The Role of MicroRNAs in Cerebellar Development and Autism Spectrum Disorder During Embryogenesis (Q38989159)

8 September 2017

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title

The Role of MicroRNAs in Cerebellar Development and Autism Spectrum Disorder During Embryogenesis (English)

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8 September 2017

autism spectrum disorder

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Lena Constantin

1

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publication date

24 October 2016

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8 September 2017

Molecular Neurobiology

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https://scigraph.springernature.com/pub.10.1007/s12035-016-0220-9

8 September 2017

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cites work

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Radially expanding transglial calcium waves in the intact cerebellum

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Glia-synapse interaction through Ca2+-permeable AMPA receptors in Bergmann glia

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Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain

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Dicer Is Required for Normal Cerebellar Development and to Restrain Medulloblastoma Formation

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Site-specific DICER and DROSHA RNA products control the DNA-damage response

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Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog

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Purkinje-cell-derived Sonic hedgehog regulates granule neuron precursor cell proliferation in the developing mouse cerebellum

21 January 2018

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Sonic hedgehog patterning during cerebellar development

21 January 2018

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The miR-17/92 polycistron is up-regulated in sonic hedgehog-driven medulloblastomas and induced by N-myc in sonic hedgehog-treated cerebellar neural precursors

21 January 2018

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The miR-17~92 cluster collaborates with the Sonic Hedgehog pathway in medulloblastoma

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MicroRNA-199b-5p impairs cancer stem cells through negative regulation of HES1 in medulloblastoma

21 January 2018

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MiR-34a targeting of Notch ligand delta-like 1 impairs CD15+/CD133+ tumor-propagating cells and supports neural differentiation in medulloblastoma

21 January 2018

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Sonic Hedgehog regulates Hes1 through a novel mechanism that is independent of canonical Notch pathway signalling.

21 January 2018

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Progenitor cell proliferation in the retina is dependent on Notch-independent Sonic hedgehog/Hes1 activity

21 January 2018

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A GLI1-p53 inhibitory loop controls neural stem cell and tumour cell numbers

21 January 2018

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Gli2 is a novel regulator of sox2 expression in telencephalic neuroepithelial cells.

21 January 2018

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The micro-RNA 199b-5p regulatory circuit involves Hes1, CD15, and epigenetic modifications in medulloblastoma.

21 January 2018

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MicroRNA Biogenesis and Hedgehog-Patched Signaling Cooperate to Regulate an Important Developmental Transition in Granule Cell Development.

21 January 2018

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MiR-34a deficiency accelerates medulloblastoma formation in vivo

21 January 2018

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MicroRNA 22 regulates cell cycle length in cerebellar granular neuron precursors.

21 January 2018

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N-myc is a key switch regulating the proliferation cycle of postnatal cerebellar granule cell progenitors

21 January 2018

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21 January 2018

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Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years--Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012.

21 January 2018

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The familial risk of autism

21 January 2018

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Autism as a strongly genetic disorder: evidence from a British twin study

21 January 2018

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Evidence for autosomal recessive inheritance in 46 families with multiple incidences of autism

21 January 2018

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21 January 2018

The genetics of autism

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Common genetic variants, acting additively, are a major source of risk for autism

21 January 2018

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The co-morbidity burden of children and young adults with autism spectrum disorders

21 January 2018

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Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

21 January 2018

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Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders.

21 January 2018

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Fragile X in a survey of 75 autistic males.

21 January 2018

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Molecular and cytogenetic analyses of autism in Taiwan.

21 January 2018

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Most genetic risk for autism resides with common variation

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Consensus paper: pathological role of the cerebellum in autism

21 January 2018

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Neuroanatomic observations of the brain in autism: a review and future directions

21 January 2018

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Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study.

21 January 2018

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Purkinje cell size is reduced in cerebellum of patients with autism

21 January 2018

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Regional alterations in purkinje cell density in patients with autism

21 January 2018

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The cerebellum contributes to higher functions during development: evidence from a series of children surgically treated for posterior fossa tumours.

21 January 2018

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Neuropsychological consequences of cerebellar tumour resection in children: cerebellar cognitive affective syndrome in a paediatric population

21 January 2018

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Persistent cognitive dysfunction secondary to cerebellar injury in patients treated for posterior fossa tumors in childhood.

21 January 2018

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The pathophysiologic mechanism of cerebellar mutism

21 January 2018

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Injury to the premature cerebellum: outcome is related to remote cortical development

21 January 2018

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Regional cerebellar volumes predict functional outcome in children with cerebellar malformations.

21 January 2018

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The cerebellum, sensitive periods, and autism.

21 January 2018

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Decreased connectivity and cerebellar activity in autism during motor task performance

21 January 2018

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Differential effects of developmental cerebellar abnormality on cognitive and motor functions in the cerebellum: an fMRI study of autism.

21 January 2018

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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice

21 January 2018

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Loss of Tsc2 in Purkinje cells is associated with autistic-like behavior in a mouse model of tuberous sclerosis complex.

21 January 2018

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Autistic-Like Traits and Cerebellar Dysfunction in Purkinje Cell PTEN Knock-Out Mice

21 January 2018

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Cerebellar Purkinje cell p75 neurotrophin receptor and autistic behavior.

