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Assessing the requirements of prenatal UBE3A expression for rescue of behavioral phenotypes in a mouse model for Angelman syndrome

https://doi.org/10.1186/s13229-020-00376-9
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33/33 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.

2 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.

The 33 checked references that resolve
resolves10.1002/ajmg.a.31074
Angelman syndrome 2005: Updated consensus for diagnostic criteria
resolves10.1002/ajmg.1320320235
Angelman and Prader‐Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion
resolves10.1002/ajmg.1320280407
Is angelman syndrome an alternate result of del(15)(qllql3)?
resolves10.1038/ng0197-70
UBE3A/E6-AP mutations cause Angelman syndrome
resolves10.1038/ng0997-14
The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain
resolves10.1093/hmg/dds130
Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a
resolves10.1038/nature13975
Towards a therapy for Angelman syndrome by targeting a long non-coding RNA
resolves10.1038/nature10726
Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
resolves10.1002/aur.2203
Prenatal treatment path for angelman syndrome and other neurodevelopmental disorders
resolves10.1172/JCI80554
Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model
resolves10.1002/cne.23507
Allelic specificity of Ube3a Expression In The Mouse Brain During Postnatal Development
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
resolves10.1006/nbdi.2001.0463
Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice
resolves10.1186/s13229-018-0231-7
A behavioral test battery for mouse models of Angelman syndrome: a powerful tool for testing drugs and novel Ube3a mutants
resolves10.1016/j.bbr.2012.12.052
Behavioral deficits in an Angelman syndrome model: Effects of genetic background and age
resolves10.1038/s41598-017-08825-x
Strain-dependence of the Angelman Syndrome phenotypes in Ube3a maternal deficiency mice
resolves10.1093/hmg/ddn117
Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors
resolves10.1016/j.nbd.2010.08.002
Loss of dopaminergic neurons and resulting behavioural deficits in mouse model of Angelman syndrome
resolves10.1172/JCI83541
Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model
resolves10.1038/12703
Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety
resolves10.1093/hmg/ddm288
The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology
resolves10.1002/1096-9861(20001002)425:4<479::AID-CNE2>3.0.CO;2-3
Vascular niche for adult hippocampal neurogenesis
resolves10.1038/35067582
A unified hypothesis on the lineage of neural stem cells
resolves10.1369/jhc.2010.955609
The Neural Stem/Progenitor Cell Marker Nestin Is Expressed in Proliferative Endothelial Cells, but Not in Mature Vasculature
resolves10.1242/bio.20122287
A <i>Nestin-cre</i> transgenic mouse is insufficient for recombination in early embryonic neural progenitors
resolves10.1186/s13072-017-0134-4
Genomic imprinting does not reduce the dosage of UBE3A in neurons
resolves10.1186/s13229-019-0277-1
Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes
resolves10.1038/s41593-019-0425-0
Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome
resolves10.1016/j.cell.2015.06.045
An Autism-Linked Mutation Disables Phosphorylation Control of UBE3A
resolves10.1523/JNEUROSCI.5746-12.2013
Modeling Transformations of Neurodevelopmental Sequences across Mammalian Species
resolves10.1016/j.lfs.2015.10.025
Men and mice: Relating their ages
resolves10.1038/nrn1787
Critical period plasticity in local cortical circuits
resolves10.1146/annurev-neuro-061010-113813
Critical-Period Plasticity in the Visual Cortex
The 2 references without a DOI — listed, not checked
no DOI — not checkedWang T, van Woerden GM, Elgersma Y, Borst JGG. Enhanced transmission at the Calyx of held synapse in a mouse model for Angelman syndrome. Front Cell Neurosci. 2018;11:1–19.
no DOI — not checkedHensch TK, Bilimoria PM. Re-opening windows: manipulating critical periods for brain development. Cerebrum. 2012;2012:11.
What this badge says. CiteStamped means the CHECKABLE references of this work were clean at the dated check: each resolved to a known work in a public registry, and none carried a retraction notice at that time. It says nothing about the quality, findings, or importance of the work itself, and nothing about references deposited without a DOI.

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