ライフサイエンスコーパス: long interspersed nuclear element

1 to a repetitive transposable element (LINE; long interspersed nuclear element).

2 ere located in repeat regions (8 of these in long interspersed nuclear elements).

3 uman genome, such as SINE-VNTR-Alu (SVA) and long interspersed nuclear element 1 (L1), is unknown.

4 genous retrotransposable elements, including long interspersed nuclear element 1 (LINE-1 or L1) and h

5 Long interspersed nuclear element 1 (LINE-1 or L1) is an

6 Lyon has proposed that long interspersed nuclear element 1 (LINE-1 or L1) repea

7 are encoded by the mammalian retrotransposon long interspersed nuclear element 1 (LINE-1 or L1); both

8 ear ribonucleoprotein polypeptide N, and the long interspersed nuclear element 1 (LINE-1) in genomic

9 cripts correlated with overexpression of the long interspersed nuclear element 1 (LINE-1) retrotransp

10 Long interspersed nuclear element 1 (LINE-1; L1) retrotr

11 f cells that do not produce VSV DNA with the long interspersed nuclear element 1 and their infection

12 L1s (LINE-1: Long Interspersed Nuclear Element 1) are present in all

13 nslated region of a primate-specific LINE-1 (long interspersed nuclear element 1) retrotransposon, su

14 Long interspersed nuclear elements 1 (L1) are active ret

15 Furthermore, long interspersed nuclear elements 1 retrotransposition

16 Long interspersed nuclear element-1 (L1) retrotransposon

17 Long interspersed nuclear element-1 (LINE-1 or L1) retro

18 Methylation levels of long interspersed nuclear element-1 (LINE-1) and the Alu

19 repetitive sequences ("repeats"), including Long Interspersed Nuclear Element-1 (LINE-1) elements, a

20 In brain neurons, it was found that active long interspersed nuclear element-1 (LINE-1) lacked CW m

21 3 patients using a modified version of human long interspersed nuclear element-1 (LINE-1) quantitive

22 he 3' terminal exon contains sequence from a long interspersed nuclear element-1 (LINE-1) retrotransp

23 ATMmvp2b) and genome-wide DNA methylation in long interspersed nuclear element-1 (LINE1) repetitive e

24 f RNA binding is expected for all vertebrate long interspersed nuclear element-1 elements, since resi

25 cytosine-phosphate-guanine-3' (CpG) sites of long interspersed nuclear element-1 repetitive sequences

26 genetic regulatory network of murine LINE-1 (long interspersed nuclear element-1), an active mammalia

27 we show that an engineered human LINE-1 (for long interspersed nuclear element-1; also known as L1) e

28 Long interspersed nuclear elements-1 (L1s) are highly re

29 Long interspersed nuclear elements-1 (LINE-1 or L1s) are

30 LINE-1s (long interspersed nuclear elements-1) are abundant non-L

31 ements, such as high-flexibility regions and long interspersed nuclear element 1s, suggesting that co

32 at repetitive sequences, including short and long interspersed nuclear elements and LTR elements, seg

33 tributions of CW methylations in introns and long interspersed nuclear elements are also cell-type sp

34 atal blood cards revealed significantly more long interspersed nuclear element CpG methylations in in

35 alf of genes within isochores rich in AT and long interspersed nuclear elements displayed programmed

36 n of genes and transcripts and enrichment of long interspersed nuclear element (LINE) and long termin

37 long terminal repeat (LTR) retrotransposon, long interspersed nuclear element (LINE) and short inter

38 gous recombination (NAHR) between paralogous long interspersed nuclear element (LINE) or human endoge

39 Finally, we observed overexpression of long interspersed nuclear element (LINE) sequences in Cs

40 nrichment at specific genomic repeats [e.g., long interspersed nuclear element (LINE)-1 repeats] were

41 Because high densities of long interspersed nuclear element (LINE)-1 transposon se

42 We find that these loci are among the most long interspersed nuclear element (LINE)-dense regions o

43 The long interspersed nuclear element (LINE-1) (L1) clade of

44 tion arose from the antisense insertion of a long interspersed nuclear element (LINE-1) (or L1) into

45 ort interspersed nuclear elements (SINE) and long interspersed nuclear elements (LINE), but not in lo

46 We analyzed the distribution of long interspersed nuclear elements (LINE)-1 (L1) along m

47 Long interspersed nuclear elements (LINE-1 or L1) compri

48 Long interspersed nuclear elements (Line-1 or L1s) accou

49 reak fusion junction in 22Rv1 cells revealed long interspersed nuclear elements (LINE-1) flanking the

50 methylation changes, including CpG sites in long interspersed nuclear elements (LINE-1) retrotranspo

51 Long interspersed nuclear elements (LINE-1s or L1s) are

52 DAC that induced the most hypomethylation of long interspersed nuclear elements (LINE; R = 0.94, P <

53 Long interspersed nuclear elements [LINE-1 (L1)] are abu

54 t mutant mouse spastic carries a full-length long interspersed nuclear element (LINE1) retrotransposo

55 prenatal pollutants (PM2.5, PM10, NO2, O3), long interspersed nuclear elements (LINE1) and AluYb8 DN

56 Long interspersed nuclear elements (LINEs or L1s) compri

57 short interspersed nuclear elements (SINEs), long interspersed nuclear elements (LINEs) and the endog

58 ding within isochores rich in GC and poor in long interspersed nuclear elements (LINEs) did not chang

59 e repressive H3K9me3 histone modification on long interspersed nuclear elements (LINEs) in germ cells

60 tioning of centromeres, pericentromeres, and long interspersed nuclear elements (LINEs) to the neutro

61 short interspersed nuclear elements (SINEs), long interspersed nuclear elements (LINEs), and low-copy

62 e from non-LTR retrotransposons, also called long interspersed nuclear elements (LINEs), from Beta vu

63 h process primarily mediated by transposable long interspersed nuclear elements (LINEs).

64 We have identified 9652 full-length long interspersed nuclear elements (LINEs).

65 acilitated in part by common repeats such as long interspersed nuclear elements (LINEs).

66 lation between GR rates and the abundance of long interspersed nuclear elements (LINEs)/short intersp

67 oss of exons, with 7 deletion endpoints near long interspersed nuclear elements or long terminal repe

68 Finally, we also show that long interspersed nuclear elements or short interspersed

69 t target of homologous recombination between long interspersed nuclear element sequences resulting in

70 of MITEs are clearly distinct from short or long interspersed nuclear elements (SINEs or LINEs), the

71 iated with transcriptional regulators and in long interspersed nuclear elements, suggesting that thes