Search results for "MUTATION"
showing 10 items of 2830 documents
Improved constructions of mixed state quantum automata
2009
Quantum finite automata with mixed states are proved to be super-exponentially more concise rather than quantum finite automata with pure states. It was proved earlier by A. Ambainis and R. Freivalds that quantum finite automata with pure states can have an exponentially smaller number of states than deterministic finite automata recognizing the same language. There was an unpublished ''folk theorem'' proving that quantum finite automata with mixed states are no more super-exponentially more concise than deterministic finite automata. It was not known whether the super-exponential advantage of quantum automata is really achievable. We prove that there is an infinite sequence of distinct int…
Efficient algorithm for learning simple regular expressions from noisy examples
1994
We present an efficient algorithm for finding approximate repetitions in a given sequence of characters. First, we define a class of simple regular expressions which are of star-height one and do not contain union operations, and a stochastic mutation process of a given length over a string of characters. Then, assuming that a given string of characters is obtained corrupted by the defined mutation process from some long enough word generated by a simple regular expression, we try to restore the expression. We prove that to within some reasonable accuracy it is always possible if the length of the mutation process is bounded comparing to the length of the example. We provide an algorithm by…
Finitary Representations and Images of Transitive Finitary Permutation Groups
1999
Abstract We characterize the point stabilizers and kernels of finitary permutation representations of infinite transitive groups of finitary permutations. Moreover, the number of such representations is determined.
Large-scale network functional interactions during distraction and reappraisal in remitted bipolar and unipolar patients.
2017
Objectives The human brain is organized into large-scale networks that dynamically interact with each other. Extensive evidence has shown characteristic changes in certain large-scale networks during transitions from internally directed to externally directed attention. The aim of the present study was to compare these context-dependent network interactions during emotion regulation and to examine potential alterations in remitted unipolar and bipolar disorder patients. Methods We employed a multi-region generalized psychophysiological interactions analysis to quantify connectivity changes during distraction vs reappraisal pair-wise across 90 regions placed throughout the four networks of i…
The broad-spectrum antiinfective drug artesunate interferes with the canonical nuclear factor kappa B (NF-κB) pathway by targeting RelA/p65.
2015
Infection with human cytomegalovirus (HCMV) is a serious medical problem, particularly in immunocompromised individuals and neonates. The success of standard antiviral therapy is hampered by low drug compatibility and induction of viral resistance. A novel strategy is based on the exploitation of cell-directed signaling inhibitors. The broad antiinfective drug artesunate (ART) offers additional therapeutic options such as oral bioavailability and low levels of toxic side-effects. Here, novel ART-derived compounds including dimers and trimers were synthesized showing further improvements over the parental drug. Antiviral activity and mechanistic aspects were determined leading to the followi…
Gefitinib in lung cancer therapy. Clinical results, predictive markers of response and future perspectives.
2009
Over the past few years, epidermal growth factor receptor has emerged as one of the most important targets in tumorgenesis and several drugs targeting signal transduction pathways have been developed. The first among these agents to be approved for the treatment of NSCLC was gefitinib, a potent, selective and reversible inhibitor of HER1/EGFR tyrosine kinase activity. The review summarizes its clinical development and the new therapeutic options, with particular focus on predictive markers of susceptibility to this drug.
Toward a Rationale for the PTC124 (Ataluren) Promoted Readthrough of Premature Stop Codons: A Computational Approach and GFP-Reporter Cell-Based Assay
2014
The presence in the mRNA of premature stop codons (PTCs) results in protein truncation responsible for several inherited (genetic) diseases. A well-known example of these diseases is cystic fibrosis (CF), where approximately 10% (worldwide) of patients have nonsense mutations in the CF transmembrane regulator (CFTR) gene. PTC124 (3-(5-(2-fluorophenyl)-1,2,4-oxadiazol-3-yl)-benzoic acid), also known as Ataluren, is a small molecule that has been suggested to allow PTC readthrough even though its target has yet to be identified. In the lack of a general consensus about its mechanism of action, we experimentally tested the ability of PTC124 to promote the readthrough of premature termination c…
Analysis of Protected Accidental Transients in the EFIT Reactor With the RELAP5 Thermal-Hydraulic Code
2008
The European Facility for Industrial Transmutation (EFIT) is aimed at demonstrating the feasibility of transmutation process through the Accelerator Driven System (ADS) route on an industrial scale. The conceptual design of this reactor of about 400 MW thermal power is under development in the frame of the European EUROTRANS Integrated Project of the EURATOM Sixth Framework Program (FP6). EFIT is a pool-type reactor cooled by forced circulation of lead in the primary system where the heat is removed by steam generators installed inside the reactor vessel. The reactor power is sustained by a spallation neutron source supplied by a proton beam impinging on a lead target at the core centre. A …
Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis
2006
Familial haemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous disorder characterised by constitutive defects in cellular cytotoxicity resulting in fever, hepatosplenomegaly and cytopenia, and the outcome is fatal unless treated by chemoimmunotherapy followed by haematopoietic stem‐cell transplantation. Since 1999, mutations in the perforin gene giving rise to this disease have been identified; however, these account only for 40% of cases. Lack of a genetic marker hampers the diagnosis, suitability for transplantation, selection of familial donors, identification of carriers, genetic counselling and prenatal diagnosis. Mutations in the Munc13–4 gene have recently been des…
Histopathological progression of hidradenitis suppurativa/acne inversa
2021
It is generally acknowledged that the first morphological change of hidradenitis suppurativa/acne inversa (HS/AI) consists of infundibular plugging of the folliculosebaceous apocrine apparatus, which is followed by acute and chronic inflammation, cysts with sinus formation, and fibrosis. Alternatively, it has been hypothesized that HS/AI is primarily a neutrophilic autoinflammatory disease and that the follicular plugging typical of this disease is secondary to inflammation.To review the sequence of the changes that mark the disease development, we have performed a histopathologic study on the surgical material from a series of axillary and inguinal/perineal cases.The histologic material fr…