ライフサイエンスコーパス: nonneural

1 different human cell lines, both neural and nonneural.

2 It is concluded that neural and nonneural A1, A2a, A2b, and A3Rs may participate in the

3 egions independently drive the expression in nonneural and in neural cells, such that the emission an

4 tic regulation of IEGs may influence diverse nonneural and neural biologic processes.

5 essive reduction and reciprocal expansion in nonneural and neural ectoderm, respectively, in snailhou

6 ral patterning genes, BMP2/4 and chordin, in nonneural and neural ectoderm, respectively, of chordate

7 Cells with c-Kit-LI were nonneural and seemed to be common precursors for longitu

8 -PNS myelin antibody, but not by delivery of nonneural antibodies.

9 hich is a component of neural progenitor and nonneural BAF complexes, cannot replace BAF53b's role in

10 en intact and SCN-lesioned mice to show that nonneural (behavioral or bloodborne) signals are adequat

11 of the virus life cycle in neural (N18) and nonneural (BHK) cells.

12 differentiation and placement of the neural-nonneural border.

13 ma, 1 unspecified type) were the most common nonneural cancers.

14 type II cadherins (with the exception of the nonneural Cdh5) in the developing and adult mouse brain.

15 In both neural and nonneural cell lines, the activity-regulated cytoskeleta

16 in primary human neurons and in neuronal and nonneural cell lines.

17 vels of PAM expression characterized several nonneural cell populations as well, including limb mesod

18 tem cells with myoblast cells also generated nonneural cell progeny.

19 e single-channel and whole-cell levels, in a nonneural cell type.

20 Only when GiPSCs were directed to nonneural cell types did we observe sustained expression

21 Both neural and nonneural cell types have been successfully engineered t

22 that sel-12 is expressed in most neural and nonneural cell types in all developmental stages.

23 physiological functions both in neurons and nonneural cell types.

24 red including polymer-encapsulated cells and nonneural cells (that is, adrenal chromaffin cells) or g

25 l precursor cells to arise intermingled with nonneural cells [7,8].

26 src pre-mRNA is both negatively regulated in nonneural cells and positively regulated in neurons.

27 easingly realized that bioelectric events in nonneural cells are critical for pattern regulation, but

28 ular responses to guidance cues, not only in nonneural cells but also in pathfinding neurons.

29 Two-way communication between neurons and nonneural cells called glia is essential for axonal cond

30 tial for determining the fates of neural and nonneural cells during development and in the adult.

31 differentiating astrocyte progenitors and in nonneural cells expressing AQP4 transgenically.

32 In vitro studies of nonneural cells have suggested that the long allele may

33 e viral replication and spread in neurons or nonneural cells in reproductive tissue.

34 ripheral and central nervous systems, and in nonneural cells infected by T. cruzi, including cardiac

35 is due, in part, to long-term repression in nonneural cells mediated by the repressor protein REST/N

36 Although the enhancer was active in specific nonneural cells of the notochord when placed with APPb g

37 The aberrant ALK expression in nonneural cells results from chromosomal translocations

38 ically reengineered BoNTs can be targeted to nonneural cells to selectively inhibit hormone secretion

39 ng CNS intrinsic neural cells, CNS intrinsic nonneural cells, and CNS extrinsic cells that enter from

40 on of the type II sodium channel promoter in nonneural cells, and the REST/CoREST complex may mediate

41 yogenesis, REST is expressed ubiquitously in nonneural cells, but is down-regulated during differenti

42 L1 is also expressed by nonneural cells, but its function outside of the nervous

43 hreonine kinase rapidly activated by E(2) in nonneural cells, functions as a downstream node for E(2)

44 cal methods of autophagy induction used with nonneural cells, such as starvation, simply result in ne

45 form CD4(+) T lymphocytes and other types of nonneural cells.

46 revented expression of L1 gene constructs in nonneural cells.

47 roteins as inhibitors of miR-7 processing in nonneural cells.

48 Neuroblasts also enhance NT-3 production by nonneural cells.

49 t of membrane-bound organelles in neural and nonneural cells.

50 s a surprising variety of neurons, glia, and nonneural cells.

51 gnition and contributing to exon skipping in nonneural cells.

52 nd nuclear proteins isolated from neural and nonneural cells; (iii) the effect of the negative regula

53 erfamily members, are utilized in neural and nonneural contexts, nervous system-specific diversificat

54 NS), as well as other neural crest cells and nonneural crest-derived lineages.

55 rces, investigators have proposed the use of nonneural donor sources for use in neural transplantatio

56 , deltaNp63 is required for specification of nonneural ectoderm and its up-regulation suppresses neur

57 are specified at the interface of neural and nonneural ectoderm and together contribute to the periph

58 he secreted molecule Tiarin, produced by the nonneural ectoderm at border of the anterior and lateral

59 e found that interactions between neural and nonneural ectoderm can generate neural crest cells, with

60 es an integrative understanding of the human nonneural ectoderm development and a model for embryonic

61 ernative model combining mesoderm expansion, nonneural ectoderm expansion, and neural plate adhesion

62 urface ectoderm are specified along a common nonneural ectoderm trajectory based on cell density.

