Sentence examples for Two dba from inspiring English sources

Following that, two DBA algorithms are designed for object-based coding quality control in which weighted bits are allocated to prioritized single or group of video objects.

We predict the wallaby has four DBB genes, one DAA gene and two DBA genes.

Only a single DAA gene was identified 1 Mb away from the cluster of DAB genes and two DBA genes were identified.

MHC class II genes are found on nine of the sequenced BACs and include at least one DMA, one DMB, seven DAB, four DBB, one DAA and two DBA genes.

For performance evaluation in terms of average delay, average queue size, loss rate and utilization, five DBA schemes are simulated, namely AP-Sort DBA, interleaved polling with adaptive cycle time (IPACT), dynamic bandwidth allocation with a modified grant table generation algorithm and fair-excess allocation (DBA2-FE), Sort-DBA and double phase polling algorithm (DPA).

Only one of these five DBA patients is alive.

We analyzed the p53 pathway in erythroid cells from six DBA patients – three with mutant RPS19 (RPS19+/mut) and three with mutant RPL11 (RPL11+/Mut).

This study was performed on four DBA patients, carrying two missense (p.Arg62Trp and p.Arg101His), one frameshift and a splice site mutations (c.58delG and c.1-1G>A), respectinely, in RPS19.

We analysed the gene expression profiles of dermal fibroblasts isolated from four DBA patients carrying mutations in RPS19, in comparison to those obtained from six healthy individuals.

Dermal biopsies were obtained from the four DBA patients and from six healthy controls after informed consent during surgery for medical reasons that were not connected with this study.

Abnormal expression of genes related to apoptosis was also reported in bone marrow CD34+ cells isolated from three DBA patients with mutations in RPS19 and in remission from the disease (Gazda et al., 2006), and in a previous study by our group focused on unraveling the gene expression alterations in fibroblasts isolated from DBA patients with RPS19 mutations (Avondo et al., 2009).