ライフサイエンスコーパス: compartmentation

1 related redox signaling is tightly wedded to compartmentation.

2 evelopment that coincides with Purkinje cell compartmentation.

3 l probe of G protein-coupled receptor (GPCR) compartmentation.

4 cts of anatomical diffusion barriers on cAMP compartmentation.

5 modulation and the effect of electrodynamic compartmentation.

6 duced in the thymus, irrespective of antigen compartmentation.

7 f influx, efflux, synthesis, degradation and compartmentation.

8 duction of ABA degradation, modification, or compartmentation.

9 hesized to reveal information about myowater compartmentation.

10 erimentally measured diffusion rates on cAMP compartmentation.

11 o the complexity of subcellular and cellular compartmentation.

12 vergent and ill-defined aspect of plant cell compartmentation.

13 that mucosal DCs play a crucial role in this compartmentation.

14 indicating tissue-specific regulation of SUS compartmentation.

15 ins within the glycosome and the function of compartmentation.

16 The first level is subcellular compartmentation.

17 ned to the nucleus, they demonstrate altered compartmentation after carcinogen treatment, in cancers,

18 KAPs) provide a molecular mechanism for cAMP compartmentation, allowing for the precise control of PK

19 Compartmentation along both the mediolateral and rostroc

20 s an important role in chloroplast phosphate compartmentation and ATP synthesis, which affect plant g

21 investigated and modeled subcellular calcium compartmentation and Ca2+ movement under steady-state co

22 patibility, which is characterized by hyphal compartmentation and cell lysis, is induced.

23 bition, repression of conidiation and hyphal compartmentation and death (HCD).

24 mpatibility and significantly reduced hyphal compartmentation and death rates.

25 ed GRN expression, including changes in cell compartmentation and decreased secretion of GRN protein.

26 Compartmentation and dynamics of cAMP and PKA signaling

27 al model of fluorescent potentiometric probe compartmentation and dynamics using a bis-oxonol-type in

28 context both of current models of metabolic compartmentation and engineering.

29 ved understanding of plant lipid metabolism, compartmentation and function are discussed.

30 times measurements, information on molecular compartmentation and mobility can be gleaned.

31 However, subcellular compartmentation and protein modification may differ in

32 hat enhances co-enzyme affinity, subcellular compartmentation and stability.

33 led aspartate and lactate indicates cellular compartmentation and thus selective vulnerability of mit

34 ability of arginine but by a tight metabolic compartmentation at the systemic level.

35 1 h after wounding, indicating that loss of compartmentation barrier makes the structure unstable; s

36 ic to T. brucei in the absence of glycosomal compartmentation because of the intrinsic lack of feedba

37 R2IIIb), differences in cell type of origin, compartmentation by alternate translation, the affinity

38 s the first demonstration that Purkinje cell compartmentation can be altered by mutation; therefore,

39 ective membrane fusion underlies subcellular compartmentation, cell growth, neurotransmission and hor

40 cluding those required for the cytoskeleton, compartmentation, cell-cycle control, proteolysis, prote

41 Compartmentation contributes to selectivity because Pkh1

42 ed in the cardiac myocyte dyadic space, cAMP compartmentation did occur, but only when diffusion was

43 strate that neuronal LRP undergoes selective compartmentation during neuronal maturation and suggest

44 gonist-stimulated NO signaling, likely via a compartmentation effect.

45 cytoplasm, as related to the electrodynamic compartmentation effects, might explain the morphologica

46 olism often presents a complex cell-specific compartmentation essential to accomplish the biosynthesi

47 he importance of polyglutamylation in folate compartmentation, folate homeostasis and folate-dependen

48 The potential importance of metabolic compartmentation for attempts to engineer phenylpropanoi

49 The importance of this subcellular compartmentation has not been directly tested in vivo.

50 e an overview of the advances in subcellular compartmentation, identifying the gaps in our knowledge

51 lowers, and suggest a role for intracellular compartmentation in auxin biosynthesis.

