ライフサイエンスコーパス: chromosome abnormality

1 some transmission is often associated with a chromosome abnormality.

2 of EMC with a t(9;17)(q22;q11.2) as the sole chromosome abnormality.

3 ited increased sister-chromatid exchange and chromosome abnormalities.

4 istinct genetic subgroups based on recurrent chromosome abnormalities.

5 ISH and PCR rapid tests for the detection of chromosome abnormalities.

6 rst-trimester miscarriages result from fetal chromosome abnormalities.

7 ogic correlations were associated with these chromosome abnormalities.

8 large number of subtypes defined by specific chromosome abnormalities.

9 diverse histopathology accompanied by severe chromosome abnormalities.

10 T cells with reduced Ikaros activity display chromosome abnormalities.

11 types, most often in association with other chromosome abnormalities.

12 igin of malignancies characterized by clonal chromosome abnormalities.

13 e identification of numerical and structural chromosome abnormalities.

14 Thirteen of 21 patients (62%) had additional chromosome abnormalities (ACAs); all coanalyzed PRalpha/

15 Sex chromosome abnormalities also have been observed to co-o

16 cyclin D1 overexpression is associated with chromosome abnormalities, although a causal effect has n

17 dy was designed to compare the prevalence of chromosome abnormalities among the offspring of women wi

18 leads to DNA replication stress, structural chromosome abnormalities and chromosome missegregation.

19 gly suggested by the association of CHD with chromosome abnormalities and high recurrence risk.

20 least 8% of all human conceptions have major chromosome abnormalities and the frequency of chromosoma

21 pressor gene responsible for the i12p marker chromosome abnormality and development of FISH probes fo

22 c mechanisms by which tumors evolve, such as chromosome abnormalities, and allow for heterogeneity be

23 Chromosome abnormalities are frequently associated with

24 We previously described a chromosome abnormality disrupting the kainate class iono

25 in the formation of structural or numerical chromosome abnormalities during meiosis.

26 er studies suggest that patients may acquire chromosome abnormalities during the course of their dise

27 Many chromosome abnormalities, especially translocations of i

28 NA replication fork progression and prevents chromosome abnormalities from occurring when DNA replica

29 high degree of heterogeneity with respect to chromosome abnormalities, gene mutations and changes in

30 Molecular characterization of recurrent chromosome abnormalities has identified new candidate on

31 gies for first-trimester screening for fetal chromosome abnormalities have improved the detection rat

32 tly dedicated to investigating the role of X chromosome abnormalities (i.e. monosomy rates and inacti

33 siblings and detailed molecular analyses of chromosome abnormalities identified in autistic subjects

34 omal translocation is one of the most common chromosome abnormalities identified in leukemia.

35 while CEM and drug-resistant cell lines had chromosome abnormalities in common, indicating a common

36 Chromosome abnormalities in humans are strikingly associ

37 Characterization of chromosome abnormalities in leukemia and lymphoma have c

38 g (NHEJ) is associated with the incidence of chromosome abnormalities in mutant rodent cells.

39 brain, but the cause and the consequence of chromosome abnormalities in the CNS are poorly defined.

40 wer of SKY in resolving the full spectrum of chromosome abnormalities in tumors.

41 the initial discovery of its disruption by a chromosome abnormality in a person with schizophrenia, w

42 The t(8;21) chromosome abnormality in acute myeloid leukemia targets

43 Aneuploidy is the most common chromosome abnormality in humans, and is the leading gen

44 Chromosome abnormalities include highly aberrant structu

45 n increase in spontaneous and damage-induced chromosome abnormalities including the frequency of trir

46 Prenatal diagnosis for chromosome abnormality is routinely undertaken by full k

47 er is lagging behind the discoveries made on chromosome abnormalities of prostate cancer.

48 elative to CIN(-) CRC cells, with structural chromosome abnormalities precipitating chromosome misseg

49 e, leukocyte count at the time of diagnosis, chromosome abnormalities, remission status, or length of

50 lect for hepatocytes with specific numerical chromosome abnormalities, rendering them differentially

51 Chromosome abnormalities resulting in gene fusions are c

52 this disorder are heterogeneous and include chromosome abnormalities, single gene disorders, and ter

53 rom Bloom's syndrome cells results in severe chromosome abnormalities, such that sister chromatids re

54 to understand the recombination patterns for chromosome abnormalities, there is a lack of multilocus

55 th chemotherapy, the presence of a secondary chromosome abnormality was associated with longer comple

56 a likely fate of embryonic NPCs with severe chromosome abnormalities, was observed only in Xrcc5-/-

57 ught to clear newly postmitotic neurons with chromosome abnormalities, we found a 38% increase in the

58 responsible for this heterogeneous class of chromosome abnormality, we coupled high-resolution array

59 uced in cells from surrounding regions, many chromosome abnormalities were discernable.

60 ly 40% of UL have non-random, tumor-specific chromosome abnormalities which have allowed classificati