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1 seful tool for chromosome identification and karyotype analysis.
2 rearrangements could be detected by standard karyotype analysis.
3 nd numerical chromosomal integrity by banded karyotype analysis.
4 or numerical chromosome changes based on SKY karyotyping analysis.
5  secondary genetic events, by using spectral karyotyping analysis.
6 mined by metaphase spread assay and spectral karyotyping analysis.
7 analysis yielded results more often than did karyotype analysis (87.4% vs. 70.5%, P<0.001) and provid
8         Using electrophoretic techniques for karyotype analysis, a highly dimorphic chromosome pair t
9                                          For karyotype analysis, a pool of human chromosome painting
10 ons in either the VHL or Ras genes, although karyotype analysis and chromosome painting revealed the
11                                              Karyotype analysis and fluorescence in situ hybridizatio
12 nomic hybridization (CGH) studies, Q-banding karyotype analysis, and autofusions of representative cl
13 ssessment of pluripotency factor expression, karyotype analysis, and pathogen/sterility testing was c
14                                              Karyotype analysis confirmed that this sequence was pres
15                                              Karyotype analysis coupled with fluorescence in situ hyb
16                       DNA fingerprinting and karyotype analysis demonstrated that immortalized hVFE w
17  trisomy index from pooled cytogenetic data (karyotype analysis) from 2 large cohorts of patients wit
18                                     Spectral karyotype analysis identified approximately 33% of neuro
19                                              Karyotype analysis indicated that cells lacking one copy
20                                  Single-cell karyotype analysis indicates that these CNVs appear to a
21 ine models of human carcinogenesis, however, karyotype analysis is technically demanding because mous
22                                       Unlike karyotype analysis, microarray analysis does not require
23                             As compared with karyotype analysis, microarray analysis provided a relat
24                                      In eSNP karyotyping analysis, none of the predicted copy number
25                     Using aCGH, we performed karyotype analysis of 33 small cell lung cancer (SCLC) t
26  abnormality is routinely undertaken by full karyotype analysis of chromosomes from cultured cells; p
27 ybridization for the X and Y chromosomes and karyotype analysis of cultured osteoblasts confirmed the
28                                    Metaphase karyotype analysis of fetal cells obtained by amniocente
29                                              Karyotype analysis of hTERT corneal fibroblasts identifi
30  SKY substantially improves the precision of karyotype analysis of malignant cells, which in turn lea
31                                              Karyotype analysis of MSCs revealed the development of t
32                                              Karyotype analysis of the S(10:11) generation detected a
33                        Furthermore, spectral karyotype analysis of the tumors shows that the tumors h
34                                              Karyotype analysis of three of the cell lines revealed t
35                          Based on marker and karyotype analysis of tumor samples, a significant fract
36 hromosomes in the primary tumor and spectral karyotyping analysis of derived cell lines identify chro
37                                     Spectral karyotyping analysis of metaphase chromosomes from prima
38 ARA in leukemogenesis, we performed spectral karyotyping analysis of myeloid leukemias from hMRP8-PML
39 operate with PML-RARA, we performed spectral karyotyping analysis of myeloid leukemias from transgeni
40                                The pillar of karyotype analysis rests on chromosome banding technique
41 mparative genomic hybridization and spectral karyotype analysis reveal that genomic copy number loss
42 terized Pr1A subtilisin of M. anisopliae and karyotype analysis revealed that Pr1A and Pr1B are locat
43                                              Karyotype analysis revealed that this phenotype was sign
44                                  Comparative karyotyping analysis revealed that chromosome organizati
45                                     G-banded karyotype analysis should be reserved for patients with
46                                     Spectral karyotype analysis showed frequent intrachromosomal fusi
47                                              Karyotype analysis showed that increased chromosome numb
48                                              Karyotype analysis showed that the cells were of human a
49    Consistent with this hypothesis, spectral karyotype analysis (SKY) of lymphomas derived from Lck-B
50 chromosomal aberrations as shown by spectral karyotyping analysis, suggesting changes beyond neu sign
51      Microarray analysis is more likely than karyotype analysis to provide a genetic diagnosis, prima
52                                           By karyotype analysis, two independently derived cell lines
53 me instability might drive tumour evolution, karyotype analysis using single-cell sequencing technolo
54 o transfer cycles of 692 women who underwent karyotyping analysis using Giemsa-Trypsin-Leishman (GTL)
55 gement of the 24 blocks can be obtained from karyotype analysis via comparative chromosome painting e
56                                    Follow-up karyotype analysis was done on all samples.
57 e lymphoblastic leukemia of infancy in which karyotype analysis was technically unsuccessful and did
58                                              Karyotype analysis, which includes identifying aneuploid
59       This notion was confirmed by molecular karyotype analysis, which revealed gross chromosomal alt