950 resultados para M2-m3 Loop


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Il lavoro svolto nella presente tesi di laurea magistrale consiste nella modellazione e simulazione numerica, tramite il software commericale COMSOL MULTIPHYSICS, di un reservoir geotermico a bassa entalpia sfruttato mediante un impianto di teleriscaldamento a pompa di calore accoppiato ad un sistema open-loop.

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In questo lavoro viene presentato un recente modello di buco nero che implementa le proprietà quantistiche di quelle regioni dello spaziotempo dove non possono essere ignorate, pena l'implicazione di paradossi concettuali e fenomenologici. In suddetto modello, la regione di spaziotempo dominata da comportamenti quantistici si estende oltre l'orizzonte del buco nero e suscita un'inversione, o più precisamente un effetto tunnel, della traiettoria di collasso della stella in una traiettoria di espansione simmetrica nel tempo. L'inversione impiega un tempo molto lungo per chi assiste al fenomeno a grandi distanze, ma inferiore al tempo di evaporazione del buco nero tramite radiazione di Hawking, trascurata e considerata come un effetto dissipativo da studiarsi in un secondo tempo. Il resto dello spaziotempo, fuori dalla regione quantistica, soddisfa le equazioni di Einstein. Successivamente viene presentata la teoria della Gravità Quantistica a Loop (LQG) che permetterebbe di studiare la dinamica della regione quantistica senza far riferimento a una metrica classica, ma facendo leva sul contenuto relazionale del tessuto spaziotemporale. Il campo gravitazionale viene riformulato in termini di variabili hamiltoniane in uno spazio delle fasi vincolato e con simmetria di gauge, successivamente promosse a operatori su uno spazio di Hilbert legato a una vantaggiosa discretizzazione dello spaziotempo. La teoria permette la definizione di un'ampiezza di transizione fra stati quantistici di geometria spaziotemporale, applicabile allo studio della regione quantistica nel modello di buco nero proposto. Infine vengono poste le basi per un calcolo in LQG dell'ampiezza di transizione del fenomeno di rimbalzo quantistico all'interno del buco nero, e di conseguenza per un calcolo quantistico del tempo di rimbalzo nel riferimento di osservatori statici a grande distanza da esso, utile per trattare a posteriori un modello che tenga conto della radiazione di Hawking e, auspicatamente, fornisca una possibile risoluzione dei problemi legati alla sua esistenza.

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Il software Smart-M3, ereditato dal progetto europeo SOFIA, conclusosi nel 2011, permette di creare una piattaforma d'interoperabilità indipendente dal tipo di dispositivi e dal loro dominio di utilizzo e che miri a fornire un Web Semantico di informazioni condivisibili fra entità software e dispositivi, creando ambienti intelligenti e collegamenti tra il mondo reale e virtuale. Questo è un campo in continua ascesa grazie al progressivo e regolare sviluppo sia della tecnologia, nell'ambito della miniaturizzazione dei dispositivi, che delle potenzialità dei sistemi embedded. Questi sistemi permettono, tramite l'uso sempre maggiore di sensori e attuatori, l'elaborazione delle informazioni provenienti dall’esterno. È evidente, come un software di tale portata, possa avere una molteplicità di applicazioni, alcune delle quali, nell’ambito della Biomedica, può esprimersi nella telemedicina e nei sistemi e-Heath. Per e-Health si intende infatti l’utilizzo di strumenti basati sulle tecnologie dell'informazione e della comunicazione, per sostenere e promuovere la prevenzione, la diagnosi, il trattamento e il monitoraggio delle malattie e la gestione della salute e dello stile di vita. Obiettivo di questa tesi è fornire un set di dati che mirino ad ottimizzare e perfezionare i criteri nella scelta applicativa di tali strutture. Misureremo prestazioni e capacità di svolgere più o meno velocemente, precisamente ed accuratamente, un particolare compito per cui tale software è stato progettato. Ciò si costruisce sull’esecuzione di un benchmark su diverse implementazioni di Smart-M3 ed in particolare sul componente centrale denominato SIB (Semantic Information Broker).

