ライフサイエンスコーパス: neural-specific

1 ng protein SCG10 (superior cervical ganglia, neural specific 10) was found to directly interact with

2 SCG10 (superior cervical ganglia neural-specific 10 protein) is a neuron specific member

3 Neural-specific ablation of C9orf72 in conditional C9orf

4 A neural-specific activating subunit, p35, of cyclin-depen

5 e present study shows that Cdk5 bound to its neural specific activator p35 not only binds to Munc-18

6 immediate 3' flanking sequence produce full neural specific activity that is down-regulated by GABA

7 The tuba1a gene encodes a neural-specific alpha-tubulin isoform whose expression i

8 ated B(DeltaI)/B(DeltaI) mice by replacing a neural-specific alternative exon with the PGK-Neo casset

9 r target of the analgesic acetaminophen is a neural-specific, alternatively spliced isoform of cycloo

10 partate (NMDA) receptor 2B (NR2B) subunit is neural-specific and differentially regulated.

11 n cells retain their neural fate and express neural-specific antigens.

12 previously available models to further study neural-specific aspects of CS.

13 The NEUROGENINS (NGNs) are neural-specific basic helix-loop-helix (bHLH) transcript

14 MATH1 is a neural-specific basic helix-loop-helix transcription fac

15 c and cDNA mouse and human clones encoding a neural-specific bHLH protein, human BHLHB5 was cloned an

16 on of the Hes5 and Mash1 genes, which encode neural-specific bHLH proteins, decrease and increase, re

17 Mash1, a neural-specific bHLH transcription factor, is essential

18 Neural-specific, but not skeletal muscle-specific, delet

19 Neurogranin/RC3 is a neural-specific Ca(2+)-sensitive calmodulin (CaM)-bindin

20 The type I adenylyl cyclase (I-AC) is a neural-specific, Ca2+-stimulated enzyme that couples int

21 Neurogranin is a neural-specific, calmodulin (CaM)-binding protein that i

22 tion and expression in chromaffin cells of a neural specific Cdk5 activator, p25, led to a strong inc

23 Nectin-like 1 (Necl-1) is a neural-specific cell adhesion molecule that is expressed

24 By using neural specific conditional mouse mutants, we show that

25 e isomerase-like protein that may bind TH, a neural-specific cytoskeletal protein, and two hypophysio

26 Here we show that neural-specific deletion of FIP200 resulted in cerebella

27 Mice with a neural-specific deletion of paxillin are also postnatal

28 We report that neural-specific deletion of sirtuin 6 (Sirt6) in mice le

29 Here we show that neural-specific deletion of the BTB/POZ zinc-finger tran

30 blasts from the cell cycle and expression of neural-specific differentiation markers.

31 To address this, we created mice with a neural-specific disruption of STAT3 (STAT3(N-/-)).

32 transgenic mice that express FAAH under the neural specific enolase promoter.

33 enhancer from the developmentally regulated neural-specific esrrga gene.

34 Splicing of neural-specific exons is differentially regulated in neu

35 s that are necessary and sufficient to drive neural-specific expression during gastrulation in transg

36 own for any vertebrate gene how the onset of neural-specific expression in early gastrula embryos is

37 Neural-specific expression of the mouse regulatory type-

38 al visual system) is a key mediator of these neural-specific extensions.

39 a calmodulin binding protein thought to be a neural-specific factor involved in learning and memory.

40 To investigate neural-specific functions of ERK2 in the brain, we used

41 data thus suggest that CSPP1 is involved in neural-specific functions of primary cilia.

42 contains specific recognition sites for two neural-specific GAP-43 mRNA-binding proteins.

43 ional MAPK pathways in NGF induction of this neural specific gene.

44 Interestingly, expression of one neural-specific gene (synaptobrevin), which is normally

45 orly understood small transmembrane proteins neural-specific gene 1 and 2 (Nsg1/NEEP21 and Nsg2/P19).

46 cription factors in CRMs faithfully predicts neural-specific gene activity.

47 oss-of-function mutations in CTNND2 target a neural-specific gene and are associated with the transfo

48 critical role in the activation of anterior neural-specific gene expression and that alkalinization

49 Injected Xski RNA was able to induce neural-specific gene expression directly in ectodermal e

50 First, RT-PCR was used to examine neural-specific gene expression in planar explants in wh

51 hich interruption of BMP signaling activates neural-specific gene expression is not understood.

52 Second, neural-specific gene expression was examined in isolates

53 ha gene could represent the first identified neural-specific gene induced by TR4.

54 re identified and the expression of the most neural-specific gene, Sof-elav1, was characterized durin

55 by directly targeting an extensive array of neural-specific genes as well as genes of developmental

56 le genes, it also precludes the induction of neural-specific genes by regulating the expression of PR

57 ifying complexes to repress transcription of neural-specific genes during early development.

