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1                                         This intercompartmental antagonism was functionally submaxima
2 onstrate mechanisms by which plants maintain intercompartmental aromatic amino acid homeostasis, and
3 y increased in LMNCs, in contrast to similar intercompartmental CD8(+) memory function.
4 sociated transcription factors that initiate intercompartmental cellular stress responses.
5 cross-validation, estimated total clearance, intercompartmental clearance (Q), and volumes of distrib
6 ic signaling factor involved in coordinating intercompartmental communication between plastids and th
7 he major signalling pathways responsible for intercompartmental communication between the cell envelo
8  we conducted a CellChat analysis to uncover intercompartmental communication patterns and generated
9                One important role of the NAA intercompartmental cycle appears to be osmoregulatory, a
10                                              Intercompartmental cycling of tumor cells may represent
11  regulation of individual vitamers and their intercompartmental distribution, we anticipate that thes
12 s sporulation provides a dramatic example of intercompartmental DNA transport, in which SpoIIIE moves
13            Phe accumulation had multifaceted intercompartmental effects on aromatic amino acid metabo
14 les between intracompartmental reactions and intercompartmental exchange and is robust across a wide
15 ith fast particle exchange, the role of slow intercompartmental exchange remains poorly understood.
16                                              Intercompartmental force coupling in the physiologic dir
17  in epithelial cells had opposite impacts on intercompartmental homeostasis in the prostate.
18 ffect on individual cell fate, indicating an intercompartmental impact of mucosal-wide BMP antagonism
19 ntegrative approach holds promise to explore intercompartmental interactions in other cancers with va
20 r in vitro study of kidney intracellular and intercompartmental interactions using differentiated hum
21 rve the structural integrity and to minimize intercompartmental leaks of metabolites.
22 with arteriovenous (AV) accesses, the median intercompartmental mass transfer coefficient (Kc) was 79
23 olecules within the recipient extends beyond intercompartmental movements within the substrate myceli
24 tion of the enzymes that participate in this intercompartmental one-carbon metabolism, and animal mod
25                            Moreover, we show intercompartmental phenotypic differences in CMV-specifi
26 l compartment (Vc), clearance (SCL), and the intercompartmental rate constants Kcp and Kpc was used.
27 poIVB protein is a critical component of the intercompartmental signal-transduction pathway that acti
28 otal in lung inflammation, but mechanisms of intercompartmental signaling are not understood.
29 sociated fibroblast-pEMT axis as a nexus for intercompartmental signaling that reprograms pEMT cells
30           This work reveals the mechanism of intercompartmental signalling and provides a unified mod
31                      SpoIVB is essential for intercompartmental signalling in the sigma(K)-checkpoint
32                      One function is that of intercompartmental signalling of pro-delta K processing.
33          The BofC protein acts negatively on intercompartmental signalling of pro-sigma(K) processing
34       SpoIVB is the critical determinant for intercompartmental signalling of pro-sigmaK processing d
35                              Mutations in an intercompartmental signalling process generate a set of
36 oposed a model for BofC's functional role in intercompartmental signalling.
37 mentalization is a complex process involving intercompartmental signalling; models based on changes i
38  (V1) while drug accumulates in V2 and V3 to intercompartmental steady-state, is necessary for effect
39  To learn more about the specificity of this intercompartmental step, we have examined the subcellula
40 stead, low BHTC levels trigger a coordinated intercompartmental transcriptional response manifested i
41 mbranes from a PEP4 yeast strain, indicating intercompartmental transfer.
42 our of the enrolled patients exhibited rapid intercompartmental transitioning of the disease reflecte
43 specific isoforms, have novel mechanisms for intercompartmental translocation, have distinct endogeno
44 s allowed the demonstration of reconstituted intercompartmental transport coupled to the function of
45 in a temporally ordered manner, and that the intercompartmental transport factor Sec18p/N-ethylmaleim
46 nd C1-metabolism, and thirdly, assessment of intercompartmental transport fluxes of pyruvate, acetyl-
47 egrated control of CREB-H function, coupling intercompartmental transport in the cytoplasm with stabi