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Correction : The 2019 and 2021 International workshops on Alport syndrome
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Daga, Sergio (University of Siena) ;
Ding, Jie (Peking University First Hospital) ;
Deltas, Constantinos (University of Cyprus Medical School) ;
Savige, Judy (The University of Melbourne) ;
Lipska-Ziętkiewicz, Beata S. (Medical University of Gdańsk) ;
Hoefele, Julia (Technical University of Munich) ;
Flinter, Frances (Guys' and St Thomas' NHS Foundation Trust) ;
Gale, Daniel P. (UK Renal Registry) ;
Aksenova, Marina (Y. Veltischev Research and Clinical Institute for Pediatrics at the Pirogov Russian National Research Medical University) ;
Kai, Hirofumi (Kumamoto University) ;
Perin, Laura (University of Southern California) ;
Barua, Moumita (University of Toronto) ;
Torra Balcells, Roser (Institut d'Investigació Biomèdica Sant Pau) ;
Miner, Jeff H. (Washington University School of Medicine) ;
Massella, Laura (Bambino Gesù Children's Hospital-IRCCS) ;
Ljubanović, Danica Galešić (University of Zagreb School of Medicine) ;
Lennon, Rachel (The University of Manchester) ;
Weinstock, Andrè B. (Alport Syndrome Foundation) ;
Knebelmann, Bertrand (Paris University) ;
Cerkauskaite, Agne (Vilnius University Hospital Santariskiu Clinics) ;
Gear, Susie (Alport UK, Tetbury, UK) ;
Gross, Oliver (University Medicine Goettingen) ;
Turner, A. Neil (University of Edinburgh) ;
Baldassarri, Margherita (Azienda Ospedaliero-Universitaria Senese) ;
Pinto, Anna Maria (Azienda Ospedaliero-Universitaria Senese) ;
Renieri, Alessandra (Azienda Ospedaliero-Universitaria Senese) ;
Universitat Autònoma de Barcelona
2023 -  10.1038/s41431-023-01286-z
European Journal of Human Genetics, Vol. 32 (january 2023) , p. 130
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10 p, 1.7 MB |
The 2019 and 2021 International Workshops on Alport Syndrome
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Daga, Sergio (University of Siena) ;
Ding, Jie (Peking University First Hospital) ;
Savige, Judy (The University of Melbourne) ;
Lipska-Ziętkiewicz, Beata S. (Medical University of Gdańsk) ;
Hoefele, Julia (Technical University of Munich) ;
Flinter, Frances (Guys' and St Thomas' NHS Foundation Trust) ;
Gale, Daniel (UK Renal Registry. Rare Renal Disease Registry) ;
Aksenova, Marina (Y. Veltischev Research and Clinical Institute for Pediatrics at the Pirogov Russian National Research Medical University) ;
Kai, Hirofumi (Kumamoto University) ;
Perin, Laura (University of Southern California) ;
Barua, Moumita (University of Toronto) ;
Torra Balcells, Roser (Institut d'Investigació Biomèdica Sant Pau) ;
Miner, Jeff H. (Washington University School of Medicine) ;
Massella, Laura (Bambino Gesù Children's Hospital) ;
Ljubanović, Danica Galešić (University of Zagreb) ;
Lennon, Rachel (The University of Manchester) ;
Weinstock, Andrè B. (Alport Syndrome Foundation) ;
Knebelmann, Bertrand (Paris University, Paris, France) ;
Cerkauskaite, Agne (Vilnius University Hospital Santariskiu Clinics) ;
Gear, Susie (Alport UK, Tetbury, UK) ;
Gross, Oliver (University Medical Center Göttingen) ;
Turner, A. Neil (University of Edinburgh) ;
Baldassarri, Margherita (Azienda Ospedaliero-Universitaria Senese) ;
Pinto, Anna Maria (Azienda Ospedaliero-Universitaria Senese) ;
Renieri, Alessandra (Azienda Ospedaliero-Universitaria Senese) ;
Universitat Autònoma de Barcelona
In 1927 Arthur Cecil Alport, a South African physician, described a British family with an inherited form of kidney disease that affected males more severely than females and was sometimes associated with hearing loss. [...]
