Page last updated: 2024-08-18

isomethyleugenol and Muscular Atrophy, Spinal

isomethyleugenol has been researched along with Muscular Atrophy, Spinal in 11 studies

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (18.18)18.2507
2000's6 (54.55)29.6817
2010's3 (27.27)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Peng, C; Wong, CC1
Allmang, C; Barkats, M; Cavarelli, J; Cura, V; Gribling-Burrer, AS; Huttin, A; Leichter, M; Massenet, S; Schlotter, F; Troffer-Charlier, N; Wurth, L1
Côté, J; Hubers, L; Laframboise, J; Sanchez, G; Timbers, J; Valderrama-Carvajal, H1
Autexier, C; Bachand, F; Boisvert, FM; Boulanger, MC; Cleroux, P; Cote, J; Richard, S1
Groves, MR; Sattler, M; Sinning, I; Sprangers, R1
Israël, M1
Androphy, EJ; Coon, K; Francis, JW; Lince, D; Lorson, CL; Young, PJ1
Boisvenue, S; Côté, J; Deschênes-Furry, J; Tadesse, H1
Bates, G; Lehrach, H1
Di Rocco, A; Simpson, DM1
Dreyfuss, G; Friesen, WJ; Massenet, S; Paushkin, S; Wyce, A1

Reviews

3 review(s) available for isomethyleugenol and Muscular Atrophy, Spinal

ArticleYear
The story of protein arginine methylation: characterization, regulation, and function.
    Expert review of proteomics, 2017, Volume: 14, Issue:2

    Topics: Arginine; Cardiovascular Diseases; DNA Repair; Humans; Mass Spectrometry; Methylation; Multiple Sclerosis; Muscular Atrophy, Spinal; Neoplasms; Protein Processing, Post-Translational; Protein-Arginine N-Methyltransferases; Proteins; Proteomics; Signal Transduction

2017
Trinucleotide repeat expansions and human genetic disease.
    BioEssays : news and reviews in molecular, cellular and developmental biology, 1994, Volume: 16, Issue:4

    Topics: Adult; Age of Onset; Base Sequence; Child; Embryonic and Fetal Development; Fragile X Syndrome; Genetic Diseases, Inborn; Humans; Huntington Disease; Infant, Newborn; Intellectual Disability; Male; Methylation; Middle Aged; Molecular Sequence Data; Muscular Atrophy, Spinal; Myotonic Dystrophy; Repetitive Sequences, Nucleic Acid; Spermatozoa; Spinocerebellar Degenerations

1994
AIDS-associated vacuolar myelopathy.
    AIDS patient care and STDs, 1998, Volume: 12, Issue:6

    Topics: Diagnosis, Differential; Disease Progression; HIV Infections; Humans; Male; Methylation; Muscular Atrophy, Spinal; Parasympatholytics; Physical Therapy Modalities; Vitamin B 12

1998

Other Studies

8 other study(ies) available for isomethyleugenol and Muscular Atrophy, Spinal

ArticleYear
SECIS-binding protein 2 interacts with the SMN complex and the methylosome for selenoprotein mRNP assembly and translation.
    Nucleic acids research, 2017, May-19, Volume: 45, Issue:9

    Topics: Glutathione Peroxidase; Glutathione Peroxidase GPX1; HEK293 Cells; HeLa Cells; Humans; Methylation; Models, Biological; Muscular Atrophy, Spinal; Protein Binding; Protein Biosynthesis; Ribonucleoproteins; RNA-Binding Proteins; Selenoproteins; SMN Complex Proteins; Spinal Cord

2017
HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.
    Human molecular genetics, 2011, Feb-01, Volume: 20, Issue:3

    Topics: Animals; Base Sequence; Cell Cycle; Cell Cycle Proteins; Cell Line; ELAV Proteins; ELAV-Like Protein 4; Fluorescent Antibody Technique; Gene Expression; Gene Knockdown Techniques; Immunoblotting; Methylation; Mice; Muscular Atrophy, Spinal; Mutation; Nerve Growth Factors; Neurites; Phenotype; Polymerase Chain Reaction; Protein Interaction Domains and Motifs; Protein-Arginine N-Methyltransferases; Retinol-Binding Proteins; RNA, Messenger; RNA, Small Interfering; Signal Transduction; Survival of Motor Neuron 1 Protein

