Home About us Contact
|
Home About us Contact | ||
|
|
||
Mutual Exclusion (mutual + exclusion)
Selected AbstractsMutual exclusion of t(11;18)(q21;q21) and numerical chromosomal aberrations in the development of different types of primary gastric lymphomasBRITISH JOURNAL OF HAEMATOLOGY, Issue 4 2003Max I. Schreuder Summary., Gastric non-Hodgkin's lymphomas can be divided histologically into mucosa-associated lymphoid tissue (MALT) lymphoma (ML) and diffuse large cell lymphoma (DLCL) with or without evidence of preceding/accompanying ML (DLCL + ML). We studied the incidence of the most frequent structural chromosomal aberration in ML, t(11;18)(q21;q21), and numerical aberrations of seven chromosomes in 36 ML, 39 DLCL + ML and ten gastric DLCL cases, by dual-colour interphase fluorescence in situ hybridization (FISH) and reverse transcriptase polymerase chain reaction (RT-PCR). t(11;18)(q21;q21) was exclusively detected in ML (FISH 22%; RT-PCR 24%), being completely absent in DLCL + ML and DLCL. No other translocations involving 11q21 or 18q21 and other partner chromosomes were detected by FISH. In lymphomas harbouring t(11;18)(q21;q21), this translocation was the sole genetic abnormality. In contrast, 45% of the t(11;18)(q21;q21)-negative ML showed trisomies, especially of chromosome 3 and 18. In DLCL + ML with separate small and large cell components, trisomies were either detected in both components or occurred exclusively in large tumour cells. Our results suggest that ML can be divided in lymphomas characterized by the t(11;18)(q21;q21), which are unlikely to transform into high-grade tumours, and t(11;18)(q21;q21)-negative ML that may develop into DLCL + ML after the acquisition of additional genetic aberrations. [source] A robust monitor construct with runtime fault detection,CONCURRENCY AND COMPUTATION: PRACTICE & EXPERIENCE, Issue 5 2006Jiannong Cao Abstract The monitor concept provides a structured and flexible high-level programming construct to control concurrent accesses to shared resources. It has been widely used in a concurrent programming environment for implicitly ensuring mutual exclusion and explicitly achieving process synchronization. This paper proposes an extension to the monitor construct for detecting runtime errors in monitor operations. Monitors are studied and classified according to their functional characteristics. A taxonomy of concurrency control faults over a monitor is then defined. The concepts of a monitor event sequence and a monitor state sequence provide a uniform approach to history information recording and fault detection. Rules for detecting various types of faults are defined. Based on these rules, fault-detection algorithms are developed. A prototypical implementation of the proposed monitor construct with runtime fault detection mechanisms has been developed in Java. We shall briefly report our experience with and the evaluation of the robust monitor prototype. Copyright © 2005 John Wiley & Sons, Ltd. [source] Efficient probabilistic reasoning in BNs with mutual exclusion and context-specific independenceINTERNATIONAL JOURNAL OF INTELLIGENT SYSTEMS, Issue 8 2004Carmel Domshlak Prior work has shown that context-specific independence (CSI) in Bayes networks can be exploited to speed up belief updating. We examine how networks with variables exhibiting mutual exclusion (e.g., "selector variables"), as well as CSI, can be efficiently updated. In particular, directed-path singly connected and polytree networks that have an additional common selector variable can be updated in linear time (given null and general conjunctive evidence, respectively), where quadratic time would be needed without the mutual exclusion requirement. The above results have direct applications, as such network topologies can be used in predicting the ramifications of user selection in some multimedia data browsing systems. © 2004 Wiley Periodicals, Inc. Int J Int Syst 19: 703,725, 2004. [source] Null model analysis of communities on gradientsJOURNAL OF BIOGEOGRAPHY, Issue 6 2004James G. Sanderson Abstract Aim, I employed a novel null model and metric to uncover unusual species co-occurrence patterns in a herpetofaunal assemblage of 49 species collected at discrete elevations along a gradient. Location, Mount Kupe, Cameroon. Methods, Using a construction algorithm that started from a matrix of 0s, a sample null space of 25,000 unique null matrices was generated by simultaneously conserving (1) the number of occurrences of each species, (2) site richness and (3) species range spans derived from the observed incidence matrix. I then compared the number of times each pair of confamilial species co-occurred in the null space with the same number derived from the observed incidence matrix. Two cases dealing with embedded absences in species ranges were tested: (1) embedded absences were maintained, and (2) embedded absences were assumed to be sampling omissions and were replaced by presences. Results, In the observed absence/presence assemblage there were 147 possible confamilial species pairs. Therefore, 5% or eight were expected by chance alone to have co-occurrence patterns that differed from chance expectations by chance alone. Of these confamilial species pairs, 38 were congeneric and so 5% or two were expected to differ from chance expectations. For case (1) 16, and for case (2) 17 confamilial species pairs' co-occurrence patterns differed significantly from chance expectations. For case (1) nine congeneric species pairs, and for case (2) 10 congeneric pairs differed significantly from chance expectations. For case (1) four, and for case (2) five congeneric species pairs formed checkerboards (patterns of mutual exclusion). Results from case (1) were a proper subset of case (2) indicating that sampling omissions did not alter greatly the results. Main conclusions, I have demonstrated that null models are valuable tools to analyse ecological communities provided that proper models are employed. The choice of the appropriate null space to analyse distributions is critical. The null model employed to analyse birds on islands of an archipelago can be adapted to analyse species along gradients provided an additional range constraint is added to the null model. Moreover, added precision to results can be obtained by analysing each species pair separately, particularly those in the same family or genus, as opposed to applying a community-wide metric to the faunal assemblage. My results support some of the speculations of previous authors who were unable to demonstrate their suspicions analytically. [source] Biomechanical warfare in ecology; negative interactions between species by habitat modificationOIKOS, Issue 5 2007B. K. Van Wesenbeeck Since the introduction of the term ecosystem engineering by Jones et al. many studies have focused on positive, facilitative interactions caused by ecosystem engineering. Much less emphasis has been placed on the role of ecosystem engineering in causing negative interactions between species. Here, we report on negative interactions between two well known ecosystem engineers occurring at the interface of salt marsh and intertidal flat (i.e. common cordgrass Spartina anglica and lugworms Arenicolamarina), via modification of their joint habitat. A field survey indicated that, although both species share a common habitat, they rarely co-occur on small spatial scales (<1 m). Experiments in the field and in mesocosms reveal that establishment of small Spartina plants is inhibited in Arenicola -dominated patches because of low sediment stability induced by the lugworms. In turn, Arenicola establishment in Spartina -dominated patches is limited by high silt content, compactness and dense rooting of the sediment caused by Spartina presence. Our results show that negative interactions by modification of the environment can result in rapid mutual exclusion, particularly if adverse effects of habitat modification are strong and if both species exhibit positive feedbacks. This illustrates the potential for negative interactions via the environment to affect community composition. [source] | ||||||||||