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Institution

University of Bologna

EducationBologna, Emilia-Romagna, Italy
About: University of Bologna is a education organization based out in Bologna, Emilia-Romagna, Italy. It is known for research contribution in the topics: Population & Galaxy. The organization has 38387 authors who have published 115176 publications receiving 3460869 citations. The organization is also known as: Università di Bologna & UNIBO.


Papers
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Journal ArticleDOI
TL;DR: Intestinal permeability, which is a feature of intestinal barrier function, is increasingly recognized as being of relevance for health and disease, and therefore, this topic warrants more attention.
Abstract: Data are accumulating that emphasize the important role of the intestinal barrier and intestinal permeability for health and disease. However, these terms are poorly defined, their assessment is a matter of debate, and their clinical significance is not clearly established. In the present review, current knowledge on mucosal barrier and its role in disease prevention and therapy is summarized. First, the relevant terms ‘intestinal barrier’ and ‘intestinal permeability’ are defined. Secondly, the key element of the intestinal barrier affecting permeability are described. This barrier represents a huge mucosal surface, where billions of bacteria face the largest immune system of our body. On the one hand, an intact intestinal barrier protects the human organism against invasion of microorganisms and toxins, on the other hand, this barrier must be open to absorb essential fluids and nutrients. Such opposing goals are achieved by a complex anatomical and functional structure the intestinal barrier consists of, the functional status of which is described by ‘intestinal permeability’. Third, the regulation of intestinal permeability by diet and bacteria is depicted. In particular, potential barrier disruptors such as hypoperfusion of the gut, infections and toxins, but also selected over-dosed nutrients, drugs, and other lifestyle factors have to be considered. In the fourth part, the means to assess intestinal permeability are presented and critically discussed. The means vary enormously and probably assess different functional components of the barrier. The barrier assessments are further hindered by the natural variability of this functional entity depending on species and genes as well as on diet and other environmental factors. In the final part, we discuss selected diseases associated with increased intestinal permeability such as critically illness, inflammatory bowel diseases, celiac disease, food allergy, irritable bowel syndrome, and – more recently recognized – obesity and metabolic diseases. All these diseases are characterized by inflammation that might be triggered by the translocation of luminal components into the host. In summary, intestinal permeability, which is a feature of intestinal barrier function, is increasingly recognized as being of relevance for health and disease, and therefore, this topic warrants more attention.

1,186 citations

Journal ArticleDOI
TL;DR: Bone scintigraphy enables the diagnosis of cardiac ATTR amyloidosis to be made reliably without the need for histology in patients who do not have a monoclonal gammopathy, and proposes noninvasive diagnostic criteria that are applicable to the majority of patients with this disease.
Abstract: Background—Cardiac transthyretin (ATTR) amyloidosis is a progressive and fatal cardiomyopathy for which several promising therapies are in development. The diagnosis is frequently delayed or missed...

1,185 citations

Journal ArticleDOI
17 May 2010-PLOS ONE
TL;DR: Evidence is provided for the fact that the ageing process deeply affects the structure of the human gut microbiota, as well as its homeostasis with the host's immune system, because of its crucial role in the host physiology and health status.
Abstract: Background: Age-related physiological changes in the gastrointestinal tract, as well as modifications in lifestyle, nutritional behaviour, and functionality of the host immune system, inevitably affect the gut microbiota, resulting in a greater susceptibility to infections. Methodology/Principal Findings: By using the Human Intestinal Tract Chip (HITChip) and quantitative PCR of 16S rRNA genes of Bacteria and Archaea, we explored the age-related differences in the gut microbiota composition among young adults, elderly, and centenarians, i.e subjects who reached the extreme limits of the human lifespan, living for over 100 years. We observed that the microbial composition and diversity of the gut ecosystem of young adults and seventy-years old people is highly similar but differs significantly from that of the centenarians. After 100 years of symbiotic association with the human host, the microbiota is characterized by a rearrangement in the Firmicutes population and an enrichment in facultative anaerobes, notably pathobionts. The presence of such a compromised microbiota in the centenarians is associated with an increased inflammatory status, also known as inflammageing, as determined by a range of peripheral blood inflammatory markers. This may be explained by a remodelling of the centenarians’ microbiota, with a marked decrease in Faecalibacterium prauznitzii and relatives, symbiotic species with reported anti-inflammatory properties. As signature bacteria of the long life we identified specifically Eubacterium limosum and relatives that were more than ten-fold increased in the centenarians. Conclusions/Significance: We provide evidence for the fact that the ageing process deeply affects the structure of the human gut microbiota, as well as its homeostasis with the host’s immune system. Because of its crucial role in the host physiology and health status, age-related differences in the gut microbiota composition may be related to the progression of diseases and frailty in the elderly population.

