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Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies.
Ayoglu, Burcu; Chaouch, Amina; Lochmüller, Hanns; Politano, Luisa; Bertini, Enrico; Spitali, Pietro; Hiller, Monika; Niks, Eric H; Gualandi, Francesca; Pontén, Fredrik; Bushby, Kate; Aartsma-Rus, Annemieke; Schwartz, Elena; Le Priol, Yannick; Straub, Volker; Uhlén, Mathias; Cirak, Sebahattin; 't Hoen, Peter A C; Muntoni, Francesco; Ferlini, Alessandra; Schwenk, Jochen M; Nilsson, Peter; Al-Khalili Szigyarto, Cristina.
Afiliação
  • Ayoglu B; Affinity Proteomics, SciLifeLab, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Chaouch A; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Lochmüller H; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Politano L; Cardiomiology and Medical Genetics, Department of Experimental Medicine, Second University of Naples, Naples, Italy.
  • Bertini E; Unit of Neuromuscular and Neurodegenerative Disorders, Department of Neurosciences, Bambino Gesú Children's Hospital, Rome, Italy.
  • Spitali P; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Hiller M; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Niks EH; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
  • Gualandi F; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Pontén F; SciLifeLab, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
  • Bushby K; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Aartsma-Rus A; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Schwartz E; Ariadne Diagnostics, Rockville, MD, USA.
  • Le Priol Y; Elsevier, Amsterdam, The Netherlands.
  • Straub V; Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK.
  • Uhlén M; Affinity Proteomics, SciLifeLab, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Cirak S; Research Center for Genetic Medicine, Childrens National Medical Center, Washington, DC, USA.
  • 't Hoen PA; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Muntoni F; The Dubowitz Neuromuscular Centre, UCL Institute of Child Health, London, UK.
  • Ferlini A; Unit of Medical Genetics, Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
  • Schwenk JM; Affinity Proteomics, SciLifeLab, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Nilsson P; Affinity Proteomics, SciLifeLab, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden.
  • Al-Khalili Szigyarto C; Department of Proteomics, School of Biotechnology KTH-Royal Institute of Technology, Stockholm, Sweden caks@kth.se.
EMBO Mol Med ; 6(7): 918-36, 2014 Jul.
Article em En | MEDLINE | ID: mdl-24920607
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Sanguíneas / Distrofia Muscular de Duchenne Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Sanguíneas / Distrofia Muscular de Duchenne Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article