Imprinted genes, cognition and behaviour (Q51975646)

19 April 2018

title

Imprinted genes, cognition and behaviour (English)

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19 April 2018

author

Anthony R Isles

series ordinal

1

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19 April 2018

author name string

Wilkinson LS

series ordinal

2

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19 April 2018

publication date

1 August 2000

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19 April 2018

Trends in Cognitive Sciences

published in

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19 April 2018

volume

4

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19 April 2018

issue

8

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19 April 2018

page(s)

309-318

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19 April 2018

Gametic imprinting in mammals

cites work

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genomic imprinting in mammalian development: a parental tug-of-war

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Towards a molecular understanding of Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Imprinting in Angelman and Prader-Willi syndromes

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

On the parental origin of de novo mutation in man.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The complex pathology of trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Glomerular-specific imprinting of the mouse gsalpha gene: how does this relate to hormone resistance in albright hereditary osteodystrophy?

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Distribution of parthenogenetic cells in the mouse brain and their influence on brain development and behavior.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genomic imprinting and the differential roles of parental genomes in brain development

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

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/10.1016/S1364-6613(00)01504-7

7 January 2021

Analysis and identification of imprinted genes.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genomic imprinting in the brain

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The neuroanatomy of autism: a voxel-based whole brain analysis of structural scans

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

A lack of cerebral lateralization in schizophrenia is within the normal variation in brain maturation but indicates late, slow maturation

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

A role for the Ras signalling pathway in synaptic transmission and long-term memory

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Sex Specific X Chromosome Expression Caused by Genomic Imprinting

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Mother and father in surprise genetic agreement

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genes and social skills

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

1 reference

7 January 2021

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Functional imprinting and epigenetic modification of the human SNRPN gene

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The Angelman syndrome candidate gene, UBE3AIE6-AP, is imprinted in brain

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Evidence for Uniparental, Paternal Expression of the Human GABAA Receptor Subunit Genes, Using Microcell-Mediated Chromosome Transfer

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

A model system to study genomic imprinting of human genes

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Xp deletions associated with autism in three females

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Concordance by sex in sibling pairs with schizophrenia is paternally inherited. Evidence for a pseudoautosomal locus

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Imprinting and anticipation. Are they relevant to genetic studies of schizophrenia?

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Anticipation and imprinting in schizophrenia

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Clinical evidence of genomic imprinting in Tourette's syndrome

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Sex of parent transmission effect in Tourette's syndrome: evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genomic imprinting and audiogenic seizures in mice

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The Ras Guanine nucleotide Exchange Factor CDC25Mm is present at the synaptic junction.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Ca(2 )-dependent routes to Ras: mechanisms for neuronal survival, differentiation, and plasticity?

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Human PEG1/MEST, an imprinted gene on chromosome 7

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Peg3/Pw1 is an imprinted gene involved in the TNF-NFkappaB signal transduction pathway.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Ubiquitin C-terminal hydrolase is an immediate-early gene essential for long-term facilitation in Aplysia

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2.

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Arrest of Cell Growth by Necdin, a Nuclear-Protein Expressed in Postmitotic Neurons

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

Visuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotype

1 reference

https://api.crossref.org/works/10.1016/S1364-6613(00)01504-7

7 January 2021

10.1016/S1364-6613(00)01504-7

Identifiers

DOI

1 reference

19 April 2018

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19 April 2018