Page last updated: 2024-08-24

adenosine and Fragile X Syndrome

adenosine has been researched along with Fragile X Syndrome in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Armida, M; Bagni, C; Borreca, A; Boussadia, Z; Ferrante, A; Mallozzi, C; Martire, A; Pacini, L; Pedini, G; Pezzola, A; Popoli, P; Varani, K; Vincenzi, F1
Jin, P; Kang, Y; Li, Y; Shu, Q; Song, H; Wang, M; Wu, H; Xu, T; Yang, W; Zhang, F1
Mackie, K; Min, KT; Straiker, A1
Astbury, C; Bass, HN; Gao, H; Jamehdor, MR; Liang, S; Qu, Y1
Carson, NL; Chudley, AE; Dawson, AJ; Mogk, RL1

Other Studies

5 other study(ies) available for adenosine and Fragile X Syndrome

ArticleYear
Adenosine A
    Translational psychiatry, 2021, 02-05, Volume: 11, Issue:1

    Topics: Adenosine; Animals; Cognition; Disease Models, Animal; Fragile X Mental Retardation Protein; Fragile X Syndrome; Hippocampus; Mice; Mice, Inbred C57BL; Mice, Knockout; Receptor, Adenosine A2A

2021
Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets.
    Human molecular genetics, 2018, 11-15, Volume: 27, Issue:22

    Topics: Adenosine; Animals; Cerebral Cortex; Disease Models, Animal; Epigenomics; Fragile X Mental Retardation Protein; Fragile X Syndrome; Gene Expression Regulation; Genome; Humans; Mice; Proteolysis; RNA-Binding Proteins; RNA, Messenger; Transcriptome

2018
Fmr1 deletion enhances and ultimately desensitizes CB(1) signaling in autaptic hippocampal neurons.
    Neurobiology of disease, 2013, Volume: 56

    Topics: Adenosine; Animals; Baclofen; Data Interpretation, Statistical; Electrophysiological Phenomena; Excitatory Postsynaptic Potentials; Fragile X Mental Retardation Protein; Fragile X Syndrome; GABA Agonists; Hippocampus; Methoxyhydroxyphenylglycol; Mice; Mice, Knockout; Neurons; Receptor, Cannabinoid, CB1; Receptors, Metabotropic Glutamate; Synapses

2013
A pseudo-full mutation identified in fragile X assay reveals a novel base change abolishing an EcoRI restriction site.
    The Journal of molecular diagnostics : JMD, 2008, Volume: 10, Issue:5

    Topics: Adenosine; Base Sequence; Blotting, Southern; Child, Preschool; DNA Mutational Analysis; DNA Restriction-Modification Enzymes; Female; Fragile X Mental Retardation Protein; Fragile X Syndrome; Humans; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Sequence Homology, Nucleic Acid; Trinucleotide Repeat Expansion

2008
Transmission of the FRAXA haplotype from three nonpenetrant brothers to their affected grandsons: an update with AGG interspersion analysis.
    American journal of medical genetics, 1998, Jan-06, Volume: 75, Issue:1

    Topics: Adenosine; Alleles; Base Composition; Base Sequence; Chromosome Fragility; Deoxyribonucleases, Type II Site-Specific; Female; Fragile X Syndrome; Genetic Linkage; Genetic Markers; Guanosine; Haplotypes; Humans; Male; Molecular Sequence Data; Pedigree; Sequence Analysis, DNA; Trinucleotide Repeats

1998