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1 inase (ROP18 and ROP16, respectively) is the key molecule.
2 to future structure-function studies of this key molecule.
3 s elicit pathogenesis and platelet CD40 is a key molecule.
4 "jumpstarted" by the selective activation of key molecules.
6 idation of distinct neuronal roles played by key molecules already well known to immunologists (e.g.,
7 in imaging technology with probes that image key molecules and molecular based events that are fundam
9 complex remodelling process, with a focus on key molecules and pathways that might be suitable target
11 elegans model should yield new insights into key molecules and their possible implications in parasit
12 3 (IRF3) and nuclear factor (NF)-kB, that is key molecules and transcription factors involved in the
14 ty is associated with selective exclusion of key molecules, and that manipulation of transport can en
15 build a presynaptic terminal has been made, key molecules are recruited to assemble synaptic vesicle
17 d alopecia, we examined expression levels of key molecules associated with hair follicle differentiat
18 of the stress response kinase p38-MAPK, both key molecules associated with ultraviolet radiation derm
20 le fundamental regulators, such as SOX9, are key molecules both in mice and humans, the way in which
21 onging to the TNF family (BAFF) represents a key molecule by which macrophages and DCs directly regul
23 tor of mitochondrial calcium uniporter, as a key molecule conferring cancer cells with resistance to
24 therapeutic dosing of AE, whereas IGF-1 is a key molecule coupled to gene expression of other molecul
25 eptor interacting protein 3 kinase (RIP3), a key molecule critical for the assembly of the necrosome
28 creasing evidence have pointed out CD25 as a key molecule during this transdifferentiation process, h
32 ning the GC response in mice have identified key molecules expressed on follicular dendritic cells th
34 Thus, our findings establish IKK-gamma as a key molecule for adapting an oncoprotein-specific signal
35 llular process is still unclear, Beclin 1, a key molecule for autophagy, has been suggested to play a
37 id organ homeostasis and identify RANKL as a key molecule for controlling the plasticity of the immun
39 th 5' AMP-activated protein kinase (AMPK), a key molecule for energy sensing that negatively regulate
42 have previously identified fibronectin as a key molecule for incorporation of LTBP1 and TGF-beta int
45 d cyclophilin ligand interactor (TACI), is a key molecule for plasma cell maintenance and is required
49 ne (and related phytochelatins) could act as key molecules for ensuring the effective formation of HM
50 iced leader (SL) RNA and the large rRNAs are key molecules for mRNA maturation and protein synthesis,
51 roteins (TRAPs) that have been implicated as key molecules for parasite motility and adhesion onto ho
52 ese results suggest that IRS-1 and IRS-2 are key molecules for the TbetaR-V/LRP-1-mediated growth inh
54 ts the acquisition of adaptation by removing key molecules from the hair bundle that serve a temporar
55 ing chemical logic to remind how these seven key molecules function as mobile packets of cellular cur
56 These findings have identified HDAC6 as a key molecule gating the effects of acute stress on synap
59 s, stem cells and mitochondria interact with key molecules governing genome integrity, 'stemness' and
61 owever, the regulatory role of miRNAs on the key molecules implicated in kidney fibrosis remains poor
63 ifferences in the expression or induction of key molecules implicated in viral induction of interfero
66 ol regulatory element-binding protein 2 is a key molecule in aggravating proinflammatory responses in
69 plasticity, and prostaglandin E2 (PGE2) is a key molecule in COX-2-meduated synaptic modification.
71 and degraded poly ADP ribose polymerase-1 (a key molecule in DNA repair and cell survival), leading t
72 tion of poly-ADP ribose polymerase (PARP), a key molecule in DNA repair, led to ovarian cancer patien
73 osure in CD8 T cells, with STAT4 acting as a key molecule in driving optimal antigen-specific respons
74 in gene, Rax, was previously identified as a key molecule in early eye formation in mice and humans.
75 nicotinamide adenine dinucleotide (NAD(+), a key molecule in energy and redox metabolism) decrease wi
76 n vitro and induce the expression of nNOS, a key molecule in gastrointestinal motility regulation.
77 mania spp., the spliced-leader (SL) RNA is a key molecule in gene expression donating its 5'-terminal
78 report that mice deficient in lymphotoxin, a key molecule in gut immunity, were resistant to DIO.
