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Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model

25/25 checkable references clean · checked 2026-07-23

Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.

The 25 checked references that resolve

resolves10.1016/j.braindev.2003.09.014

Neurological aspects of the Angelman syndrome

resolves10.1038/ng0598-15

An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript

resolves10.1371/journal.pgen.1004039

Truncation of Ube3a-ATS Unsilences Paternal Ube3a and Ameliorates Behavioral Defects in the Angelman Syndrome Mouse Model

resolves10.1093/hmg/dds130

Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a

resolves10.1016/j.tins.2011.04.001

Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes

resolves10.1038/nature10784

Drugs to awaken a paternal gene

resolves10.1038/nature10726

Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons

resolves10.1038/nature13975

Towards a therapy for Angelman syndrome by targeting a long non-coding RNA

resolves10.1016/j.tins.2012.03.005

Sensitive time-windows for susceptibility in neurodevelopmental disorders

resolves10.1038/npp.2014.231

Monoamine-Sensitive Developmental Periods Impacting Adult Emotional and Cognitive Behaviors

resolves10.1126/science.1138389

Reversal of Neurological Defects in a Mouse Model of Rett Syndrome

resolves10.1016/j.cell.2012.08.045

Pathogenic SYNGAP1 Mutations Impair Cognitive Development by Disrupting Maturation of Dendritic Spine Synapses

resolves10.1006/bbrc.1997.7111

A Transgenic Mouse Line That Retains Cre Recombinase Activity in Mature Oocytes Irrespective of thecreTransgene Transmission

resolves10.1016/j.bbr.2012.12.052

Behavioral deficits in an Angelman syndrome model: Effects of genetic background and age

resolves10.1016/S0896-6273(00)80596-6

Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation

resolves10.1038/nn1845

Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of αCaMKII inhibitory phosphorylation

resolves10.1006/dbio.2002.0597

Efficient Recombination in Diverse Tissues by a Tamoxifen-Inducible Form of Cre: A Tool for Temporally Regulated Gene Activation/Inactivation in the Mouse

resolves10.1016/j.biopsych.2012.01.021

Reversal of Impaired Hippocampal Long-Term Potentiation and Contextual Fear Memory Deficits in Angelman Syndrome Model Mice by ErbB Inhibitors

resolves10.1016/j.nbd.2012.04.002

Ampakines promote spine actin polymerization, long-term potentiation, and learning in a mouse model of Angelman syndrome

resolves10.1371/journal.pone.0027221

Adeno-Associated Virus-Mediated Rescue of the Cognitive Defects in a Mouse Model for Angelman Syndrome

resolves10.1016/j.neuron.2012.03.014

Fragile X Syndrome Therapeutics S(C)TEP through the Developmental Window

resolves10.1073/pnas.0511189103

<i>Disc1</i> is mutated in the 129S6/SvEv strain and modulates working memory in mice

resolves10.1016/j.neuron.2007.04.015

Behavioral Phenotypes of Disc1 Missense Mutations in Mice

resolves10.1523/JNEUROSCI.5746-12.2013

Modeling Transformations of Neurodevelopmental Sequences across Mammalian Species

resolves10.1146/annurev-neuro-061010-113813

Critical-Period Plasticity in the Visual Cortex

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