ライフサイエンスコーパス: copy number abnormality

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1 s were found to bias the spectrum of genomic copy number abnormalities.

2 to detect allelic imbalance and chromosomal copy number abnormalities.

3 r laboratory for array CGH and found to have copy-number abnormalities.

4 The frequency of specific copy number abnormalities [+4, del(6q23.3-6q25.3), +12,

5 rofiles were correlated with genome-wide DNA copy number abnormalities and clinical and outcome featu

6 molecular level, myeloma is characterized by copy number abnormalities and recurrent translocations i

7 tions/deletions, chromosomal translocations, copy number abnormalities, and zygosity changes in a sin

8 We identify two loci where copy number abnormalities are correlated with poor survi

9 he rate of diagnosis of patients with genome copy number abnormalities as the cause of developmental

10 rom 45 AA and 196 EA MM patients for somatic copy number abnormalities associated with poor outcome.

11 Plots of BAC end-sequences density identify copy number abnormalities at high resolution.

12 In this study, we compared the genome-wide copy number abnormalities between 29 human and 10 canine

13 mutations by PCR-capillary sequencing, EGFR copy number abnormalities by fluorescence and chromogeni

14 The most commonly shared copy number abnormalities (CNAs) in all types were losse

15 a Wnt pathway signature and those harboring copy number abnormalities (CNAs) of potential prognostic

16 Copy number abnormalities (CNAs) represent an important

17 Copy number abnormalities (CNAs) such as somatically-acq

18 precursor ALL, we evaluated gene expression, copy number abnormalities (CNAs), and DNA methylation.

19 genomic hybridization (aCGH) to investigate copy number abnormalities (CNAs), one of the most promin

20 pically showed different patterns of genomic copy number abnormalities (CNAs), with the CNAs acquired

21 The number of copy number abnormalities does not correlate with the la

22 arative genomic hybridization summarizes DNA copy number abnormalities in a tumor by mapping them to

23 To determine genomewide miRNA DNA copy number abnormalities in cancer, 283 known human miR

24 describes analyses of associations of genome copy number abnormalities in ovarian cancers with clinic

25 genetic lesions affecting the same genes or copy number abnormality in different subclones.

26 yses have identified a high frequency of DNA copy-number abnormalities in ALL, but the prognostic imp

27 Finally, we identified high frequency copy number abnormalities of Dicer1, Argonaute2, and oth

28 Subsequent analysis pinpoints suspected DNA copy number abnormalities of specific samples and chromo

29 Copy number abnormalities play an important role in pati

30 Thus, detection and mapping of copy number abnormalities provide an approach for associ

31 Frequent copy number abnormalities targeting cancer-associated ge

32 A copy-number abnormality was identified as a predictor of

33 Using copy-number abnormalities, we identified a predictor of

34 DNA copy number abnormalities were identified using microarr

35 More than 50 recurring copy-number abnormalities were identified, most commonly

36 We found two classes of copy number abnormalities: whole chromosome and partial

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