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1 t, similar to FMF patients, retains the full PYRIN domain.
2 Their N termini vary, but most have a pyrin domain.
3 90-amino-acid N-terminal sequence called the PYRIN domain.
4 pha2-alpha3 loop is not a general feature of pyrin domains.
5 two zebrafish caspases containing N-terminal pyrin domains.
6 nod-like receptor family member containing a pyrin domain 3 (NLRP3) inflammasome in a protracted mann
7 diated by the NOD-like receptor containing a pyrin domain 3 (NLRP3) inflammasome, although exactly ho
9 gomerization domain-like receptor containing pyrin domain 3 (NLRP3) inflammasomes and induces the rel
11 elanoma 2 and Nod-like receptor containing a pyrin domain 3 are partially required for caspase-1 acti
12 otide-binding domain and leucine-rich repeat pyrin domain 3 are simultaneously present in the same in
13 lood leukocytes and encodes a protein with a pyrin domain, a nucleotide-binding site (NBS, NACHT subf
15 sist of three functional domains including a pyrin domain, an NACHT domain, and a leucine-rich repeat
16 amily member that contains an amino-terminal pyrin domain and a carboxy-terminal oligonucleotide/olig
17 N-terminal region that contains a predicted pyrin domain and a putative nuclear localization signal.
18 ein containing a caspase recruitment domain) pyrin domain and the IFI16-double stranded DNA complex h
19 unexpected auto-inhibitory function for the pyrin domain, and provide the first genetic evidence lin
21 this response by interacting with the IFI16 pyrin domain, blocking its oligomerization upon DNA sens
22 200 domain of AIM2 binds to DNA, whereas the pyrin domain (but not that of the other PYHIN family mem
23 ing dsDNA, only the Aim2 protein through its pyrin domain can form an inflammasome to activate caspas
24 gomerization domain, leucine rich repeat and pyrin domain containing 1 (NLRP1), NLRP3, and nucleotide
25 these sensors, including NLRP1 (NLR family, pyrin domain containing 1), are described to form an inf
26 ng the NOD-like receptor NLRP10 (NLR family, pyrin domain containing 10); however, the mechanism by w
27 merization domain (NOD)-like receptor family pyrin domain containing 12 (NLRP12) plays a protective r
29 ucine-rich repeat containing protein family, pyrin domain containing 3 (NLRP3) (cryopyrin or NALP3) a
30 uble deficiency of Nod like receptor family, pyrin domain containing 3 (NLRP3) and caspase 8 inPstpip
32 n and leucine rich repeat containing family, pyrin domain containing 3 (NLRP3) inflammasome as an ess
33 ding domain, leucine-rich-containing family, pyrin domain containing 3 (NLRP3) inflammasome complex a
34 cell sensor leucine-rich-containing family, pyrin domain containing 3 (NLRP3) inflammasome controls
36 is a key to induce NOD-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome in macrop
37 itin, activate the NOD-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome in primed
39 leucine-rich repeat containing gene family, pyrin domain containing 3 (NLRP3) inflammasome to induce
41 oligomerization domain-like receptor family, pyrin domain containing 3 (NLRP3) inflammasome-dependent
42 of Tat in priming and activating NLR family pyrin domain containing 3 (NLRP3) inflammasomes in micro
43 ammasome system, mediated by the NLR family, pyrin domain containing 3 (NLRP3) initiating protein, wa
44 leotide-binding domain, leucine-rich repeat, pyrin domain containing 3 (NLRP3) is a key component of
46 rm depended on the NOD-like receptor family, pyrin domain containing 3 (NLRP3) sensor and the apoptos
47 components of the NOD-like receptor family, pyrin domain containing 3 (NLRP3), and absent in melanom
49 Activation of the NOD-like receptor family, pyrin domain containing 3 (NLRP3)/caspase-1 inflammasome
