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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  reveal how coordinated miRNA regulation and neural-specific alternative polyadenylation (APA) of a s
10 r target of the analgesic acetaminophen is a neural-specific, alternatively spliced isoform of cycloo
11 ntify independent and opposing roles for two neural-specific and differentially expressed non-coding
12 partate (NMDA) receptor 2B (NR2B) subunit is neural-specific and differentially regulated.
13 y probe ADARs, harnessing brain organoids as neural specific, and teratomas as pan-tissue development
14 n cells retain their neural fate and express neural-specific antigens.
15 previously available models to further study neural-specific aspects of CS.
16                   The NEUROGENINS (NGNs) are neural-specific basic helix-loop-helix (bHLH) transcript
17                                   MATH1 is a neural-specific basic helix-loop-helix transcription fac
18 c and cDNA mouse and human clones encoding a neural-specific bHLH protein, human BHLHB5 was cloned an
19 on of the Hes5 and Mash1 genes, which encode neural-specific bHLH proteins, decrease and increase, re
20                                     Mash1, a neural-specific bHLH transcription factor, is essential
21                                              Neural-specific, but not skeletal muscle-specific, delet
22                         Neurogranin/RC3 is a neural-specific Ca(2+)-sensitive calmodulin (CaM)-bindin
23      The type I adenylyl cyclase (I-AC) is a neural-specific, Ca2+-stimulated enzyme that couples int
24                             Neurogranin is a neural-specific, calmodulin (CaM)-binding protein that i
25 tion and expression in chromaffin cells of a neural specific Cdk5 activator, p25, led to a strong inc
26                  Nectin-like 1 (Necl-1) is a neural-specific cell adhesion molecule that is expressed
27  transcriptomics data to infer and visualize neural-specific cell-cell communication.
28 ciliary network presents a wealth of new and neural-specific ciliary signaling proteins and yields ne
29 the inference, visualization and analysis of neural-specific communication networks among pre-defined
30                                     By using neural specific conditional mouse mutants, we show that
31 e isomerase-like protein that may bind TH, a neural-specific cytoskeletal protein, and two hypophysio
32                            Here we show that neural-specific deletion of FIP200 resulted in cerebella
33                                  Mice with a neural-specific deletion of paxillin are also postnatal
34                               We report that neural-specific deletion of sirtuin 6 (Sirt6) in mice le
35                            Here we show that neural-specific deletion of the BTB/POZ zinc-finger tran
36 blasts from the cell cycle and expression of neural-specific differentiation markers.
37      To address this, we created mice with a neural-specific disruption of STAT3 (STAT3(N-/-)).
38                                    Despite a neural-specific down-regulation of adr-2 during developm
39 emethylation was essential for commissioning neural-specific enhancers in proximity to master neurode
40  transgenic mice that express FAAH under the neural specific enolase promoter.
41  enhancer from the developmentally regulated neural-specific esrrga gene.
42                                   Therefore, neural-specific exon 5 splicing and depletion of BAK1 pr
43                                  Splicing of neural-specific exons is differentially regulated in neu
44 s that are necessary and sufficient to drive neural-specific expression during gastrulation in transg
45 own for any vertebrate gene how the onset of neural-specific expression in early gastrula embryos is
46                                              Neural-specific expression of the mouse regulatory type-
47  to increase TRIM46 proteins, leading to its neural-specific expression.
48 al visual system) is a key mediator of these neural-specific extensions.
49 a calmodulin binding protein thought to be a neural-specific factor involved in learning and memory.
50  of small "Z" exons in Agrin, resulting in a neural-specific form of this extracellular proteoglycan
51                               To investigate neural-specific functions of ERK2 in the brain, we used
52  data thus suggest that CSPP1 is involved in neural-specific functions of primary cilia.
53  contains specific recognition sites for two neural-specific GAP-43 mRNA-binding proteins.
54 ional MAPK pathways in NGF induction of this neural specific gene.
55             Interestingly, expression of one neural-specific gene (synaptobrevin), which is normally
56 orly understood small transmembrane proteins neural-specific gene 1 and 2 (Nsg1/NEEP21 and Nsg2/P19).
57 cription factors in CRMs faithfully predicts neural-specific gene activity.
58 oss-of-function mutations in CTNND2 target a neural-specific gene and are associated with the transfo
59  critical role in the activation of anterior neural-specific gene expression and that alkalinization
60         Injected Xski RNA was able to induce neural-specific gene expression directly in ectodermal e
61            First, RT-PCR was used to examine neural-specific gene expression in planar explants in wh
62 hich interruption of BMP signaling activates neural-specific gene expression is not understood.
63                                      Second, neural-specific gene expression was examined in isolates
64 ha gene could represent the first identified neural-specific gene induced by TR4.
65 re identified and the expression of the most neural-specific gene, Sof-elav1, was characterized durin
66  by directly targeting an extensive array of neural-specific genes as well as genes of developmental
67 le genes, it also precludes the induction of neural-specific genes by regulating the expression of PR
68 ifying complexes to repress transcription of neural-specific genes during early development.
69                               Mesodermal and neural-specific genes were not expressed in cultured ani
70 es and an additional 24.4% (11/45) were from neural-specific genes, demonstrating the utility of this
71 inal targets for these signaling pathways in neural-specific genes.
72 on and cell fate, as well as other essential neural-specific genes.
73 differential nascent expression (Bru-Seq) of neural-specific genes.
