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1 ured a long terminal repeat sequence from an intracisternal A particle (an endogenous retrovirus-like
2  in mutant mice revealed the insertion of an intracisternal A particle (IAP) element in intron 7.
3 provide evidence that mutants carry a 5.4-kb intracisternal A particle (IAP) element insertion upstre
4 defense of deleterious retrotransposition of intracisternal A particle (IAP) elements, IAP loci are h
5 hat Ahvy resulted from the integration of an intracisternal A particle (IAP) in an antisense orientat
6 plication of Ty1 elements in yeast and mouse intracisternal A particle (IAP) long terminal repeat (LT
7 murine endogenous retrovirus-L (MuERV-L) and intracisternal A particle (IAP), two autonomous long ter
8        METTL3 predominantly localizes to the intracisternal A particle (IAP)-type family of endogenou
9 mouse genome caused by a variably methylated intracisternal A particle (VM-IAP) retrotransposon.
10       Mili mutants derepress LINE-1 (L1) and intracisternal A particle and lose DNA methylation of L1
11  mutant ep gene revealed the insertion of an intracisternal A particle element in a protein-coding 3'
12 The sph(Dem) mutation is the insertion of an intracisternal A particle element in intron 10 of the er
13   The Eya1(bor) mutant hypomorph contains an intracisternal A particle insertion in intron 7 of the E
14 ement (RTE), present in a subclass of rodent intracisternal A particle retroelements, that is able to
15           In contrast, imprinted regions and intracisternal A particle retroelements, which are resis
16                           The mutation is an intracisternal A particle retroposon insertion in intron
17  splicing in scm homozygotes, with 1.5 kb of intracisternal A particle retrotransposon sequence inser
18 sine-guanine dinucleotide) methylation in an intracisternal A particle retrotransposon upstream of th
19 es from the long terminal repeat of a murine intracisternal A particle retrotransposon were not impri
20  Fused and Knobbly, result from insertion of intracisternal A particle retrotransposons into the gene
21  that are interrupted by the insertion of an intracisternal A particle sequence.
22                                              Intracisternal A particle sequences closest to those pre
23  activation of ERVs, including CpG-rich IAP (intracisternal A particle) proviruses.
24 s, which inhibit retrotransposition (RTP) of intracisternal A particles (IAP).
25          The long terminal repeats of murine intracisternal A particles (IAPs) contain an IAP proxima
26 le of P bodies in the movement of endogenous intracisternal A particles (IAPs) in mammalian cells.
27                            Major satellites, intracisternal A particles (IAPs), and imprinted genes r
28 s were cloned by inverse PCR and revealed an intracisternal A-particle (IAP) element inserted near th
29     Most but not all MEs are associated with intracisternal A-particle (IAP) elements, tending to loc
30 ined a novel element with homology to rodent intracisternal A-particle (IAP) retroelements.
31 OBEC3A, can reduce retrotransposition by the intracisternal A-particle (IAP) retrotransposon in human
32     However, some TEs in mice, including the Intracisternal A-particle (IAP) subfamily of retrotransp
33 e by a solo long terminal repeat (LTR) of an intracisternal A-particle (IAP), an endogenous retrotran
34 g a repertoire of murine variably methylated intracisternal A-particle (VM-IAP) epialleles as a model
35                                         This intracisternal A-particle element is flanked by duplicat
36                                              Intracisternal A-particle family retrotransposons were n
37 nd the RNA transport element found in rodent intracisternal A-particle LTR retrotransposons.
38           The drugs intermediately inhibited intracisternal A-particle retrotransposition but were in
39 the Gag sequence of the transposable element intracisternal A-particle.
40                                              Intracisternal A-particles (IAPs) are endogenous retrovi
41 d western blot tests for HIV-1 and the human intracisternal A-type particle (HIAP), on serum samples
42 was detected in mice containing 2 alleles of intracisternal A-type particle (IAP) retrotransposon seq
43                           The methylation of intracisternal A-type particle (IAP) sequences is mainta
44 ed in the brain and ectopically activated by intracisternal A-type particle long terminal repeats in
45 ty of engineered human LINE-1 (L1) and mouse intracisternal A-type particle retrotransposons in cultu
46 on mechanism in detail within one group, the intracisternal A-type particles (IAPs), and performing s
47 f the early transposon (ETn)/MusD family and intracisternal A-type particles (IAPs).
