Sentence examples similar to fusion and breaking from inspiring English sources

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Chávez's vision is not about outdated Western political and economic models; it is about creating revolutionary 'fusion' and breaking new ground.

A 20% cut-off was used for numerical abnormalities and 10% for fusions and break-apart probes as recommended by the European Myeloma Network FISH workshop guidelines http://www.myeloma-europe.org.org

All those three patients were also positive in FISH for both KIF5B-RET fusion and RET break-apart probes.

SQSTM1/p62 is a multifunctional adaptor protein that recruits ubiquitinated proteins and organelles to LC3II to be taken into the autophagosome and broken down after lysosome fusion [ 1, 28].

There are N (N >= 20000) protein coding genes in the human genome, even if we only consider situation of paired gene fusion breaking points occurring in both original coding regions, N2 possibilities are not acceptable.

To control the scale of the database, at this stage we only considered the situation of fusion breaking points falling into intron regions, since if the break point falls in one exon region, each different location would generate a different translation frame.

Jews and African-Americans in Hollywood and Chicago where I spent my childhood related and spent time together, worked together toward collective goals and it is only now in retrospect that this fusion seems broken.

Moreover, knockout of p53 can cause or increase chromosome end-to-end fusions and chromosomal breaks in the reprogrammed MEFs compared to wild-type iPSCs [ 55].

Do not visit an osteopath if you have a spinal fusion, osteoporosis, broken bones, bone cancer, an infection or damaged ligaments in addition to your back pain.

The concurrent involvement of MYC proto-oncogene and TCRA/D genes was confirmed by FISH on metaphases exposed to LSI MYC/IGH/CEP8 tricolor dual fusion and LSI MYC and TCRA/D break apart Vysis probes: t(8 14)(D8Z1+,5′ MYC+,3′ TCRA/D+5′ TCRA/D+,3′ MYC+)[10].

Prior breakpoint sequence analysis of the D13 GCR indicated it was a fusion between a broken chromosome V and the telomere of another chromosome, and consistent with this PFGE analysis revealed that the size of this rearranged chromosome was 1,500 Kb (Figure 4A and Table 1).

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