84 research outputs found
A problem of emphasizing features of a surface roughness by means the Discrete Wavelet Transform
When we are interested to the detection of the roughness features by means of the 3D reconstruction, based on photometric stereo techniques,
an important problem is the elimination of the brightness variation due to different light conditions which can alter the response.
This paper will concentrate on presenting results of a new method for eliminating this problem.
Every pixel of a picture gives only one number: the brightness of the corresponding point on the object, whereas the surface orientation is
described by a normal vector that has two degrees of freedom. The level of brightness depends on many factors as well as the homogeneity
of reflection properties of the material or its physical continuity and the surface smoothness or roughness.
In this work we will show how the application of the Discrete Wavelet Transform (DWT) to the processing of some images, captured
on different light conditions, permits to solve the problem of emphasizing roughness features of a metallic surface. Wavelet transforms can
model irregular data patterns such as sharp changes, better than the Fourier transforms and standard statistical procedures (e.g., parametric
and non-parametric regressions) and provide a multiresolution approximation to the data.
Here we propose, also, a non-parametric method, based on the wavelet theory, for the estimation of the threshold level of a gray levels
distribution, obtained from the intensity image matrix
Minerals from the Carpathian Mountains and from Transylvania donated by Joseph II (1785) to the museum of the Collegio Nazareno, Rome, Italy
Abstract
The mineralogical museum of the Collegio Nazareno of the Piarists Order in Rome was founded by Gian Vincenzo Petrini c. 1760. It hosted minerals and rocks the Popes had received as gifts and given to Piarists to support their teaching, as well as minerals collected from Roman and Neapolitan volcanoes. On March 24, 1769, the museum was visited by Emperor Joseph II, officially there as an incognito tourist but, in fact, to organize the election of a Pope who would abolish the Jesuit Order. On June 14, 1785 the Emperor, by now King of Hungary as well, presented eight crates of minerals from mining areas in Transylvania and Upper Hungary, i.e. Slovakia. This collection had been organized by “Baron of Born”, who also wrote down descriptions of all the specimens (mostly ores), as referred to in Petrini (1791–92). The museum of the Collegio Nazareno has survived and the royal gift is partially preserved, curated by the Gruppo Mineralogico Romano (GMR), a private association of amateurs founded in 1982. The museum now exhibits a rare collection of minerals from 18th century central Europe, organized according to systematics that just preceeded the major scientific changes brought about in mineralogy by the crystallographic approach
Clinical pharmacogenetics of methotrexate
It is well known that interindividual variability can affect the response to many drugs in relation to age, gender, diet, and organ function. Pharmacogenomic studies have also documented that genetic polymorphisms can exert clinically significant effects in terms of drug resistance, efficacy and toxicity by modifying the expression of critical gene products (drug-metabolizing enzymes, transporters, and target molecules) as well as pharmacokinetic and pharmacodynamic parameters. A growing body of in vitro and clinical evidence suggests that common polymorphisms in the folate gene pathway are associated with an altered response to methotrexate (MTX) in patients with malignancy and autoimmune disease. Such polymorphisms may also induce significant MTX toxicity requiring expensive monitoring and treatment. Although the available data are not conclusive, they suggest that in the future MTX pharmacogenetics could play a key role in clinical practice by improving and tailoring treatment. This review describes the genetic polymorphisms that significantly influence MTX resistance, efficacy, and toxicity
The Role of Target Therapy in the Treatment of Gastrointestinal Noncolorectal Cancers: Clinical Impact and Cost Consideration
Gastrointestinal (GI) tumors are among the leading cause of death in cancer patients worldwide. Particularly, gastric cancer (GC) is the third cause of cancer deaths, whereas esophageal neoplasm is the eighth leading most common cancer worldwide and its incidence, especially adenocarcinoma type, is continuously increasing. Also, Hepatocellular carcinoma, Cholangiocarcinoma and pancreatic cancer represent a very interesting model to multidisciplinary approach and recently new drugs are used in their treatment. Currently, new clinical trials are designed including classic chemotherapy in association with either small molecule inhibitors (i.e. Tyrosine Kinase inhibitors) and/or monoclonal antibody (i.e. anti-EGFR antibody). Moreover, a comprehensive list of new molecules for target therapy is included in this issue. The development of new treatment modalities (multidisciplinary approach) and targeted therapy approaches have contributed to improving the outcome in these cancer diseases. During the past few years, remarkable progress in molecular biology of malignancy, the discovery of specific targets, and the resulting development of systemic drugs that block critical kinases and several molecular pathways have all contributed to progress in cancer treatment, also in GI non-colorectal cancer treatment
Le lesioni polipoidi della colecisti: problemi diagnostici e terapeutici
Le lesioni polipoidi della colecisti costituiscono un’entità eterogenea di difficile definizione diagnostica preoperatoria. L’indicazione
chirurgica è discutibile ma in alcuni casi obbligatoria .
