Researchposted Oct 26, 2020
Relevance of cancer cachexia models – muscle whole genome gene expression in human and animal cachexia
Rogier L.C. Plas, Guido Hooiveld, Renger F. Witkamp, Klaske van Norren
Under Review
at
Researchupdated Oct 12, 2020
TRAPPC11-related muscular dystrophy with hypoglycosylation of alpha-dystroglycan in skeletal muscle and brain.
Pinki Munot, Nadine McCrea, Silvia Torelli, Adnan Manzur, Caroline Sewry, Darren Chambers, Lucy Feng, and 13 more authors
Under Review
at
Researchposted Sep 28, 2020
Sarcoglycan A Mutation in Miniature Dachshund Dogs Causes Limb Girdle Muscular Dystrophy 2D
James R Mickelson, Katie M Minor, Ling T Guo, Steven G Friedenberg, Jonah N Cullen, Amanda Ciavarella, Lydia E Hambrook, and 4 more authors
Under Review
at
Researchupdated Sep 14, 2020
Complementary NAD+ Replacement Strategies Fail to Functionally Protect Dystrophin-Deficient Muscle
David Frederick, Alan V. McDougal, Melisa Semenas, Johanna Vappiani, Andrea Nuzzo, John C. Ulrich, Eugene L. Stewart, and 4 more authors
Published
at
Researchupdated Jun 26, 2020
X-linked muscular dystrophy in a Labrador Retriever strain: phenotypic and molecular characterization.
Inès Barthelemy, Nadège Calmels, Robert B. Weiss, Laurent Tiret, Adeline Vulin, Nicolas Wein, Cécile Peccate, and 11 more authors
Published
at
Researchupdated Jun 15, 2020
Exercise promotes satellite cell contribution to myofibers in a load-dependent manner
Evi Masschelein, Gommaar D'Hulst, Joel Zvick, Laura Hinte, Inés Soro-Arnaiz, Tatiane Gorski, Ferdinand von Meyenn, and 2 more authors
Published
at
Methodologyupdated May 28, 2020
Optimized method for extraction of exosomes from human primary muscle cells
Laura Le Gall, Zamalou Gisele Ouandaogo, Ekene Anakor, Owen Connolly, Gillian Butler Browne, Jeanne Laine, William John Duddy, and 1 more authors
Published
at
Researchposted May 22, 2020
A Newly Built rAAV-SaCas9 Genome Editing System Enables Muscle-Directed Gene Editing to Improve Muscular Atrophy
Shaoting Weng, Xingyu Li, Yitian Zhao, Feng Gao, Mengmeng Shi, Haoxiang Yang, Liqiang Han, and 2 more authors
Under Review
at
Researchposted May 20, 2020
Human Laminin-111 and Laminin-211 protein therapy prevents muscle disease progression in an immune deficient mouse model of LAMA2-CMD
Pamela Barraza-Flores, Hailey J. Hermann, Christina R. Bates, Tyler G. Allen, Timothy T. Grunert, Dean J. Burkin
Under Review
at
Researchposted Apr 23, 2020
SMN-deficiency disrupts SERCA2 expression and intracellular Ca2+ signaling in cardiomyocytes from SMA mice and patient-derived iPSCs
Guzal Khayrullina, Kasey E Moritz, James F. Schooley, Naheed Fatima, Coralie Viollet, Nikki McCormack, Jeremy T. Smyth, and 4 more authors
Under Review
at