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Closure of loop ileostomy can be safely performed using sutures or staplers. The aim of the present study was to compare the cost effectiveness of three different techniques.

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Invariant Natural Killer T cells (iNKT) are a versatile lymphocyte subset with important roles in both host defense and immunological tolerance. They express a highly conserved TCR which mediates recognition of the non-polymorphic, lipid-binding molecule CD1d. The structure of human iNKT TCRs is unique in that only one of the six complementarity determining region (CDR) loops, CDR3beta, is hypervariable. The role of this loop for iNKT biology has been controversial, and it is unresolved whether it contributes to iNKT TCR:CD1d binding or antigen selectivity. On the one hand, the CDR3beta loop is dispensable for iNKT TCR binding to CD1d molecules presenting the xenobiotic alpha-galactosylceramide ligand KRN7000, which elicits a strong functional response from mouse and human iNKT cells. However, a role for CDR3beta in the recognition of CD1d molecules presenting less potent ligands, such as self-lipids, is suggested by the clonal distribution of iNKT autoreactivity. We demonstrate that the human iNKT repertoire comprises subsets of greatly differing TCR affinity to CD1d, and that these differences relate to their autoreactive functions. These functionally different iNKT subsets segregate in their ability to bind CD1d-tetramers loaded with the partial agonist alpha-linked glycolipid antigen OCH and structurally different endogenous beta-glycosylceramides. Using surface plasmon resonance with recombinant iNKT TCRs and different ligand-CD1d complexes, we demonstrate that the CDR3beta sequence strongly impacts on the iNKT TCR affinity to CD1d, independent of the loaded CD1d ligand. Collectively our data reveal a crucial role for CDR3beta for the function of human iNKT cells by tuning the overall affinity of the iNKT TCR to CD1d. This mechanism is relatively independent of the bound CD1d ligand and thus forms the basis of an inherent, CDR3beta dependent functional hierarchy of human iNKT cells.

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Benzodiazepines act at the major isoforms of GABA type A receptors where they potentiate the current evoked by the agonist GABA. The underlying mechanism of this potentiation is poorly understood, but hypothesized to be related to the mechanism that links agonist binding to channel opening in these ligand activated ion channels. The loop F of the ?(1) and the ?(2) subunit have been implicated in channel gating, and loop F of the ?(2) subunit in the modulation by benzodiazepines. We have identified the conservative point mutation Y168F located N-terminally of loop F in the ?(1) subunit that fails to affect agonist properties. Interestingly, it disrupts modulation by benzodiazepines, but leaves high affinity binding to the benzodiazepine binding site intact. Modulation by barbiturates and neurosteroids is also unaffected. Residue ?(1) Y168 is not located either near the binding pockets for GABA, or for benzodiazepines, or close to the loop F of the ?(2) subunit. Our results support the fact, that broader regions of ligand gated receptors are conformationally affected by the binding of benzodiazepines. We infer that also broader regions could contribute to signaling from GABA agonist binding to channel opening.

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The aim of this study was to assess the changes in inclination of the maxillary second (M2) and third (M3) molars after orthodontic treatment of Class II Division 1 malocclusion with extraction of maxillary first molars.

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Stereology is an essential method for quantitative analysis of lung structure. Adequate fixation is a prerequisite for stereological analysis to avoid bias in pulmonary tissue, dimensions and structural details. We present a technique for in situ fixation of large animal lungs for stereological analysis, based on closed loop perfusion fixation.

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Unique as snowflakes, learning communities are formed in countless ways. Some are designed specifically for first-year students, while others offer combined or clustered upper-level courses. Most involve at least two linked courses, and some add residential and social components. Many address core general education and basic skills requirements. Learning communities differ in design, yet they are similar in striving to enhance students' academic and social growth. First-year learning communities foster experiences that have been linked to academic success and retention. They also offer unique opportunities for librarians interested in collaborating with departmental faculty and enhancing teaching skills. This article will explore one librarian's experiences teaching within three first-year learning communities at Buffalo State College.

