(Q35575191)

8 August 2017

1 reference

title

Genomic imprinting and the social brain (English)

1 reference

8 August 2017

0 references

William Davies

2

0 references

Anthony R Isles

object named as

Anthony R Isles

series ordinal

1

0 references

author name string

Lawrence S Wilkinson

series ordinal

3

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 December 2006

1 reference

Philosophical Transactions of the Royal Society B

8 August 2017

number of pages

9

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

8 August 2017

volume

361

1 reference

8 August 2017

issue

1476

1 reference

8 August 2017

page(s)

2229-2237

1 reference

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

8 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Imprinted gene expression in the brain

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Imprinted Nesp55 influences behavioral reactivity to novel environments

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Imprinted genes and mother-offspring interactions

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

The nose knows who's who: chemosensory individuality and mate recognition in mice

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Epigenetic regulation of mammalian genomic imprinting

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Sociality and the evolution of intelligence

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

How does the brain deal with the social world?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Are XX and XY brain cells intrinsically different?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Effects of X-monosomy and X-linked imprinting on superior temporal gyrus morphology in Turner syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

What good is genomic imprinting: the function of parent-specific gene expression

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Angelman syndrome: a review of the clinical and genetic aspects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Imprinted genes and mental dysfunction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Genomic imprinting, maternal care, and brain evolution

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

The evolution of X-linked genomic imprinting

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Neural control of tongue movement with respect to respiration and swallowing

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Imprinted genes, cognition and behaviour.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Pw1/Peg3 is a potential cell death mediator and cooperates with Siah1a in p53-mediated apoptosis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Kinship and genomic imprinting.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Parental antagonism, relatedness asymmetries, and genomic imprinting

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Primate brain evolution: genetic and functional considerations.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Prader-Willi syndrome: consensus diagnostic criteria.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Behaviour problems in Angelman syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Somatic mutation favors the evolution of diploidy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Completion of mouse embryogenesis requires both the maternal and paternal genomes

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Role of paternal and maternal genomes in mouse development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Lesions of the dorsal noradrenergic bundle simultaneously enhance and reduce responsivity to novelty in a food preference test

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Angelman's syndrome in infancy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Genomic imprinting and the strange case of the insulin-like growth factor II receptor

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Paternal kin discrimination in wild baboons.

12 July 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Sex chromosome genes directly affect brain sexual differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

21 January 2018

Resourceful imprinting.

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Sexually dimorphic gene expression in mouse brain precedes gonadal differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Prader‐Willi syndrome and the evolution of human childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Urinary odour preferences in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

A possible role for imprinted genes in inbreeding avoidance and dispersal from the natal area in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Imprinted gene in postnatal growth role

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Brainstem mechanisms underlying feeding behaviors

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Kin recognition and the 'armpit effect': evidence of self-referent phenotype matching.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Novelty seeking behavior in the rat is dependent upon the integrity of the noradrenergic system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Genotype-dependent sex differentiation of dopaminergic neurons in primary cultures of embryonic mouse brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Wild female baboons bias their social behaviour towards paternal half-sisters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Parent-Offspring Conflict

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

An Ecological Model of Female-Bonded Primate Groups

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Genomic imprinting, sex-biased dispersal, and social behavior.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1764840

Sex Specific X Chromosome Expression Caused by Genomic Imprinting

26 September 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Parent-Specific Gene Expression and the Triploid Endosperm

21 January 2018

1 reference

https://api.crossref.org/works/10.1098%2FRSTB.2006.1942

Sex-biased dispersal and inbreeding avoidance in birds and mammals

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17118935

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17118935

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1098/RSTB.2006.1942

1 reference

8 August 2017

1 reference

8 August 2017

1 reference