Page last updated: 2024-11-08

serine and Fragile X Syndrome

serine has been researched along with Fragile X Syndrome in 8 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)

Research Excerpts

ExcerptRelevanceReference
"Fragile X syndrome is caused by loss of FMR1 protein expression."1.31Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties. ( Higashijima, K; Ishizuka, A; Siomi, H; Siomi, MC, 2002)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (12.50)29.6817
2010's6 (75.00)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Nolin, SL1
Napoli, E1
Flores, A1
Hagerman, RJ1
Giulivi, C1
Bostrom, CA1
Majaess, NM1
Morch, K1
White, E1
Eadie, BD1
Christie, BR1
Kang, JY1
Chadchankar, J1
Vien, TN1
Mighdoll, MI1
Hyde, TM1
Mather, RJ1
Deeb, TZ1
Pangalos, MN1
Brandon, NJ1
Dunlop, J1
Moss, SJ1
Sharma, A1
Hoeffer, CA1
Takayasu, Y1
Miyawaki, T1
McBride, SM1
Klann, E1
Zukin, RS1
Yuskaitis, CJ1
Beurel, E1
Jope, RS1
Coffee, RL1
Williamson, AJ1
Adkins, CM1
Gray, MC1
Page, TL1
Broadie, K1
Ronesi, JA1
Collins, KA1
Hays, SA1
Tsai, NP1
Guo, W1
Birnbaum, SG1
Hu, JH1
Worley, PF1
Gibson, JR1
Huber, KM1
Siomi, MC1
Higashijima, K1
Ishizuka, A1
Siomi, H1

Other Studies

8 other studies available for serine and Fragile X Syndrome

ArticleYear
Deficits in Prenatal Serine Biosynthesis Underlie the Mitochondrial Dysfunction Associated with the Autism-Linked
    International journal of molecular sciences, 2021, May-30, Volume: 22, Issue:11

    Topics: 5' Untranslated Regions; Adult; Amniocentesis; Amniotic Fluid; Autistic Disorder; Citric Acid Cycle;

2021
Rescue of NMDAR-dependent synaptic plasticity in Fmr1 knock-out mice.
    Cerebral cortex (New York, N.Y. : 1991), 2015, Volume: 25, Issue:1

    Topics: Animals; Fragile X Mental Retardation Protein; Fragile X Syndrome; Glycine; Hippocampus; Long-Term P

2015
Deficits in the activity of presynaptic γ-aminobutyric acid type B receptors contribute to altered neuronal excitability in fragile X syndrome.
    The Journal of biological chemistry, 2017, 04-21, Volume: 292, Issue:16

    Topics: Aged; Aged, 80 and over; Animals; Behavior, Animal; Disease Models, Animal; Fragile X Mental Retarda

2017
Dysregulation of mTOR signaling in fragile X syndrome.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010, Jan-13, Volume: 30, Issue:2

    Topics: Adaptor Proteins, Signal Transducing; Animals; CA1 Region, Hippocampal; Carrier Proteins; Cell Cycle

2010
Evidence of reactive astrocytes but not peripheral immune system activation in a mouse model of Fragile X syndrome.
    Biochimica et biophysica acta, 2010, Volume: 1802, Issue:11

    Topics: Animals; Astrocytes; Brain; Cytokines; Disease Models, Animal; Female; Fragile X Mental Retardation

2010
In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation.
    Human molecular genetics, 2012, Feb-15, Volume: 21, Issue:4

    Topics: Animals; Animals, Genetically Modified; Brain; Cytoskeleton; Disease Models, Animal; Drosophila mela

2012
Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome.
    Nature neuroscience, 2012, Jan-22, Volume: 15, Issue:3

    Topics: Analysis of Variance; Animals; Carrier Proteins; Cycloheximide; Disease Models, Animal; Electric Sti

2012
Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties.
    Molecular and cellular biology, 2002, Volume: 22, Issue:24

    Topics: Amino Acid Sequence; Animals; Casein Kinase II; Cell Fractionation; Cell Line; DNA-Binding Proteins;

2002