Sentence examples for acquisition of defects from inspiring English sources

Exact(2)

1) The acquisition of defects in HSCs is regulated by the peripheral demands for B-cell.

It is believed that the acquisition of defects in the regulation of these processes is important in the process of carcinogenesis.

Similar(58)

The reconstruction of defect profiles based on ultrasonic guided waves means the acquisition of defect profiles and parameters from ultrasonic guided wave inspection signals, and it is the key for the inversion of ultrasonic guided waves.

The transformation process is often associated with the acquisition of additional defects (e.g. del6p as demonstrated in patient #29, or micro-deletions of chromosomes 4 and 19 as demonstrated in patient #38).

Therefore, CHFR inactivation is expected to participate in the acquisition of chromosomal defects and a chromosomal instability phenotype in cancer.

All cancers result from the cumulative acquisition of molecular defects within a basic core of cellular functions that control proliferation, apoptosis, and invasiveness (Hanahan and Weinberg, 2000).

Alternatively, the distinct nuclear contexts occupied by DAZ and DAZL during male meiosis (XY body versus fully paired bivalents, respectively) may underlie a different propensity for the acquisition of epigenetic defects between both determinants.

Although the role of DNA damage and the DDR in this process has not been extensively explored experimentally, increased genomic instability due to the acquisition of DDR defects has been proposed to play a role in the acquisition of these traits based on human patient data (Halazonetis et al., 2008).

Therefore, the premise of combining olaparib and bevacizumab is based on the rationale that direct targeting of PARP by olaparib and indirect sensitisation to olaparib by acquisition of HR defects by bevacizumab will be therapeutically beneficial, and pragmatism as bevacizumab is incorporated into standard-of-care treatments in tumour types that PARP inhibitors have potential to be effective.

Although strictly speaking not required for an approach in which chimeras serve as an endpoint, we decided to maintain this quality control as a means to identify ESC clones with impaired germline-competence caused by loss of pluripotency or the acquisition of genetic defects during culture and manipulation.

By the age of 60 years, 90% of patients will have developed refractory cytopenia and multilineage dysplasia that meets standard criteria and is often associated with the acquisition of additional genetic defects.

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