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INTRODUCTION: The ultrastructure of venous valves and walls in chronic venous disease was investigated. METHODS: Consecutive patients were categorised into one of three groups (group A: patients with C1 venous disease in accordance with CEAP (Clinical severity, Etiology, Anatomy, Pathophysiology); group B: C2 and C3; group C: C4, C5 and C6). The terminal or preterminal valve and adjacent vessel wall was harvested from the great saphenous vein. Sections were examined with a transmission electron microscope. The volumes of elastin and of collagen per unit surface area of valve were assessed, as well as the surface endothelium of valve and vessel wall. RESULTS: The study population consisted of 17 patients. The elastin ratio was analysed by means of stereology. Mean values were: in group A, 0.45 μm3/m2; in group B, 0.67 μm3/m2; in group C, 0.97 μm3/m2. The ratio was similar for collagen (A, 15.7 μm3/m2; B, 26.8 μm3/m2; C, 30.1 μm3/m2). Surface analysis of the valve endothelium and the adjacent vessel wall endothelium showed a trend towards increasing damage with more severe disease. CONCLUSIONS: With progression of venous disease, the valve elastin content, assessed morphologically, seems to increase, and the endothelium of the venous valve and the vein wall tend to show more damage.

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OBJECTIVE: To analyze myoelectric activity of the ileum, cecum, proximal loop of the ascending colon (PLAC), and spiral colon in cows with naturally occurring cecal dilatation-dislocation (CDD) and compare findings with those in healthy cows. ANIMALS: 8 CDD-affected and 6 healthy control cows. PROCEDURES: Immediately after diagnosis, CDD-affected cows underwent surgery; control cows underwent a similar surgical procedure. Before completion of surgery, 8 bipolar silver electrodes were implanted in the ileum (n = 2), cecum (1), PLAC (1), and spiral colon (4) of each cow. Beginning the day after surgery, intestinal myoelectric activity was recorded daily (8-hour period) for 4 days; data were analyzed by use of specialized software programs. Quantitative variables of myoelectric activity were compared between groups. RESULTS: Cows of both groups recovered without complications after surgery. In control cows, physiologic myoelectric activity was recorded in all intestinal segments on all days after surgery. Apparently normal myoelectric activity was evident in the ileum of CDD-affected cows on the first day after surgery, but myoelectric activity patterns in the cecum, PLAC, and spiral colon were variable with no organized cyclic myoelectric patterns, incomplete or normally organized migrating myoelectric complexes, and slow normalization over time. CONCLUSIONS AND CLINICAL RELEVANCE: After surgery for CDD, normal myoelectric patterns were disrupted in the large intestine of cows, especially in the spiral colon. Clinical recovery with effective transit of ingesta occurred before normalization of myoelectric activity in the large intestine. Therapeutic protocols for restoration or normalization of spiral colon motility should be developed for treatment of CDD-affected cattle.

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Protein scaffolds that support molecular recognition have multiple applications in biotechnology. Thus, protein frames with robust structural cores but adaptable surface loops are in continued demand. Recently, notable progress has been made in the characterization of Ig domains of intracellular origin--in particular, modular components of the titin myofilament. These Ig belong to the I(intermediate)-type, are remarkably stable, highly soluble and undemanding to produce in the cytoplasm of Escherichia coli. Using the Z1 domain from titin as representative, we show that the I-Ig fold tolerates the drastic diversification of its CD loop, constituting an effective peptide display system. We examine the stability of CD-loop-grafted Z1-peptide chimeras using differential scanning fluorimetry, Fourier transform infrared spectroscopy and nuclear magnetic resonance and demonstrate that the introduction of bioreactive affinity binders in this position does not compromise the structural integrity of the domain. Further, the binding efficiency of the exogenous peptide sequences in Z1 is analyzed using pull-down assays and isothermal titration calorimetry. We show that an internally grafted, affinity FLAG tag is functional within the context of the fold, interacting with the anti-FLAG M2 antibody in solution and in affinity gel. Together, these data reveal the potential of the intracellular Ig scaffold for targeted functionalization.