Fragile X-related proteins regulate mammalian circadian behavioral rhythms. - Wikidata - wikimedia - TriplyDB

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

http://www.wikidata.org/entity/Q36744675

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PML regulates PER2 nuclear localization and circadian function Circadian organization of behavior and physiology in Drosophila Altered Neuronal and Circuit Excitability in Fragile X Syndrome.Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.Synchronization of Biological Clock Neurons by Light and Peripheral Feedback Systems Promotes Circadian Rhythms and Health Sleep and sleep disorders in rare hereditary diseases: a reminder for the pediatrician, pediatric and adult neurologist, general practitioner, and sleep specialist Ribonucleoprotein complexes that control circadian clocks Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus Synaptic plasticity in sleep: learning, homeostasis and disease Fragile X Proteins FMRP and FXR2P Control Synaptic GluA1 Expression and Neuronal Maturation via Distinct Mechanisms.Linking neural activity and molecular oscillations in the SCN.Fragile X mental retardation protein is required for rapid experience-dependent regulation of the potassium channel Kv3.1b Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P Circuit level defects in the developing neocortex of Fragile X mice.Fragile X Mental Retardation Protein expression in the retina is regulated by light Sleep, plasticity and the pathophysiology of neurodevelopmental disorders: the potential roles of protein synthesis and other cellular processes.In vivo monitoring of multi-unit neural activity in the suprachiasmatic nucleus reveals robust circadian rhythms in Period1⁻/⁻ mice.New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.Sleep in Neurodevelopmental Disorders.Prevalence, nature, and correlates of sleep problems among children with fragile X syndrome based on a large scale parent survey.Melatonin as a Novel Interventional Candidate for Fragile X Syndrome with Autism Spectrum Disorder in Humans Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.Short- and long-term memory are modulated by multiple isoforms of the fragile X mental retardation protein Genetic analysis of sleep.Circadian rhythm-dependent alterations of gene expression in Drosophila brain lacking fragile X mental retardation protein Concise review: Fragile X proteins in stem cell maintenance and differentiation Protein interactome reveals converging molecular pathways among autism disorders.The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice.Altered neocortical rhythmic activity states in Fmr1 KO mice are due to enhanced mGluR5 signaling and involve changes in excitatory circuitry FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124 Common genetic variants in ARNTL and NPAS2 and at chromosome 12p13 are associated with objectively measured sleep traits in the elderly.MBD5 haploinsufficiency is associated with sleep disturbance and disrupts circadian pathways common to Smith-Magenis and fragile X syndromes.FMR1, circadian genes and depression: suggestive associations or false discovery?Comprehensive motor testing in Fmr1-KO mice exposes temporal defects in oromotor coordination The Drosophila FMRP and LARK RNA-binding proteins function together to regulate eye development and circadian behavior Behavioral Phenotype of Fmr1 Knock-Out Mice during Active Phase in an Altered Light/Dark Cycle.Altered hippocampal synaptic plasticity in the FMR1 gene family knockout mouse models.Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs.Temporal requirements of the fragile x mental retardation protein in modulating circadian clock circuit synaptic architecture.Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.

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P2860

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

http://www.wikidata.org/entity/Q36744675

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name

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

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Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

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type

label

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

@ast

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

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prefLabel

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

@ast

Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

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J.AJHG.2008.06.003

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American Journal of Human Genetics

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Fragile X-related proteins regulate mammalian circadian behavioral rhythms.

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Ben A Oostra

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Cheng Chi Lee

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Corinne Jud

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David L Nelson

http://www.w3.org/2001/XMLSchema#string

Filippo Tamanini

http://www.w3.org/2001/XMLSchema#string

Jing Zhang

http://www.w3.org/2001/XMLSchema#string

Johanna H Meijer

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Krista Kaasik

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Mariska J Vansteensel

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Zhe Fang

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P2860

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

The basic-helix-loop-helix-PAS orphan MOP3 forms transcriptionally active complexes with circadian and hypoxia factors

FXR1, an autosomal homolog of the fragile X mental retardation gene

CLOCK and NPAS2 have overlapping roles in the suprachiasmatic circadian clock

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

Coordination of circadian timing in mammals

NPAS2: an analog of clock operative in the mammalian forebrain.

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association

Comparative genomic sequence analysis of the FXR gene family: FMR1, FXR1, and FXR2

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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43-52

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1

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circadian rhythm

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2443847

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