অনুসন্ধান ফলাফলগুলি - B. Udd
- প্রদর্শন 1 - 4 ফলাফল এর 4
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1
Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression অনুযায়ী Daphne Wijnbergen, Mridul Johari, Ozan Özışık, Peter A.C. ‘t Hoen, Friederike Ehrhart, Anaı̈s Baudot, Chris T. Evelo, B. Udd, Marco Roos, Eleni Mina
প্রকাশিত 2025Artigo -
2
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy অনুযায়ী Phillipa J. Lamont, B. Udd, Francis Mastaglia, Marjolein Visser, Peter Hedera, Thomas Voït, Leslie Bridges, V. Fabian, Annemieke J.M. Rozemüller, Nigel G. Laing
প্রকাশিত 2005Artigo -
3
Mutations in DNMT3B Modify Epigenetic Repression of the D4Z4 Repeat and the Penetrance of Facioscapulohumeral Dystrophy অনুযায়ী Marlinde L. van den Boogaard, Richard J.L.F. Lemmers, Judit Balog, Mariëlle Wohlgemuth, Mari Auranen, Satomi Mitsuhashi, Patrick J. van der Vliet, Kirsten R. Straasheijm, Rob F. P. van den Akker, Marjolein Kriek, Marlies E.Y. Laurense-Bik, Vered Raz, Monique M. van Ostaijen-ten Dam, Kerstin Hansson, E.L. van der Kooi, Sari Kiuru‐Enari, B. Udd, Maarten J. D. van Tol, Ichizo Nishino, Rabi Tawil, Stephen J. Tapscott, Baziel G.M. van Engelen, Silvère M. van der Maarel
প্রকাশিত 2016Artigo -
4
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy অনুযায়ী Jorge Alonso‐Pérez, Lídia González-Quereda, Luca Bello, Michela Guglieri, Volker Straub, P. Gallano, Claudio Semplicini, Elena Pegoraro, Vittoria Zangaro, Andrés Nascimento, C. Ortez, Giacomo P. Comi, Leroy ten Dam, Marjolein Visser, Anneke J. van der Kooi, Cristina Garrido, Manuela Santos, Ulrike Schara, Andrea Gangfuß, Nicoline Løkken, J. Storgaard, John Vissing, Benedikt Schoser, Gabriele Dekomien, B. Udd, Johanna Palmio, Adele D'Amico, Luisa Politano, Vincenzo Nigro, Claudio Bruno, Chiara Panicucci, Anna Sárközy, Omar Abdel‐Mannan, Alicia Alonso‐Jiménez, Kristl G. Claeys, David Gómez‐Andrés, Francina Munell, Laura Costa-Comellas, Jana Haberlová, Marie Rohlenová, De Vos Elke, Jan De Bleecker, Cristina Domínguez‐González, Giorgio Tasca, Claudia Weiß, Nicolas Deconinck, Roberto Fernández‐Torrón, Adolfo López de Munaín, Ana Camacho, Béla Melegh, Kinga Hadzsiev, Lea Leonardis, Blaž Koritnik, Matteo Garibaldi, Juan C. de León-Hernández, Edoardo Malfatti, Arturo Fraga-Bau, Isabelle Richard, Isabel Illa, Jordi Díaz-Manera
প্রকাশিত 2020Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
Biology
Gene
Genetics
Internal medicine
Medicine
Anatomy
Bioinformatics
Biophysics
Biopsy
Cardiomyopathy
Cohort
Cohort study
Compound heterozygosity
Computational biology
Congenital myopathy
DNMT3B
Disease
Epigenetics
Facioscapulohumeral muscular dystrophy
Gene expression
Genotype
Heart failure
Human genetics
Inclusion body myositis
MYH7
Methylation
Methyltransferase
Muscle biopsy
Muscle weakness
Muscular dystrophy