In questo studio abbiamo analizzato i dati clinici relativi a 25
pazienti sottoposti consecutivamente a colecistectomia laparoscopica
per formazioni polipoidi. Ciò al fine di evidenziare la possibile correlazione fra aspetto ecografico e valutazione istopatologica e di definire
l’indicazione terapeutica
Correction of Mutant p63 in EEC Syndrome Using siRNA Mediated Allele-Specific Silencing Restores Defective Stem Cell Function
Ectrodactyly-Ectodermal dysplasia-Clefting (EEC) syndrome is a rare autosomal dominant disease caused by heterozygous mutations in the p63 gene and characterized by limb defects, orofacial clefting, ectodermal dysplasia, and ocular defects. Patients develop progressive total bilateral limbal stem cell deficiency, which eventually results in corneal blindness. Medical and surgical treatments are ineffective and of limited benefit. Oral mucosa epithelial stem cells (OMESCs) represent an alternative source of stem cells capable of regenerating the corneal epithelium and, combined with gene therapy, could provide an attractive therapeutic avenue. OMESCs from EEC patients carrying the most severe p63 mutations (p.R279H and p.R304Q) were characterized and the genetic defect of p.R279H silenced using allele-specific (AS) small interfering RNAs (siRNAs). Systematic screening of locked nucleic acid (LNA)-siRNAs against R279H-p63 allele in (i) stable WT-\u394Np63\u3b1-RFP and R279H-\u394Np63\u3b1-EGFP cell lines, (ii) transient doubly transfected cell lines, and (iii) p.R279H OMESCs, identified a number of potent siRNA inhibitors for the mutant allele, which had no effect on wild-type p63. In addition, siRNA treatment led to longer acquired life span of mutated stem cells compared to controls, less accelerated stem cell differentiation in vitro, reduced proliferation properties, and effective ability in correcting the epithelial hypoplasia, thus giving rise to full thickness stratified and differentiated epithelia. This study demonstrates the phenotypic correction of mutant stem cells (OMESCs) in EEC syndrome by means of siRNA mediated AS silencing with restoration of function. The application of siRNA, alone or in combination with cell-based therapies, offers a therapeutic strategy for corneal blindness in EEC syndrome
Biliverdin Protects against Liver Ischemia Reperfusion Injury in Swine
Ischemia reperfusion injury (IRI) in organ transplantation remains a serious and unsolved problem. Organs that undergo significant damage during IRI, function less well immediately after reperfusion and tend to have more problems at later times when rejection can occur. Biliverdin has emerged as an agent that potently suppress IRI in rodent models. Since the use of biliverdin is being developed as a potential therapeutic modality for humans, we tested the efficacy for its effects on IRI of the liver in swine, an accepted and relevant pre-clinical animal model. Administration of biliverdin resulted in rapid appearance of bilirubin in the serum and significantly suppressed IRI-induced liver dysfunction as measured by multiple parameters including urea and ammonia clearance, neutrophil infiltration and tissue histopathology including hepatocyte cell death. Taken together, our findings, in a large animal model, provide strong support for the continued evaluation of biliverdin as a potential therapeutic in the clinical setting of transplantation of the liver and perhaps other organs
Minerals from the Carpathian Mountains and from Transylvania donated by Joseph II (1785) to the museum of the Collegio Nazareno, Rome, Italy
A randomized phase 3 study on the optimization of the combination of bevacizumab with FOLFOX/OXXEL in the treatment of patients with metastatic colorectal cancer-OBELICS (Optimization of BEvacizumab scheduLIng within Chemotherapy Scheme).
BACKGROUND: Despite the improvements in diagnosis and treatment, colorectal cancer (CRC) is the second cause of cancer deaths in both sexes. Therefore, research in this field remains of great interest. The approval of bevacizumab, a humanized anti-vascular endothelial growth factor (VEGF) monoclonal antibody, in combination with a fluoropyrimidine-based chemotherapy in the treatment of metastatic CRC has changed the oncology practice in this disease. However, the efficacy of bevacizumab-based treatment, has thus far been rather modest. Efforts are ongoing to understand the better way to combine bevacizumab and chemotherapy, and to identify valid predictive biomarkers of benefit to avoid unnecessary and costly therapy to nonresponder patients. The BRANCH study in high-risk locally advanced rectal cancer patients showed that varying bevacizumab schedule may impact on the feasibility and efficacy of chemo-radiotherapy. METHODS/DESIGN: OBELICS is a multicentre, open-label, randomised phase 3 trial comparing in mCRC patients two treatment arms (1:1): standard concomitant administration of bevacizumab with chemotherapy (mFOLFOX/OXXEL regimen) vs experimental sequential bevacizumab given 4 days before chemotherapy, as first or second treatment line. Primary end point is the objective response rate (ORR) measured according to RECIST criteria. A sample size of 230 patients was calculated allowing reliable assessment in all plausible first-second line case-mix conditions, with a 80% statistical power and 2-sided alpha error of 0.05. Secondary endpoints are progression free-survival (PFS), overall survival (OS), toxicity and quality of life. The evaluation of the potential predictive role of several circulating biomarkers (circulating endothelial cells and progenitors, VEGF and VEGF-R SNPs, cytokines, microRNAs, free circulating DNA) as well as the value of the early [(18)F]-Fluorodeoxyglucose positron emission tomography (FDG-PET) response, are the objectives of the traslational project. DISCUSSION: Overall this study could optimize bevacizumab scheduling in combination with chemotherapy in mCRC patients. Moreover, correlative studies could improve the knowledge of the mechanisms by which bevacizumab enhance chemotherapy effect and could identify early predictors of response. EudraCT Number: 2011-004997-27 TRIAL REGISTRATION: ClinicalTrials.gove number, NCT01718873
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