1,180 citations

Journal ArticleDOI
TL;DR: The development of the concept of microbial fuel cell into a wider range of derivative technologies, called bioelectrochemical systems, is described, introducing briefly microbial electrolysis cells, microbial desalination cells and microbial electrosynthesis cells.

1,180 citations

Journal ArticleDOI
Martin Peifer1, Lynnette Fernandez-Cuesta1, Martin L. Sos1, Julie George1, Danila Seidel1, Lawryn H. Kasper, Dennis Plenker1, Frauke Leenders1, Ruping Sun2, Thomas Zander1, Roopika Menon3, Mirjam Koker1, Ilona Dahmen1, Christian Müller1, Vincenzo Di Cerbo2, Hans Ulrich Schildhaus1, Janine Altmüller1, Ingelore Baessmann1, Christian Becker1, Bram De Wilde4, Jo Vandesompele4, Diana Böhm3, Sascha Ansén1, Franziska Gabler1, Ines Wilkening1, Stefanie Heynck1, Johannes M. Heuckmann1, Xin Lu1, Scott L. Carter5, Kristian Cibulskis5, Shantanu Banerji5, Gad Getz5, Kwon-Sik Park6, Daniel Rauh7, Christian Grütter7, Matthias Fischer1, Laura Pasqualucci8, Gavin M. Wright9, Zoe Wainer9, Prudence A. Russell10, Iver Petersen11, Yuan Chen11, Erich Stoelben, Corinna Ludwig, Philipp A. Schnabel, Hans Hoffmann, Thomas Muley, Michael Brockmann, Walburga Engel-Riedel, Lucia Anna Muscarella12, Vito Michele Fazio12, Harry J.M. Groen13, Wim Timens13, Hannie Sietsma13, Erik Thunnissen14, Egber Smit14, Daniëlle A M Heideman14, Peter J.F. Snijders14, Federico Cappuzzo, C. Ligorio15, Stefania Damiani15, John K. Field16, Steinar Solberg17, Odd Terje Brustugun17, Marius Lund-Iversen17, Jörg Sänger, Joachim H. Clement11, Alex Soltermann18, Holger Moch18, Walter Weder18, Benjamin Solomon19, Jean-Charles Soria20, Pierre Validire, Benjamin Besse20, Elisabeth Brambilla21, Christian Brambilla21, Sylvie Lantuejoul21, Philippe Lorimier21, Peter M. Schneider1, Michael Hallek1, William Pao22, Matthew Meyerson23, Matthew Meyerson5, Julien Sage6, Jay Shendure24, Robert Schneider2, Robert Schneider25, Reinhard Büttner1, Jürgen Wolf1, Peter Nürnberg1, Sven Perner3, Lukas C. Heukamp1, Paul K. Brindle, Stefan A. Haas2, Roman K. Thomas1 
TL;DR: This study implicates histone modification as a major feature of SCLC, reveals potentially therapeutically tractable genomic alterations and provides a generalizable framework for the identification of biologically relevant genes in the context of high mutational background.
Abstract: Small-cell lung cancer (SCLC) is an aggressive lung tumor subtype with poor prognosis(1-3). We sequenced 29 SCLC exomes, 2 genomes and 15 transcriptomes and found an extremely high mutation rate of 7.4 +/- 1 protein-changing mutations per million base pairs. Therefore, we conducted integrated analyses of the various data sets to identify pathogenetically relevant mutated genes. In all cases, we found evidence for inactivation of TP53 and RB1 and identified recurrent mutations in the CREBBP, EP300 and MLL genes that encode histone modifiers. Furthermore, we observed mutations in PTEN, SLIT2 and EPHA7, as well as focal amplifications of the FGFR1 tyrosine kinase gene. Finally, we detected many of the alterations found in humans in SCLC tumors from Tp53 and Rb1 double knockout mice(4). Our study implicates histone modification as a major feature of SCLC, reveals potentially therapeutically tractable genomic alterations and provides a generalizable framework for the identification of biologically relevant genes in the context of high mutational background.

1,177 citations


Authors

Showing all 39076 results

NameH-indexPapersCitations
Anil K. Jain1831016192151
H. S. Chen1792401178529
Stefan Schreiber1781233138528
Alvio Renzini16290895452
David H. Adams1551613117783
Roberto Romero1511516108321
Thomas E. Starzl150162591704
Paolo Boffetta148145593876
Kypros H. Nicolaides147130287091
J. Fraser Stoddart147123996083
Fabio Finelli147542111128
Jack Hirsh14673486332
Kjell Fuxe142147989846
Andrew Ivanov142181297390
Peter Lang140113698592
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023398
20221,031
20217,486
20207,099
20196,390
20185,737