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Page last updated: 2024-08-17

lysine and Limb-Girdle Muscular Dystrophies

lysine has been researched along with Limb-Girdle Muscular Dystrophies in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Garcia-Garcia, J; Khan, W; Overå, KS; Sjøttem, E1
Antonioli, M; Ciccosanti, F; Corazzari, M; De La Torre, R; Dentice, M; Di Rienzo, M; Ding, H; Ferlini, A; Fimia, GM; Fusco, C; Germani, F; Kulesz-Martin, M; Liu, Y; Mandriani, B; Mari, M; Merla, G; Neri, M; Orhon, I; Pellico, MT; Piacentini, M; Refolo, G; Reggiori, F; Romagnoli, A1
Hayashi, YK; Matsuda, C; Minami, N; Mitsuhashi, H; Nishino, I; Noguchi, S; Nonaka, I; Shalaby, S1
Bierhaus, A; Friess, U; Haslbeck, KM; Heuss, D; Kirchner, A; Nawroth, PP; Neundörfer, B; Pauli, E; Schleicher, ED1
Briggs, CE; Darras, BT; Duncan, DR; Kang, PB; Kunkel, LM; Lidov, HG; Rabbat, JC1

Other Studies

5 other study(ies) available for lysine and Limb-Girdle Muscular Dystrophies

ArticleYear
Generation of the short TRIM32 isoform is regulated by Lys 247 acetylation and a PEST sequence.
    PloS one, 2021, Volume: 16, Issue:5

    Topics: Acetylation; Cell Line; HEK293 Cells; Humans; Lysine; Muscular Dystrophies, Limb-Girdle; Protein Binding; Protein Isoforms; Protein Processing, Post-Translational; Transcription Factors; Tripartite Motif Proteins; Ubiquitin-Protein Ligases; Ubiquitination

2021
Autophagy induction in atrophic muscle cells requires ULK1 activation by TRIM32 through unanchored K63-linked polyubiquitin chains.
    Science advances, 2019, Volume: 5, Issue:5

    Topics: Adaptor Proteins, Signal Transducing; Animals; Autophagy; Autophagy-Related Protein-1 Homolog; Cell Line; Cell Transdifferentiation; Humans; Lysine; Mice; Mice, Knockout; Muscular Dystrophies, Limb-Girdle; Myoblasts; Protein Binding; RNA Interference; RNA, Small Interfering; Ubiquitin-Protein Ligases; Ubiquitination

2019
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient.
    Journal of neuropathology and experimental neurology, 2009, Volume: 68, Issue:6

    Topics: Actinin; Animals; Arginine; Chlorocebus aethiops; Connectin; COS Cells; Cytoskeletal Proteins; DNA Mutational Analysis; Exons; Female; Humans; Immunoprecipitation; Japan; Lysine; Male; Microfilament Proteins; Middle Aged; Molecular Sequence Data; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; NAD; Protein Structure, Tertiary; Serine; Transfection; Two-Hybrid System Techniques

2009
The RAGE pathway in inflammatory myopathies and limb girdle muscular dystrophy.
    Acta neuropathologica, 2005, Volume: 110, Issue:3

    Topics: Adult; Aged; Dermatomyositis; Glycation End Products, Advanced; Humans; Immunohistochemistry; Leukocytes, Mononuclear; Lysine; Middle Aged; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophies, Limb-Girdle; Myositis; NF-kappa B; Polymyositis; Receptor for Advanced Glycation End Products; Receptors, Immunologic; Regeneration; Signal Transduction; Transcriptional Activation

2005
A novel mutation in two families with limb-girdle muscular dystrophy type 2C.
    Neurology, 2006, Jul-11, Volume: 67, Issue:1

    Topics: Adolescent; Child; Child, Preschool; Connectin; DNA Mutational Analysis; Exons; Family Health; Female; Glutamic Acid; Humans; Lysine; Male; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation

2006