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Institution

University of Pavia

EducationPavia, Italy
About: University of Pavia is a education organization based out in Pavia, Italy. It is known for research contribution in the topics: Population & Large Hadron Collider. The organization has 21173 authors who have published 52524 publications receiving 1610492 citations. The organization is also known as: Università degli Studi di Pavia & Università di Pavia.


Papers
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Journal ArticleDOI
TL;DR: The immunological aspects of CFS are discussed and an immunological hypothesis for the disease processes is offered and may explain some of the manifestations such as fatigue and flu-like symptoms and influence NK activity.

263 citations

Journal ArticleDOI
TL;DR: An adaptive isogeometric collocation method is explored that is based on local hierarchical refinement of NURBS basis functions and collocation points derived from the corresponding multi-level Greville abscissae, and introduces the concept of weighted collocation that can be consistently developed from the weighted residual form and the two-scale relation of B-splines.

262 citations

Book ChapterDOI
TL;DR: Methods for isolation, ex vivo expansion, phenotypic characterization, and viral infection of MSCs from mouse bone marrow are described and a method for preparation of conditioned and concentrated conditioned medium from M SCs is described.
Abstract: Mesenchymal stem cells (MSCs) are defined as self-renewing and multipotent cells capable of differentiating into multiple cell types, including osteocytes, chondrocytes, adipocytes, hepatocytes, myocytes, neurons, and cardiomyocytes. MSCs were originally isolated from the bone marrow stroma but they have recently been identified also in other tissues, such as fat, epidermis, and cord blood. Several methods have been used for MSC isolation. The most common method is based on the ability of the MSCs to selectively adhere to plastic surfaces. Phenotypic characterization of MSCs is usually carried out using immunocytochemical detection or fluorescence-activated cell sorting (FACS) analysis of cell surface molecule expression. However, the lack of specific markers renders the characterization of MSCs difficult and sometimes ambiguous. MSCs posses remarkable expansion potential in culture and are highly amenable to genetic modification with various viral vectors rendering them optimal vehicles for cell-based gene therapy. Most importantly, MSC plasticity and the possibility to use them as autologous cells render MSCs suitable for cell therapy and tissue engineering. Furthermore, it is known that MSCs produce and secrete a great variety of cytokines and chemokines that play beneficial paracrine actions when MSCs are used for tissue repair. In this chapter, we describe methods for isolation, ex vivo expansion, phenotypic characterization, and viral infection of MSCs from mouse bone marrow. We also describe a method for preparation of conditioned and concentrated conditioned medium from MSCs. The conditioned medium can be easily tested both in vitro and in vivo when a particular paracrine effect (i.e., cytoprotection) is hypothesized to be an important mechanism of action of the MSCs and/or screened to identify a target paracrine/autocrine mediator.

262 citations

Journal ArticleDOI
TL;DR: Two stronger uncertainty relations are given, relating to the sum of variances, whose lower bound is guaranteed to be nontrivial whenever the two observables are incompatible on the state of the system.
Abstract: The Heisenberg-Robertson uncertainty relation expresses a limitation in the possible preparations of the system by giving a lower bound to the product of the variances of two observables in terms of their commutator. Notably, it does not capture the concept of incompatible observables because it can be trivial; i.e., the lower bound can be null even for two noncompatible observables. Here we give two stronger uncertainty relations, relating to the sum of variances, whose lower bound is guaranteed to be nontrivial whenever the two observables are incompatible on the state of the system.

262 citations

Journal ArticleDOI
01 May 2006-Blood
TL;DR: Observations suggest that JAK2 (V617F) may constitutively activate granulocytes and by this means mobilize CD34(+) cells in myeloproliferative disorders.

261 citations


Authors

Showing all 21348 results

NameH-indexPapersCitations
Giacomo Bruno1581687124368
Melody A. Swartz1481304103753
Peter J. Schwartz147647107695
Marco Zanetti1451439104610
Th. Müller1441798125843
Chiara Mariotti141142698157
Silvia G. Priori140515120642
Kevin Varvell138132593740
Alberto Messineo134151196492
Franco Ligabue134140495389
Michele Arneodo134133993977
Roberto Tenchini133139094541
Bruce Yabsley133119184889
Philip McGuire13388160813
Antonio Limosani133118183668
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023114
2022312
20213,299
20203,182
20192,732
20182,483