic day (E)3.5.

21 nalyses, using nuclear extracts derived from gizzards at various stages in development, showed that t

22 Bmp4 is not expressed in the developing gizzard but is expressed in the rest of the gut includin

23 t treatment, full-length recombinant chicken gizzard CaD overexpressed in insect cells (High-FiveTM)

24 l and C-terminal deletion mutants of chicken-gizzard CaD revealed that the major myosin-binding site

25 Unphosphorylated turkey gizzard caldesmon (3 microM) significantly reduced mean

26 tatic interactions to the effects of chicken gizzard calponin on the kinetics of actin polymerization

27 Ectopic BMP4 in the gizzard caused a thinning of the muscularis.

28 Chronic exposure of the phasic (gizzard) cells to endothelin-1 prolonged the time to pea

29 om a single progenitor can populate both the gizzard (chicken stomach) and the small intestine early

30 In the gizzard coincident with the shift in expression from the

31 did not detect ecto-apyrase in immunolabeled gizzard cryosections.

32 the reconstituted Ac:Tm filament formed with gizzard-derived Tm, we discuss two possible mechanisms f

33 crease in SRF protein and mRNA levels during gizzard development by Western and Northern blot analyse

34 es for canonical signaling in the developing gizzard, duodenum, and large intestine in chick were tes

35 The sequence homology between the gizzard ecto-ATPase and CD39 was confirmed by Western bl

36 antibodies that recognize the 66 kDa chicken gizzard ecto-ATPase monomer strengthened the hypothesis

37 antibodies, both raised against the chicken gizzard ecto-ATPase, were evaluated for their ability to

38 hnic mesoderm resulted in the failure of the gizzard epithelium to form microvilli.

39 nic contracting aorta and phasic contracting gizzard exclusively express the leucine zipper positive

40 Early during development, the chicken gizzard expresses the splice-in MYPT isoform, and GTPgam

41 Proteolytic gizzard heavy meromyosin regulatory light chains were pa

42 ng of both beta beta and gamma gamma chicken gizzard homodimers.

43 23 splicing as the rat portal vein and avian gizzard implement the fast program of gene expression in

44 ls of the fast-phasic contractile phenotype (gizzard), in which the central alternative exon is skipp

45 om that observed in seeds obtained from dove gizzards, indicating that seed passage through cougar gu

46 of Bapx1 in the proventriculus results in a gizzard-like morphology and inhibits the normal proventr

47 he sFv recognizes a single 100-kD protein in gizzard lysates.

48 ve apyrase) in Western blots of both chicken gizzard membrane extracts and partially purified anion e

49 Viral misexpression of Sox9 in the gizzard mesoderm is sufficient to specify epithelium cha

50 noggin down-regulates Sox9 expression in the gizzard mesoderm.

51 he chick, Tcf4 is expressed in the posterior gizzard mesoderm.

52 k of differentiation of smooth muscle in the gizzard mesoderm.

53 s and a decrease in proliferation within the gizzard mesoderm.

54 roperties of permeabilized strips of chicken gizzard muscle in rigor and in the presence of MgADP.

55 directly resolved and visualized cardiac and gizzard muscle Tm on filamentous Ac in the position that

56 The results with gizzard muscle were similar after thiophosphorylation of

57 Bapx1 (Nkx3.2) is expressed in the gizzard musculature but not in the proventriculus or mid

58 cally interact with the S2 domain in chicken gizzard myosin and nonmuscle myosin IIA (MYH-9) but exhi

59 Gizzard myosin regulatory light chain (RLC) was labeled

60 Chicken gizzard myosin regulatory light chain (RLC) was labeled

61 Regulatory light chain from chicken gizzard myosin was covalently modified with iodoacetamid

62 prepared by proteolytic digestion of chicken gizzard myosin with between 5 and 95% heavy chain cleava

63 steine mutants of the smooth muscle (chicken gizzard) myosin regulatory light chain and performing el

64 een actin, MgADP, and smooth muscle (chicken gizzard) myosin subfragment 1 (smS1).