79 ated candidate genes and select one, EGR1, a key molecule in hippocampus-related learning and memory,
80 ld the acyl-NAD adduct which is considered a key molecule in INH action, providing a better understan
81 y endocytic proteins, it is not considered a key molecule in mediating the major forms of endocytosis
82 immunoglobulin E (IgE) was identified as the key molecule in mediating what are now described as type
83 ported that S-adenosylmethionine (AdoMet), a key molecule in methylation reactions and polyamine bios
85 the DRGs of diabetic mice at 8 mo of age, a key molecule in pain signaling, and this effect was also
87 r data suggest that myocardial MDA5 may be a key molecule in protecting the heart from direct viral i
89 vator receptor (uPAR) has been shown to be a key molecule in regulating plasminogen-mediated extracel
92 These data strongly suggest that Cas-L is a key molecule in T cell migration induced by the ligation
95 nsforming growth factor-beta (TGF-beta) as a key molecule in the development and progression of hepat
97 ese results demonstrate that galectin-3 is a key molecule in the host defense against pneumococcal in
102 oid protein (Abeta) has been implicated as a key molecule in the neurodegenerative cascades of Alzhei
105 G protein-coupled receptor (KSHV-GPCR) is a key molecule in the pathogenesis of Kaposi's sarcoma, pl
107 inositol-4,5-bisphosphate (PtdIns-4,5-P2), a key molecule in the phosphoinositide signalling pathway,
111 expression of Lyn, indicating that Lyn is a key molecule in the regulation of BCR-mediated signaling
112 is a G-protein-coupled receptor (GPCR) and a key molecule in the regulation of energy homeostasis.
115 -associated protein of 25 kDa (SNAP-25) is a key molecule in the soluble N-ethylmaleimide-sensitive f
116 f cytokinesis, Plo1p is thus implicated as a key molecule in the spatial and temporal coordination of
118 AR signaling and suggest that betaARK1 is a key molecule in the transition of myocardial hypertrophy
119 our data suggest that C5a(desArg) acts as a key molecule in the triggering of local inflammation as
123 kin 1 receptor-associated kinase 1(IRAK1), a key molecule in TLR/IL-1R-mediated signaling, is phospho
124 ynthesis of S-adenosylmethionine (AdoMet), a key molecule in transmethylation reactions and polyamine
127 To validate and quantitate the expression of key molecules in a wide range of samples, we have develo
129 (cysteine-aspartate-specific proteases) are key molecules in apoptosis and require proteolytic remov
130 ctivated protein kinase, that alterations in key molecules in both GLUT4 trafficking and insulin sign
133 Noncoding RNAs (ncRNAs) are emerging as key molecules in human cancer, with the potential to ser
134 summary, this study identifies SREBPs as the key molecules in regulating angiogenesis in response to
135 ogical or genetic inhibition of ROCK1 and 2, key molecules in Rho signaling, resulted in neuroblastom
137 creasingly important to the functionality of key molecules in signaling, cell growth, and cell death.
139 aromatic hydrocarbons (PAHs) are regarded as key molecules in the astrochemical evolution of the inte
140 the intracellular concentrations of several key molecules in the bone formation cascade, we examined
141 ew risk loci could lead to identification of key molecules in the development of Barrett's oesophagus
143 d protein kinase Clambda (PKC-lambda), three key molecules in the insulin-signaling pathway, and was
144 ENU (N-ethyl-N-nitrosourea), have disclosed key molecules in the TLR signaling pathways and helped u
145 ponses is poorly understood, in part because key molecules in this mode of signal transduction, the m
146 habditis elegans have implicated a number of key molecules in this process, including the nutrient-se
147 netic mechanism studies have identified more key molecules (including Osterix, beta-catenin, and soni
148 tial to life because of its role in numerous key molecules, including DNA and RNA; indeed, organisms
152 t also suppressed the expression of IL-7R, a key molecule involved in controlling intestinal ILC home
157 ancer metastasis; therefore, identifying the key molecules involved during this process promises to a
158 Recent studies have highlighted some of the key molecules involved in all of these pathogenic proces
159 to evaluate the expression and activation of key molecules involved in cell survival and proliferatio
160 and ZAP-70 also associated differently with key molecules involved in cytoskeletal and calcium signa
161 temic immunosuppression by downregulation of key molecules involved in DC differentiation and suppres
163 harmacological inhibition against a panel of key molecules involved in galvanotaxis further revealed
165 ome biosynthetic aspects of T. cruzi mucins, key molecules involved in parasite protection and virule
166 he brain and thus controls the expression of key molecules involved in receptor signaling and spine m
167 t of NM, and (2) the expression of two other key molecules involved in regulating neuronal [Ca(2+)](i
168 r adapters capable of binding to enzymes and key molecules involved in signal transduction, maintaini
171 Transcriptomics revealed downregulation of key molecules involved in T cell receptor (TCR) signalin
172 NA microarray analysis is starting to reveal key molecules involved in the accumulation of free chole
173 ated in part through increased expression of key molecules involved in the class II MHC pathway via i
174 in the striatum, we suggest that they may be key molecules involved in the expression of the dyskines
175 on on Th17 cells and inhibited expression of key molecules involved in the generation of pathogenic T
176 aken together, these results have identified key molecules involved in the group II mGluR-induced pot
179 gnaling systems as well as the processing of key molecules involved in the pathology of the disease.
