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N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer's disease

Genome Biology, 2021-01, Vol.22 (1), p.17-17, Article 17

2021

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A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies

Nature neuroscience, 2021-10, Vol.24 (10), p.1377-1391

2021

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Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA

Human molecular genetics, 2007-05, Vol.16 (9), p.1124-1131

2007

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Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias

Neurobiology of aging, 2020-05, Vol.89, p.142.e1-142.e7

2020

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Drosophila CHIP protects against mitochondrial dysfunction by acting downstream of Pink1 in parallel with Parkin

The FASEB journal, 2017-12, Vol.31 (12), p.5234-5245

2017

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Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy

Annals of neurology, 2020-12, Vol.88 (6), p.1132-1143

2020

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Attitudes of medical professionals toward fragile X carrier screening and genetic counseling in China

Journal of community genetics, 2024-04, Vol.15 (2), p.177-185

2024

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Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum

Human molecular genetics, 2012-12, Vol.21 (26), p.5500-5510

2012

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UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia

PloS one, 2016-02, Vol.11 (2), p.e0149039-e0149039

2016

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Eg5 UFMylation promotes spindle organization during mitosis

Cell death & disease, 2024-07, Vol.15 (7), p.544-13, Article 544

2024

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A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder

Cell reports (Cambridge), 2023-12, Vol.42 (12), p.113445-113445, Article 113445

2023

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Fragile x mental retardation protein regulates proliferation and differentiation of adult neural stem/progenitor cells

PLoS genetics, 2010-04, Vol.6 (4), p.e1000898-e1000898

2010

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MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm

BMC medical genomics, 2013-09, Vol.6 (1), p.36-36, Article 36

2013

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Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima

Neurobiology of disease, 2020-09, Vol.143, p.105013, Article 105013

2020

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Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration

PloS one, 2013-04, Vol.8 (4), p.e62572

2013

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A small molecule enhances RNA interference and promotes microRNA processing

Nature biotechnology, 2008-08, Vol.26 (8), p.933-940

2008

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Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity

Neurobiology of disease, 2019-10, Vol.130, p.104493-104493, Article 104493

2019

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miR-25 alleviates polyQ-mediated cytotoxicity by silencing ATXN3

FEBS letters, 2014-12, Vol.588 (24), p.4791-4798

2014

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Drosophila Netrin-B controls mushroom body axon extension and regulates courtship-associated learning and memory of a Drosophila fragile X syndrome model

Molecular brain, 2019-05, Vol.12 (1), p.52-52, Article 52

2019

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Characteristics of autonomic dysfunction in neuronal intranuclear inclusion disease

Frontiers in neurology, 2023-06, Vol.14, p.1168904-1168904

2023

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Evaluation of the role of FMR1 CGG repeat allele in Parkinson’s disease from the Chinese population

Frontiers in aging neuroscience, 2023-07, Vol.15, p.1234027-1234027

2023

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Argonaute 1 regulates the fate of germline stem cells in Drosophila

Development (Cambridge), 2007-12, Vol.134 (23), p.4265-4272

2007

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TTTCA Repeat Expansion of SAMD12 in a New Benign Adult Familial Myoclonic Epilepsy Pedigree

Frontiers in neurology, 2020-02, Vol.11, p.68-68

2020

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Inhibition of Transglutaminase Exacerbates Polyglutamine-Induced Neurotoxicity by Increasing the Aggregation of Mutant Ataxin-3 in an SCA3 Drosophila Model

Neurotoxicity research, 2015-04, Vol.27 (3), p.259-267

2015

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Fragile X mental retardation protein modulates the fate of germline stem cells in Drosophila

Human molecular genetics, 2007-08, Vol.16 (15), p.1814-1820

2007

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N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer's disease

A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies

Single nucleotide polymorphism associated with mature miR-125a alters the processing of pri-miRNA

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementias

Drosophila CHIP protects against mitochondrial dysfunction by acting downstream of Pink1 in parallel with Parkin

Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy

Attitudes of medical professionals toward fragile X carrier screening and genetic counseling in China

Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum

UBA5 Mutations Cause a New Form of Autosomal Recessive Cerebellar Ataxia

Eg5 UFMylation promotes spindle organization during mitosis

A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder

Fragile x mental retardation protein regulates proliferation and differentiation of adult neural stem/progenitor cells

MicroRNA/mRNA profiling and regulatory network of intracranial aneurysm

Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima

Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration

A small molecule enhances RNA interference and promotes microRNA processing

Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicity

miR-25 alleviates polyQ-mediated cytotoxicity by silencing ATXN3

Drosophila Netrin-B controls mushroom body axon extension and regulates courtship-associated learning and memory of a Drosophila fragile X syndrome model

Characteristics of autonomic dysfunction in neuronal intranuclear inclusion disease

Evaluation of the role of FMR1 CGG repeat allele in Parkinson’s disease from the Chinese population

Argonaute 1 regulates the fate of germline stem cells in Drosophila

TTTCA Repeat Expansion of SAMD12 in a New Benign Adult Familial Myoclonic Epilepsy Pedigree

Inhibition of Transglutaminase Exacerbates Polyglutamine-Induced Neurotoxicity by Increasing the Aggregation of Mutant Ataxin-3 in an SCA3 Drosophila Model

Fragile X mental retardation protein modulates the fate of germline stem cells in Drosophila

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