52 We have examined three markers of cerebellar compartmentation in En-2 mutant mice: the Zebrin II and

53 damental cellular mechanisms that link lipid compartmentation in hepatocytes to liver damage and dise

54 CXCR4 expression and cytokine responses, and compartmentation in secondary lymphoid organs was normal

55 tool for exploring ROS dynamics, the role of compartmentation in the modulation of the redox environm

56 w that T cell activation leads to a striking compartmentation in the rafts of activated T cell recept

57 s manuscript discusses aspects of functional compartmentation in the regulation of metabolism.

58 The existence of spatial compartmentation in the rhombic lip and the interplay be

59 demonstrate that this prerequisite is genome compartmentation into two epigenetically defined chromat

60 How exactly compartmentation is achieved, however, has remained a my

61 lso the evidence on which the concept of ATP compartmentation is based.

62 lasm of cells, but in plants its subcellular compartmentation is far from clear.

63 ds are wider and multilaminate, the standard compartmentation is present.

64 ecific antigen zebrin II (i.e., aldolase C), compartmentation is reflected in alternating zebrin II+

65 Characterization of Golgi compartmentation markers indicates altered colocalizatio

66 rent subcellular compartments and that their compartmentation may affect their access to arachidonic

67 This compartmentation may permit determining in which tissue

68 ion of flavin metabolism and its subcellular compartmentation, may also provide the basis for a more

69 C1 was shown to have defects in endocytosis, compartmentation, nuclear distribution, and conidiation.

70 es of inflammation can alter the subcellular compartmentation of 5-lipoxygenase.

71 we assessed the expression, regulation, and compartmentation of AC isoforms in rat aortic smooth mus

72 s investigated by studying the intracellular compartmentation of AdoMet as well as the mode of hypera

73 Genes involved in complexation and compartmentation of arsenic were up-regulated by AsIII,

74 t the pathway responsible for the functional compartmentation of beta2-AR-PKA signaling sequentially

75 s anatomical features analogous to the Kranz compartmentation of C4 plants, and phosphoenolpyruvate c

76 iac myocytes, T-tubules confer the necessary compartmentation of Ca(2+) signals, which allows sarcome

77 ution of beta(2)ARs in heart failure changes compartmentation of cAMP and might contribute to the fai

78 We conclude that compartmentation of cAMP can provide a quantitative expl

79 proteins (AKAPs) play important roles in the compartmentation of cAMP signaling, anchoring protein ki

80 ion of cAMP may be a function of appropriate compartmentation of cAMP signaling.

81 determinant of the amplitude, duration, and compartmentation of cAMP-mediated signaling.

82 scarinic receptor (M(2)R) activation involve compartmentation of cAMP.

83 Compartmentation of carbohydrate metabolism has been sho

84 lasma membrane topography, but their role in compartmentation of caveolae-resident signaling componen

85 ociation may represent a novel mechanism for compartmentation of cGMP-mediated signaling and regulati

86 This compartmentation of cyclic nucleotide signaling is accom

87 c GMP, regulate the amplitude, duration, and compartmentation of cyclic nucleotide-mediated signaling

88 nd highlight the importance of intracellular compartmentation of DAG in causing lipotoxicity and hepa

89 Analysis of the cellular compartmentation of DAG revealed that DAG increased in t

90 ecific substrate utilization and subcellular compartmentation of DLK suggest that specific mixed line

91 chemic myocardium and document the metabolic compartmentation of downstream products of fatty acyl ch

92 Compartmentation of ET-1 signaling complexes may explain

93 immunocytochemistry, and by determining the compartmentation of expressed cathepsin B fused to green

94 e root are major sites for the intracellular compartmentation of folates.

