ライフサイエンスコーパス: subcompartment

1 en the Vg1 3' untranslated region and the ER subcompartment.

2 e of SP might be heightened in this striatal subcompartment.

3 tuning protein exit or retention within each subcompartment.

4 , indicating that BKPyV accumulated in an ER subcompartment.

5 us associations with potentially any nuclear subcompartment.

6 ast subsequently being detected in an acidic subcompartment.

7 dendrites, where it was restricted to the ER subcompartment.

8 anism for the specification of other somitic subcompartments.

9 he assembly and maintenance of the different subcompartments.

10 evealed interdigitating axonal and dendritic subcompartments.

11 membranes of both the sorting and recycling subcompartments.

12 ys that target proteins to other chloroplast subcompartments.

13 combinations of interstripe and thin stripe subcompartments.

14 ntain structurally and functionally distinct subcompartments.

15 imented streaming forms distinct cytoplasmic subcompartments.

16 zation of different ion channels in specific subcompartments.

17 unclear how signaling is coordinated at both subcompartments.

18 erns of histone marks and segregate into six subcompartments.

19 the localization of Met in specific synaptic subcompartments.

20 proportions of protein partners in cellular subcompartments.

21 the discrete input pathways for different FB subcompartments.

22 utputs to be quantified in specific cellular subcompartments.

23 ambiguously to one of the four mitochondrial subcompartments.

24 nal regulators in the specification of these subcompartments.

25 ate heretofore uncharacterized proepicardial subcompartments.

26 instead organize into functionally distinct subcompartments.

27 s, which are distributed into four different subcompartments.

28 ulus is dependent on segregation of synaptic subcompartments.

29 hogen-induced alterations of specific tissue subcompartments.

30 dorsal compartment (71%) and in the lateral subcompartment (24%) of the ventral XII.

31 endocytic system into biochemically distinct subcompartments allows for spatial and temporal control

32 The differentiation of physically distinct subcompartments also contributes to peroxisome diversifi

33 ecting the Igh locus to a repressive nuclear subcompartment and inducing the Igh locus to decontract.

34 otein)) are localized to their own endosomal subcompartment and interact with a wide range of protein

35 rticipate in the formation of this matrisome subcompartment and its striatofugal projections.

36 ntinual fusion and fission of stable, "like" subcompartments and provides a mechanism to grow the Gol

37 to the fates of the three distinct nucleolar subcompartments and their associated protein machineries

38 ion became preferentially associated with A2 subcompartments and were constrained to the relative pro

39 re dynamically organized into shared nuclear subcompartments, and movement into or out of these facto

40 wever, many such RNP bodies contain internal subcompartments, and the mechanism of their formation re

41 These hematopoietic subcompartments are composed of erythroblasts surroundin

42 n channel localization in distinct dendritic subcompartments are largely unknown.

43 Second, A1 and A2 subcompartments are segregated in 3D space through diffe

44 Prx1 distribution to distinct mitochondrial subcompartments are unknown.

45 on of altered distributions within metabolic subcompartments as well as conventional metabonomics con

46 ess, superficial, and deep layers of defined subcompartments at baseline and follow-up in ACL-injured

47 The mean CVs for the subcompartments before and after exclusion of artifacts

48 cking OCAM show a redistribution of synaptic subcompartments, but the total area occupied by axonal i

49 cific mRNAs in microscopically selected lung subcompartments by complementary DNA or RNA hybridizatio

50 x maintains Golgi enzymes in different Golgi subcompartments by retrograde protein trafficking.

51 he favoring nuclear differentiation and that subcompartments can be self-organized as a consequence o

52 We conclude that Golgi subcompartments can separate one from the other.

53 synapses appear to be spatially isolated in subcompartments delineated by astrocyte processes.

54 nto acinar cells, whereas cells in the trunk subcompartment differentiate into endocrine and duct cel

55 Scattering kinetics of Golgi subcompartments during microtubule disassembly and reass

56 omote Rab2-mediated vesicle budding at a VTC subcompartment enriched in recycling cargo.

57 atches (or striosomes) are limbic-associated subcompartments enriched in mu opioid receptors.