2022 - 10.1038/s41431-022-01075-0
European Journal of Human Genetics, march 2022, p. 1-10
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Functional and molecular heterogeneity of D2R neurons along dorsal ventral axis in the striatum
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Puighermanal, Emma (Universitat Autònoma de Barcelona. Institut de Neurociències) ;
Castell, Laia (Université Montpellier) ;
Esteve-Codina, Anna (Centre de Regulació Genòmica) ;
Melser, Su (Université de Bordeaux) ;
Kaganovsky, Konstantin (Stanford University School of Medicine) ;
Zussy, Charleine (Université Montpellier) ;
Boubaker-Vitre, Jihane (Université Montpellier) ;
Gut, Marta (Universitat Pompeu Fabra) ;
Rialle, Stephanie (Université Montpellier) ;
Kellendonk, Christoph (New York State Psychiatric Institute) ;
Sanz, Elisenda (Universitat Autònoma de Barcelona. Institut de Neurociències) ;
Quintana Romero, Albert (Universitat Autònoma de Barcelona. Institut de Neurociències) ;
Marsicano, Giovanni (Université de Bordeaux) ;
Martin, Miquel (Université Montpellier) ;
Rubinstein, Marcelo (University of Michigan Medical School) ;
Girault, Jean-Antoine (Institut du Fer à Moulin) ;
Ding, Jun B. (Stanford University School of Medicine) ;
Valjent, Emmanuel (Université Montpellier)
Action control is a key brain function determining the survival of animals in their environment. In mammals, neurons expressing dopamine D2 receptors (D2R) in the dorsal striatum (DS) and the nucleus accumbens (Acb) jointly but differentially contribute to the fine regulation of movement. [...]
2020 - 10.1038/s41467-020-15716-9
Nature communications, Vol. 11 (april 2020)
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15 p, 1.5 MB |
Room-temperature tunnel magnetoresistance across biomolecular tunnel junctions based on ferritin
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Karuppannan, Senthil kumar (National University of Singapore. Department of Chemistry) ;
Pasula, Rupali Reddy (Nanyang Technological University. School of Chemical and Biomedical Engineering) ;
Herng, Tun Seng (National University of Singapore. Department of Materials Science and Engineering) ;
Ding, Jun (National University of Singapore. Department of Materials Science and Engineering) ;
Chi, Xiao (Singapore Synchrotron Light Source) ;
Del Barco, Enrique (University of Central Florida. Department of Physics) ;
Roche, Stephan (Institut Català de Nanociència i Nanotecnologia) ;
Yu, Xiaojiang (Singapore Synchrotron Light Source) ;
Yakovlev, Nikolai (Institute of Materials Research and Engineering (Singapur, Singapur)) ;
Lim, Sierin (Nanyang Technological University. School of Chemical and Biomedical Engineering) ;
Nijhuis, Christian A. (University of Twente. Department of Molecules and Materials)
We report exceptionally large tunnel magnetoresistance (TMR) for biomolecular tunnel junctions based on ferritins immobilized between Ni and EGaIn electrodes. Ferritin stores iron in the form of ferrihydrite nanoparticles (NPs) and fulfills the following roles: (a) it dictates the tunnel barrier, (b) it magnetically decouples the NPs from the ferromagnetic (FM) electrode, (c) it stabilizes the NPs, and (d) it acts as a spin filter reducing the complexity of the tunnel junctions since only one FM electrode is required. [...]
2021 - 10.1088/2515-7639/abfa79
JPhys materials, Vol. 4, issue 3 (April 2021) , art. 035003
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23 p, 797.0 KB |
Decelerating Autumn CO2 Release With Warming Induced by Attenuated Temperature Dependence of Respiration in Northern Ecosystems
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Liu, Dan (Chinese Academy of Sciences. Key Laboratory of Alpine Ecology, Institute of Tibetan Plateau Research) ;
Piao, Shilong (Chinese Academy of Sciences. Center for Excellence in Tibetan Earth Science) ;
Wang, Tao (Chinese Academy of Sciences. Center for Excellence in Tibetan Earth Science) ;
Wang, Xuhui (Laboratoire des Sciences du Climat et de l'Environnement) ;
Wang, Xiaoyi (Chinese Academy of Sciences. Key Laboratory of Alpine Ecology, Institute of Tibetan Plateau Research) ;
Ding, Jinzhi (Chinese Academy of Sciences. Key Laboratory of Alpine Ecology, Institute of Tibetan Plateau Research) ;
Ciais, Philippe (Laboratoire des Sciences du Climat et de l'Environnement) ;
Peñuelas, Josep (Centre de Recerca Ecològica i d'Aplicacions Forestals) ;
Janssens, Ivan (University of Antwerp. Department of Biology)
Feedbacks from the carbon cycle in boreal and arctic ecosystems can significantly affect climate change, but the effects of climate change on the high-latitude carbon cycle during the dormant period remain uncertain. [...]
