Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0162871 (abdominal aortic aneurysm)
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Plantains and bananas (Musa spp. sect. eumusa) originated from intra- and interspecific hybridization between two wild diploid species, M. acuminata Colla. and M. balbisiana Colla., which contributed the A and B genomes, respectively. Polyploidy and hybridization have given rise to a number of diploid, triploid, and tetraploid clones with different permutations of the A and B genomes. Thus, dessert and highland bananas are classified mainly as AAA, plantains are AAB, and cooking bananas are ABB. Classification of Musa into genomic groups has been based on morphological characteristics. This study aimed to identify RAPD (random amplified polymorphic DNA) markers for the A and B genomes. Eighty 10-mer Operon primers were used to amplify DNA from M. acuminata subsp. burmannicoides clone 'Calcutta 4' (AA genomes) and M. balbisiana clone 'Honduras' (BB genomes). Three primers (A17, A18, and D10) that produced unique genome-specific fragments in the two species were identified. These primers were tested in a sample of 40 genotypes representing various genome combinations. The RAPD markers were able to elucidate the genome composition of all the genotypes. The results showed that RAPD analysis can provide a quick and reliable system for genome identification in Musa that could facilitate genome characterization and manipulations in breeding lines.
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PMID:Identification of RAPD markers linked to A and B genome sequences in Musa L. 1108 65

The purpose of this study is to examine the plan quality and monitor unit with sliding window IMRT and RapidArc (RA) treatment plans using American Association Physicists in Medicine TG119 test suite DICOM-RT images and structure sets. The structure set includes multi-target (superior, central, inferior), prostate, head and neck and C-shape. Plans were performed with Eclipse planning system using AAA algorithm with the plan goals specified in TG119. The plan results for multitarget shows that the D99 is greater than the plan goal for all the targets. The D10 is less than the plan goal for superior and inferior targets in both IMRT and RA plans. The D10 is 5% more with IMRT plan and 7% more with RA plan for central target in comparison with plan goal. The plan results for prostate shows that D95 is greater than the plan goal for both IMRT and RA plans. The D5 is less than the plan goal for IMRT plan and almost equal to plan goal for RA plan. The D30 is less than the plan goal for bladder and rectum in both the plans. The D10 is higher than the plan goal by 1.9% and 2.5% in IMRT and RA plan for rectum. The plan results for head and neck shows that the D99 and D90 were greater than the plan goal for PTV. The spinal cord and parotid doses were less than the plan goal in both the plans. The plan results for C-shape shows that the D95 was greater than the plan goal and D10 was less than the plan goal for PTV. The dose to central core was less than the plan goal in both IMRT and RA plans. Both the IMRT and RapidArc plans have met the plan goal for all the target and normal structures. RapidArc optimization and treatment planning requires more time than the IMRT plan. The monitor unit calculated by the RapidArc plan is less compared to IMRT plan, which reduces the treatment error caused by patient motion during treatment and integral dose.
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PMID:Comparison of IMRT and Rapidarc treatment plans using AAPM task group test suites. 2172 24