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Andreas Roos

Showing results (41-50 of 209) with videos related to

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Annals of the New York Academy of Sciences|January 10, 2018
Clinical and research strategies for limb-girdle congenital myasthenic syndromesEmily O'Connor, Ana Töpf, René P Zahedi, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variantAndreas Roos, Miriam Elbracht, Michael Baudis, et al.
Journal of Neuromuscular Diseases|November 9, 2020
Diagnosing X-linked Myotubular Myopathy - A German 20-year Follow Up ExperienceAndrea Gangfuss, Dirk Schmitt, Andreas Roos, et al.
Nature Communications|May 18, 2019
Proteome-wide detection of S-nitrosylation targets and motifs using bioorthogonal cleavable-linker-based enrichment and switch techniqueRuzanna Mnatsakanyan, Stavroula Markoutsa, Kim Walbrunn, et al.
Biomolecules|January 25, 2025
Proteomic Profiling Towards a Better Understanding of Genetic Based Muscular Diseases: The Current Picture and a Look to the FutureMarc Pauper, Andreas Hentschel, Malte Tiburcy, et al.
Thrombosis Journal|February 2, 2024
Causes of death after first time venous thromboembolismFrida Lonnberg, Andreas Roos, Maria Farm, et al.
Acta Neuropathologica|November 30, 2016
Towards a functional pathology of hereditary neuropathiesJoachim Weis, Kristl G Claeys, Andreas Roos, et al.
Human Molecular Genetics|February 21, 2018
MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretionEmily O'Connor, Vietxuan Phan, Isabell Cordts, et al.
International Journal of Cardiology|January 14, 2017
Investigations, findings, and follow-up in patients with chest pain and elevated high-sensitivity cardiac troponin T levels but no myocardial infarctionAndreas Roos, Anton Hellgren, Farshid Rafatnia, et al.
Biomolecules|October 26, 2024
A Deficiency in Glutamine-Fructose-6-Phosphate Transaminase 1 (Gfpt1) in Skeletal Muscle Results in Reduced Glycosylation of the Delta Subunit of the Nicotinic Acetylcholine Receptor (AChRδ)Stephen Henry Holland, Ricardo Carmona-Martinez, Kaela O'Connor, et al.
Pageof 21

Showing results (41-50 of 209) with videos related to

Sort By:
Pageof 21
Annals of the New York Academy of Sciences|January 10, 2018
Clinical and research strategies for limb-girdle congenital myasthenic syndromesEmily O'Connor, Ana Töpf, René P Zahedi, et al.
American Journal of Medical Genetics. Part A|August 14, 2008
A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variantAndreas Roos, Miriam Elbracht, Michael Baudis, et al.
Journal of Neuromuscular Diseases|November 9, 2020
Diagnosing X-linked Myotubular Myopathy - A German 20-year Follow Up ExperienceAndrea Gangfuss, Dirk Schmitt, Andreas Roos, et al.
Nature Communications|May 18, 2019
Proteome-wide detection of S-nitrosylation targets and motifs using bioorthogonal cleavable-linker-based enrichment and switch techniqueRuzanna Mnatsakanyan, Stavroula Markoutsa, Kim Walbrunn, et al.
Biomolecules|January 25, 2025
Proteomic Profiling Towards a Better Understanding of Genetic Based Muscular Diseases: The Current Picture and a Look to the FutureMarc Pauper, Andreas Hentschel, Malte Tiburcy, et al.
Thrombosis Journal|February 2, 2024
Causes of death after first time venous thromboembolismFrida Lonnberg, Andreas Roos, Maria Farm, et al.
Acta Neuropathologica|November 30, 2016
Towards a functional pathology of hereditary neuropathiesJoachim Weis, Kristl G Claeys, Andreas Roos, et al.
Human Molecular Genetics|February 21, 2018
MYO9A deficiency in motor neurons is associated with reduced neuromuscular agrin secretionEmily O'Connor, Vietxuan Phan, Isabell Cordts, et al.
International Journal of Cardiology|January 14, 2017
Investigations, findings, and follow-up in patients with chest pain and elevated high-sensitivity cardiac troponin T levels but no myocardial infarctionAndreas Roos, Anton Hellgren, Farshid Rafatnia, et al.
Biomolecules|October 26, 2024
A Deficiency in Glutamine-Fructose-6-Phosphate Transaminase 1 (Gfpt1) in Skeletal Muscle Results in Reduced Glycosylation of the Delta Subunit of the Nicotinic Acetylcholine Receptor (AChRδ)Stephen Henry Holland, Ricardo Carmona-Martinez, Kaela O'Connor, et al.
Pageof 21