Results 121 to 130 of about 231,256 (313)
In the present work, we have identified a transcriptional signature based on the differential expression of six genes (BCL2&MAST4, HSH2D&LAT2, METRN&PITPNM2) that would facilitate the early detection of T‐cell acute lymphoblastic leukemia (T‐ALL) patients prone to a poor treatment response and could be implemented at diagnosis, along with other risk ...
Antonio Lahera +11 more
wiley +1 more source
Optimal designs for estimating critical effective dose under model uncertainty in a dose response study [PDF]
Toxicologists have been increasingly using a class of models to describe a continuous response in the last few years. This class consists of nested nonlinear models and is used for estimating various parameters in the models or some meaningful function ...
Shpilev, Piter +3 more
core +2 more sources
An Equivalence Theorem and A Sequential Algorithm for A-Optimal Experimental Designs on Manifolds
Selecting input data points in the context of high-dimensional, nonlinear, and complex data in Riemannian space is challenging. While optimal experimental design theory is well-established in Euclidean space, its extension to Riemannian manifolds remains
Jingwen Zhang, Yaping Wang
doaj +1 more source
EXOSC10, an essential nuclear RNA exosome‐associated 3′‐5′ exoribonuclease, is inhibited by the anticancer drug 5‐fluorouracil (5‐FU), and EXOSC10 depletion increases 5‐FU sensitivity. The colon‐cancer variant EXOSC10S402T, located in a proteolysis motif, is stable and nuclear but nonfunctional in vivo.
Radhika Sain +10 more
wiley +1 more source
D-optimal Design for Polynomial Regression: Choice of Degree and Robustness [PDF]
In this paper we show that for D-optimal design, departures from the design are much less important than a depar-ture from a model. As a consequence, we propose, based on D-optimality, a rule for choosing the regression degree.
Weinberg Allen, Anna, Antille, Gerard
core
We analyze cisplatin–DNA adducts (CDAs) and double‐strand breaks (DSBs) in a cell‐cycle‐dependent manner. We find that CDAs form similarly across all cell cycle phases. DSBs arise only in S‐phase. CDAs might not directly impair DSB repair, but S‐phase DSB lesions evolve in the presence of CDAs and disrupt repair in G2, also causing radiosensitization ...
Ye Qiu +10 more
wiley +1 more source
Maximin and Bayesian optimal designs for regression models [PDF]
For many problems of statistical inference in regression modelling, the Fisher information matrix depends on certain nuisance parameters which are unknown and which enter the model nonlinearly.
Dette, Holger +2 more
core
Intratumour heterogeneity complicates precision management of advanced endometrial cancer. Circulating tumor DNA (ctDNA) offers a minimally invasive strategy to capture tumor evolution and therapeutic resistance. Here, we compare tumor‐agnostic NGS with tumor‐informed ddPCR, outlining their relative sensitivity, concordance, and clinical implications ...
Carlos Casas‐Arozamena +15 more
wiley +1 more source
Optimal designs for dose finding experiments in toxicity studies [PDF]
We construct optimal designs for estimating fetal malformation rate, prenatal death rate and an overall toxicity index in a toxicology study under a broad range of model assumptions.
Dette, Holger +2 more
core
Sequences Converging to $D$-Optimal Designs of Experiments
Fedorov (Theory of Optimal Experiments (1972)) gives a sequence of designs converging to a $D$-optimal design. Several modifications of that sequence are given to improve the speed of convergence. The analogous sequence for estimating some of the parameters is shown to converge to a $D$-optimal design, whether or not all the parameters are estimable ...
openaire +2 more sources