58 Mesodermal and neural-specific genes were not expressed in cultured ani

59 es and an additional 24.4% (11/45) were from neural-specific genes, demonstrating the utility of this

60 inal targets for these signaling pathways in neural-specific genes.

61 on and cell fate, as well as other essential neural-specific genes.

62 Gli3 binds inertly to previously identified neural-specific Gli enhancers, demonstrating the accessi

63 ugh a non-neural toll-like receptor, linking neural-specific glycan expression to a kinase activity t

64 on of Tollo/Toll-8 into null embryos rescues neural-specific glycan expression.

65 duces a pattern of incompletely defined, but neural specific, glycan expression in the Drosophila emb

66 However, mechanisms controlling embryonic neural-specific glycosylation are unknown.

67 haracterization of a mutation that abolishes neural-specific glycosylation in the Drosophila embryo d

68 l cells are deficient in PTB, they express a neural-specific homologue of PTB (nPTB).

69 Here we report that neural-specific inactivation of two murine post-transcri

70 Using murine neural-specific inactivation of Xrcc1, a factor that is

71 ins in the CNS, we provide evidence that the neural-specific interpretation of morphogen signaling re

72 paradigm appears to conceptually explain the neural-specific interpretation of pleiotropic signaling

73 ase in the immunohistochemical signal of the neural-specific isoform of Neuroglian, which is generate

74 ein) conditional-null allele and showed that neural-specific knockout of nucleostemin predisposes emb

75 ll, Ramos et al. (2015) demonstrate that the neural-specific lncRNA Pnky regulates neuronal different

76 Here, we identify Pinky (Pnky) as a neural-specific lncRNA that regulates neurogenesis from

77 , as they are fully abrogated in mice with a neural-specific loss of function of HDAC6.

78 We used antibodies against the neural specific markers Hu C/D, neurofilament, and SV2 t

79 d de novo generation of cells that expressed neural-specific markers and exhibited neuronal morpholog

80 nant-negative GSK3 induces the expression of neural-specific markers and inhibits the expression of B

81 he time taken for the onset of expression of neural-specific markers.

82 ical division and the onset of expression of neural-specific markers.

83 These findings define a neural-specific mechanism of cell death whereby Pin1 cou

84 HuC is a neural-specific member of the Elav family of RNA-binding

85 Munc18-1, a neural-specific member of the Sec1/Munc18 protein family

86 specific RNA-binding proteins comprise three neural specific members called HuD, HuC, and Hel-N1.

87 Syntaxin1A, a neural-specific N-ethylmaleimide-sensitive factor attach

88 n all Nogo isoforms that can interact with a neural-specific Nogo-66 receptor, the receptor for the a

89 als with mutations in MeCP2 may underlie the neural-specific pathology of RTT.

90 isms by which MeCP2 dysfunction leads to the neural-specific phenotypes of RTT remain poorly understo

91 d after intracerebroventricular injection in neural-specific POMC-deficient (Pomc(-/-)Tg/+) and globa

92 The same cells express phc2, a neural specific prohormone convertase, which suggests th

93 Drosophila melanogaster neural-specific protein, ELAV, has been shown to regulat

94 ctor pathways in NIH3T3 fibroblasts for this neural-specific Ras family member.

95 We have isolated the gene that encodes the neural-specific RNA binding protein HuD in the mouse (El

96 elav-like neuronal protein 1) gene encodes a neural-specific RNA binding protein that is expressed in

97 the determinants required to recreate proper neural-specific RNA processing seen with the endogenous

98 The vertebrate and neural-specific Ser/Arg (SR)-related protein nSR100/SRRM

99 put as a context-specific determinant of the neural-specific Shh response and differential Gli-bindin

100 ssed in neural cells and is required for the neural-specific splicing of the c-src N1 exon.

101 rotein, ELAV, has been shown to regulate the neural-specific splicing of three genes: neuroglian (nrg

102 n mesodermal cells the potential to activate neural-specific target genes upon Shh, retinoid, or bone

103 Alpha1-tubulin expression occurs in a neural-specific, temporally regulated, and regeneration-

104 Thus, XBF-1 is a neural-specific transcription factor that can independen

105 Herein, we discovered that the neural-specific transcription factor, Engrailed 1 (EN1),

106 Wild-type mouse nodes strongly induce the neural-specific transcription factors Sox2 and Sox3 in t

107 factor 1 (NZF-1) is a member of a family of neural-specific transcription factors that contain multi

108 udes the first exon, is sufficient to direct neural-specific transcription.

109 or proper regulation of a Deformed-dependent neural-specific transcriptional enhancer.

110 In addition, two neural-specific transcripts, GAP-43 and SCG-10, are syne

111 Examples include the neural-specific TRK receptors, the VEGF and angiopoietin