Zobrazeno 1 - 10
of 44
pro vyhledávání: '"John Colling"'
Autor:
Debra Ann Fadool, Louis John Colling
Synopsis Our olfactory system not only detects chemicals in the external environment but also subserves to detect the chemicals in our internal environment - the chemistry of energy homeostasis and metabolism. Olfaction guides our eating behavior usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74caf59a8283a1382735b42a3e91638e
https://doi.org/10.1016/b978-0-12-809324-5.23770-x
https://doi.org/10.1016/b978-0-12-809324-5.23770-x
Autor:
Diana Eggers, Simon Moons, Miguel Pérez, Juan A. de Ferrer, Thomas Gruenenwald, Jean-Francois Viot, Karsten Groenke, Tilly Borsboom-Patel, Kate Niedermann, Alain Bouvy, Diederik Schowanek, Johanna Martinsson, John Colling, Bjoern Miller, Christine Schneider, Philip Mckeown
Publikováno v:
The International Journal of Life Cycle Assessment. 23:867-886
Cradle-to-gate life cycle inventories (LCIs) for the production of a series of common surfactants used in European detergents and personal care products have been voluntarily compiled by 14 major companies collaborating within ERASM ( www.erasm.org )
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a5c8ccce40fa4d1216d9e8f2837e7d
https://doi.org/10.1007/s11367-017-1384-x
https://doi.org/10.1007/s11367-017-1384-x
Autor:
Diederik Schowanek, Tilly Borsboom-Patel, Alain Bouvy, John Colling, Juan Antonio de Ferrer, Diana Eggers, Karsten Groenke, Thomas Gruenenwald, Johanna Martinsson, Philip Mckeown, Bjoern Miller, Simon Moons, Kate Niedermann, Miguel Pérez, Christine Schneider, Jean-Francois Viot
Publikováno v:
The International Journal of Life Cycle Assessment. 23:887-889
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43d32f4b7968b2169d3acd65ddd7de7e
https://doi.org/10.1007/s11367-018-1437-9
https://doi.org/10.1007/s11367-018-1437-9
Autor:
Holger Hummerich, Helen Speedy, Tracy Campbell, Lee Darwent, Elizabeth Hill, Steven Collins, Christiane Stehmann, Gabor G Kovacs, Michael D Geschwind, Karl Frontzek, Herbert Budka, Ellen Gelpi, Adriano Aguzzi, Sven J van der Lee, Cornelia M van Duijn, Pawel P Liberski, Miguel Calero, Pascual Sanchez-Juan, Elodie Bouaziz-Amar, Jean-Louis Laplanche, Stéphane Haïk, Jean-Phillipe Brandel, Angela Mammana, Sabina Capellari, Anna Poleggi, Anna Ladogana, Maurizio Pocchiari, Saima Zafar, Stephanie Booth, Gerard H Jansen, Aušrinė Areškevičiūtė, Eva Løbner Lund, Katie Glisic, Piero Parchi, Peter Hermann, Inga Zerr, Brian S Appleby, Jiri Safar, Pierluigi Gambetti, John Collinge, Simon Mead
Publikováno v:
PLoS ONE, Vol 19, Iss 7, p e0304528 (2024)
Human prion diseases are rare, transmissible and often rapidly progressive dementias. The most common type, sporadic Creutzfeldt-Jakob disease (sCJD), is highly variable in clinical duration and age at onset. Genetic determinants of late onset or slo
Externí odkaz:
https://doaj.org/article/a8105e366d44473aa02be9676f81d759
Autor:
Emma Jones, Elizabeth Hill, Jacqueline Linehan, Tamsin Nazari, Adam Caulder, Gemma F. Codner, Marie Hutchison, Matthew Mackenzie, Michael Farmer, Thomas Coysh, Michael Wiggins De Oliveira, Huda Al-Doujaily, Malin Sandberg, Emmanuelle Viré, Thomas J. Cunningham, Emmanuel A. Asante, Sebastian Brandner, John Collinge, Simon Mead
Publikováno v:
Neurobiology of Disease, Vol 190, Iss , Pp 106363- (2024)
Sporadic Creutzfeldt-Jakob disease (sCJD), the most common human prion disease, is thought to occur when the cellular prion protein (PrPC) spontaneously misfolds and assembles into prion fibrils, culminating in fatal neurodegeneration. In a genome-wi
Externí odkaz:
https://doaj.org/article/44274454a3b548c1acc3170aed6ccfe8
Autor:
Graham S. Jackson, Jacqueline Linehan, Sebastian Brandner, Emmanuel A. Asante, Jonathan D. F. Wadsworth, John Collinge
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Transgenic mice over-expressing human PRNP or murine Prnp transgenes on a mouse prion protein knockout background have made key contributions to the understanding of human prion diseases and have provided the basis for many of the fundamenta
Externí odkaz:
https://doaj.org/article/436ec582413448b5a496b4820ef97f59
Autor:
Szymon W. Manka, Wenjuan Zhang, Adam Wenborn, Jemma Betts, Susan Joiner, Helen R. Saibil, John Collinge, Jonathan D. F. Wadsworth
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-11 (2022)
High-resolution structures of mammalian prions have remained elusive. Here, Manka et al. report the cryo-EM structure of infectious RML prion fibrils from mice. Structural similarity with recently reported infectious 263K prion fibrils from hamsters
Externí odkaz:
https://doaj.org/article/9b6eb942195b4bc19be04c9aa47b9d02
Autor:
Madeleine Reilly, Iryna Benilova, Azadeh Khalili-Shirazi, Christian Schmidt, Parvin Ahmed, Daniel Yip, Parmjit S. Jat, John Collinge
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract There is an urgent need to develop disease-modifying therapies to treat neurodegenerative diseases which pose increasing challenges to global healthcare systems. Prion diseases, although rare, provide a paradigm to study neurodegenerative de
Externí odkaz:
https://doaj.org/article/6c3d427e537748449f547bcad8e6d4f9
Autor:
François Kroll, Athanasios Dimitriadis, Tracy Campbell, Lee Darwent, John Collinge, Simon Mead, Emmanuelle Vire
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Prion diseases are fatal neurodegenerative conditions that affect humans and animals. Rapid and accurate sequencing of the prion gene PRNP is paramount to human prion disease diagnosis and for animal surveillance programmes. Current methods
Externí odkaz:
https://doaj.org/article/9e9fbd6a422948078a3fa174ad017576
Autor:
Silvia A Purro, Michael Farmer, Elizabeth Noble, Claire J Sarell, Megan Powell, Daniel Yip, Lauren Giggins, Leila Zakka, David X Thomas, Mark Farrow, Andrew J Nicoll, Dominic Walsh, John Collinge
Publikováno v:
PLoS ONE, Vol 18, Iss 11, p e0294465 (2023)
Oligomers formed from monomers of the amyloid β-protein (Aβ) are thought to be central to the pathogenesis of Alzheimer's disease (AD). Unsurprisingly for a complex disease, current mouse models of AD fail to fully mimic the clinical disease in hum
Externí odkaz:
https://doaj.org/article/8af80f9aedd94ca28f2439779fee4821