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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 diverse histopathology accompanied by severe chromosome abnormalities.
9 T cells with reduced Ikaros activity display chromosome abnormalities.
10 large number of subtypes defined by specific 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 k degradation induces DNA breaks and various chromosome abnormalities.
15 Thirteen of 21 patients (62%) had additional chromosome abnormalities (ACAs); all coanalyzed PRalpha/
16                                          Sex chromosome abnormalities also have been observed to co-o
17  cyclin D1 overexpression is associated with chromosome abnormalities, although a causal effect has n
18 dy was designed to compare the prevalence of chromosome abnormalities among the offspring of women wi
19 nactivation of p53 signaling, which leads to chromosome abnormalities and aggressive phenotypes.
20  leads to DNA replication stress, structural chromosome abnormalities and chromosome missegregation.
21 gly suggested by the association of CHD with chromosome abnormalities and high recurrence risk.
22 least 8% of all human conceptions have major chromosome abnormalities and the frequency of chromosoma
23 pressor gene responsible for the i12p marker chromosome abnormality and development of FISH probes fo
24 c mechanisms by which tumors evolve, such as chromosome abnormalities, and allow for heterogeneity be
25                                              Chromosome abnormalities are frequently associated with
26 undamental insight into the origins of human chromosome abnormalities, as well as a practical tool wi
27                    We previously described a chromosome abnormality disrupting the kainate class iono
28  in the formation of structural or numerical chromosome abnormalities during meiosis.
29 er studies suggest that patients may acquire chromosome abnormalities during the course of their dise
30                                         Many chromosome abnormalities, especially translocations of i
31  for the ability of ETAA1 to prevent mitotic chromosome abnormalities following replicative stress.
32 NA replication fork progression and prevents chromosome abnormalities from occurring when DNA replica
33 high degree of heterogeneity with respect to chromosome abnormalities, gene mutations and changes in
34      Molecular characterization of recurrent chromosome abnormalities has identified new candidate on
35 gies for first-trimester screening for fetal chromosome abnormalities have improved the detection rat
36 was enriched for participants with high-risk chromosome abnormalities (HRCAs).
37 tly dedicated to investigating the role of X chromosome abnormalities (i.e. monosomy rates and inacti
38  siblings and detailed molecular analyses of chromosome abnormalities identified in autistic subjects
39 omal translocation is one of the most common chromosome abnormalities identified in leukemia.
40  underlies elevated rates of infertility and chromosome abnormalities in children of older women.
41  while CEM and drug-resistant cell lines had chromosome abnormalities in common, indicating a common
42                                              Chromosome abnormalities in humans are strikingly associ
43                          Characterization of chromosome abnormalities in leukemia and lymphoma have c
44 g (NHEJ) is associated with the incidence of chromosome abnormalities in mutant rodent cells.
45  brain, but the cause and the consequence of chromosome abnormalities in the CNS are poorly defined.
46 wer of SKY in resolving the full spectrum of chromosome abnormalities in tumors.
47 the initial discovery of its disruption by a chromosome abnormality in a person with schizophrenia, w
48                                  The t(8;21) chromosome abnormality in acute myeloid leukemia targets
49          Trisomy 12 is the most common whole-chromosome abnormality in human pluripotent stem cells.
50                Aneuploidy is the most common chromosome abnormality in humans, and is the leading gen
51                                              Chromosome abnormalities include highly aberrant structu
52 n increase in spontaneous and damage-induced chromosome abnormalities including the frequency of trir
53                       Prenatal diagnosis for chromosome abnormality is routinely undertaken by full k
54 er is lagging behind the discoveries made on chromosome abnormalities of prostate cancer.
55 elative to CIN(-) CRC cells, with structural chromosome abnormalities precipitating chromosome misseg
56 e, leukocyte count at the time of diagnosis, chromosome abnormalities, remission status, or length of
57 lect for hepatocytes with specific numerical chromosome abnormalities, rendering them differentially
58                                              Chromosome abnormalities resulting in gene fusions are c
59 , reduced RAD51 focus formation, spontaneous chromosome abnormalities, sensitivity to PARP inhibitors
60  this disorder are heterogeneous and include chromosome abnormalities, single gene disorders, and ter
61 rom Bloom's syndrome cells results in severe chromosome abnormalities, such that sister chromatids re
62 to understand the recombination patterns for chromosome abnormalities, there is a lack of multilocus
63 Mosaicism involving numerical and structural chromosome abnormalities was detected in 82% of the embr
64 th chemotherapy, the presence of a secondary chromosome abnormality was associated with longer comple
65  a likely fate of embryonic NPCs with severe chromosome abnormalities, was observed only in Xrcc5-/-
66 ught to clear newly postmitotic neurons with chromosome abnormalities, we found a 38% increase in the
67  responsible for this heterogeneous class of chromosome abnormality, we coupled high-resolution array
68 uced in cells from surrounding regions, many chromosome abnormalities were discernable.
69 ly 40% of UL have non-random, tumor-specific chromosome abnormalities which have allowed classificati