acetylcysteine and Distal Myopathies

acetylcysteine has been researched along with Distal Myopathies in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cho, A; Christine, M; Malicdan, V; Miyakawa, M; Nishino, I; Noguchi, S; Nonaka, I	1
Azakir, BA; Di Fulvio, S; Kinter, J; Sinnreich, M	1

Other Studies

2 other study(ies) available for acetylcysteine and Distal Myopathies

Article	Year
Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy. Human molecular genetics, 2017, 08-15, Volume: 26, Issue:16 Topics: Acetylcysteine; Animals; Disease Models, Animal; Distal Myopathies; Humans; Mice; Mice, Knockout; Multienzyme Complexes; Muscle Proteins; Muscle, Skeletal; Muscular Atrophy; N-Acetylneuraminic Acid; Oxidative Stress; Reactive Oxygen Species	2017
Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells. The Journal of biological chemistry, 2012, Mar-23, Volume: 287, Issue:13 Topics: Acetylcysteine; Alleles; Amino Acid Substitution; Antineoplastic Agents; Boronic Acids; Bortezomib; Cells, Cultured; Cysteine Proteinase Inhibitors; Distal Myopathies; Dysferlin; Humans; Membrane Proteins; Muscle Fibers, Skeletal; Muscle Proteins; Muscular Atrophy; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Proteolysis; Pyrazines; RNA, Messenger	2012

Article

Year

Sialic acid deficiency is associated with oxidative stress leading to muscle atrophy and weakness in GNE myopathy.

Human molecular genetics, 2017, 08-15, Volume: 26, Issue:16

Topics: Acetylcysteine; Animals; Disease Models, Animal; Distal Myopathies; Humans; Mice; Mice, Knockout; Multienzyme Complexes; Muscle Proteins; Muscle, Skeletal; Muscular Atrophy; N-Acetylneuraminic Acid; Oxidative Stress; Reactive Oxygen Species

2017

Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells.

The Journal of biological chemistry, 2012, Mar-23, Volume: 287, Issue:13

Topics: Acetylcysteine; Alleles; Amino Acid Substitution; Antineoplastic Agents; Boronic Acids; Bortezomib; Cells, Cultured; Cysteine Proteinase Inhibitors; Distal Myopathies; Dysferlin; Humans; Membrane Proteins; Muscle Fibers, Skeletal; Muscle Proteins; Muscular Atrophy; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Proteasome Endopeptidase Complex; Proteasome Inhibitors; Proteolysis; Pyrazines; RNA, Messenger

2012