1,131 research outputs found
Energy Management in Buildings: Lessons Learnt for Modeling and Advanced Control Design
This paper presents a comparative analysis of different modeling and control techniques that can be used to tackle the energy efficiency and management problems in buildings. Multiple resources are considered, from generation to storage, distribution and delivery. In particular, it is shown what are the real needs and advantages of adopting different techniques, based on different applications, type of buildings, boundary conditions. This contribution is based widely on the experience performed by the authors in the recent years in dealing with existing residential, commercial and tertiary filed buildings, with application ranging from local temperature control up to smart grids where buildings are seen as an active node of the grid thanks to their ability to shape the thermal and electrical profile in real time. As for control models, a wide range of modeling techniques are here investigated and compared, from linear time-invariant models, to time-varying, to nonlinear ones. Similarly, control techniques include adaptive ones and real-time predictive ones
Automated shape modeling and analysis of brain ventricles : findings in the spectrum from normal cognition to Alzheimer disease
Many efforts have been spent to investigate the causes and mechanisms of Alzheimer Disease (AD). Therapies to slow down the cognitive decline have proved more effective during the early stage of the disease: consequently, biomarkers for early diagnosis are desirable. Growing evidence of the correlation between the progression of AD and the loss of neurons in specific areas of the brain has been reported. Clinical MR images are a valuable tool for the estimation of volume loss and shape changes in brain structures: tissue degeneration due to AD has been shown both in gray and white matter. Investigating changes in these areas might increase our knowledge on the progression of AD. The delineation of white and gray matter structures remains a challenging task in elderly: the reduced contrast between white and gray matter yields to error-prone (semi-)automatic segmentations. Manual delineation is more subjective and time consuming. The analysis of brain ventricles could lead to more reproducible results since the contrast between CSF and the rest of the parenchyma remains sharp. Focus of this research was to investigate changes in the ventricular shape within different populations (controls, MCIs, and ADs), and across the spectrum of cognitive impairment.Stichting Beeldverwerkering, Leiden Medis medical imaging systems bv., Leiden Foundation Imago, Oegstgeest Internationale Stichting Alzheimer Onderzoek (ISAO) Bio-Imaging Technologies bv., LeidenUBL - phd migration 201
A concise enantioselective synthesis of (+)-endo-brevicomin accomplished by a tellurium/metal exchange reaction
A homoenolate generated by tellurium/lithium exchange reaction was employed in a straightforward enantioselective synthesis of (+)-endo-brevicomin in 70% yield and 84.4% e.e.Um homoenolato gerado pela reação de troca telúrio/lítio foi aplicado na síntese enantioseletiva do (+)-endo-brevicomin com 70% de rendimento isolado e 84,4% de e.e.FAPESPCNPqCoordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES
On the Microscopic Origin of Cholesteric Pitch
We present a microscopic analysis of the instability of the nematic phase to
chirality when molecular chirality is introduced perturbatively. We show that
previously neglected short-range biaxial correlations play a crucial role in
determining the cholesteric pitch. We propose an order parameter which
quantifies the chirality of a molecule.Comment: RevTeX 3.0, 4 pages, one included eps figure. Published versio
Glycan-independent role of calnexin in the intracellular retention of Charcot-Marie-tooth 1A Gas3/PMP22 mutants
Missense point mutations in Gas3/PMP22 are responsible for the peripheral neuropathies Charcot-Marie-Tooth 1A and Dejerine Sottas syndrome. These mutations induce protein misfolding with the consequent accumulation of the proteins in the endoplasmic reticulum and the formation of aggresomes. During folding, Gas3/PMP22 associates with the lectin chaperone calnexin. Here, we show that calnexin interacts with the misfolded transmembrane domains of Gas3/PMP22, fused to green fluorescent protein, in a glycan-independent manner. In addition, photobleaching experiments in living cells revealed that Gas3/PMP22-green fluorescent protein mutants are mobile but diffuse at almost half the diffusion coefficient of wild type protein. Our results support emerging models for a glycan-independent chaperone role for calnexin and for the mechanism of retention of misfolded membrane proteins in the endoplasmic reticulum
PMH59 HEALTH RELATED QUALITY OF LIFE IN PATIENTS TREATED WITH ANTIPSYCHOTIC DRUGS: RESULTS AT BASELINE FROM THE COMETA STUDY
Immunohistochemical evidence of a cytokine and chemokine network in three patients with Erdheim-Chester disease: Implications for pathogenesis.
OBJECTIVE:
Erdheim-Chester disease (ECD) is a rare form of non-Langerhans' cell histiocytosis (LCH) of unknown etiology, characterized by diffuse histiocyte infiltration of bones and soft tissue. The purpose of this study was to assess cell proliferation and expression of cytokines, chemokines, and chemokine receptors that may potentially be important in histiocyte accumulation in ECD lesions.
METHODS:
Biopsies were performed on 3 patients with ECD. The diagnosis of the disease was based on clinical signs including typical radiologic osteosclerosis, and on the detection of foamy CD68+,CD1a- non-Langerhans' cell histiocytes on histologic examination. The expression of the proliferation marker Ki-67 as well as of selected chemokine/chemokine receptor pairs and cytokines was analyzed by immunohistochemistry.
