ライフサイエンスコーパス: functional cell

1 ions, subject to the complexities of a fully functional cell.

2 easome system is essential for maintaining a functional cell.

3 cells with either cDNA alone resulted in non-functional cells.

4 propose a possible explanation for these non-functional cells.

5 nversion, and an inability to produce mature functional cells.

6 neral mechanism to eliminate differentiated, functional cells.

7 g to repopulate the alveolar epithelium with functional cells.

8 ocyte maturation to CD4 single positive (SP) functional cells.

9 Functional cell adhesion and leukocyte transmigration as

10 ledge from developmental biology to generate functional cells and tissues that could be used for rege

11 atode populations lacking defined classes of functional cells, and for genetic screens.

12 e recombinase (Cre)-mediated excision led to functional, cell- and tissue-specific loss of alpha7 nAC

13 cellular activity in a hemagglutination (HA) functional cell assay of bacterial adhesion.

14 d calcium fluctuations may form the basis of functional cell assemblies.

15 selective and dynamic control of distributed functional cell assemblies.

16 efficient nucleation of fiber subunits into functional, cell-associated amyloid.

17 The presence of functional, cell-associated IL-1 alpha activity in infec

18 The functional cell-based assay Receptor Selection and Ampli

19 Using a functional cell-based assay, we have identified two nove

20 Ab response, a bridging ELISA, as well as a functional cell-based assay, were constructed.

21 LCN leads to increased cell-cell adhesion in functional cell-based assays and disruption of cell pola

22 This includes functional cell-based assays and the evaluation of molec

23 In addition, most functional cell-based assays designed to characterize th

24 ptor kinase interacting ArfGAP 1) gene using functional cell-based assays involving coexpression of G

25 We found that functional cell-based assays of three point mutants affe

26 To test this hypothesis, we have utilized a functional cell-based endocytosis assay and identified t

27 were designed and assessed for inhibition of functional cell-based Gli1-mediated transcription and se

28 presents a new tool for rapid measurement of functional cell-based responses and parallel separation

29 A functional cell-based screen identified 3-(4-chloropheny

30 In the present study, a high-throughput, functional, cell-based assay for identifying Maxi-K chan

31 nist activity using a chimeric receptor in a functional, cell-based, high-throughput assay.

32 hat such cells may ultimately predominate if functional cells become exhausted.

33 Because functional cells cannot be deprived of ATP, we have knoc

34 an ionically tight interface necessary for a functional cell-cell channel.

35 If Cx34.7 forms functional cell-cell channels between cones, it would pr

36 ssociated mutation, Ser-85-Cys (S85C), forms functional cell-cell channels in paired Xenopus oocytes.

37 Functional cell-cell communication developed between WB

38 Here we show that functional cell-cell interaction between NPCs and NSCs t

39 Z progenitor cells may be one anatomical and functional cell class.

40 These results suggest that a limited set of functional cell classes emerges in macaque prefrontal co

41 and programmed cell death (PCD) to produce a functional cell corpse.

42 orphological localization to the synapse and functional cell culture assays, but their role in embryo

43 of the fact that HEI-C-depleted cells retain functional cell cycle checkpoints, as these cells arrest

44 be2S slows down APC substrate degradation in functional cell-cycle extracts.

45 by a continuous replacement of short-lived, functional cells during chronic MCMV infection.

46 tivity is not responsible for the paucity of functional cells even in end-stage liver disease.

47 proposed device was loaded and cultured with functional cells for drug response investigation and org

48 ve major potential as an unlimited source of functional cells for many biomedical applications; howev

49 eding behaviour by dynamic reorganization of functional cell groups in the hypothalamus.

50 Strategies to expand functional cells have focused on discovering and control

51 Pertussis toxin-treated Th2 cells were functional cells, however, and when directly instilled i

52 an integrate into the embryo and form mature functional cells in the animal.

53 tability and potential to differentiate into functional cells in vitro (hepatocytes) and in vivo (hep

54 A functional cell is requisite for TSWV infection and cell

55 However, its role in mature functional cells is poorly studied.

56 on the availability of these factors in the functional cell lines employed.

57 In most cases, limitations in functional cell longevity will necessitate periodic repl

58 rocess during which fully differentiated and functional cells lose aspects of their identity while ga

59 Varicella-zoster virus (VZV) encodes a functional cell membrane Fc receptor called glycoprotein

60 lar bioenergetics is proposed that occurs in functional cells not exposed to catastrophic DNA damage.

61 rompted in vitro efforts to produce the main functional cells of the liver: hepatocyte-like cells (He

62 ow efficiently they may be differentiated to functional cells of various lineages.

63 an easy and rapid method for engineering of functional, cell-permeable peptides and demonstrates the

64 ntiation and establishment of structural and functional cell polarity; components of the apical micro

65 rived lymphoid compartments contained normal functional cell populations as determined by the presenc

66 F-kappaB activation was not due to a lack of functional cell/protein because NF-kappaB was appropriat

67 ely integrate to translate pMHC stimuli into functional cell responses.