21 January 2018

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Cadm1-expressing synapses on Purkinje cell dendrites are involved in mouse ultrasonic vocalization activity

21 January 2018

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Autism-relevant social abnormalities and cognitive deficits in engrailed-2 knockout mice

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Behavioral flexibility in a mouse model of developmental cerebellar Purkinje cell loss

21 January 2018

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Repetitive behavior and increased activity in mice with Purkinje cell loss: a model for understanding the role of cerebellar pathology in autism

21 January 2018

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Genetic effects on cerebellar structure across mouse models of autism using a magnetic resonance imaging atlas

21 January 2018

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Heterogeneous dysregulation of microRNAs across the autism spectrum.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Spatial navigation of staggerer and normal mice during juvenile and adult stages.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Gene and miRNA expression profiles in autism spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Serum microRNA profiles in children with autism

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism

21 January 2018

1 reference

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Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MicroRNA expression profiles classify human cancers

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

En2 knockout mice display neurobehavioral and neurochemical alterations relevant to autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Loss of GABAergic neurons in the hippocampus and cerebral cortex of Engrailed-2 null mutant mice: implications for autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Decreased number of interneurons and increased seizures in neuropilin 2 deficient mice: implications for autism and epilepsy.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

staggerer phenotype in retinoid-related orphan receptor alpha-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MicroRNA-21 is induced by rapamycin in a model of tuberous sclerosis (TSC) and lymphangioleiomyomatosis (LAM).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MicroRNA-mediated dysregulation of neural developmental genes in HPRT deficiency: clues for Lesch-Nyhan disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

An activity-regulated microRNA, miR-188, controls dendritic plasticity and synaptic transmission by downregulating neuropilin-2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

A direct molecular link between the autism candidate gene RORa and the schizophrenia candidate MIR137.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Genetics of childhood disorders: XLVIII. Learning and memory, Part 1: Fragile X syndrome update

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

The fragile X gene and its function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Association of tuberous sclerosis of temporal lobes with autism and atypical autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Neuro-epileptic determinants of autism spectrum disorders in tuberous sclerosis complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Genotype and psychological phenotype in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Rett syndrome: clinical and molecular update

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

How commonly are known medical conditions associated with autism?

21 January 2018

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https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Autism and known medical conditions: myth and substance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Evidence that fragile X mental retardation protein is a negative regulator of translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Phosphorylation influences the translation state of FMRP-associated polyribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Analysis of neocortex in three males with the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Synaptic regulation of protein synthesis and the fragile X protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Altered synaptic plasticity in a mouse model of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Specificity of cerebellar vermian abnormalities in autism: a quantitative magnetic resonance imaging study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Decreased cerebellar posterior vermis size in fragile X syndrome: correlation with neurocognitive performance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Cerebellar LTD and Learning-Dependent Timing of Conditioned Eyelid Responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

G quadruplex RNA structures in PSD-95 mRNA: potential regulators of miR-125a seed binding site accessibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

A critical role for PSD-95/AKAP interactions in endocytosis of synaptic AMPA receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Molecular dissociation of the role of PSD-95 in regulating synaptic strength and LTD

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Activity-dependent PSD formation and stabilization of newly formed spines in hippocampal slice cultures.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

TSC2 mediates cellular energy response to control cell growth and survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

mTOR signaling in growth control and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Tuberous sclerosis complex proteins control axon formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Regulable neural progenitor-specific Tsc1 loss yields giant cells with organellar dysfunction in a model of tuberous sclerosis complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Excitatory/inhibitory synaptic imbalance leads to hippocampal hyperexcitability in mouse models of tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Autism and tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Cerebellar lesions in tuberous sclerosis complex: neurobehavioral and neuroimaging correlates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Cortical Tubers: Windows into Dysregulation of Epilepsy Risk and Synaptic Signaling Genes by MicroRNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MicroRNAs are critical regulators of tuberous sclerosis complex and mTORC1 activity in the size control of the Xenopus kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

The MicroRNA-17-92 cluster enhances axonal outgrowth in embryonic cortical neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MeCP2, a key contributor to neurological disease, activates and represses transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Disruption of DNA-methylation-dependent long gene repression in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MeCP2 binds to non-CG methylated DNA as neurons mature, influencing transcription and the timing of onset for Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Gene length matters in neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MeCP2-dependent transcriptional repression regulates excitatory neurotransmission.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Loss of activity-induced phosphorylation of MeCP2 enhances synaptogenesis, LTP and spatial memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Selective impact of MeCP2 and associated histone deacetylases on the dynamics of evoked excitatory neurotransmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MECP2 duplication phenotype in symptomatic females: report of three further cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Cerebellar and cerebral abnormalities in Rett syndrome: a quantitative MR analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Rett syndrome: cerebellar pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Enhanced cell death in MeCP2 null cerebellar granule neurons exposed to excitotoxicity and hypoxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Speech and motor disturbances in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Genome-wide analysis reveals methyl-CpG-binding protein 2-dependent regulation of microRNAs in a mouse model of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

miR-199a Links MeCP2 with mTOR Signaling and Its Dysregulation Leads to Rett Syndrome Phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Transgenic miR132 alters neuronal spine density and impairs novel object recognition memory

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Memory formation and retention are affected in adult miR-132/212 knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

MicroRNA-9 modulates Cajal-Retzius cell differentiation by suppressing Foxg1 expression in mouse medial pallium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12035-016-0220-9

Hamartin, the product of the tuberous sclerosis 1 (TSC1) gene, interacts with tuberin and appears to be localized to cytoplasmic vesicles

21 January 2018

1 reference

12 December 2020

Sequential roles for Fgf4, En1 and Fgf8 in specification and regionalisation of the midbrain.

1 reference

12 December 2020

FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression.

1 reference

12 December 2020

Sonic hedgehog regulates the growth and patterning of the cerebellum

1 reference

12 December 2020

Abnormal development of dendritic spines in FMR1 knock-out mice

1 reference

12 December 2020

Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex

1 reference

12 December 2020

Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, 14 sites, United States, 2002.

1 reference

12 December 2020

10.1007/S12035-016-0220-9

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1 reference

PubMed ID

27774573