2011
Symmetrical dimethylarginine methylation is required for the localization of SMN in Cajal bodies and pre-mRNA splicing.
    The Journal of cell biology, 2002, Dec-23, Volume: 159, Issue:6

    Topics: Antibodies; Arginine; Cell Nucleus; Coiled Bodies; DNA; Dose-Response Relationship, Drug; Down-Regulation; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; Fibroblasts; Fluorescent Antibody Technique, Indirect; HeLa Cells; Humans; Mass Spectrometry; Methylation; Microscopy, Fluorescence; Muscular Atrophy, Spinal; Precipitin Tests; RNA Splicing; RNA, Messenger; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Transfection

2002
High-resolution X-ray and NMR structures of the SMN Tudor domain: conformational variation in the binding site for symmetrically dimethylated arginine residues.
    Journal of molecular biology, 2003, Mar-21, Volume: 327, Issue:2

    Topics: Arginine; Binding Sites; Crystallography, X-Ray; Cyclic AMP Response Element-Binding Protein; Glycine; Humans; Methylation; Models, Molecular; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Nuclear Magnetic Resonance, Biomolecular; Protein Binding; Protein Conformation; Protein Folding; Protein Structure, Tertiary; RNA-Binding Proteins; SMN Complex Proteins

2003
Genetic adaptation controlled by methylations and acetylations at the nuclear and cytosolic levels: a hypothetical model.
    Neurochemical research, 2003, Volume: 28, Issue:3-4

    Topics: Acetylation; Adaptation, Physiological; Animals; Cell Nucleus; Cytosol; Gene Expression Regulation; Gene Silencing; Humans; Methylation; Models, Genetic; Muscular Atrophy, Spinal

2003
The Ewing's sarcoma protein interacts with the Tudor domain of the survival motor neuron protein.
    Brain research. Molecular brain research, 2003, Nov-06, Volume: 119, Issue:1

    Topics: Animals; Arginine; Binding Sites; Cell Line, Tumor; Cell Nucleus; Cells, Cultured; Cyclic AMP Response Element-Binding Protein; Exons; Humans; Methylation; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Neurons; Peptides; Protein Binding; Protein Structure, Tertiary; Rats; RNA-Binding Protein EWS; RNA-Binding Proteins; RNA, Antisense; SMN Complex Proteins; Survival of Motor Neuron 1 Protein

2003
KH-type splicing regulatory protein interacts with survival motor neuron protein and is misregulated in spinal muscular atrophy.
    Human molecular genetics, 2008, Feb-15, Volume: 17, Issue:4

    Topics: Amino Acid Sequence; Animals; Arginine; Base Sequence; Binding Sites; Cell Line; Cyclic AMP Response Element-Binding Protein; DNA Primers; Gene Expression Regulation; Humans; Methylation; Mice; Mice, Knockout; Mice, Mutant Strains; Molecular Chaperones; Molecular Sequence Data; Motor Neurons; Muscular Atrophy, Spinal; Mutation; Nerve Tissue Proteins; Protein Structure, Tertiary; Protein-Arginine N-Methyltransferases; RNA Stability; RNA-Binding Proteins; RNA, Messenger; Sequence Homology, Amino Acid; SMN Complex Proteins; Survival of Motor Neuron 1 Protein; Trans-Activators

2008
SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets.
    Molecular cell, 2001, Volume: 7, Issue:5

    Topics: Amino Acid Sequence; Arginine; Autoantigens; Cyclic AMP Response Element-Binding Protein; Enzyme Inhibitors; HeLa Cells; Humans; Methylation; Molecular Sequence Data; Muscular Atrophy, Spinal; Nerve Tissue Proteins; Protein Binding; Recombinant Fusion Proteins; Ribonucleoproteins, Small Nuclear; RNA-Binding Proteins; SMN Complex Proteins; snRNP Core Proteins; Substrate Specificity

2001