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1 rase RNA) and a protein subunit named hTERT (human telomerase reverse transcriptase).
2 telomerase RNA; hTER) and the core protein (human telomerase reverse transcriptase).
3 onucleotide that targets the RNA template of human telomerase reverse transcriptase.
4 2)D(3)) decreases the mRNA expression of the human telomerase reverse transcriptase.
5 responds to a peptide sequence derived from human telomerase reverse transcriptase.
6 exes, the MRP ribonucleoprotein ribozyme and human telomerase reverse transcriptase.
7 quantitative polymerase chain reaction using human telomerase reverse transcriptase.
8 tion of two genes, asparagine synthetase and human telomerase reverse transcriptase.
9 T-oligo also inhibited mRNA expression of human telomerase reverse transcriptase, a catalytic subu
10 ptide tumor antigen vaccine derived from the human telomerase reverse transcriptase and the antiapopt
11 e restriction decreased expression of hTERT (human telomerase reverse transcriptase) and increased ex
12 ly enriched for expression of Ki-67, ZAP-70, human telomerase reverse transcriptase, and telomerase a
13 espan in human cancer cells, thus validating human telomerase reverse transcriptase as an important t
14 e "insertion in fingers domain" (IFD) in the human telomerase reverse transcriptase catalytic subunit
16 that alteration of the carboxyl terminus of human telomerase reverse transcriptase does not affect t
17 ential for malignant behavior, expression of human telomerase reverse transcriptase enabled cells fro
18 ause c-Myc can activate transcription of the human telomerase reverse transcriptase gene (hTERT), we
19 t promoted c-Myc-dependent expression of the human telomerase reverse transcriptase gene (hTERT).
20 t is recruited by Myc to the promoter of the human telomerase reverse transcriptase gene, and p300/CB
21 hromosome clone containing the entire hTERT (human telomerase reverse transcriptase) gene was introdu
24 1 and the core components of telomerase, the human telomerase reverse transcriptase (hTERT) and assoc
25 hTR adopts a new conformation on binding to human telomerase reverse transcriptase (hTERT) and recon
26 enic HLA-DR-restricted peptides derived from human telomerase reverse transcriptase (hTERT) and refer
28 zation, the cells were exposed to retroviral human telomerase reverse transcriptase (hTERT) and/or SV
29 and RAS signaling pathways and activation of human telomerase reverse transcriptase (hTERT) are commo
30 ulated expression and telomerase activity of human telomerase reverse transcriptase (hTERT) are hallm
33 ty reflects E6-enhanced transcription of the human telomerase reverse transcriptase (hTERT) catalytic
35 de and optical methods to measure changes in human telomerase reverse transcriptase (hTERT) gene expr
38 t binds to and regulates the activity of the human telomerase reverse transcriptase (hTERT) gene prom
39 cell life span, telomerase, was modified by human telomerase reverse transcriptase (hTERT) gene tran
40 by the ectopic expression of telomerase via human telomerase reverse transcriptase (hTERT) gene tran
42 and also by transcriptionally activating the human telomerase reverse transcriptase (hTERT) gene, whi
43 tuting G-quadruplexes in the promoter of the human telomerase reverse transcriptase (hTERT) gene.
45 c cells (DCs) transfected with mRNA encoding human telomerase reverse transcriptase (hTERT) have been
46 cribed increased mRNA expression of CSF1R in human telomerase reverse transcriptase (hTERT) immortali
47 Here we report that ectopic expression of human telomerase reverse transcriptase (hTERT) in BMSSCs
48 pression of mutant H-Ras), and expression of human telomerase reverse transcriptase (hTERT) in combin
49 se chain reaction (RT-PCR) for expression of human telomerase reverse transcriptase (hTERT) in medias
50 brary to knock down factors cooperating with human telomerase reverse transcriptase (hTERT) in the im
51 e neuronal conversion, whereas expression of human telomerase reverse transcriptase (hTERT) induces i
54 f the mechanisms governing expression of the human telomerase reverse transcriptase (hTERT) is import
60 ariants of the active full-length isoform of human telomerase reverse transcriptase (hTERT) may be ex
61 ecular analyses showed that leptin increased human telomerase reverse transcriptase (hTERT) mRNA expr
63 that 1,25(OH)(2)VD(3) decreases the level of human telomerase reverse transcriptase (hTERT) mRNA, the
65 model to show that FTSECs immortalized with human telomerase reverse transcriptase (hTERT) plus SV40
66 enoviral system, we recently showed that the human telomerase reverse transcriptase (hTERT) promoter
68 /3 capsid for enhanced tumor transduction, a human telomerase reverse transcriptase (hTERT) promoter
69 recently demonstrated that E6 activates the human telomerase reverse transcriptase (hTERT) promoter
70 factors in the regulation of the activity of human telomerase reverse transcriptase (hTERT) promoter
71 e viral replication, is under control of the human telomerase reverse transcriptase (hTERT) promoter.
