受强制性开放获取政策约束的文章 - Luciano Merlini了解详情
无法在其他位置公开访问的文章：3 篇
查看
Expanding the clinical and genetic spectrum of pathogenic variants in STIM1
C Ticci, D Cassandrini, A Rubegni, B Riva, G Vattemi, S Matà, G Ricci, ...
Muscle & Nerve 64 (5), 567-575, 2021
强制性开放获取政策： Fondazione Telethon, Italy, Government of Italy
查看
Macrophages: a minimally invasive tool for monitoring collagen VI myopathies
F Gualandi, R Curci, P Sabatelli, E Martoni, M Bovolenta, MN Maraldi, ...
Muscle & nerve 44 (1), 80-84, 2011
强制性开放获取政策： Fondazione Telethon, Italy
查看
Protein aggregates and autophagy involvement in a family with a mutation in Z-band alternatively spliced PDZ-motif protein
D Cassandrini, L Merlini, F Pilla, V Cenni, S Santi, C Faldini, FM Santorelli, ...
Neuromuscular Disorders 31 (1), 44-51, 2021
强制性开放获取政策： Government of Italy
可在其他位置公开访问的文章：49 篇
查看
Guidelines for the use and interpretation of assays for monitoring autophagy
DJ Klionsky, K Abdelmohsen, A Abe, MJ Abedin, H Abeliovich, ...
Autophagy 12 (1), 1-222, 2016
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health, US …
查看
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
P Grumati, L Coletto, P Sabatelli, M Cescon, A Angelin, E Bertaggia, ...
Nature medicine 16 (11), 1313-1320, 2010
强制性开放获取政策： Fondazione Telethon, Italy
查看
Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study
I Dierick, J Baets, J Irobi, A Jacobs, E De Vriendt, T Deconinck, L Merlini, ...
Brain 131 (5), 1217-1227, 2008
强制性开放获取政策： Research Foundation (Flanders)
查看
Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies
M Zimoń, J Baets, M Auer-Grumbach, J Berciano, A Garcia, E Lopez-Laso, ...
Brain 133 (6), 1798-1809, 2010
强制性开放获取政策： US National Institutes of Health, Austrian Science Fund, Research Foundation …
查看
Early onset collagen VI myopathies: Genetic and clinical correlations
L Brinas, P Richard, S Quijano‐Roy, C Gartioux, C Ledeuil, E Lacène, ...
Annals of neurology 68 (4), 511-520, 2010
强制性开放获取政策： National Institute of Health and Medical Research, France
查看
Mutation spectrum in the large GTPase dynamin 2, and genotype–phenotype correlation in autosomal dominant centronuclear myopathy
J Böhm, V Biancalana, ET DeChene, M Bitoun, CR Pierson, E Schaefer, ...
Human mutation 33 (6), 949-959, 2012
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
查看
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies
P Sabatelli, SK Gara, P Grumati, A Urciuolo, F Gualandi, R Curci, ...
Journal of Investigative Dermatology 131 (1), 99-107, 2011
强制性开放获取政策： German Research Foundation, Fondazione Telethon, Italy
查看
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle
E Mattioli, M Columbaro, C Capanni, NM Maraldi, V Cenni, K Scotlandi, ...
Cell Death & Differentiation 18 (8), 1305-1315, 2011
强制性开放获取政策： Fondazione Telethon, Italy
查看
Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis
P Sabatelli, F Gualandi, SK Gara, P Grumati, A Zamparelli, E Martoni, ...
Matrix Biology 31 (3), 187-196, 2012
强制性开放获取政策： German Research Foundation, Fondazione Telethon, Italy
查看
NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models
A Zulian, E Rizzo, M Schiavone, E Palma, F Tagliavini, B Blaauw, ...
Human Molecular Genetics 23 (20), 5353-5363, 2014
强制性开放获取政策： Fondazione Telethon, Italy
查看
NaV1. 4 mutations cause hypokalaemic periodic paralysis by disrupting IIIS4 movement during recovery
JR Groome, F Lehmann-Horn, C Fan, M Wolf, V Winston, L Merlini, ...
Brain 137 (4), 998-1008, 2014
强制性开放获取政策： US National Institutes of Health
查看
Alisporivir rescues defective mitochondrial respiration in Duchenne muscular dystrophy
M Schiavone, A Zulian, S Menazza, V Petronilli, F Argenton, L Merlini, ...
Pharmacological Research 125, 122-131, 2017
强制性开放获取政策： Fondazione Telethon, Italy
查看
Cyclosporine A in Ullrich congenital muscular dystrophy: Long‐term results
L Merlini, P Sabatelli, A Armaroli, S Gnudi, A Angelin, P Grumati, ...
Oxidative medicine and cellular longevity 2011 (1), 139194, 2011
强制性开放获取政策： Fondazione Telethon, Italy
查看
Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis
A Citterio, A Arnoldi, E Panzeri, L Merlini, MG D’Angelo, O Musumeci, ...
Journal of neurology 262, 2684-2690, 2015
强制性开放获取政策： Government of Italy
查看
The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series
RN Villar-Quiles, M von Der Hagen, C Métay, V Gonzalez, S Donkervoort, ...
Neurology 95 (11), e1512-e1527, 2020
强制性开放获取政策： US National Institutes of Health, German Research Foundation, National …
查看
Monoamine oxidase inhibition prevents mitochondrial dysfunction and apoptosis in myoblasts from patients with collagen VI myopathies
E Sorato, S Menazza, A Zulian, P Sabatelli, F Gualandi, L Merlini, ...
Free radical biology and medicine 75, 40-47, 2014
强制性开放获取政策： Fondazione Telethon, Italy, Government of Italy
查看
Autophagy activation in COL6 myopathic patients by a low-protein-diet pilot trial
S Castagnaro, C Pellegrini, M Pellegrini, M Chrisam, P Sabatelli, S Toni, ...
Autophagy 12 (12), 2484-2495, 2016
强制性开放获取政策： Fondazione Telethon, Italy, Government of Italy
出版信息和资助信息由计算机程序自动确定