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1 locus that includes TERC, which encodes the telomerase RNA component.
2 copying a short template sequence within its telomerase RNA component.
3 igoadenylate)-linked antisense against human telomerase RNA component (2-5A-anti-hTER) was investigat
4 able cell line overexpressing both the human telomerase RNA component and the N-terminally biotinylat
5 omoter interactions (7SK), telomere biology (telomerase RNA component) and inflammatory gene regulati
6 DKC1, while heterozygous mutations in TERC (telomerase RNA component) and TERT (telomerase reverse t
7 s that cause reduced levels of TERC/hTR, the telomerase RNA component, are found in most TBD patients
8 of NP oligonucleotide (GRN163) against human telomerase RNA component as a telomerase inhibitor and p
10 he regulation of telomerase activity and the telomerase RNA component as leukocytes were stimulated t
13 yethyl oligonucleotides complementary to the telomerase RNA component diffuse across cell membranes w
14 in the telomerase reverse transcriptase and telomerase RNA component genes have been observed at a h
17 tion, telomerase activity, expression of the telomerase RNA component (hTR) and telomere length were
18 ribonucleoprotein complex that includes the telomerase RNA component (hTR) and the telomerase cataly
20 s we found a heterogeneous expression of the telomerase RNA component (hTR) within the basal layer, w
21 ound to regulate the maturation of the human telomerase RNA component (hTR), a noncoding RNA required
26 UC1 and PyMT (MMT mice) but deficient in the telomerase RNA component, mTerc, on the C57BL/6 backgrou
28 and expression of the recently cloned mouse telomerase RNA component (mTR) in two different transgen
29 omerase in normal and neoplastic growth, the telomerase RNA component (mTR) was deleted from the mous
31 h respect to both Wrn and Terc (encoding the telomerase RNA component), telomere dysfunction elicits
32 1 (rs9419958 P = 9.1 x 10(-11)) and with the telomerase RNA component TERC (rs1317082, P = 1.1 x 10(-
33 receptor tyrosine kinase, downregulates the telomerase RNA component TERC, confers genomic stability
34 on of telomere-length maintenance molecules [telomerase RNA component ( Terc; P < 0.01), P23 ( P = 0.
40 d DC cells overcome a critical limitation in telomerase RNA component (TERC) levels to restore telome
42 the synthesis and enzymatic stabilization of telomerase RNA component (TERC), a therapeutically relev
43 telomerase reverse transcriptase (TERT), the telomerase RNA component (TERC), and the TERC-binding pr
48 Determination of the structure of the yeast telomerase RNA component TLC1 has been hampered by its l
50 Here we show that genetic depletion of the telomerase RNA component (TR) in the zebrafish results i
51 d cultured cells from mice deficient for the telomerase RNA component, we found that G-strand overhan
52 s new function for TERT does not require the telomerase RNA component, which encodes the template for