8,606 research outputs found
RIC-HSCT for MF/SS
Advanced-stage mycosis fungoides and Sezary syndrome (MF/SS) have a poor prognosis. Allogeneic hematopoietic stem cell transplantation (HSCT), particularly using a reduced-intensity conditioning (RIC) regimen, is a promising treatment for advanced-stage MF/SS. We performed RIC-HSCT in nine patients with advanced MF/SS. With a median follow-up period of 954days after HSCT, the estimated 3-year overall survival was 85.7% (95% confidence interval, 33.4-97.9%) with no non-relapse mortality. Five patients relapsed after RIC-HSCT; however, in four patients whose relapse was detected only from the skin, persistent complete response was achieved in one patient, and the disease was manageable in other three patients by the tapering of immunosuppressants and donor lymphocyte infusion, suggesting that graft-versus-lymphoma effect and "down-staging" effect from advanced stage to early stage by HSCT improve the prognosis of advanced-stage MF/SS. These results suggest that RIC-HSCT is an effective treatment for advanced MF/SS
Genotypic status of mF fibroblasts.
A) Alignment of one base substitution in murine mF fibroblasts (fibro-apc-mute track) versus murine nF fibroblasts (fibro-normal track) by the Integrative Genomics Viewer (IGV) and graphic report showed detection of the mutation. B) VEP analysis and Web results (summary pie charts with statistics and results table) of base substitution in murine mF fibroblasts. Only mutations (divided in categories based on their predicted impact on protein functions using snpEff (Cingolani et al, 2012) and classified ‘‘high” (“The variant was assumed to have disruptive impact in the protein, probably causing protein truncation, loss of function or triggering nonsense mediated decay”) were considered. Alignment of one base substitution in murine mF fibroblasts (fibro-apc-mute track) versus murine nF fibroblasts (fibro-normal track) by the Integrative Genomics Viewer (IGV) and graphic report shows detection of the mutation. C) Western blot analysis showing the truncated APC protein (~100 kDa) in mF fibroblasts, nF fibroblasts, Co cells and in Min/+ mouse intestine. Cingolani P., Platts A., Wang LL., Coon M., Nguyen T., Wang, L., Land SJ., Lu X. and Ruden DM. (2012). A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff. Fly (Austin) 6, 80–92. (TIF)</p
Sign Retention in Classical MF-DFA
In this paper, we propose a one-dimensional (1D) multifractal sign retention detrending fluctuation analysis algorithm (MF-S-DFA). The proposed method is based on conventional multifractal detrending fluctuation analysis (MF-DFA). As negative values may exist in the calculation in the original MF-DFA model, sign retention is considered to improve performance. We evaluate the two methods based on time series constructed by p-model multiplication cascades. The results indicate that the generalized Hurst exponent H(q), the scale exponent τ(q) and the singular spectrum f(α) estimated by MF-S-DFA behave almost consistently with the theoretical values. Moreover, we also employ distance functions such as DH and Dτ. The results prove that MF-S-DFA achieves more accurate estimation. In addition, we present various numerical experiments by transforming parameters such as nmax, q and p. The results imply that MF-S-DFA obtains more excellent performance than that of conventional MF-DFA in all cases. Finally, we also verify the high feasibility of MF-S-DFA in ECG signal classification. Through classification of normal and abnormal ECG signals, we further corroborate that MF-S-DFA is more effective than conventional MF-DFA
Modified MF-DFA Model Based on LSSVM Fitting
This paper proposes a multifractal least squares support vector machine detrended fluctuation analysis (MF-LSSVM-DFA) model. The system is an extension of the traditional MF-DFA model. To address potential overfitting or underfitting caused by the fixed-order polynomial fitting in MF-DFA, LSSVM is employed as a superior alternative for fitting. This approach enhances model accuracy and adaptability, ensuring more reliable analysis results. We utilize the p model to construct a multiplicative cascade time series to evaluate the performance of MF-LSSVM-DFA, MF-DFA, and two other models that improve upon MF-DFA from recent studies. The results demonstrate that our proposed modified model yields generalized Hurst exponents h(q) and scaling exponents τ(q) that align more closely with the analytical solutions, indicating superior correction effectiveness. In addition, we explore the sensitivity of MF-LSSVM-DFA to the overlapping window size s. We find that the sensitivity of our proposed model is less than that of MF-DFA. We find that when s exceeds the limited range of the traditional MF-DFA, h(q) and τ(q) are closer than those obtained in MF-DFA when s is in a limited range. Meanwhile, we analyze the performances of the fitting of the two models and the results imply that MF-LSSVM-DFA achieves a better outstanding performance. In addition, we put the proposed MF-LSSVM-DFA into practice for applications in the medical field, and we found that MF-LSSVM-DFA improves the accuracy of ECG signal classification and the stability and robustness of the algorithm compared with MF-DFA. Finally, numerous image segmentation experiments are adopted to verify the effectiveness and robustness of our proposed method
Oral screening for leukoplakia and oral cancer with and without Toluidine blue test: a community-based individual randomized trial
A case-cohort study for the disease natural history of adenoma-carcinoma and de novo carcinoma and surveillance of colon and rectum after polypectomy: implication for efficacy of colonoscopy
Unplanned readmission within the most recent postoperative year of heart transplant patients in Taiwan
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