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 t also to determine the precise positions of chromosomal breakpoints.

11 when colocated with evolutionarily conserved chromosomal breakpoints.

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

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

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

15 The chromosomal breakpoints and joining sites in the index a

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

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

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

19 The chromosomal breakpoint approach provides a basis for anc

20 Chromosomal breakpoints are often mapped near purine-pyr

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

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

23 Evolutionary chromosomal breakpoints between CFA1 and the correspondi

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

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

26 tructure in array data and developed a novel chromosomal breakpoint detection algorithm, LDcnv, which

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

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

29 Eighteen chromosomal breakpoints have been cloned and sequenced.

30 ally-occurring H-DNA-forming sequence from a chromosomal breakpoint hotspot in the human c-MYC oncoge

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

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

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

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

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

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

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

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

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

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

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

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

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

44 Since the chromosomal breakpoint lay between these two structures,

45 The chromosomal breakpoint lies in an Alu family repeat loca

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

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

48 he rearranged SegDup sequences and the exact chromosomal breakpoint locations, which coincide with va

49 Chromosomal breakpoints (n = 467) generating imbalances

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

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

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

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

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

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

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

57 , the full sequence rearrangements and exact chromosomal breakpoints of 22q11.2DS (including all comm

58 The chromosomal breakpoints overlap with areas of elevated t

59 Combinatorial diversity among chromosomal breakpoints produces varying fusions.

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

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

62 Our understanding of chromosomal breakpoint target selection comes primarily

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

64 mean shift in genetic intensities to locate chromosomal breakpoints, the step of which is referred t

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

66 Approximately 300 chromosomal breakpoints were localized to the regions af

67 Chromosomal breakpoints were primarily assigned by simul

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