63 more pronounced in the neural plate than in nonneural ectoderm, and the pattern of cell division bec

64 tion of the otic placode is derived from the nonneural ectoderm, the neural folds also contribute cel

65 d at the border between the neural plate and nonneural ectoderm, where they initiate a distinct progr

66 originates at the border between neural and nonneural ectoderm.

67 in addition to the pan-neuronal marker Hu in nonneural ectoderm.

68 ith swirl/bmp2b mutants exhibiting almost no nonneural ectoderm.

69 n, within the neural plate as well as within nonneural ectodermal progenitor populations, resulting i

70 umental for the measurement of artifacts and nonneural effects in functional imaging, and more recent

71 ors have been demonstrated in the neural and nonneural elements of pain pathways.

72 n of chemokines/receptors in both neural and nonneural elements of the peripheral nervous system play

73 , and biases individual progenitors toward a nonneural fate, without altering the expression of multi

74 at direct the repression of N1 splicing in a nonneural HeLa cell extract.

75 nce can occur in response to both neural and nonneural inputs.

76 were differentially expressed in neural and nonneural layers of the jejunum, ileum, colon, and cecum

77 ld type for these two parameters in cells of nonneural lineage (immortalized primate Vero cells).

78 lex formation at oriS in cells of neural and nonneural lineage, we used nuclear extracts of HSV-infec

79 20 gene to date have been largely limited to nonneural malignant and nonmalignant cells.

80 arcinoma (2 of 12, 17%) were the most common nonneural malignant neoplasms.

81 s that have traditionally been classified as nonneural may express neurofilament and that the basilar

82 release from adrenomedullary cells through a nonneural mechanism.

83 the intrinsic dynamic behavior of mammalian nonneural microtubules, we purified tubulin from culture

84 GM2 is expressed in both neural and nonneural mouse cells and tissues.

85 lysis suggests that the previously described nonneural/neural ectodermal interaction specifying the n

86 In contrast, experiments with four nonneural "normal" cell lines and four cancer cell lines

87 ever, aneuploid cells might instead be glia, nonneural, or dying cells, which are irrelevant to direc

88 ive, rather than a guidance, function during nonneural organogenesis.

89 ly, transplanting cells--of either neural or nonneural origin--that intrinsically secrete missing or

90 al organizing cell groups of both neural and nonneural origin.

91 To ensure that the ectoderm was from nonneural regions, we utilized extraembryonic ectoderm (

92 Our finding that ngn2 can instruct nonneural retinal pigment epithelial cells to differenti

93 Ectopic expression of ngn2 in nonneural, retinal pigment epithelial cell culture trigg

94 vent reactivation from latency in neural and nonneural sites and would thus prevent transmission to o

95 otemporal changes in Vmem distribution among nonneural somatic tissues regulate pattern formation and

96 ata demonstrate a previously uncharacterized nonneural stretch reflex in gastric muscles and provide

97 pression for both of the mammalian genes are nonneural, suggesting that the functions of the mammalia

98 as a mitogen, a motogen, and a morphogen in nonneural systems, HGF/SF can function as a guidance and

99 ations into LPA signaling both in neural and nonneural systems.

100 ans sleep, energetic stores are allocated to nonneural tasks with a resultant drop in the overall fat

101 nce and significance of GABA(A) receptors in nonneural tissue is less clear.

102 s, but not in tumors or cancer cell lines of nonneural tissue origin.

103 The ciliary body of the eye is a nonneural tissue that is derived from the anterior rim o

104 no acid decarboxylase (L-AADC) in neural and nonneural tissue, on blood pressure and orthostatic tole

105 er, torsin is expressed in a wide variety of nonneural tissues and is strictly conserved across speci

106 function of human semaphorins A(V) and IV in nonneural tissues and their role in the pathogenesis of

107 ghly oncogenic, when aberrantly expressed in nonneural tissues as a fusion protein with nucleophosphi

108 a diffusible attractant in the meninges, the nonneural tissues covering the nervous system, and to a

109 a role in the silencing of L1 expression in nonneural tissues during early development but also can

110 pted chronobiologists to investigate whether nonneural tissues possess intrinsic circadian clocks, wh

111 sat1 is expressed in a variety of neural and nonneural tissues, most of which are involved in reprodu

112 r, DLG4 is also expressed in a wide range of nonneural tissues, suggesting that the protein may have

113 To explore whether netrin-1 organizes nonneural tissues, we examined its role in mammary gland

114 ferentially in a variety of human neural and nonneural tissues.

115 central nervous system (CNS), compared with nonneural tissues.

116 riched in CNS ECs compared with ECs in other nonneural tissues.

117 LN-agrin is expressed in both neural and nonneural tissues.

118 re known to be involved in cell signaling in nonneural tissues.

119 evt-2 is widely expressed in both neural and nonneural tissues.

120 pinal cord and for molybdoenzyme activity in nonneural tissues.

121 1lacZ in the brain and ectopic expression in nonneural tissues.

122 RNA expression, nor did the vast majority of nonneural tissues.

123 Nonneural tumors that metastasize to the central nervous

124 have recently been shown to directly affect nonneural wound healing.