2018 - 10.1029/2018GL077447
Geophysical Research Letters, Vol. 45, Issue 11 (June 2018) , p. 5562-5571
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Advances and unmet needs in genetic, basic and clinical science in Alport syndrome : report from the 2015 International Workshop on Alport Syndrome
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Gross, Oliver (University Medicine Goettingen (Germany)) ;
Kashtan, Clifford E. (University of Minnesota Medical School (USA)) ;
Rheault, Michelle N. (University of Minnesota Medical School (USA)) ;
Flinter, Frances (Guy's and St Thomas' NHS Foundation Trust (United Kingdom)) ;
Savige, Judith (The University of Melbourne (Australia)) ;
Miner, Jeffrey H. (Washington University School of Medicine (USA)) ;
Torra Balcells, Roser (Institut d'Investigació Biomèdica Sant Pau) ;
Ars, Elisabet (Institut d'Investigació Biomèdica Sant Pau) ;
Deltas, Constantinos (University of Cyprus) ;
Savva, Isavella (University of Cyprus) ;
Perin, Laura (University of Southern California, Children's Hospital Los Angeles (USA)) ;
Renieri, Alessandra (University of Siena (Italy)) ;
Ariani, Francesca (University of Siena (Italy)) ;
Mari, Francesca (University of Siena (Italy)) ;
Baigent, Colin (University of Oxford (United Kingdom)) ;
Judge, Parminder (University of Oxford (United Kingdom)) ;
Knebelman, Bertrand (Université Paris Descartes (France)) ;
Heidet, Laurence (Clinique Maurice Lamy, Hôpital Necker-Enfants Malades (France)) ;
Lagas, Sharon (Alport Syndrome Foundation (USA)) ;
Blatt, Dave (Alport Foundation of Australia) ;
Ding, Jie (Peking University First Hospital (China)) ;
Zhang, Yanqin (Peking University First Hospital (China)) ;
Gale, Daniel (University College London-Centre for Nephrology (United Kingdom)) ;
Prunotto, Marco (F. Hoffmann-La Roche Ltd. Roche Pharma Research & Early Development (Switzerland)) ;
Xue, Yong (Global Clinical Development. Sanofi Genzyme (The Netherlands)) ;
Schachter, Asher D. (Novartis Institutes for BioMedical Research (USA)) ;
Morton, Lori C. G. (Regeneron Pharmaceuticals (USA)) ;
Blem, Jacqui (Regulus Therapeutics (USA)) ;
Huang, Michael (Regulus Therapeutics (USA)) ;
Liu, Shiguang (Sanofi-Genzyme R&D Center (USA)) ;
Vallee, Sebastien (Discovery Biology. Shire (USA)) ;
Renault, Daniel (FEDERG (Belgium)) ;
Schifter, Julia (Alport Israel) ;
Skelding, Jules (Alport UK (United Kingdom)) ;
Gear, Susie (Alport UK (United Kingdom)) ;
Friede, Tim (University Medical Center Goettingen (Germany)) ;
Turner, A. Neil (University of Edinburgh (United Kingdom)) ;
Lennon, Rachel (University of Manchester (United Kingdom)) ;
Universitat Autònoma de Barcelona
Alport syndrome (AS) is a genetic disease characterized by haematuric glomerulopathy variably associated with hearing loss and anterior lenticonus. It is caused by mutations in the COL4A3, COL4A4 or COL4A5 genes encoding the α3α4α5(IV) collagen heterotrimer. [...]
2017 - 10.1093/ndt/gfw095
Nephrology Dialysis Transplantation, Vol. 32, Issue 6 (June 2017) , p. 916-924
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