58 Twelve patients had detailed lymphocyte subcompartments evaluated.

59 nm-thick zone that potentially constitutes a subcompartment for achieving locally elevated [Ca(2+) ]

60 e represented as occurring in two myoplasmic subcompartments for Ca(2+) distribution, one (T-space) a

61 ry infection period, to examine the anatomic subcompartment from which these cells are depleted, and

62 viorally relevant information onto dendritic subcompartments; global synaptic upscaling by deprivatio

63 e in these regions, which contain a membrane subcompartment harboring the early assembly factor PratA

64 Our results indicate that each Golgi subcompartment has a distinct phospholipid composition d

65 olarization, but the developmental origin of subcompartments in axons and dendrites is less well unde

66 ical response and the recovery of lymphocyte subcompartments in patients with metastatic melanoma.

67 ulates the levels of the protein in specific subcompartments, in particular the one containing the ac

68 ive oxygen species (ROS), the major cellular subcompartments involved and the overall cellular respon

69 obal scale but also within specific neuronal subcompartments, involving a wide range of molecules and

70 ondria; (iii) the mitochondria-associated ER subcompartment is enriched in enzymatic activities invol

71 tes because RNA contributed by relevant lung subcompartments is enriched.

72 ect positioning of CLL cells within lymphoid subcompartments is essential for the transmission of the

73 ganization of eukaryotic cells into distinct subcompartments is vital for all functional processes, a

74 tial segment (AIS) is a specialized neuronal subcompartment located at the beginning of the axon that

75 Similarly, the ventromedial subcompartment mainly rostrally, and the dorsal compartm

76 ate, suggesting that migration to functional subcompartments may influence gene expression.

77 Nuclear subcompartments may play a role by offering rich microen

78 per, a technique for isolating RNA from lung subcompartments obtained by microdissection is described

79 Dissociation of proteins from the other subcompartments occurred with faster kinetics but commen

80 also result from the existence of a specific subcompartment of endoplasmic reticulum regulating Icrac

81 CD1 family (CD1a-e) localizes to a distinct subcompartment of endosomes.

82 rcinoma cells with a growth factor-dependent subcompartment of malignant cells designated HCT116b tha

83 renewing tissues of the body contain a small subcompartment of self-maintaining stem cells, upon whic

84 ion of C/EBPalpha in the non-heterochromatic subcompartment of the cell nucleus.

85 ndent gata2b expression within the hemogenic subcompartment of the dorsal aorta that is in turn requi

86 se activity itself, are highly enriched in a subcompartment of the endoplasmic reticulum (ER) that is

87 This may indicate that a specialized subcompartment of the endoplasmic reticulum functions as

88 ow that presenilins are highly enriched in a subcompartment of the endoplasmic reticulum that is asso

89 r cytoplasmic structure or possibly a unique subcompartment of the endoplasmic reticulum, and a cell-

90 t nuclear membranes lose their identity as a subcompartment of the ER during mitosis.

91 I to yield GlcN-PI, is largely confined to a subcompartment of the ER that appears to be associated w

92 and endogenous Vg1 mRNA is associated with a subcompartment of the ER.

93 (+) T cell loss predominated in the effector subcompartment of the GI mucosa, in distinction to the i

94 also provide evidence that the cristae are a subcompartment of the inner membrane.

95 The core subcompartment of the nucleus accumbens (NAcore) contrib

96 otoneuron pool, comprising the ventrolateral subcompartment of the nXII, was consistently and heavily

97 of caveolae microdomains, which represent a subcompartment of the plasma membrane.

98 ae are vesicular organelles that represent a subcompartment of the plasma membrane.

99 the dorsal compartment and the ventromedial subcompartment of the ventral compartment, where BDA lab

100 via the indirect pathway to the dorsolateral subcompartment of the ventral pallidum (dlVP) and throug

101 We investigated whether subcompartments of AT within the thigh are determinants

102 ments in solitary cells, multiple cells, and subcompartments of cells.

103 It is well-established that subcompartments of endoplasmic reticulum (ER) are in phy

104 BM CD34(+) cells belonging to four subcompartments of increasing RNA content within the G0

105 sed to identify proteins targeted to various subcompartments of mammalian cells, including the NE.

106 e immunoreactivity (LIR) labels all cellular subcompartments of neurons and microglia, including thei

107 re differentially regulated across different subcompartments of neurons.

108 n size and differentiate into the definitive subcompartments of the AOTU, BU, and EB.

109 allows CD1 to sample lipid Ags from various subcompartments of the endocytic system.

