ライフサイエンスコーパス: chromosome deletion

1 sity (LOH) in developing lymphocytes through chromosome deletion.

2 identified in about 70% of individuals with chromosome deletion.

3 nt(s) of virtually any naturally occurring Y chromosome deletion.

4 was previously shown to be amorphic using a chromosome deletion.

5 ency events such as oligonucleotide-mediated chromosome deletions.

6 1 have short telomeres and elevated rates of chromosome deletions.

7 12 Dm3 mutations were associated with large chromosome deletions.

8 s and high resolution mapping using a set of chromosome deletions.

9 r consequences of "simple" cancer-associated chromosome deletions.

10 Chromosome deletion and microdeletion syndromes account

11 me cancers have a specific tendency to whole-chromosome deletion and regain or to mitotic recombinati

12 ide transposition events but instead yielded chromosome deletion and translocation events involving t

13 To circumvent this problem, we used chromosome deletions and duplications from D. melanogast

14 ed very high rates of aneuploidy, as well as chromosome deletions and duplications.

15 deletion, we examined a panel of men with Y chromosome deletions and known testicular pathologies us

16 a new approach to develop animal models with chromosome deletions, and a potential therapeutic strate

17 Chromosome deletions are the most common genetic events

18 Y chromosome deletions arise frequently in human populatio

19 This approach demonstrates the utility of chromosome deletions as reagents for mapping and charact

20 transcript exon in a previously described X chromosome deletion associated with autism, and the cere

21 In patients with chromosome deletion at the FZD9 locus, aberrant methylat

22 ng evidence for the non-random clustering of chromosome deletion breakpoints with CCG-repeats, and su

23 ved in the mouse, we were able to engineer a chromosome deletion (Df1) spanning a segment of the muri

24 We used chromosome deletion/duplication and P element insertion

25 In most of the common chromosome deletion/duplication syndromes, the rearrange

26 Chromosome deletions, duplications and inversions can be

27 es undergo breakage in mitosis, resulting in chromosome deletions, duplications, and translocations.

28 These studies demonstrate the utility of chromosome deletions for complex trait analysis.

29 ved when the wild-type allele was removed by chromosome deletion from the E2A heterozygous mice, a re

30 Chromosome deletions have several applications in the ge

31 monstrated the effectiveness of Cre-mediated chromosome deletion in the LOH assay for HEB function in

32 unts of 40 000-100 000 per mL, we detected Y-chromosome deletions in leucocyte DNA similar in locatio

33 In the two men in whom Y-chromosome deletions in leucocyte DNA were detected, we

34 The Y-chromosome deletions in these two men are de-novo mutati

35 in 11q23.3, FRA11B, has been shown to cause chromosome deletions in vivo, its expression being assoc

36 Females with partial X-chromosome deletions, in whom this critical locus is del

37 Mice bearing an X chromosome deletion of Hdac6 (Hdac6-/Y) and MTECs from t

38 In addition, duplications of the X chromosome, deletions of chromosomes 9 and 10, and trans

39 In the remaining four cases, X-chromosome deletions prevented interpretation (n = 3), o

40 Thus, the Cre-mediated chromosome deletion provides a new and effective method

41 When present as a single copy in the chromosome, deletions removing as few as two amino acids

42 erm DNA was tested, and it showed the same Y-chromosome deletion seen in leucocytes.

43 were ordered using the P1-derived artificial chromosome deletion series.

44 on of abnormal spermatogenesis in men with Y chromosome deletions suggests that genes important for s

45 In 10-15% of cases, Y chromosome deletions that encompass critical spermatogen

46 hese intervals are defined by interstitial Y-chromosome deletions that impair or extinguish spermatog

47 that aberrant methylation can cooperate with chromosome deletions to silence TSG.

48 y epithelial cell line NOG8 to create random chromosome deletion/translocation.

49 Chromosome deletion was triggered by Cre/loxP-mediated i

50 No Y-chromosome deletions were detected in the fathers of the

51 The heterozygous chromosome deletion within the band 22q11 (del22q11) is

52 , five lines of outbred XY(d) females with Y chromosome deletions Y(Del(Y)1Ct)-Y(Del(Y)5Ct) that depl