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   1  a specific PET ligand for the assessment of translocator protein.                                   
     2 exoprotein and a cognate TpsB outer membrane translocator protein.                                   
     3  AhR-hsp90, AhR-XAP2, and/or AhR-AhR nuclear translocator protein.                                   
     4 acking the aryl hydrocarbon receptor nuclear translocator protein.                                   
     5 ween pRb and the AhR but not the AhR nuclear translocator protein.                                   
     6 de (DPA-714) is a radioligand for the 18-kDa translocator protein.                                   
     7 1 polymorphism in the gene encoding the 18Kd translocator protein.                                   
     8 ceptor and aryl hydrocarbon receptor nuclear translocator proteins.                                  
     9                    Typhimurium chaperone and translocator proteins.                                  
    10 ation is associated with increased levels of translocator protein 18 kDa (TSPO) and binding sites for
    11  (PET) imaging with radiotracers that target translocator protein 18 kDa (TSPO) has become a popular 
    12 ssion tomography (PET) studies targeting the translocator protein 18 kDa (TSPO) have been limited by 
  
    14 d can be monitored through expression of the translocator protein 18 kDa (TSPO) on activated microgli
    15 ET imaging of brown adipose tissue (BAT) and translocator protein 18 kDa (TSPO) via a combination of 
  
  
    18 ro evaluated for their potential to bind the translocator protein 18 kDa (TSPO), a protein today reco
    19 ssion tomography with (11)C-PBR28 to measure translocator protein 18 kDa (TSPO), a putative biomarker
  
  
  
    23 some BDZs also bind mitochondrial receptors [translocator protein (18 kDa) (TSPO)] and promote the sy
  
  
  
    27 (PET) radiotracer [11C]PBR28, which binds to translocator protein, a molecular marker that is up-regu
    28 at is consistent with the biodistribution of translocator protein and yields a dose burden that is co
    29 cterial cells HrpJ controls the secretion of translocator proteins and inside plant cells it suppress
    30 structure and topology of the outer membrane translocator proteins and the large exoproteins that the
    31 iple systems indicates that the pore-forming translocator proteins are exported before effectors, but
  
  
    34 following the binding of the AhR/AhR nuclear translocator protein (ARNT) heterodimer to dioxin respon
    35  (AHR) and aryl hydrocarbon receptor nuclear translocator protein (ARNT) were coexpressed in the yeas
  
  
  
  
    40 n patients, and could explain the overlap in translocator protein binding values between patients wit
  
    42 here when PET imaging was performed with the translocator protein-binding radioligand (18)F-GE180.   
  
    44 f interest and voxel-wise comparison, 18-kDa translocator protein-binding was higher in high affinity
  
  
    47 as to test for an association between 18 kDa translocator protein brain positron emission tomography 
    48 e secretion channel because the pore-forming translocator proteins can still be secreted while effect
    49 on channel protein or the adenine nucleotide translocator protein could not be demonstrated by immuno
  
  
  
    53 ecretion system, or with mutants lacking the translocator proteins, do not develop clinical disease, 
  
  
  
    57 hogenic E. coli is unique in that one of the translocator proteins, EspA, polymerizes to form an exte
  
    59 ar within the EPEC LEE region: CesD, for the translocator proteins EspB and EspD; CesT, for the effec
    60  N terminus of the type III secretion system translocator proteins EspB, EspD, and EspA mediate prote
    61 carbon receptor and aryl hydrocarbon nuclear translocator protein expression are not responsible for 
  
  
    64 lter nuclear AhR levels or hAhR/hAhR nuclear translocator protein heterodimer DRE-binding activity as
  
    66 m Salmonella and is therefore likely to be a translocator protein in the type-III secretion system of
    67 ion of the aryl hydrocarbon receptor nuclear translocator protein in vivo by adenovirus-mediated RNA 
    68 es pilus protein and no longer secretes four translocator proteins in culture, and it fails to inject
  
  
    71 he recruitment and stable association of the translocator protein IpaB at the TTSA needle tip in the 
  
    73 trigger recruitment of the first hydrophobic translocator protein, IpaB, to the tip complex where it 
  
  
    76 ic members of the Yersinia genus require the translocator protein LcrV for proper function of the typ
    77 ibition does not alter hAhR and hAhR nuclear translocator protein levels or TCDD-induced down-regulat
    78 GE180 for imaging activated microglia (18-kD translocator protein ligand [TSPO]) and static 30- to 60
    79 ement, were examined using a specific 18-kDa translocator protein ligand, (11)C-PBR28, and T1-weighte
  