110 Translocation of Ca2+ between distinct subcompartments of the endoplasmic reticulum is mediated

111 tively, human CD34(+) cells were isolated in subcompartments of the G0 /G1 phase of the cell cycle by

112 IIIbeta and PI4KIIalpha localize to discrete subcompartments of the Golgi complex in Madin-Darby cani

113 f several viruses that assemble in different subcompartments of the Golgi, as well as subcellular fra

114 -G was prominent in both proximal and distal subcompartments of the IS, where it colocalized with eit

115 ands the tight junction proteome and defines subcompartments of the junction.

116 aptic density proteins in the core and shell subcompartments of the nucleus accumbens were compared w

117 several hundreds of proteins in the various subcompartments of the organelle.

118 ng ventricular zone (VZ) and outer and inner subcompartments of the outer subventricular zone (OSVZ)

119 These subcompartments of the plasma membrane are characterized

120 These subcompartments of the plasma membrane are characterized

121 that caveolae function as signal transducing subcompartments of the plasma membrane.

122 of ZO-1 are embedded in different functional subcompartments of the tight junction.

123 ction as both lipid biosynthesis and storage subcompartments of thylakoid membranes.

124 n, is accompanied by the separation of Golgi subcompartments one from another.

125 e manner or is targeted to specific neuronal subcompartments or synaptic sites to affect circuit func

126 the assignment of 818 proteins into the four subcompartments: outer membrane, inner membrane, interme

127 ganize, we analyzed distributions of nuclear subcompartment proteins and assayed for caspase-induced

128 or caspase-induced cleavage of major nuclear subcompartment proteins during late erythropoiesis, in c

129 havior; similar regions within a dorsomedial subcompartment provide a domain-independent reconfigurat

130 king of NMDARs in this endoplasmic reticulum subcompartment requires both CASK and SAP97.

131 To demonstrate tumor subcompartment resolution, we validated the predicted tu

132 the glomerulus into the axonal and dendritic subcompartments, respectively.

133 -alpha activity, yet the isoparental HCT116b subcompartment showed similar levels of TGF-alpha expres

134 rised of stacked cisternal membranes forming subcompartments specialized for posttranslational proces

135 ing conformational and kinetic variations to subcompartment-specific actions of C/EBPalpha or any pro

136 gomeric cargo is central to the mechanism of subcompartment specification.

137 nylation activities within the mitochondrial subcompartments, suggesting localized regulatory functio

138 localized to the endoplasmic reticulum (ER) subcompartment termed mitochondria-associated ER membran

139 a wider range of processes and environmental subcompartments than most previous models and considers

140 lum into a specialized endoplasmic reticulum subcompartment that bypasses somatic Golgi, merging inst

141 The endoplasmic reticulum (ER) consists of subcompartments that have distinct protein constituents,

142 regulated by the cellular organization into subcompartments that impose barriers to diffusion, can l

143 and equally importantly, upon what cellular subcompartments the projections target.

144 When Rab2 binds to a VTC subcompartment, the subsequent recruitment of PKCiota/la

145 to promote transport within the dendritic ER subcompartment, thereby restricting alpha7 trafficking t

146 enetic polymers encapsulated within targeted subcompartments to produce chemically organized multi-ti

147 ain; and (iv) the mitochondria-associated ER subcompartment, unlike bulk ER, is capable of the de nov

148 as detected in peroxisomes, but not in an ER subcompartment, using immunofluorescence microscopy.

149 This endoplasmic reticulum subcompartment was composed of highly mobile vesicles co

150 tions, drug penetration into the various CNS subcompartments was not statistically different between

151 Dendritic subcompartments were composed predominately of dendritic

152 The axonal subcompartments were composed primarily of ORC processes

153 This work defines the nuclear periphery as a subcompartment where dangerous DNA elements can be handl

154 ts that these islands are highly specialized subcompartments where cell adhesion events, in concert w

155 interchromatin space is composed of nuclear subcompartments, which are defined by several distinctiv

156 l progenitors were present in G0 or early G1 subcompartments, while lineage-restricted granulomonocyt

157 ineate a potential transiently proliferating subcompartment within the basal cell compartment of the

158 se data show that SERCA2b is associated in a subcompartment within the sarcoplasmic reticulum of card

159 und between different tissue compartments or subcompartments within a given tissue.

160 ng for OMP and MAP2 revealed two distinctive subcompartments within glomeruli: an axonal compartment

161 unique proteins that associate with specific subcompartments within organelles.

162 ed the liposome localization in intratumoral subcompartments within spheroids.

163 er with computational modeling, to show that subcompartments within the nucleolus represent distinct,