48 seudoknot from the gag-pro junction of mouse intracisternal A-type particles (mIAP), an endogenous re
49                            A retrovirus-like intracisternal-A particle (IAP) family sequence was also
50 x(J) mice as a result of the insertion of an intracisternal-A particle (IAP) into intron 5 of Usp14.
51  the CTE and which is part of a novel murine intracisternal-A particle (IAP) retroelement, inserted w
52 ate that this effect represses expression of intracisternal-A particle endogenous retrovirus elements
53                                              Intracisternal-A-particle-related envelope-encoding (IAP
54 demonstrate that inhibiting NAA synthesis by intracisternal administration of a locked nucleic acid a
55 ocused on neuronal injury resulting from the intracisternal administration of aluminum maltolate to N
56 u and neurofilament protein aggregates using intracisternal administration of aluminum maltolate to r
57 n the blood (<24 h) underscores the value of intracisternal administration of IL-1RA for therapeutic
58   In addition, we demonstrated that a single intracisternal administration of interleukin-1 receptor
59 sed in a canine model of NPE produced by the intracisternal administration of veratrine.
60                                              Intracisternal application of BDNF also causes similar a
61 to time-matched vehicle control experiments, intracisternal application of SB-269970 (30-300 microg k
62 denosine or knock-down of AC-5 expression by intracisternal AS-ODN.
63  by stress responses that deplete glucose or intracisternal calcium or otherwise disrupt glycoprotein
64 .), inhibited significantly Fos-LI evoked by intracisternal capsaicin administration.
65 also more potent than astressin at reversing intracisternal CRF- and abdominal surgery-induced delay
66           Many of these cells also contained intracisternal crystalline pole-like inclusions similar
67                      Twenty-four hours after intracisternal delivery of autologous EPCs, basilar arte
68 eplacement can be achieved via less-invasive intracisternal delivery of CSF1Ri-resistant murine and i
69 nse granular aggregates within cisternae and intracisternal filament bundles associated with trans-Go
70  accumulation of moderate-density content or intracisternal granules.
71                           In conscious rats, intracisternal (i.c) WIN55,212-2 (3, 10, 30 mug/rat) eli
72       Experimental meningitis was induced by intracisternal (i.c.) administration of lipopolysacchari
73                                              Intracisternal (i.c.) injection of astressin (10 microg/
74                  We previously reported that intracisternal (i.c.) injection of peptide YY (PYY) and
75 ed the influence of repeated phasic CRDs and intracisternal (ic) CRF on the spontaneous discharge rat
76 er a 24 h-fasting, GLP-1 was administered by intracisternal (ic)-injection immediately after the soli
77                                              Intracisternal IL-10 in concentrations >1 microg signifi
78 ocalized to the ER and delimit the prolamine intracisternal inclusion granules (PB-ER), whereas glute
79  within the ER lumen and their assembly into intracisternal inclusion granules are unknown, but the i
80                                              Intracisternal infection of infant rats with increasing
81  the pial brain surface following controlled intracisternal infusions in anesthetized animals.
82 l male, n = 30) under anesthesia received an intracisternal injection of a fluorescent tracer (Texas
83                                     A single intracisternal injection of adeno-associated virus carry
84                       We found that biweekly intracisternal injection of basic fibroblast growth fact
85                    However, 5 days after the intracisternal injection of blood into rabbits to mimic
86                                     After an intracisternal injection of CTOP (micro antagonist), nor
87 ed ultrasound (FUS) to rats that received an intracisternal injection of fluorescent CSF tracers (dex
88 pairment of CSF dynamics were restored after intracisternal injection of macrophage colony-stimulatin
89                                      We used intracisternal injection of superparamagnetic iron oxide
90                                              Intracisternal injections are well suited for extracellu
91   Comparison of a ure1 mutant with H99 after intracisternal inoculation into corticosteroid-treated r
92  fluid (CSF)-mediated administration routes (intracisternal, intrathecal, or intracerebroventricular)
93     In a rat model of raised ICP, created by intracisternal kaolin injection, mechanical thresholds w
94 travenous IL-10 (1 mg/kg) in two doses after intracisternal LOS significantly reduced CSF TNF-alpha a
95                                              Intracisternal magna injection, the conventional techniq
96                            Pretreatment with intracisternal nor-BNI 0.32 mg significantly blocked bot
97  larger animal, we treated beagle dogs using intracisternal or intracerebroventricular delivery.
98  of solute movement in mouse brain following intracisternal or intraparenchymal solute injection.
99                                              Intracisternal RX 77368 significantly increased acid out
100                        Our data suggest that intracisternal transplantation of SVZ cells provides an