4,874 research outputs found
Pre-therapy process and outcome: A review of research instruments and findings
Pre-Therapy aims at stimulating psychological contact in persons suffering psychosis. We offer a review of Pre-Therapy research instruments and findings. The Pre-Therapy Rating Scale (PTRS, Prouty, 1994) and the Evaluation Criterion for the Pre-Therapy Interview (ECPI, Dinacci, 1997) have been the two most frequently used instruments for the assessment of psychological contact. PTRS scores seem more reliable than ECPI scores, but all manuals need revision. Particular attention is needed for the rating of nonverbal behavior. A preliminary evaluation of the structure of the PTRS indicates that it is two-dimensional rather than three-dimensional. The PTRS and the ECPI can be regarded as measures of communicative contact but also as measures of the meaningfulness of communication. Preliminary outcome studies suggest that pre-post and comparative effect sizes of Pre-Therapy are large for communicative contact, but the number of participants in these studies is generally low, as is the number of systematic case studies
Tiled QR factorization algorithms
This work revisits existing algorithms for the QR factorization of
rectangular matrices composed of p-by-q tiles, where p >= q. Within this
framework, we study the critical paths and performance of algorithms such as
Sameh and Kuck, Modi and Clarke, Greedy, and those found within PLASMA.
Although neither Modi and Clarke nor Greedy is optimal, both are shown to be
asymptotically optimal for all matrices of size p = q^2 f(q), where f is any
function such that \lim_{+\infty} f= 0. This novel and important complexity
result applies to all matrices where p and q are proportional, p = \lambda q,
with \lambda >= 1, thereby encompassing many important situations in practice
(least squares). We provide an extensive set of experiments that show the
superiority of the new algorithms for tall matrices
Cell cycle specific radiosensitisation by the disulfiram and copper complex
The disulfiram and copper complex (DSF:Cu) has emerged as a potent
radiosensitising anti-cancer agent. The ability of copper to stabilise DSF in a planar
conformation and to inhibit DNA replication enzymes stimulated our investigation of
the effect of DSF:Cu on cell cycle regulation. Flow cytometry and immunoblotting were
used to assess the effect of DSF:Cu on cell cycle progression of the neuroblastoma cell
line SK-N-BE(2c) and the glioma cell line UVW. Treatment with 0.1 and 0.3 μM DSF:Cu
inhibited DNA synthesis in SK-N-BE(2c) and UVW cells, respectively. The increased
potency of ionising radiation treatment induced by DSF:Cu and/or gemcitabine was
determined by clonogenic assay. Treatment with 0.3 μM DSF:Cu resulted in greater
radiation kill, exemplified by dose enhancement factor values of 2.64 and 2.84 in SKN-BE(2c)
and UVW cells, respectively. Although DSF:Cu failed to sensitise S phase
cells to irradiation, we observed that DSF:Cu radiosensitisation was potentiated by
the S phase-specific cytotoxic drug gemcitabine. The efficacy of the combination
treatment consisting of DSF:Cu, gemcitabine and ionising radiation was scheduledependent.
Together, these results describe cell cycle specific radiosensitisation by
DSF:Cu. The well-established toxicity profiles of DSF and gemcitabine should facilitate
their evaluation as a combination treatment in patients undergoing radiotherapy
Extracting partition statistics from semistructured data
The effective grouping, or partitioning, of semistructured data is of fundamental importance when providing support for queries. Partitions allow items within the data set that share common structural properties to be identified efficiently. This allows queries that make use of these properties, such as branching path expressions, to be accelerated. Here, we evaluate the effectiveness of several partitioning techniques by establishing the number of partitions that each scheme can identify over a given data set. In particular, we explore the use of parameterised indexes, based upon the notion of forward and backward bisimilarity, as a means of partitioning semistructured data; demonstrating that even restricted instances of such indexes can be used to identify the majority of relevant partitions in the data
Pressure buildup during CO2 injection in brine aquifers using the Forchheimer equation
If geo-sequestration of CO2 is to be employed as a key emissions reduction method in the global effort to mitigate climate change, simple yet robust screening of the risks of disposal in brine aquifers will be needed. There has been significant development of simple analytical and semi-analytical techniques to support screening analysis and performance assessment for potential carbon sequestration sites. These techniques have generally been used to estimate the size of CO2 plumes for the purpose of leakage rate estimation. A common assumption has been that both the fluids and the geological formation are incompressible. Consequently, calculation of pressure distribution requires the specification of an arbitrary radius of influence. In this talk, a new similarity solution is derived using the method of matched asymptotic expansions. By allowing for slight compressibility in the fluids and formation, the solution improves on previous work by not requiring the specification of an arbitrary radius of influence. A large-time approximation of the solution is then extended to account for non-Darcy inertial effects using the Forchheimer equation. Both solutions are verified by comparison with finite difference solutions. The results show that inertial losses will often be comparable, and sometimes greater than, the viscous Darcy-like losses associated with the brine displacement, although this is strongly dependent on formation porosity and permeability
Evaluation of melanin-targeted radiotherapy in combination with radiosensitizing drugs for the treatment of melanoma
The incidence of malignant melanoma is rising faster than that of any other cancer in the United States. An [131I]-labeled benzamide - [131I]MIP-1145 - selectively targets melanin, reduces melanoma tumor burden and increases survival in preclinical models. Our purpose was to determine the potential of radiosensitizers to enhance the anti-tumor efficacy of [131I]MIP-1145. Melanotic (A2058) and amelanotic (A375 and SK-N-BE(2c)) cells were treated with [131I]MIP-1145 as a single agent or in combination with drugs with radiosenitizing potential. Cellular uptake of [131I]MIP-1145 and toxicity were assessed in monolayer culture. The interaction between radiosensitizers and [131I]MIP-1145 was evaluated by combination index analysis in monolayer cultures and by delayed growth of multicellular tumor spheroids. [131I]MIP-1145 was taken up by and was toxic to melanotic cells but not amelanotic cells. Combination treatments comprising [131I]MIP-1145 with the topoisomerase inhibitor topotecan or the PARP-1 inhibitor AG014699 resulted in synergistic clonogenic cell kill and enhanced delay of the growth of spheroids derived from melanotic melanoma cells. The proteasome inhibitor bortezomib had no synergistic cytotoxic effect with [131I]MIP-1145 and failed to enhance the delay of spheroid growth. Following combination treatment of amelanotic cells, neither synergistic clonogenic cell kill nor enhanced growth delay of spheroids was observed
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