72 te telomerase activity without alteration of human telomerase reverse transcriptase (hTERT) protein e
73 ignalling network consistent with a model of human telomerase reverse transcriptase (hTERT) repressio
74 n-of-function mutations in the TEN-domain of human telomerase reverse transcriptase (hTERT) that disr
75 ously expressed transcriptional regulator of human telomerase reverse transcriptase (hTERT) that is t
76 sition established that hTR remains bound to human telomerase reverse transcriptase (hTERT) throughou
77 lastoma gene (pRb) and ectopic expression of human telomerase reverse transcriptase (hTERT) to immort
78 Here we used retroviral overexpression of human telomerase reverse transcriptase (hTERT) to immort
80 ession of Bmi-1 in MECs led to activation of human telomerase reverse transcriptase (hTERT) transcrip
82 ol vector, and immortalized HAECs containing human telomerase reverse transcriptase (hTERT) were comp
83 the catalytic component of human telomerase human telomerase reverse transcriptase (hTERT), and colo
84 dation of p53, transcriptional activation of human telomerase reverse transcriptase (hTERT), and degr
85 telomerase RNA [hTR]), the catalytic subunit human telomerase reverse transcriptase (hTERT), and telo
86 the catalytic component of human telomerase, human telomerase reverse transcriptase (hTERT), extends
87 as mediated by the induced overexpression of human telomerase reverse transcriptase (hTERT), has perm
89 tion of expression of the catalytic subunit, human telomerase reverse transcriptase (hTERT), is sugge
90 ntaining cyclin-dependent kinase (Cdk) 4 and human telomerase reverse transcriptase (hTERT), resultin
93 ts both the transcription and translation of human telomerase reverse transcriptase (hTERT), the cata
94 vel link between HMGA2 and the regulation of human telomerase reverse transcriptase (hTERT), the cata
99 we showed the superior in vitro survival of human telomerase reverse transcriptase (hTERT)-transduce
106 icient induction of the telomerase component human telomerase reverse transcriptase (hTERT); T cell a
107 ial components, a catalytic protein subunit [human telomerase reverse transcriptase (hTERT)] and a te
108 e protein catalytic component of telomerase [human telomerase reverse transcriptase (hTERT)] are requ
109 ression of the telomerase catalytic subunit [human telomerase reverse transcriptase (hTERT)] expressi
111 ation is the transcriptional upregulation of human telomerase reverse transcriptase, hTERT, and the r
113 ression of the telomerase catalytic subunit (human telomerase reverse transcriptase; hTERT) in human
116 ta (CK1delta) blocks primary ciliogenesis in human telomerase reverse transcriptase immortalized reti
117 tant form of CDK4 or knockdown of p16 in the human telomerase reverse transcriptase-immortalized NPE
119 ressing the catalytic subunit of telomerase (human telomerase reverse transcriptase) in primary human
120 go may be mediated through POT1/TRF2 and via human telomerase reverse transcriptase inhibition throug
122 targeted the 3-prime untranslated region of human telomerase reverse transcriptase mRNA and decrease
123 The ability of 1,25(OH)(2)D(3) to decrease human telomerase reverse transcriptase mRNA and to suppr
125 ression of the telomerase catalytic subunit (human telomerase reverse transcriptase or hTERT) and sub
126 th temperature-sensitive large T antigen and human telomerase reverse transcriptase (OSEtsT/hTERT).
127 ation of four genetic alterations, including human telomerase reverse transcriptase overexpression, b
128 escent protein/TRAIL fusion protein from the human telomerase reverse transcriptase promoter (designa
129 bit c-Myc E-box-mediated transactivation and human telomerase reverse transcriptase promoter activity
130 r system TTS (TTF1 gene under the control of human telomerase reverse transcriptase promoter and huma
131 onstrate that Pyk2 is capable of driving the human telomerase reverse transcriptase promoter, resulti
132 of the human telomerase RNA subunit and the human telomerase reverse transcriptase protein (hTERT) d
135 ombined advantages of the TRAIL gene and the human telomerase reverse transcriptase target, Ad/gTRAIL
137 nted using tissue reconstruction techniques; human telomerase reverse transcriptase was required for
138 present evidence that the overexpression of human telomerase reverse transcriptase was sufficient to
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