(Q36455952)

14 August 2017

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title

Modes of imprinted gene action in learning disability (English)

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14 August 2017

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Isles AR

1

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14 August 2017

Humby T

series ordinal

2

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14 August 2017

publication date

1 May 2006

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Journal of Intellectual Disability Research

14 August 2017

published in

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14 August 2017

volume

50

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14 August 2017

issue

Pt 5

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14 August 2017

page(s)

318-325

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

14 August 2017

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21 January 2018

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Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome.

21 January 2018

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Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

21 January 2018

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Angelman syndrome: a review of the clinical and genetic aspects

21 January 2018

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Placental-specific IGF-II is a major modulator of placental and fetal growth.

21 January 2018

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Resourceful imprinting.

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Coadaptation in mother and infant regulated by a paternally expressed imprinted gene.

21 January 2018

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Influence of X chromosome and hormones on human brain development: a magnetic resonance imaging and proton magnetic resonance spectroscopy study of Turner syndrome.

21 January 2018

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Prenatal protein malnourished rats show changes in sleep/wake behavior as adults

21 January 2018

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Xlr3b is a new imprinted candidate for X-linked parent-of-origin effects on cognitive function in mice

21 January 2018

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Epigenetic regulation of mammalian genomic imprinting

21 January 2018

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Dendritic morphology is altered in hippocampal neurons following prenatal compromise

21 January 2018

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Genomic imprinting: implications for human disease

21 January 2018

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21 January 2018

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Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis

21 January 2018

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The paradox of Prader-Willi syndrome: a genetic model of starvation

21 January 2018

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Calculation difficulties in children of very low birthweight: a neural correlate.

21 January 2018

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Cortical anomalies associated with visuospatial processing deficits.

21 January 2018

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Imprinted genes and mother-offspring interactions

21 January 2018

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Imprinted genes, cognition and behaviour.

21 January 2018

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Imprinted gene in postnatal growth role

21 January 2018

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

21 January 2018

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Epigenetics and human disease

21 January 2018

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Maternal nutrient restriction reduces concentrations of amino acids and polyamines in ovine maternal and fetal plasma and fetal fluids

21 January 2018

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Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest

21 January 2018

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Disruption of imprinting caused by deletion of the H19 gene region in mice

21 January 2018

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Long-term metabolic consequences of being born small for gestational age.

21 January 2018

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Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

21 January 2018

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Completion of mouse embryogenesis requires both the maternal and paternal genomes

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

The imprinted signaling protein XL alpha s is required for postnatal adaptation to feeding.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Identification of a cluster of X-linked imprinted genes in mice

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Genomic imprinting: parental influence on the genome

21 January 2018

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Birth weight and cognitive function in the British 1946 birth cohort: longitudinal population based study

21 January 2018

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Cognition, academic progress, behavior and self-concept at 14 years of very low birth weight children

21 January 2018

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The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

The relationship of prenatal and perinatal complications to cognitive functioning at age 7 in the New England Cohorts of the National Collaborative Perinatal Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Identification of novel imprinted genes in a genome-wide screen for maternal methylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

An investigation of executive function abilities in adults with Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Looking back in time: outcome of a national cohort of very preterm infants born in The Netherlands in 1983.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Early nutrition, epigenetic changes at transposons and imprinted genes, and enhanced susceptibility to adult chronic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Cognitive abilities and genotype in a population-based sample of people with Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Neurological aspects of the Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

Type 2 (non-insulin-dependent) diabetes mellitus, hypertension and hyperlipidaemia (syndrome X): relation to reduced fetal growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2006.00843.X

10.1111/J.1365-2788.2006.00843.X

21 January 2018

Identifiers

DOI

1 reference

14 August 2017

1 reference