ライフサイエンスコーパス: telomerase RNA component

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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 DKC1, while heterozygous mutations in TERC (telomerase RNA component) and TERT (telomerase reverse t

5 of NP oligonucleotide (GRN163) against human telomerase RNA component as a telomerase inhibitor and p

6 ng telomerase activity and for targeting the telomerase RNA component as an anti-cancer therapy.

7 he regulation of telomerase activity and the telomerase RNA component as leukocytes were stimulated t

8 The template domain of the telomerase RNA component dictates synthesis of species-s

9 yethyl oligonucleotides complementary to the telomerase RNA component diffuse across cell membranes w

10 Telomerase RNA components have been identified from many

11 erase activity in combination with the human telomerase RNA component hTR.

12 tion, telomerase activity, expression of the telomerase RNA component (hTR) and telomere length were

13 ribonucleoprotein complex that includes the telomerase RNA component (hTR) and the telomerase cataly

14 The human telomerase RNA component (hTR) is present in normal soma

15 s we found a heterogeneous expression of the telomerase RNA component (hTR) within the basal layer, w

16 complex controls the stability of the human telomerase RNA component (hTR/TERC).

17 In addition to the human telomerase RNA component (hTR; ref.

18 Overexpression of the telomerase RNA component, hTR, demonstrated that this pr

19 UC1 and PyMT (MMT mice) but deficient in the telomerase RNA component, mTerc, on the C57BL/6 backgrou

20 ns of telomerase-deficient mice null for the telomerase RNA component, mTERC.

21 and expression of the recently cloned mouse telomerase RNA component (mTR) in two different transgen

22 omerase in normal and neoplastic growth, the telomerase RNA component (mTR) was deleted from the mous

23 stions regarding the mechanisms by which the telomerase RNA component supports tumorigenesis.

24 h respect to both Wrn and Terc (encoding the telomerase RNA component), telomere dysfunction elicits

25 1 (rs9419958 P = 9.1 x 10(-11)) and with the telomerase RNA component TERC (rs1317082, P = 1.1 x 10(-

26 In addition, we confirmed the telomerase RNA component (TERC) as a gene associated wit

27 r telomerase reverse transcriptase (Tert) or telomerase RNA component (Terc) genes.

28 The telomerase RNA component (TERC) is a critical determinan

29 d DC cells overcome a critical limitation in telomerase RNA component (TERC) levels to restore telome

30 lomerase reverse transcriptase (TERT) or the telomerase RNA component (TERC) telomerase genes.

31 telomerase reverse transcriptase (TERT), the telomerase RNA component (TERC), and the TERC-binding pr

32 Telomerase RNA component (TERC), the RNA component and T

33 sm level in mice doubly null for Atm and the telomerase RNA component (Terc).

34 is required for the 3'-end maturation of the telomerase RNA component (TERC).

35 Determination of the structure of the yeast telomerase RNA component TLC1 has been hampered by its l

36 When the yeast telomerase RNA component, TLC1, is deleted, telomeres sh

37 Here we show that genetic depletion of the telomerase RNA component (TR) in the zebrafish results i

38 d cultured cells from mice deficient for the telomerase RNA component, we found that G-strand overhan

39 s new function for TERT does not require the telomerase RNA component, which encodes the template for

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