ライフサイエンスコーパス: chromosomal breakpoint

1 on of the CLDN14 gene isoform at the 21q22.1 chromosomal breakpoint.

2 ing factor acetylhydrolase (Pafah1a2) at the chromosomal breakpoint.

3 in addition to regions flanking interspecies chromosomal breakpoints.

4 tion was observed for markers within 5 cM of chromosomal breakpoints.

5 gnition of conserved sequences found at many chromosomal breakpoints.

6 ally an oblate ellipsoid, which binds DNA at chromosomal breakpoints.

7 ce homology, also known as microhomology, at chromosomal breakpoints.

8 ase II poisons in the initiation of leukemic chromosomal breakpoints.

9 2 Mb of distal Xp11.21 and spanned two IP1 X-chromosomal breakpoints.

10 when colocated with evolutionarily conserved chromosomal breakpoints.

11 To further define the chromosomal breakpoints among the VCFS patients, we deve

12 at DNA sites proximal to a defined leukemic chromosomal breakpoint and displayed a sequence specific

13 sun was located close to the chromosomal breakpoint and within the inversion, thereby

14 The chromosomal breakpoints and joining sites in the index a

15 ed to identify any association between their chromosomal breakpoints and known AID target sequences.

16 ization of origins of early DNA replication, chromosomal breakpoints and transfer RNAs.

17 ssociated with MEN2A, MEN2B, or FMTC, or the chromosomal breakpoints and translocations associated wi

18 Chromosomal breakpoints are often mapped near purine-pyr

19 ults suggest that genomic rearrangements and chromosomal breakpoints are readily identified and annot

20 There appears to be a dramatic clustering of chromosomal breakpoints at 3pl4.2 in and immediately dis

21 Evolutionary chromosomal breakpoints between CFA1 and the correspondi

22 The process of identifying the evolutionary chromosomal breakpoints between CFA1 and the relevant hu

23 To map chromosomal breakpoints, characterize the add(14)(q32) m

24 close to, if not identical with, one of the chromosomal breakpoints giving rise to the DM.

25 ine the relationship between CpG islands and chromosomal breakpoints giving rise to the DM.

26 Eighteen chromosomal breakpoints have been cloned and sequenced.

27 lding preferences of oligonucleotides from a chromosomal breakpoint hotspot in the human c-MYC oncoge

28 Cloning and characterization of the 8;21 chromosomal breakpoint identified AML1 on chromosome 21

29 and a balanced X;9 translocation placed the chromosomal breakpoint in a 500 kb region flanked by D9S

30 Mapping of a chromosomal breakpoint in a somatic cell line establishe

31 also oncogenic, having been isolated from a chromosomal breakpoint in human T-cell leukaemia.

32 mily which includes: human p54, encoded at a chromosomal breakpoint in the B-cell lymphoma cell line,

33 o explore further this hypothesis, we mapped chromosomal breakpoints in 38 uterine leiomyomata with r

34 rder to identify a gene involved in PCG, the chromosomal breakpoints in a patient with a balanced tra

35 By cloning the chromosomal breakpoints in an MM cell line, we show that

36 tellites are associated with the majority of chromosomal breakpoints in cancer.

37 persed over a 400-bp region, consistent with chromosomal breakpoints in human diseases.

38 In fact, the identification of recurring chromosomal breakpoints in leukaemias and lymphomas has

39 In a fraction of these translocations, the chromosomal breakpoint is located within the 5' noncodin

40 Since the chromosomal breakpoint lay between these two structures,

41 The chromosomal breakpoint lies in an Alu family repeat loca

42 Consistent with these data, we observe chromosomal breakpoint locations are biased away from H3

43 a Clara, CA, USA) were used to determine the chromosomal breakpoint locations in tumours with MR.

44 Chromosomal breakpoints (n = 467) generating imbalances

45 existence of functional constraints on where chromosomal breakpoints occur or from the existence of r

46 early DNA replication and among sites where chromosomal breakpoints occur.

47 By defining the chromosomal breakpoint of a balanced t(10;12) translocat

48 We have mapped within this region the chromosomal breakpoint of a balanced translocation patie

49 Notch, TAN1, was initially identified at the chromosomal breakpoint of a subset of T-cell lymphoblast

50 We cloned the chromosomal breakpoint of der (14) from an LPL case (105

51 The BCL-2 gene was identified at the chromosomal breakpoint of t(14; 18)-bearing human follic

52 The chromosomal breakpoints overlap with areas of elevated t

53 Combinatorial diversity among chromosomal breakpoints produces varying fusions.

54 s, our data suggest that around one-third of chromosomal breakpoint regions may recur during avian ev

55 Moreover, analysis of the precise chromosomal breakpoints reveals 2 distinct cluster break

56 Our understanding of chromosomal breakpoint target selection comes primarily

57 odel systems, including diploid cells with a chromosomal breakpoint that has been mapped and sequence

58 The mapping of the chromosomal breakpoint to the 1.0-cM critical region def

59 Approximately 300 chromosomal breakpoints were localized to the regions af

60 Chromosomal breakpoints were primarily assigned by simul

61 ly, we observed a significant association of chromosomal breakpoints with structural variants in the