    81 Glial activation in white matter assessed by translocator protein PET significantly improves predicti
  
  
    84 progression using a second-generation 18-kDa translocator protein positron emission tomography radiot
    85  whether microglial activity, measured using translocator-protein positron emission tomography (PET) 
    86 sitron emission tomography scanning with the translocator protein radioligand 11C-PBR28 was performed
  
  
  
    90 on receptor and the aryl hydrocarbon nuclear translocator protein, suggesting that aryl hydrocarbon r
  
  
    93 pe III secretion systems rely on hydrophobic translocator proteins that form a pore in the host cell 
  
  
    96 ata for the structure of the A139T mutant of translocator protein TSPO from Rhodobacter sphaeroides s
  
    98 ectional design using (18)F-FDG (n = 43) and translocator protein (TSPO) ((18)F-GE180; n = 58) small-
    99 e ((18)F-PBR06) for detecting alterations in translocator protein (TSPO) (18 kDa), a biomarker of mic
  
  
   102 ivated, microglia increase the expression of translocator protein (TSPO) 18 kDa, thereby making the T
   103 wth, inflammation, and invasion, such as the translocator protein (TSPO) and matrix metalloproteinase
  
   105 althy volunteers, genetically stratified for translocator protein (TSPO) binding status, underwent PE
   106 es the first comprehensive quantification of translocator protein (TSPO) binding using SPECT and 6-ch
  
  
   109 line class was exploited to search for a new translocator protein (TSPO) fluorescent probe endowed wi
   110 et al. reported on a crystal structure for a translocator protein (TSPO) from Rhodobacter sphaeroides
   111 adiolabeled ligands selective for the 18 kDa translocator protein (TSPO) has become the most widely u
  
  
   114 ssion tomography (PET) imaging of the 18 kDa translocator protein (TSPO) has been used to investigate
  
   116 ective of this study was to evaluate whether translocator protein (TSPO) imaging could be used to vis
  
  
  
  
  
  
  
  
  
   126 in-3-yl)-N,N-die thylacetamide (6b), a novel translocator protein (TSPO) ligand exhibiting a 36-fold 
   127  4-phenylquinazoline-2-carboxamide series of translocator protein (TSPO) ligands have been explored f
  
   129 ol-3-ylglyoxylamides as potent and selective translocator protein (TSPO) ligands, two subsets of nove
   130 5 PET, which aims to image expression of the translocator protein (TSPO) on activated microglia in th
   131 nificant role in Alzheimer disease (AD), and translocator protein (TSPO) PET imaging allows us to qua
   132 -L-DOPA, 6-[(18)F]fluoro-m-tyrosine, and the translocator protein (TSPO) PET ligand [(18)F]DAA1106.  
  
   134 a-isosters of PK11195, the well-known 18 kDa translocator protein (TSPO) reference ligand, and synthe
   135 se of SPECT/PET imaging agents targeting the translocator protein (TSPO) that is upregulated on activ
  
   137  we investigated the involvement and role of translocator protein (TSPO), a biomarker of microglial a
  
  
   140 on tomography (PET) and radioligands for the translocator protein (TSPO), a marker for glial activati
   141 re the binding of [(11)C]PBR28 to the 18 kDa translocator protein (TSPO), a marker for microglial act
   142 PBR28, we quantified expression of the 18kDa translocator protein (TSPO), a marker of activated micro
   143 PBR28, we show increased brain levels of the translocator protein (TSPO), a marker of glial activatio
  
   145 eration tracer for PET imaging of the 18-kDa translocator protein (TSPO), a marker of neuroinflammati
  
   147 l with high affinity and selectivity for the translocator protein (TSPO), expressed on activated glia
   148 composed of the outer mitochondrial membrane translocator protein (TSPO), previously known as periphe
  
  
  
   152 ivation can be detected in vivo using 18-kDa translocator protein (TSPO)-binding radioligands and PET
  
  
  
  
  
  
  
  
  
   162 istribution volume of (11)C-PBR28 binding to translocator protein was significantly reduced compared 
   163 f (11)C-PBR28 to the microglia marker 18 kDa translocator protein, was examined using positron emissi
   164 11)C](R)PK11195-PET measures upregulation of translocator protein, which is associated with microglia
  
  
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