74  Gli3 binds inertly to previously identified neural-specific Gli enhancers, demonstrating the accessi
75 ugh a non-neural toll-like receptor, linking neural-specific glycan expression to a kinase activity t
76 on of Tollo/Toll-8 into null embryos rescues neural-specific glycan expression.
77 duces a pattern of incompletely defined, but neural specific, glycan expression in the Drosophila emb
78           To explore how loss of GM3 impacts neural-specific glycolipid glycosylation and cell signal
79    However, mechanisms controlling embryonic neural-specific glycosylation are unknown.
80 haracterization of a mutation that abolishes neural-specific glycosylation in the Drosophila embryo d
81 l cells are deficient in PTB, they express a neural-specific homologue of PTB (nPTB).
82                          Here we report that neural-specific inactivation of two murine post-transcri
83                                 Using murine neural-specific inactivation of Xrcc1, a factor that is
84 ins in the CNS, we provide evidence that the neural-specific interpretation of morphogen signaling re
85 paradigm appears to conceptually explain the neural-specific interpretation of pleiotropic signaling
86 two ways through which DLK is coupled to the neural-specific isoform JNK3 to control prodegenerative
87 ase in the immunohistochemical signal of the neural-specific isoform of Neuroglian, which is generate
88 ein) conditional-null allele and showed that neural-specific knockout of nucleostemin predisposes emb
89 ll, Ramos et al. (2015) demonstrate that the neural-specific lncRNA Pnky regulates neuronal different
90          Here, we identify Pinky (Pnky) as a neural-specific lncRNA that regulates neurogenesis from
91 propriate maintenance of Polycomb binding at neural-specific loci over the course of differentiation.
92 , as they are fully abrogated in mice with a neural-specific loss of function of HDAC6.
93               We used antibodies against the neural specific markers Hu C/D, neurofilament, and SV2 t
94 d de novo generation of cells that expressed neural-specific markers and exhibited neuronal morpholog
95 nant-negative GSK3 induces the expression of neural-specific markers and inhibits the expression of B
96 he time taken for the onset of expression of neural-specific markers.
97 ical division and the onset of expression of neural-specific markers.
98                      These findings define a neural-specific mechanism of cell death whereby Pin1 cou
99                                     HuC is a neural-specific member of the Elav family of RNA-binding
100                                  Munc18-1, a neural-specific member of the Sec1/Munc18 protein family
101 specific RNA-binding proteins comprise three neural specific members called HuD, HuC, and Hel-N1.
102                     However, the role of the neural-specific members HuB, HuC, and HuD (ELAVL2-4) in
103                                Syntaxin1A, a neural-specific N-ethylmaleimide-sensitive factor attach
104 , C-SRC, to yield the constitutively active, neural-specific N1-SRC kinase.
105 n all Nogo isoforms that can interact with a neural-specific Nogo-66 receptor, the receptor for the a
106 als with mutations in MeCP2 may underlie the neural-specific pathology of RTT.
107 s and substrates contribute to the primarily neural-specific phenotype of OGT-CDG.
108 isms by which MeCP2 dysfunction leads to the neural-specific phenotypes of RTT remain poorly understo
109 d after intracerebroventricular injection in neural-specific POMC-deficient (Pomc(-/-)Tg/+) and globa
110               The same cells express phc2, a neural specific prohormone convertase, which suggests th
111                      Drosophila melanogaster neural-specific protein, ELAV, has been shown to regulat
112 s a competition between HuR and the related, neural-specific proteins HuB and HuD.
113 ctor pathways in NIH3T3 fibroblasts for this neural-specific Ras family member.
114 cope variants were preferentially located in neural-specific regulatory regions.
115   We have isolated the gene that encodes the neural-specific RNA binding protein HuD in the mouse (El
116 elav-like neuronal protein 1) gene encodes a neural-specific RNA binding protein that is expressed in
117 the determinants required to recreate proper neural-specific RNA processing seen with the endogenous
118 globin), a partial functional homolog, whose neural-specific role is poorly defined.
119                           The vertebrate and neural-specific Ser/Arg (SR)-related protein nSR100/SRRM
120 put as a context-specific determinant of the neural-specific Shh response and differential Gli-bindin
121  attenuation of apoptosis competence through neural-specific splicing of the Bak1 microexon is essent
122 ssed in neural cells and is required for the neural-specific splicing of the c-src N1 exon.
123 g regulator PTBP1 in immature neurons allows neural-specific splicing of the evolutionarily conserved
124 rotein, ELAV, has been shown to regulate the neural-specific splicing of three genes: neuroglian (nrg
125 n mesodermal cells the potential to activate neural-specific target genes upon Shh, retinoid, or bone
126        Alpha1-tubulin expression occurs in a neural-specific, temporally regulated, and regeneration-
127                             Thus, XBF-1 is a neural-specific transcription factor that can independen
128               Herein, we discovered that the neural-specific transcription factor, Engrailed 1 (EN1),
129    Wild-type mouse nodes strongly induce the neural-specific transcription factors Sox2 and Sox3 in t
130  factor 1 (NZF-1) is a member of a family of neural-specific transcription factors that contain multi
131 udes the first exon, is sufficient to direct neural-specific transcription.
132 or proper regulation of a Deformed-dependent neural-specific transcriptional enhancer.
133                             In addition, two neural-specific transcripts, GAP-43 and SCG-10, are syne
134                         Examples include the neural-specific TRK receptors, the VEGF and angiopoietin

 
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