Dysregulated COMT Expression in Fragile X Syndrome.
暂无分享,去创建一个
K. H. Utami | M. Pouladi | Prabha Sampath | N. Skotte | S. Nama | M. Garcia-Miralles | N. Yusof | Niels Henning Skotte | Prabha Sampath | Sarah R Langley
[1] Samir Ruxmohan,et al. Behavioral Problems in Fragile X Syndrome: A Review of Clinical Management , 2022, Cureus.
[2] Joseph P. McCleery,et al. Genetic modifiers in rare disorders: the case of fragile X syndrome , 2020, European journal of human genetics : EJHG.
[3] K. H. Utami,et al. Elevated de novo protein synthesis in FMRP-deficient human neurons and its correction by metformin treatment , 2020, Molecular Autism.
[4] Deborah Chasman,et al. Identification of FMR1-regulated molecular networks in human neurodevelopment , 2020, Genome research.
[5] Virginia C. Salo,et al. Relations between catechol-O-methyltransferase Val158Met genotype and inhibitory control development in childhood. , 2019, Developmental psychobiology.
[6] M. Mann,et al. Integrative Analysis Identifies Key Molecular Signatures Underlying Neurodevelopmental Deficits in Fragile X Syndrome , 2019, Biological Psychiatry.
[7] B. Bardoni,et al. HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein , 2018, Nucleic acids research.
[8] Steven Taylor,et al. Association between COMT Val158Met and psychiatric disorders: A comprehensive meta‐analysis , 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[9] Heather Cody Hazlett,et al. Fragile X syndrome , 2017, Nature Reviews Disease Primers.
[10] A. Fresán,et al. The Role of a Catechol-O-Methyltransferase (COMT) Val158Met Genetic Polymorphism in Schizophrenia: A Systematic Review and Updated Meta-analysis on 32,816 Subjects , 2016, NeuroMolecular Medicine.
[11] Qi Ding,et al. Behavioral analysis of male and female Fmr1 knockout mice on C57BL/6 background , 2014, Behavioural Brain Research.
[12] B. Kolachana,et al. Biological Effects of COMT Haplotypes and Psychosis Risk in 22q11.2 Deletion Syndrome , 2014, Biological Psychiatry.
[13] M. Stanford,et al. Association of the COMT Met¹⁵⁸ allele with trait impulsivity in healthy young adults. , 2013, Molecular medicine reports.
[14] Uwe Ohler,et al. FMR1 targets distinct mRNA sequence elements to regulate protein expression , 2012, Nature.
[15] D. Licatalosi,et al. FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism , 2011, Cell.
[16] H. Rauvala,et al. Effect of S-COMT deficiency on behavior and extracellular brain dopamine concentrations in mice , 2010, Psychopharmacology.
[17] C. Freitag,et al. Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant , 2010, Journal of Neural Transmission.
[18] J. Waddington,et al. Exploratory and habituation phenotype of heterozygous and homozygous COMT knockout mice , 2007, Behavioural Brain Research.
[19] M C O'Donovan,et al. The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons , 2006, Molecular Psychiatry.
[20] D. Collier,et al. The quantification of COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression , 2006, BMC Medical Genetics.
[21] Y. Gomita,et al. Effect of methamphetamine and imipramine on cerebral ischemia-induced hyperactivity in Mongolian gerbils. , 2002, Japanese journal of pharmacology.
[22] D. Pfaff,et al. Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[23] G. Turner. Fragile X Syndrome: Diagnosis, Treatment and Research , 1997 .