50 gomerization domain, leucine-rich repeat and pyrin domain containing 3 (NRLP3) inflammasome members (
51 erization domain (NOD)-like receptor family, pyrin domain containing 3 activation in the inflammasome
53 rich repeat-containing-like receptor family, pyrin domain containing 3 and autophagosome-associated m
54 rvention targeting NOD-like receptor family, pyrin domain containing 3 inflammasome activity induces
55 he key role of the NOD-like receptor family, pyrin domain containing 3 inflammasome during acute pneu
56 n regulate hepatic steatosis; the NLR family pyrin domain containing 3 inflammasome is critically inv
57 he activity of the NOD-like receptor family, pyrin domain containing 3 inflammasome when compared wit
61 innate immune-sensing complex known as "NLR-Pyrin domain containing 3" (NLRP3) inflammasome, also kn
62 omain leucine-rich repeat containing family, pyrin domain containing 3) inflammasome complex, assembl
64 flammasomes, and that the NLRP3 (NLR family, pyrin domain containing 3) inflammasome is not involved
65 OD2 target, NLRP3 (NOD-like receptor family, pyrin domain containing 3) is of importance in the patho
66 e-recruitment domain) and NLRP3 (NLR family, pyrin domain containing 3), which are essential for casp
68 eased expression of inflammatory (NLR family pyrin domain containing 3, interleukins 1beta and 6, and
69 rich repeat-containing-like receptor family, pyrin domain containing 3-associated inflammasomes and i
70 e-1/Caspase-4- and NOD-like receptor family, pyrin domain containing 3-dependent inflammatory cell de
71 ce deficient in the NOD-like receptor family pyrin domain containing 6 (NLRP6) inflammasome feature e
72 g oligomerization domain (NOD)-like receptor pyrin domain containing family of gene 12 (Nlrp12) are a
73 salivary levels of nod-like receptor family pyrin domain containing protein (NLRP) 3, apoptosis-asso
74 tide-binding domain, leucine-rich repeat and pyrin domain containing protein (NLRP) family, which for
75 leotide-binding domain, leucine-rich repeat, pyrin domain containing protein 3 (NLRP3) inflammasome.
77 (ATG5), ATG7 and ATG16L1 but not NLR family, pyrin domain containing-3 (NALP3).We show that NOD2-medi
78 tly demonstrated that the NOD-like receptor, pyrin domain containing-3 (NLRP3) contributes to renal i
79 nding domain leucine-rich repeat containing, Pyrin domain containing-3 and for absent in melanoma 2 i
80 nding domain leucine-rich repeat containing, Pyrin domain containing-3 inflammasome, and caspase-4 ph
82 e nucleotide oligomerization domain receptor pyrin-domain containing protein 3 (NLRP3) by Salmonella
84 me components, we found that both NLR family pyrin domain-containing 3 (Nlrp3) and apoptosis-associat
85 -1beta dependent on NOD-like receptor family pyrin domain-containing 3 (NLRP3) and ASC due to the sec
86 mutations in NOD-like receptor (NLR) family, pyrin domain-containing 3 (NLRP3) cause neonatal-onset m
87 oligomerization domain-like receptor family, pyrin domain-containing 3 (NLRP3) inflammasome and conco
88 main, leucine-rich repeat-containing family, pyrin domain-containing 3 (NLRP3) inflammasome as well a
89 oligomerization domain-like receptor family, pyrin domain-containing 3 (NLRP3) inflammasome drives ma
92 omain-like receptor, leucine-rich repeat and pyrin domain-containing 3 (NLRP3) inflammasome is now no
93 g oligomerization domain-like receptor (NLR) pyrin domain-containing 3 (Nlrp3) inflammasome is though
94 leucine-rich repeat containing family (NLR), pyrin domain-containing 3 (NLRP3) inflammasome plays a k
98 n (ASC) inflammasomes, including NLR family, pyrin domain-containing 3 (NLRP3), but not NLR family, c
99 ts, including NOD-like receptor (NLR) family pyrin domain-containing 3 (NLRP3), NLRP1, NLR family CAR