RESULTS:
In all samples, Ki-67 was undetectable in CD68+ histiocytes. Conversely, these cells expressed the chemokines CCL2 (monocyte chemotactic protein 1), CCL4/macrophage inflammatory protein 1beta (MIP-1beta), CCL5/RANTES, CCL20/MIP-3alpha, and CCL19/MIP-3beta, and their counter-receptors CCR1, CCR2, CCR3, CCR5, CCR6, and CCR7. Moreover, ECD histiocytes expressed interferon-gamma-inducible 10-kd protein (CXCL10), which is specifically induced by interferon-gamma, and interleukin-6 and RANKL, which are both implicated in bone remodeling. Finally, all cases showed a Th1-type lymphocyte infiltrate.
CONCLUSION:
Our data indicate that, similar to LCH, ECD lesions are characterized by a complex cytokine and chemokine network, which may orchestrate histiocyte activation and accumulation through an autocrine loop and contribute to the pathogenesis of the disease
Effects of miRNA-15 and miRNA-16 expression replacement in chronic lymphocytic leukemia : implication for therapy
This work was supported by: Associazione Italiana Ricerca sul Cancro (AIRC) Grant 5 x mille n.9980, (to M.F., F.M. A. N., P.T. and M.N.) ; AIRC I.G. n. 14326 (to M.F.), n.10136 and 16722 (A.N.), n.15426 (to F.F.). AIRC and Fondazione CaRiCal co-financed Multi Unit Regional Grant 2014 n.16695 (to F.M.). Italian Ministry of Health 5x1000 funds (to S.Z. and F.F). A.G R. was supported by Associazione Italiana contro le Leucemie-Linfomi-Mielomi (AIL) Cosenza - Fondazione Amelia Scorza (FAS). S.M. C.M., M.C., L.E., S.B. were supported by AIRC.Peer reviewedPostprin
Inter-Strain Epigenomic Profiling Reveals a Candidate IAP Master Copy in C3H Mice.
Insertions of endogenous retroviruses cause a significant fraction of mutations in inbred mice but not all strains are equally susceptible. Notably, most new Intracisternal A particle (IAP) ERV mutagenic insertions have occurred in C3H mice. We show here that strain-specific insertional polymorphic IAPs accumulate faster in C3H/HeJ mice, relative to other sequenced strains, and that IAP transcript levels are higher in C3H/HeJ embryonic stem (ES) cells compared to other ES cells. To investigate the mechanism for high IAP activity in C3H mice, we identified 61 IAP copies in C3H/HeJ ES cells enriched with H3K4me3 (a mark of active promoters) and, among those tested, all are unmethylated in C3H/HeJ ES cells. Notably, 13 of the 61 are specific to C3H/HeJ and are members of the non-autonomous 1Δ1 IAP subfamily that is responsible for nearly all new insertions in C3H. One copy is full length with intact open reading frames and hence potentially capable of providing proteins i
Guillain-Barré syndrome in temporal association with influenza A vaccine
OBJECTIVE: To report a case of Guillain-Barré syndrome following influenza A (H1N1) 2009 vaccine. CASE DESCRIPTION: A four-year-old boy presented right thigh pain and ascending muscular weakness 15 days after the second dose of influenza A (H1N1) 2009 vaccine. The neurological examination revealed tetraparesis and areflexia. Electroneuromyography showed lower velocity and conduction blockage with small secondary axonal loss. Treated with intravenous immunoglobulin, the patient reached a plateau in the 4th day, followed by progressive muscular strength improvement. COMMENTS: The employment of large-scale influenza A (H1N1) 2009 vaccination and the preliminary reports from the American Surveillance Program suggest a significant association between Guillain-Barré syndrome and influenza A H1N1 2009 vaccination. All suspected cases of this association should be published for further evaluation. Vaccination remains the most effective method to prevent serious illness and death related to influenza.OBJETIVO: Descrever um caso de síndrome de Guillain-Barré em associação temporal com a vacina influenza A (H1N1) 2009. DESCRIÇAO DO CASO: Menino de quatro anos com queixa inicial de dor em coxa direita e perda de força muscular ascendente 15 dias após a segunda dose da vacina influenza A (H1N1) 2009. Ao exame neurológico apresentava tetraparesia e arreflexia, com predomínio em membros inferiores. A eletroneuromiografia evidenciou redução da velocidade e bloqueio de condução neuronal, com discreta perda axonal secundária. Foi tratado com imunoglobulina por via intravenosa, atingiu platô no quarto dia de evolução da doença e, depois, houve melhora progressiva da força muscular. COMENTÁRIOS: Com o emprego em larga escala da vacina influenza A (H1N1) 2009 em nosso meio e os dados preliminares do sistema de vigilância norte-americano mostrando associação temporal significante com a síndrome de Guillain-Barré, recomenda-se a descrição dos casos suspeitos dessa associação. A vacina continua sendo o método mais efetivo para prevenir doença grave e morte por influenza.Universidade Federal de São Paulo (UNIFESP)UNIFESPSciEL
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