(Q48016474)

7 February 2018

title

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. (English)

1 reference

7 February 2018

author name string

Lefebvre L

1

1 reference

7 February 2018

Viville S

2

1 reference

7 February 2018

Barton SC

3

1 reference

7 February 2018

Ishino F

4

1 reference

7 February 2018

Keverne EB

5

1 reference

7 February 2018

Surani MA

6

1 reference

7 February 2018

language of work or name

English

0 references

publication date

1 October 1998

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7 February 2018

published in

Nature Genetics

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7 February 2018

volume

20

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7 February 2018

page(s)

163-169

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7 February 2018

issue

2

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7 February 2018

https://scigraph.springernature.com/pub.10.1038/2464

exact match

0 references

cites work

Imprinted genes and regulation of gene expression by epigenetic inheritance.

1 reference

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

21 January 2018

1 reference

Human PEG1/MEST, an imprinted gene on chromosome 7

21 January 2018

1 reference

Genomic imprinting and chromosomal localization of the human MEST gene

21 January 2018

1 reference

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

21 January 2018

1 reference

Genomic structure and parent-of-origin-specific methylation of Peg1.

21 January 2018

1 reference

Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells

21 January 2018

1 reference

Dicistronic targeting constructs: reporters and modifiers of mammalian gene expression.

21 January 2018

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Derivation of completely cell culture-derived mice from early-passage embryonic stem cells

21 January 2018

1 reference

Importance of noradrenergic mechanisms in the olfactory bulbs for the maternal behaviour of mice.

21 January 2018

1 reference

Prenatal and postnatal growth failure associated with maternal heterodisomy for chromosome 7

21 January 2018

1 reference

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

21 January 2018

1 reference

Maternal uniparental disomy 7 in Silver-Russell syndrome

21 January 2018

1 reference

Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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Parental imprinting of the mouse insulin-like growth factor II gene.

21 January 2018

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Enhancement of opioid-mediated analgesia: a solution to the enigma of placentophagia

21 January 2018

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The lateral hypothalamic area revisited: ingestive behavior

21 January 2018

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Effects of hypothalamic knife cuts and experience on maternal behavior in the rat.

21 January 2018

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A defect in nurturing in mice lacking the immediate early gene fosB.

21 January 2018

1 reference

Impaired maternal behavior in mice lacking norepinephrine and epinephrine

21 January 2018

1 reference

Experimental embryological analysis of genetic imprinting in mouse development

21 January 2018

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

21 January 2018

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A candidate model for Angelman syndrome in the mouse.

21 January 2018

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Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation

21 January 2018

1 reference

Plasmid and bacteriophage vectors for excision of intact inserts

21 January 2018

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Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice

21 January 2018

1 reference

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

21 January 2018

1 reference

Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/2464

1 reference

7 February 2018

PubMed ID

9771709

1 reference

7 February 2018