Resultats globals: 4 registres trobats en 0.02 segons.
Articles, 4 registres trobats
Articles 4 registres trobats  
1.
9 p, 1.2 MB Antibodies against peripheral nerve antigens in chronic inflammatory demyelinating polyradiculoneuropathy / Querol, Luis (Institut d'Investigació Biomèdica Sant Pau) ; Siles, Ana M (Institut d'Investigació Biomèdica Sant Pau) ; Alba-Rovira, Roser (Institut d'Investigació Biomèdica Sant Pau) ; Jáuregui, Agustín (Fundación Favaloro, Buenos, Aires, Argentina) ; Devaux, Jérôme (Aix-Marseille Université) ; Faivre-Sarrailh, Catherine (Aix-Marseille Université) ; Araque,Josefa (Institut d'Investigació Biomèdica Sant Pau) ; Rojas Garcia,Ricard (Institut d'Investigació Biomèdica Sant Pau) ; Diaz Manera, Jordi (Institut d'Investigació Biomèdica Sant Pau) ; Cortés Vicente, Elena (Institut d'Investigació Biomèdica Sant Pau) ; Nogales Gadea,Gisela (Institut Germans Trias i Pujol) ; Navas Madroñal, Miquel (Institut d'Investigació Biomèdica Sant Pau) ; Gallardo Vigo, Eduard (Institut d'Investigació Biomèdica Sant Pau) ; Illa, Isabel (Institut d'Investigació Biomèdica Sant Pau)
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a heterogeneous disease in which diverse autoantibodies have been described but systematic screening has never been performed. Detection of CIDP-specific antibodies may be clinically useful. [...]
2017 - 10.1038/s41598-017-14853-4
Sientific reports, Vol. 7 (october 2017) , p. 1-9  
2.
12 p, 5.0 MB Characterization of an anti-fetal AChR monoclonal antibody isolated from a myasthenia gravis patient / Saxena, Abhishek (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Stevens, Jo (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Cetin,Hakan (Nuffield Department of Clinical Neurosciences, John Radcliffe University Hospital, Oxford) ; Koneczny, Inga (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Webster, Richard (Nuffield Department of Clinical Neurosciences, John Radcliffe University Hospital, Oxford) ; Lazaridis, Konstantinos (Hellenic Pasteur Institute) ; Tzartos, Socrates (Hellenic Pasteur Institute) ; Vrolix, Kathleen (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Nogales-Gadea, Gisela (Institut Germans Trias i Pujol. Recerca Neuromuscular i Neuropediàtrica) ; Machiels, Barbie (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Molenaar, Peter C. (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Damoiseaux, Jan (Central Diagnostic Laboratory, Maastricht University Medical Center) ; De Baets, Marc H. (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Simon-Keller, Katja (Institute of Pathology, University Medical Centre Mannheim, University of Heidelberg) ; Marx, Alexander (Institute of Pathology, University Medical Centre Mannheim, University of Heidelberg) ; Vincent, Angela (Nuffield Department of Clinical Neurosciences, John Radcliffe University Hospital, Oxford) ; Mario Losen (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ; Pilar Martinez-Martinez (Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience, Maastricht University) ;
We report here the sequence and functional characterization of a recombinantly expressed.
autoantibody (mAb 131) previously isolated from a myasthenia gravis patient by immortalization of thymic B cells using Epstein-Barr virus and TLR9 activation. The antibody is characterized by a high degree of somatic mutations as well as a 6 amino acid insertion within the VHCDR2. [...]

2017 - 10.1038/s41598-017-14350-8
Sientific reports, Vol. 7 (october 2017) , p. 1-12  
3.
13 p, 1.6 MB Delivery is key: lessons learnt from developing splice-switching antisense therapies / Godfrey, Caroline (University of Oxford. Department of Physiology, Anatomy and Genetics) ; Desviat, Lourdes R (Centro de Biología Molecular Severo Ochoa UAM-CSIC) ; Smedsrød, Bård (University of TromsØ. Department of Medical Biology) ; Piétri-Rouxel, France (Institut de Myologie, Paris) ; Denti, Michela A (Università di Trento. Centre for Integrative Biology) ; Disterer, Petra (University College London. Centre for Amyloidosis and Acute Phase Proteins) ; Lorain, Stéphanie (Institut de Myologie, Paris) ; Nogales Gadea, Gisela (Institut Germans Trias i Pujol. Grup d'Investigació en Malalties Neuromuscular i Neuropediàtriques) ; Sardone, Valentina (University College London) ; Anwar, Rayan (Drug Discovery Informatics Lap, Qasemi-Research Center, Al-Qasemi Academic College) ; EL Andaloussi, Samir (Karolinska Institute. Department of Laboratory Medicine) ; Lehto, Taavi (University of Tartu. Institute of Technology) ; Khoo, Bernard (University College London. Centre for Neuroendocrinology) ; Brolin, Camilla (University of Copenhagen. Department of Cellular and Molecular Medicine) ; van Roon-Mom, Willeke MC (Leiden University Medical Center. DEpartment of Human Genetics) ; Goyenvalle, Aurélie (Université Versailles Saint Quentin) ; Aartsma-Rus, Annemieke (Leiden University Medical Center. Department of Human Genetics) ; Arechavala-Gomeza, Virginia (Neuromuscular Disorders Group. BioCruces Health Research Insitute, Bizkaia) ; Universitat Autònoma de Barcelona
The use of splice-switching antisense therapy is highly promising, with a wealth of pre-clinical data and numerous clinical trials ongoing. Nevertheless, its potential to treat a variety of disorders has yet to be realized. [...]
2017 - 10.15252/emmm.201607199
EMBO Molecular Medicine, Vol. 9 Núm. 5 (2017) , p. 545-557  
4.
4 p, 163.0 KB McArdle disease does not affect skeletal muscle fibre type profiles in humans / Kohn, Tertius Abraham (UCT/MRC Research Unit for Exercise Science and Sports Medicine, Department of Human Biology, University of Cape Town) ; Noakes, Timothy David (UCT/MRC Research Unit for Exercise Science and Sports Medicine, Department of Human Biology, University of Cape Town) ; Rae, Dale Elizabeth (UCT/MRC Research Unit for Exercise Science and Sports Medicine, Department of Human Biology, University of Cape Town) ; Rubio, Juan Carlos (Mitochondrial and Neuromuscular Diseases Laboratory, i+12 Research Institute, Hospital 12 de Octubre) ; Santalla, Alfredo (Department of Sport Science, Universidad Pablo de Olavide) ; Nogales-Gadea, Gisela (Institut d'Investigació Biomèdica Sant Pau) ; Pinós, Tomas (Hospital Universitari Vall d'Hebron, Institut de Recerca (VHIR)) ; Martín, Miguel A. (Mitochondrial and Neuromuscular Diseases Laboratory, i+12 Research Institute, Hospital 12 de Octubre) ; Arenas, Joaquin (Mitochondrial and Neuromuscular Diseases Laboratory, i+12 Research Institute, Hospital 12 de Octubre) ; Lucia, Alejandro (European University of Madrid) ; Universitat Autònoma de Barcelona
Patients suffering from glycogen storage disease V (McArdle disease) were shown to have higher surface electrical activity in their skeletal muscles when exercising at the same intensity as their healthy counterparts, indicating more muscle fibre recruitment. [...]
2014 - 10.1242/bio.20149548
Biology Open, Vol. 3 (november 2014) , p. 1224-1227  

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