65 Recombinant chicken gizzard MYPT1 (M130) was phosphorylated in vitro by a re

66 switch coincides with the development in the gizzard of a cGMP-resistant phenotype, i.e. inability to

67 measurements showed that cultured embryonic gizzard (phasic) cells developed force more rapidly (8 +

68 change, we have measured distances between a gizzard regulatory light chain (Cys 108) and the active

69 to study the rotational dynamics of chicken gizzard regulatory light chain (RLC) bound to scallop ad

70 Engineered chicken gizzard regulatory light chain (RLC), labeled with bisio

71 Gizzard regulatory light chain was labeled with a nitrox

72 terminal domain of caldesmon (CaD-4, chicken gizzard residues 597-756) bound to tropomyosin with grea

73 LC cys177 and RLC cys154; and ELC cys177 and gizzard RLC cys108.

74 s was extracted and replaced completely with gizzard RLC labeled specifically at Cys 108 with erythro

75 yzed a series of purified mutants of chicken gizzard smooth muscle CaD generated by internal deletion

76 ion and internal deletion mutants of chicken gizzard smooth muscle CaD were systematically designed u

77 yptophan residues (W659 and W692) in chicken gizzard smooth muscle caldesmon (CaD) are located within

78 gion between residues 598-756 of the chicken gizzard smooth muscle caldesmon (CaD) molecule.

79 The ability of chicken gizzard smooth muscle caldesmon (CaD) to inhibit actomyo

80 es of C-terminal deletion mutants of chicken gizzard smooth muscle caldesmon (CaD) were made using a

81 activation, forced expression of MLC(17b) in gizzard smooth muscle cells decreased (p < 0.05) the rat

82 immunoelectron microscopy studies of chicken gizzard smooth muscle cells showed that in certain areas

83 Our findings suggest that in chicken gizzard smooth muscle cells, calponin may be an integral

84 transfected into cultured embryonic chicken gizzard smooth muscle cells.

85 single cultured chicken embryonic aortic and gizzard smooth muscle cells.

86 ntaining complexes were not present early in gizzard smooth muscle development, but appeared as devel

87 cto-ATPase enzyme, cross-linking the chicken gizzard smooth muscle ecto-ATPase with 3,3'-dithiobis(su

88 m chicken skeletal muscle myosin for that of gizzard smooth muscle heavy meromyosin (HMM) causes acti

89 Domain dynamics of the chicken gizzard smooth muscle myosin catalytic domain (heavy cha

90 Fluorescently labeled turkey gizzard smooth muscle myosin was prepared by removal of

91 o mutants of a truncated fragment of chicken gizzard smooth muscle myosin, which includes the motor d

92 eplaced by either the tail domain of chicken gizzard smooth muscle or Acanthamoeba myosin II are 20 t

93 ty were examined in goose (GG) and duck (DG) gizzard smooth muscle stored at 5 degrees C.

94 rescently colocalizes with myosin in chicken gizzard smooth muscle, and interacts with two configurat

95 dividual folded myosin molecules from turkey gizzard smooth muscle, we show that they are more compac

96 ortant role in the postmortem proteolysis of gizzard smooth muscle.

97 The ecto-ATPase from chicken gizzard (smooth muscle) was solubilized, and the 66-kDa

98 ession of the TIA and SR proteins in phasic (gizzard) smooth muscle around hatching coincided with th

99 urify with unphosphorylated SMM from chicken gizzard, suggesting that they are tightly bound.

100 Thus, purified talin head liberated from gizzard talin by calpain cleavage cosediments with F-act

101 Recombinant and native gizzard telokins were phosphorylated, in vitro, by the c

102 In chicken gizzard, the ecto-ATPase was distributed in discrete clu

103 g visceral smooth muscle cells (SMCs) during gizzard tissue development.

104 phate) (ATPgammaS) phosphorylated only adult gizzard tissue, the only tissue that did not demonstrate

105 he ratio was approximately 23-37% of that in gizzard tissue.

106 ate filaments and dense bodies isolated from gizzard tissues.

107 e a horny beak (rhamphotheca) and a muscular gizzard to acquire and process food.

108 beta beta and gamma gamma species of chicken gizzard tropomyosin concludes that their unfolding trans

109 rted on these homodimeric species of chicken gizzard tropomyosin with a single interchain disulfide c

110 mally limited to the region of the posterior gizzard under the regulation of BMP signaling from the a

111 esophagus at E3.5 but did not appear in the gizzard until E4.5.

112 ession of an activated form of BMPR1b in the gizzard upregulates Sox9 expression, while the BMP antag

113 d bacterium called J1, isolated from chicken gizzard, was noted to produce a bacteriocin (BacJ1) that

114 activity in erythrocytes, platelets, and the gizzard, we hypothesized that calmodulin increases cross

115 e BMP receptors act similarly to BMP4 in the gizzard when ectopically expressed.

116 ough the primitive esophagus to colonize the gizzard where an extensive cellular network forms.

117 rms is also developmentally regulated in the gizzard, which switches from leucine zipper positive to