受强制性开放获取政策约束的文章 - Daniel Cox了解详情
可在其他位置公开访问的文章：12 篇
Sympathetic innervation controls homeostasis of neuromuscular junctions in health and disease
MM Khan, D Lustrino, WA Silveira, F Wild, T Straka, Y Issop, E O’Connor, ...
Proceedings of the National Academy of Sciences 113 (3), 746-750, 2016
强制性开放获取政策： German Research Foundation, UK Medical Research Council, European Commission …
Identification of mutations in the MYO9A gene in patients with congenital myasthenic syndrome
E O’Connor, A Töpf, JS Müller, D Cox, T Evangelista, J Colomer, A Abicht, ...
Brain 139 (8), 2143-2153, 2016
强制性开放获取政策： UK Medical Research Council
Mutations in INPP5K, encoding a phosphoinositide 5-phosphatase, cause congenital muscular dystrophy with cataracts and mild cognitive impairment
M Wiessner, A Roos, CJ Munn, R Viswanathan, T Whyte, D Cox, ...
The American Journal of Human Genetics 100 (3), 523-536, 2017
强制性开放获取政策： UK Medical Research Council, National Institute for Health Research, UK …
Mitochondrial fragmentation enables localized signaling required for cell repair
A Horn, S Raavicharla, S Shah, D Cox, JK Jaiswal
Journal of Cell Biology 219 (5), e201909154, 2020
强制性开放获取政策： US National Institutes of Health
The beta-adrenergic agonist salbutamol modulates neuromuscular junction formation in zebrafish models of human myasthenic syndromes
G McMacken, D Cox, A Roos, J Müller, R Whittaker, H Lochmüller
Human Molecular Genetics 27 (9), 1556-1564, 2018
强制性开放获取政策： UK Medical Research Council, Wellcome Trust, Federal Ministry of Education …
High prevalence of plasma lipid abnormalities in human and canine Duchenne and Becker muscular dystrophies depicts a new type of primary genetic dyslipidemia
Z White, CH Hakim, M Theret, NN Yang, F Rossi, D Cox, GA Francis, ...
Journal of clinical lipidology 14 (4), 459-469. e0, 2020
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research …
SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human
V Phan, D Cox, S Cipriani, S Spendiff, S Buchkremer, E O'Connor, ...
Neurobiology of Disease 124, 218-229, 2019
强制性开放获取政策： UK Medical Research Council, Federal Ministry of Education and Research, Germany
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathy
A Töpf, D Cox, IT Zaharieva, V Di Leo, J Sarparanta, PH Jonson, IM Sealy, ...
Nature Genetics 56 (3), 395-407, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia, Academy of Finland …
Limb-girdle muscular dystrophy type 2B causes HDL-C abnormalities in patients and statin-resistant muscle wasting in dysferlin-deficient mice
Z White, Z Sun, E Sauge, D Cox, G Donen, D Pechkovsky, V Straub, ...
Skeletal Muscle 12 (1), 25, 2022
强制性开放获取政策： Canadian Institutes of Health Research
INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH
D Hathazi, D Cox, A d'Amico, G Tasca, R Charlton, RY Carlier, ...
Brain 144 (8), 2427-2442, 2021
强制性开放获取政策： Canadian Institutes of Health Research, Natural Sciences and Engineering …
Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy
U Moore, E Fernández-Simón, M Schiava, D Cox, H Gordish-Dressman, ...
Neuromuscular Disorders 33 (2), 199-207, 2023
强制性开放获取政策： National Institute for Health Research, UK
Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy
E Fernández-Simón, P Piñol-Jurado, R Gokul-Nath, A Unsworth, ...
Frontiers in Cell and Developmental Biology 12, 1399319, 2024
强制性开放获取政策： UK Medical Research Council
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