100 ng and oligomerization, leucine-rich repeat, pyrin domain-containing 3 (NLRP3), simultaneously and di
101 otide-binding oligomerization domain family, pyrin domain-containing 3 inflammasome activation upon H
102 is detected by the NOD-like receptor family, pyrin domain-containing 3 inflammasome and can trigger a
105 main, leucine-rich-repeat-containing family, pyrin domain-containing 3) inflammasome mediates product
107 cruitment domain-containing 4 or NLR family, pyrin domain-containing 6, are required for triggering t
109 erization domain (NOD)-like receptor family, pyrin domain-containing protein 3 (Nlrp3) expression was
112 osolic contact, and activation of NLR family pyrin domain-containing protein 3 (NLRP3) inflammasomes
113 binding oligomerization domain-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasomes
114 inding oligomerization-like receptor family, pyrin domain-containing protein 3) activation, either by
115 flammasome components Nalp3 (NACHT, LRR, and pyrin domain-containing protein 3), ASC (apoptosis-assoc
116 The SREBP-induced NOD-like receptor family pyrin domain-containing protein inflammasome and its ins
117 e activation of the NOD-like receptor family pyrin domain-containing protein inflammasome in macropha
119 t nucleotide-binding leucine-rich repeat and pyrin domain-containing receptor 12 (NLRP12) impedes alt
120 ding domain, leucine-rich-containing family, pyrin domain-containing-3 (NLRP3) inflammasome controls
121 ding domain, leucine-rich-containing family, pyrin domain-containing-3 (Nlrp3, but also known as Nalp
122 ucine-rich-repeat-containing receptor (NLR), pyrin-domain-containing 3 (NLRP3) inflammasome in human
123 merization drug AP20187, suggesting that the PYRIN domain functions as an oligomerization domain, whe
124 gy include the elucidation of the N-terminal PYRIN domain in protein-protein interactions, the descri
125 8), and Glu(16), believed critical for Pyrin/Pyrin domain interaction, are important for inflammasome
130 on the recent near-atomic structures of the PYRIN domain of ASC in the protein filament of inflammas
132 and leucine-rich repeat regions, but not the pyrin domain of CIAS1, are responsible for this inhibiti
133 weak affinity, and it is the non-DNA-binding pyrin domain of IFI16 that drives the cooperative filame
134 the structure and dynamics of the N-terminal pyrin domain of NLRP12 (NLRP12 PYD) determined using NMR
135 the structure and dynamics of the N-terminal pyrin domain of NLRP7 (NLRP7 PYD) obtained by NMR spectr
138 ty, de Almeida et al. (2015) report that the PYRIN domain-only protein (POP1) efficiently inhibits in
139 cent developments in elucidating the role of PYRIN domain-only proteins (POPs) and the related CARD-o
143 omain structure, consisting of an N-terminal pyrin domain (PYD) and a C-terminal caspase-recruitment
146 izing double-stranded DNA and its N-terminal pyrin domain (PYD) for eliciting downstream effects thro
147 ary inflammasome complexes, achieved through pyrin domain (PYD) interactions between sensors and ASC
149 on dsDNA engagement, the AIM2 amino-terminal pyrin domain (PYD) is responsible for downstream signali
150 rk of highly intercrossed filaments, whereas pyrin domain (PYD) or caspase activation and recruitment
153 recruitment domain (CARD) subfamily, and the pyrin domain (PYD) subfamily is one of the largest domai
154 ng studies on human growth hormone (hGH) and pyrin domain (PYD), and the results show how mutations a
155 uman NLRP1, mouse NLRP1b lacks an N-terminal pyrin domain (PYD), indicating that the assembly of the
169 We also show here that PAN1 binds via its PYRIN domain to ASC, an adapter protein involved in casp
171 ull-length ASC, but not its isolated CARD or PYRIN domain, with procaspase-1 induced activation of pr
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