Compounds > isomethyleugenol
Page last updated: 2024-08-18

isomethyleugenol and Decreased Muscle Tone

isomethyleugenol has been researched along with Decreased Muscle Tone in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's2 (33.33)24.3611
2020's1 (16.67)2.80

Authors

AuthorsStudies
Dong, GQ; Huang, M; Li, JX; Lu, XY; Luo, XP; Qiu, XY; Su, YY1
Birnbaum, R; Gur, H; Kidron, D; Lerman-Sagie, T; Lev, D; Malinger, G; Yanoov-Sharav, M; Yosha-Orpaz, N; Yosovich, K1
Cambi, F; Haziza, S; Hershkovitz, E; Houtz, R; Magen, S; Magnani, R; Parvari, R1
Bosio, L; Corrias, A; Crinò, A; Gargantini, L; Livieri, C; Pozzan, G; Trifirò, G1
Gillessen-Kaesbach, G; Gross, S; Horsthemke, B; Kaya-Westerloh, S; Passarge, E1
Bräutigam, C; Hoffman, GF; Hyland, K; Knust, A; Sharma, RK; Wevers, RA1

Other Studies

6 other study(ies) available for isomethyleugenol and Decreased Muscle Tone

ArticleYear
[Clinical screening and genetic diagnosis for Prader-Willi syndrome].
    Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2020, Volume: 22, Issue:9

    Topics: Cesarean Section; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Male; Methylation; Muscle Hypotonia; Prader-Willi Syndrome; Pregnancy

2020
Prenatal and postnatal presentation of PRMT7 related syndrome: Expanding the phenotypic manifestations.
    American journal of medical genetics. Part A, 2019, Volume: 179, Issue:1

    Topics: Arginine; Astrocytoma; Brachydactyly; Developmental Disabilities; Female; Fetal Growth Retardation; Humans; Infant; Infant, Newborn; Intellectual Disability; Male; Methylation; Muscle Hypotonia; Mutation; Orbital Neoplasms; Pregnancy; Protein-Arginine N-Methyltransferases

2019
Human calmodulin methyltransferase: expression, activity on calmodulin, and Hsp90 dependence.
    PloS one, 2012, Volume: 7, Issue:12

    Topics: Amino Acid Sequence; Animals; Base Sequence; Benzoquinones; Calmodulin; Cell Line; Chromosome Deletion; Chromosomes, Human, Pair 21; Craniofacial Abnormalities; Cystinuria; Green Fluorescent Proteins; HSP90 Heat-Shock Proteins; Humans; Intellectual Disability; Lactams, Macrocyclic; Methylation; Methyltransferases; Mice; Mice, Inbred ICR; Mitochondrial Diseases; Molecular Sequence Data; Muscle Hypotonia; Protein Binding; Protein Stability; Protein Structure, Tertiary; Protein Transport; Proteolysis; Recombinant Fusion Proteins; Subcellular Fractions; Transcription, Genetic

2012
Neonatal hypotonia: don't forget the Prader-Willi syndrome.
    Acta paediatrica (Oslo, Norway : 1992), 2003, Volume: 92, Issue:9

    Topics: Adult; Female; Humans; In Situ Hybridization, Fluorescence; Male; Methylation; Muscle Hypotonia; Prader-Willi Syndrome

2003
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome.
    Journal of medical genetics, 1995, Volume: 32, Issue:2

    Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Diagnosis, Differential; DNA; DNA Probes; Female; Genetic Markers; Humans; Infant; Male; Methylation; Muscle Hypotonia; Polymorphism, Restriction Fragment Length; Prader-Willi Syndrome

1995
The influence of L-dopa on methylation capacity in aromatic L-amino acid decarboxylase deficiency: biochemical findings in two patients.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Dopamine; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Hypokinesia; Levodopa; Methoxyhydroxyphenylglycol; Methylation; Muscle Hypotonia; Tetrahydrofolates; Tyrosine

2000