(Q27321157)

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Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.

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Europe PubMed Central

PubMed publication ID

22 June 2017

Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. (English)

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Europe PubMed Central

PubMed publication ID

22 June 2017

Angelman syndrome

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Jeffrey L. Noebels

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Jeffrey Noebels

9

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Yong-Hui Jiang

1

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Europe PubMed Central

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22 June 2017

Yanzhen Pan

2

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Europe PubMed Central

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22 June 2017

Li Zhu

3

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Europe PubMed Central

PubMed publication ID

22 June 2017

Luis Landa

4

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Europe PubMed Central

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22 June 2017

Jong Yoo

5

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Europe PubMed Central

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22 June 2017

Corinne Spencer

6

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Europe PubMed Central

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22 June 2017

Isabel Lorenzo

7

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Europe PubMed Central

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22 June 2017

Murray Brilliant

8

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Europe PubMed Central

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22 June 2017

Arthur L Beaudet

10

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22 June 2017

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20 August 2010

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Europe PubMed Central

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22 June 2017

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Europe PubMed Central

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22 June 2017

5

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Europe PubMed Central

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22 June 2017

8

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Europe PubMed Central

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22 June 2017

e12278

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Europe PubMed Central

PubMed publication ID

22 June 2017

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Creative Commons Attribution 4.0 International

20 August 2010

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Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism

1 reference

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Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits

1 reference

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21 March 2017

Reduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism

1 reference

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21 March 2017

15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders

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21 March 2017

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

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21 March 2017

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

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21 March 2017

Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons

1 reference

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21 March 2017

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

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21 March 2017

Angelman syndrome: a review of the clinical and genetic aspects

1 reference

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21 March 2017

The human aminophospholipid-transporting ATPase gene ATP10C maps adjacent to UBE3A and exhibits similar imprinted expression

1 reference

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21 March 2017

UBE3A/E6-AP mutations cause Angelman syndrome

1 reference

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21 March 2017

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

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21 March 2017

Engineering mouse chromosomes with Cre-loxP: range, efficiency, and somatic applications

1 reference

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21 March 2017

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

21 March 2017

Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders

1 reference

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21 March 2017

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

21 March 2017

Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

21 March 2017

Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

21 March 2017

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

7 April 2017

Altered ultrasonic vocalizations in a tuberous sclerosis mouse model of autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Ultrasonic vocalizations: a tool for behavioural phenotyping of mouse models of neurodevelopmental disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Gender influences monoallelic expression of ATP10A in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Analysis of cerebellar function in Ube3a-deficient mice reveals novel genotype-specific behaviors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Behavioral phenotyping strategies for mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

The overlapping spectrum of rett and angelman syndromes: a clinical review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Genomic rearrangements and sporadic disease

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28 September 2017

Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

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28 September 2017

Mouse chromosome engineering for modeling human disease

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28 September 2017

Mouse models of autism spectrum disorders: the challenge for behavioral genetics

1 reference

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28 September 2017

Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review

1 reference

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28 September 2017

A review of the methods of studies on infant ultrasound production and maternal retrieval in small rodents

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28 September 2017

Autism as a paradigmatic complex genetic disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: phenotypic consequences of gene dosage imbalance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Distinct phenotypes distinguish the molecular classes of Angelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Ultrasonic vocalisation emitted by infant rodents: a tool for assessment of neurobehavioural development.

1 reference

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28 September 2017

Engineering chromosomal rearrangements in mice

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28 September 2017

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Genetics of Angelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 September 2017

Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer

1 reference

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Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse

1 reference

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28 September 2017

Chromosome engineering in mice

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28 September 2017

Mice heterozygous for Atp10c, a putative amphipath, represent a novel model of obesity and type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

31 May 2018

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

31 May 2018

Angelman syndrome: correlations between epilepsy phenotypes and genotypes

1 reference

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31 May 2018

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons

1 reference

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31 May 2018

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome

1 reference

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31 May 2018

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

GABAA receptor beta3 subunit gene-deficient heterozygous mice show parent-of-origin and gender-related differences in beta3 subunit levels, EEG, and behavior

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Angelman syndrome revisited

1 reference

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21 January 2018

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

The Angelman syndrome ubiquitin ligase localizes to the synapse and nucleus, and maternal deficiency results in abnormal dendritic spine morphology

1 reference

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21 January 2018

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

1 reference

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21 January 2018

On the conflicting reports of imprinting status of mouse ATP10a in the adult brain: strain-background-dependent imprinting?

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

A type IV P-type ATPase affects insulin-mediated glucose uptake in adipose tissue and skeletal muscle in mice

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Deficit in attachment behavior in mice lacking the mu-opioid receptor gene

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Autism in Angelman syndrome: implications for autism research

1 reference

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21 January 2018

Environmental influences on the behavioral phenotype of Angelman syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Effects of environmental events on smiling and laughing behavior in Angelman syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

1 reference

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21 January 2018

The use of behavioral test batteries, II: effect of test interval

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0012278

21 January 2018

Atp10a, a gene adjacent to the PWS/AS gene cluster, is not imprinted in mouse and is insensitive to the PWS-IC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 November 2018

Ultrasonic vocalizations in rat and mouse pups.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 November 2018

Analysis of the characteristics of epilepsy in 37 patients with the molecular diagnosis of Angelman syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2924885

28 November 2018

Atp10a, the mouse ortholog of the human imprinted ATP10A gene, escapes genomic imprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two new balancer chromosomes on mouse chromosome 4 to facilitate functional annotation of human chromosome 1p

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic imprinting and the expression of affect in Angelman syndrome: what's in the smile?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The effects of cold, rotation, and genotype on the production of ultrasonic calls in infant mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20808828

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0012278

1 reference

Europe PubMed Central

PubMed publication ID

22 June 2017

2010PLoSO...512278J

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Consolidated OpenCitations Corpus – April 2017

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PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 June 2017

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