68 s compared with their parental mitochondrial-functional cells (rho(+)).

69 ese techniques will be useful in identifying functional cell-specific binding motifs and contribute t

70 d expression of genes encoding components of functional cell structures were often observed indicatin

71 uggesting that this marker does not identify functional cell subsets that produce serum interleukin-4

72 stent with the hypothesis that the number of functional cell surface alpha7 nAChRs is controlled indi

73 polymerase chain reaction, S1 nuclease, and functional cell surface binding studies showed that norm

74 pe 1 (HIV-1) coreceptor CCR5 (CCR5 -/-) lack functional cell surface CCR5 molecules and are relativel

75 ellular compartments, resulting in a loss of functional cell surface channel.

76 derivatives, can stabilize DR5 and increase functional cell surface DR5 levels, resulting in enhance

77 al requirement for N-linked glycosylation in functional cell surface expression of D1 and D5 dopamine

78 te that Kvbeta1 differentially regulates the functional cell surface expression of myocardial I(to,f)

79 transmembrane proteins RTP1 and RTP2 promote functional cell surface expression of ORs expressed in H

80 anti-DLL4 treatment reduced T cell mRNA and functional cell surface expression of the chemokine rece

81 alyzed the role of N-linked glycosylation in functional cell surface expression of the D1 and D5 dopa

82 s, but not of TCR-alpha chains, assembly and functional cell surface expression of the TCR-CD3 comple

83 the PKD1L3 and PKD2L1 is necessary for their functional cell surface expression.

84 haplotype, resulting in the formation of two functional cell surface heterodimers, HLA-DR2a (DRA*0101

85 haplotype, resulting in the formation of two functional cell surface heterodimers, HLA-DR2a (DRA*0101

86 losterism between hLHR protomers, indicating functional cell surface hLHR dimers.

87 s IL-22 and prevents binding of IL-22 to the functional cell surface IL-22R complex, which consists o

88 protein tyrosine phosphatases (RPTPs) are bi-functional cell surface molecules.

89 rom laboratory mice because of the lack of a functional cell surface receptor required for virus entr

90 , these data show that mouse DESC1 encodes a functional cell surface serine protease that may have im

91 lication error positive in both alleles lack functional cell surface TGF-beta type I (RI) and type II

92 The number of functional cell-surface NMDARs in cortical neurons incre

93 ear whether primary afferent neurons express functional cell-surface opioid receptors.

94 te that human and murine neutrophils express functional cell-surface P2X7R, which leads to ATP-induce

95 ls, indicating that the 210-kDa protein is a functional cell-surface receptor on type II cells.

96 rized a cell line, CTLL-EPO-R, that contains functional cell-surface receptors for both EPO and IL-2.

97 s can be genetically modified to overexpress functional, cell-surface Fas ligand (FasL) by adenovirus

98 ust a simple barrier for gas exchange, but a functional cell that protects alveolar epithelium from i

99 ertheless be some chance that LTD converts a functional cell to a non-functional one; in contrast, th

100 ents a valuable opportunity to replenish the functional cells to the heart.

101 cular disease that relies on the delivery of functional cells to their target site.

102 as imaged by two-photon microscopy permitted functional cell type annotation.

103 ng hematopoietic system, no direct link to a functional cell type has been made.

104 Grid cells, the most abundant functional cell type in the MEC, have hexagonally arrang

105 These suggest the existence of a novel functional cell type within the gland, that the basal/my

106 This study provides the first functional cell type-specific and spine type-specific co

107 Our findings underscore the importance of functional cell-type evaluation during stepwise differen

108 Functional cell types (FCTs) that encode similar task fe

109 ir capacity to differentiate into mature and functional cell types after transplantation.

110 ve as a unique avenue for generating diverse functional cell types for biomedical research and therap

111 ating human cells into specific homogeneous, functional cell types is challenging.

112 nduced pluripotent stem cells to defined and functional cell types is essential for future clinical a

113 urons contribute to the spiking behaviour of functional cell types of MEC neurons, such as grid cells

114 s that direct stem cell differentiation into functional cell types remains a major challenge in the f

115 icellular organisms is the specialization of functional cell types through the process of differentia

116 reproduce themselves and differentiate into functional cell types, attract much interest as potentia

117 h the activity of differentiated hippocampal functional cell types, which conjunctively encoded diffe

118 ly target and manipulate genetically defined functional cell types.

119 ll naive hESCs fail to differentiate towards functional cell types.

120 descendants that differentiate into distinct functional cell types.

121 operative in mature duct cells during which functional cells undergo "ductal retrogression" to form

122 LAM is an essential structural entity for a functional cell wall and, consequently, that the biosynt

123 f beta-lactam antibiotics, suggesting that a functional cell wall is required for Pls secretion from

124 whether mango peel is a potential source of functional cell wall polymers.

125 not need to resist osmotic challenges and a functional cell wall was not detected in these pathogens

126 odulate mitochondrial activity to maintain a functional cell wall when subjected to stresses.

127 act covalently and noncovalently to form the functional cell wall.