A global disorder of imprinting in the human female germ line (Q48864404)

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English	A global disorder of imprinting in the human female germ line	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

title

A global disorder of imprinting in the human female germ line (English)

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Europe PubMed Central

PubMed publication ID

11932746

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16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

author

David T. Bonthron

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4

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Europe PubMed Central

PubMed publication ID

11932746

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16 February 2018

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http://europepmc.org/abstract/MED/11932746

author name string

Hannah Judson

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1

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Europe PubMed Central

PubMed publication ID

11932746

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16 February 2018

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http://europepmc.org/abstract/MED/11932746

Bruce E Hayward

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2

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Europe PubMed Central

PubMed publication ID

11932746

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16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

Eamonn Sheridan

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3

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Europe PubMed Central

PubMed publication ID

11932746

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16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

language of work or name

English

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publication date

1 April 2002

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Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

published in

Nature

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Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

volume

416

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stated in

Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

issue

6880

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stated in

Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

page(s)

539-542

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Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

cites work

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

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

1 reference

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reference URL

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retrieved

21 January 2018

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

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21 January 2018

A GNAS1 imprinting defect in pseudohypoparathyroidism type IB

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21 January 2018

Androgenetic origin of hydatidiform mole

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reference URL

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retrieved

21 January 2018

Genetic mapping of a maternal locus responsible for familial hydatidiform moles

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

Repetitive complete hydatidiform mole can be biparental in origin and either male or female.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

High sensitivity mapping of methylated cytosines

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

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Crossref

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https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

Imprinting-mutation mechanisms in Prader-Willi syndrome

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retrieved

21 January 2018

Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

1 reference

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Crossref

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retrieved

21 January 2018

Maternal methylation imprints on human chromosome 15 are established during or after fertilization

1 reference

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Crossref

reference URL

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retrieved

21 January 2018

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

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

The human GNAS1 gene is imprinted and encodes distinct paternally and biallelically expressed G proteins

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteins

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21 January 2018

An imprinted antisense transcript at the human GNAS1 locus

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21 January 2018

Identification of a methylation imprint mark within the mouse Gnas locus

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Crossref

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21 January 2018

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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21 January 2018

The cell cycle control gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes

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21 January 2018

Dnmt3L and the establishment of maternal genomic imprints

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21 January 2018

A human parthenogenetic chimaera.

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21 January 2018

An imprinted locus associated with transient neonatal diabetes mellitus

1 reference

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reference URL

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retrieved

21 January 2018

Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

21 January 2018

A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F416539A

retrieved

7 January 2021

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Identifiers

DOI

10.1038/416539A

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

Altmetric DOI

10.1038/416539A

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Dimensions Publication ID

1051945129

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PubMed publication ID

11932746

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11932746

retrieved

16 February 2018

reference URL

http://europepmc.org/abstract/MED/11932746

ResearchGate publication ID

11432435

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