182 wn mechanisms by which ATP and adenosine are key molecules involved in thrombosis by regulating the a
183 mad signaling pathway, and the production of key molecules involved in tissue repair, such as type I
187 results indicate that the OAMB receptor is a key molecule mediating the octopamine's signal for appet
188 monstrating that Nemo-like kinase (NLK) is a key molecule modulating disease toxicity in spinocerebel
189 e forkhead transcription factor, FoxP3, is a key molecule necessary and sufficient for Tregs developm
190 r animal models, have identified some of the key molecules necessary for peripheral innervation and f
191 ed that Meis1 regulates the transcription of key molecules necessary for the endosomal machinery.
192 that RB deficiency altered the expression of key molecules needed for proper cellular organization an
193 ic, stochastic noise in small populations of key molecules (notably, Period mRNA near its daily minim
197 cell death converging at anoikis, including key molecules of interaction such as Beclin 1, reactive
198 nosaialic acids, is thought to be one of the key molecules of signal transduction in mammalian cells.
200 trate a sex-specific interaction between two key molecules of the human serotonergic system, and sugg
201 for characterizing the interactions between key molecules of the slit diaphragm that control glomeru
202 e of motor neurons in ALS and that targeting key molecules of this cascade may prove to be neuroprote
203 he muscle-specific kinase MuSK is one of the key molecules orchestrating neuromuscular junction (NMJ)
204 to bromodomain, testis-specific (Brdt) as a key molecule participating in chromatin remodeling durin
205 ve response may be determined, in part, by a key molecule, periostin, which maintains the integrity o
209 rtive activity, suggesting that IGF-2 is the key molecule produced by these cells that stimulates HSC
210 proach with the kinase hits identified other key molecules putatively involved in tau phosphorylation
216 Thus, our study has shown that Dcc is a key molecule required for ventral migration of early-bor
221 ype NPCs, suggesting that TSP1 is one of the key molecules responsible for astrocyte-induced neurogen
224 apparently result in the down-regulation of key molecules, such as cyclin A, which may be responsibl
226 our knowledge, cyclin D3 is identified as a key molecule targeted by autoimmunity that plays a nonre
228 e-acetylglucosaminyltransferase (LARGE) is a key molecule that binds to the N-terminal domain of alph
231 ty of cyclic AMP-dependent protein kinase, a key molecule that is known to be involved in L-LTP.
232 S, a member of the CD28 family, represents a key molecule that regulates adaptive responses to foreig
236 were combined with RNA-seq data to identify key molecules that associate with long-term durable self
239 istinct microenvironmental niches to provide key molecules that drive innate and adaptive immune resp
241 terations in the expression of Fgf8 and Shh, key molecules that establish a signaling center critical
242 y novel components of the pathway, including key molecules that function as positive or negative regu
243 ding proteins profilin and thymosin beta4 as key molecules that localize actin monomers to the leadin
244 pe 2 BBZDR/Wor rats changes in expression of key molecules that make up the nodal and paranodal appar
246 ppaB kinase alpha (IKKalpha) and IKKbeta are key molecules that predominantly mediate noncanonical an
248 data demonstrate a functional link between 2 key molecules that regulate hypoxia preconditioning and
250 alian target of rapamycin complex 1 serve as key molecules that sense cellular energy and nutrients l
252 ll proliferation and differentiation and are key molecules that target retinoid and retinoic acid rec
253 , phosphorylate and regulate the activity of key molecules that ultimately control the expression of
255 stence in their hosts while also revealing a key molecule to pursue while devising methods to improve
257 of Trk, identifying Rac GTPase as one of the key molecules whose activity is critical for cell surviv
258 r applicability of this approach for linking key molecules with defined cellular functions in another
259 ion pathways and that, specifically, several key molecules within the mitogen-activated protein kinas
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