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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 03/2018, Volume 115, Issue 12, p. E2752
Aggregation of islet amyloid polypeptide (IAPP) into amyloid fibrils in islets of Langerhans is associated with type 2 diabetes, and formation of toxic IAPP... 
Amyloidogenesis | Brain | Polypeptides | Cell survival | Neurodegenerative diseases | Toxicity | Drosophila | Diabetes mellitus | Fibrils | Amylin | Agglomeration | siRNA | Insulin | Cells | Membrane proteins | Proteins | Beta cells | Cell death | β-Amyloid | Diabetes | Diabetes mellitus (non-insulin dependent) | Alzheimer's disease | Apoptosis
Journal Article
American Journal of Pathology, ISSN 0002-9440, 03/2015, Volume 185, Issue 3, pp. 834 - 846
Journal Article
eLife, ISSN 2050-084X, 01/2017, Volume 6, Issue 1, 2017
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2015, Volume 290, Issue 24, pp. 15121 - 15132
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2015, Volume 185, Issue 3, pp. 834 - 846
Several proteins have been identified as amyloid forming in humans, and independent of protein origin, the fibrils are morphologically similar. Therefore,... 
Journal Article
Upsala Journal of Medical Sciences, ISSN 0300-9734, 07/2017, Volume 122, Issue 3, pp. 149 - 159
Journal Article
Endocrine Connections, ISSN 2049-3614, 2017, Volume 6, Issue 7, p. 458
Islet amyloid and beta cell death in type 2 diabetes are heterogeneous events, where some islets are affected early in the disease process, whereas others... 
Medical and Health Sciences | Medicin och hälsovetenskap | islet amyloid | blood flow | heterogeneity | pancreatic islets
Journal Article
by Wray, Naomi R and Ripke, Stephan and Mattheisen, Manuel and Trzaskowski, MacIej and Byrne, Enda M and Abdellaoui, Abdel and Adams, Mark J and Agerbo, Esben and Air, Tracy M and Andlauer, Till M. F and Bacanu, Silviu-Alin and Bækvad-Hansen, Marie and Beekman, Aartjan F. T and Bigdeli, Tim B and Binder, Elisabeth B and Blackwood, Douglas R. H and Bryois, Julien and Buttenschøn, Henriette N and Bybjerg-Grauholm, Jonas and Cai, Na and Castelao, Enrique and Christensen, Jane Hvarregaard and Clarke, Toni-Kim and Coleman, Jonathan I. R and Coloo-Conde, Lucía and Couvy-Duchesne, Baptiste and Craddock, Nick and Crawford, Gregory E and Crowley, Cheynna A and Dashti, Hassan S and Davies, Gail and Deary, Ian J and Degenhardt, Franziska and Derks, Eske M and DIrek, Nese and Dolan, Conor V and Dunn, Erin C and Eley, Thalia C and Eriksson, Nicholas and Escott-Price, Valentina and Kiadeh, Farnush Hassan Farhadi and Finucane, Hilary K and Forstner, Aneas J and Frank, Josef and Gaspar, H. léna A and Gill, Michael and Giusti-Roíguez, Paola and Goes, Fernando S and Gordon, Scott D and Grove, Jakob and Hall, Lynsey S and Hannon, Eilis and Hansen, Christine S. holm and Hansen, Thomas F and Herms, Stefan and Hickie, Ian B and Hoffmann, Per and Homuth, Georg and Horn, Carsten and Hottenga, Jouke-Jan and Hougaard, David M and Hu, Ming and Hyde, Craig L and Ising, Marcus and Jansen, Rick and Jin, Fulai and Jorgenson, Eric and Knowles, James A and Kohane, Isaac S and Kraft, Julia and Kretzschmar, Warren W and Krogh, Jesper and Kutalik, Zoltán and Lane, Jacqueline M and Li, Yihan and Li, Yun and Lind, Penelope A and Liu, Xiaoxiao and Lu, Leina and MacIntyre, Donald J and MacKinnon, Dean F and Maier, Robert M and Maier, Wolfgang and Marchini, Jonathan and Mbarek, Hamdi and McGrath, Patrick and McGuffin, Peter and Medland, Sarah E and Mehta, D. Ivya and Middeldorp, Christel M and Mihailov, Evelin and Milaneschi, Yuri and Milani, Lili and Mill, Jonathan and Mondimore, Francis M and Montgomery, Grant W and Mostafavi, Sara and Mullins, Niamh and Nauck, Matthias and Ng, Bernard and ... and Major Depressive Disorder Working and EQTLGEN and eQTLGen and Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium and 23andMe and the Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature genetics, ISSN 1061-4036, 2018, Volume 50, Issue 5, pp. 668 - 681
Journal Article
Journal Article
by Meddi, F and Menchaca-Rocha, A and Meninno, E and Mercado Pérez, J and Meres, M and Miake, Y and Mikhaylov, K and Milano, L and Milosevic, J and Mischke, A and Mishra, A. N and Mis̈kowiec, D and Mitu, C. M and Mlynarz, J and Mohanty, B and Molnar, L and Montano Zetina, L and Montes, E and Morando, M and Moreira De Godoy, D. A and Moretto, S and Morreale, A and Morsch, A and Muccifora, V and Mudnic, E and Muhuri, S and Mukherjee, M and Müller, H and Munhoz, M. G and Murray, S and Musa, L and Musinsky, J and Nandi, B. K and Nania, R and Nappi, E and Nattrass, C and Nayak, T. K and Nazarenko, S and Nedosekin, A and Nicassio, M and Niculescu, M and Nielsen, B. S and Nikolaev, S and Nikulin, S and Nikulin, V and Nilsen, B. S and Noferini, F and Nomokonov, P and Nooren, G and Nyanin, A and Nystrand, J and Oeschler, H and Oh, S and Oh, S. K and Okatan, A and Olah, L and Oleniacz, J and Oliveira Da Silva, A. C and Onderwaater, J and Oppedisano, C and Ortiz Velasquez, A and Oskarsson, A and Twinowski, J and Oyama, K and Sahoo, P and Pachmayer, Y and Pachr, M and Pagano, P and Paić, G and Painke, F and Pajares, C and Pal, S. K and Palmeri, A and Pant, D and Papikyan, V and Pappalardo, G. S and Pareek, P and Park, W. J and Parmar, S and Passfeld, A and Patalakha, D. I and Paticchio, V and Paul, B and Pawlak, T and Peitzmann, T and Pereira Da Costa, H and Pereira De Oliveira Filho, E and Peresunko, D and Pérez Lara, C. E and Pesci, A and Pestov, Y and Petráček, V and Petran, M and Petris, M and Petrovici, M and Petta, C and Piano, S and Pikna, M and Pillot, P and Pinazza, O and ... and ALICE Collaboration and The ALICE Collaboration and Lund University and Partikelfysik and Lunds universitet and Particle Physics
International Journal of Modern Physics A, ISSN 0217-751X, 01/2014, Volume 29, Issue 24, p. 1430044
Journal Article
Nature Genetics, ISSN 1061-4036, 03/2019, Volume 51, Issue 3, pp. 431 - 444
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of neurodevelopmental phenotypes diagnosed in more than 1% of children. Common...