95 The results support the hypothesis that compartmentation of glucokinase in the hepatocyte increa

96 ein for PFK and that this contributes to the compartmentation of glycolysis from other metabolic path

97 Compartmentation of GPCRs and AC is different in cardiom

98 s light regulation was found for the nuclear compartmentation of GUS-CRY2 fusion protein, the abundan

99 the identification of a distinct subcellular compartmentation of intracellular redox-active "labile"

100 Compartmentation of intracellular signaling pathways ser

101 Compartmentation of ion channels on the cardiomyocyte su

102 on can give new information on the molecular compartmentation of metabolites in intact tissues, inclu

103 cise regulation of the number, position, and compartmentation of mitotic membranes is a critical feat

104 chanism has been reported that regulates the compartmentation of multiple enzymes in M or BS cells.

105 The compartmentation of organic selenocompounds in specific

106 Unlike other receptor-mediated responses, compartmentation of PGE1 responses was not due to concur

107 sulin suggest 2 different isoforms of PI3-K, compartmentation of PI3-K, potentiation, or inhibition b

108 lays a foundation for studying targeting and compartmentation of PKA and other kinases and phosphatas

109 oteins has been implicated in the functional compartmentation of PKA signaling, the exact mechanism u

110 orelease of diacylglycerol further suggested compartmentation of PKC signaling, with release at the m

111 PKGI is required for cGMP-stimulated nuclear compartmentation of PKGI and phosphorylation of transcri

112 rocessing in the GA was critical for nuclear compartmentation of PKGIgamma because GA disruption with

113 e deduced from what is currently known about compartmentation of plant-cell metabolism.

114 Compartmentation of primary metabolism in developing emb

115 these preparations established intracellular compartmentation of processes to support a NAD-malic enz

116 ction are widely believed to require spatial compartmentation of protein kinase and phosphatase activ

117 d for a more complex view of the subcellular compartmentation of PTGS in plants.

118 role for granule cell raphes in parasagittal compartmentation of Purkinje cells.

119 to or rather due to differential subcellular compartmentation of reductant in the different organs.

120 To determine whether compartmentation of RhoA and Rac1 within caveolae was ne

121 of heme-oxidation and altered intracellular compartmentation of sGC as potential mechanisms.

122 reases in cAMP or, alternatively, because of compartmentation of signaling components.

123 s mounting evidence for the organization and compartmentation of signaling molecules at the plasma me

124 ulate that the mutant might have a defect in compartmentation of substrates involved in the biosynthe

125 esponsible for the loss of an Edn1-dependent compartmentation of the arch into the intermediate and v

126 the experimentally elongated neurites showed compartmentation of the axonal markers dephospho-tau and

127 We investigated the compartmentation of the catabolism of dodecanedioate (DO

128 adrenergic receptor (beta2-AR)/G(i)-mediated compartmentation of the concurrent G(s)-cAMP signaling,

129 Compartmentation of the folate-dependent de novo thymidy

130 h F-actin is suggested to be a mechanism for compartmentation of the glycolytic pathway.

131 osphate, consistent with the known lysosomal compartmentation of the molecule.

132 Instead, compartmentation of the PGE1 response in cardiac myocyte

133 At the same time, compartmentation of the Purkinje cell layer was detected

134 contribute to the molecular and subcellular compartmentation of the turnover of properly folded prot

135 Subcellular compartmentation of the ubiquitous second messenger cAMP

136 ription and quantitation of cellular calcium compartmentation patterns and movements as correlated wi

137 However, the exact mechanism by which compartmentation provides a catalytic advantage to the e

138 of versatile protein elements, weak linkage, compartmentation, redundancy, and exploratory behavior r

139 ught to develop a representation of cellular compartmentation that would accurately capture cellular

140 These results indicate that CK compartmentation to the myofibril of skeletal muscle is

141 he elucidation of the basis for carbohydrate compartmentation to the plasma membrane in a wide variet

142 enzyme activity measurements and subcellular compartmentation was parameterized to fit the sucrose, h

143 ith ZE, and no differences in subcellular Zn compartmentation were found between Zn-efficient and -in

144 glucose utilization and inorganic phosphate compartmentation with normal ATP gamma-phosphoryl dynami

145 This indicates a high level of functional compartmentation within the rat mPFC whereat many functi

146 sALMT4 expression affected malate efflux and compartmentation within the tissues, which increased Mn