(Q48864404)

16 February 2018

title

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

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16 February 2018

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16 February 2018

author name string

Hannah Judson

series ordinal

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16 February 2018

Bruce E Hayward

series ordinal

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16 February 2018

Eamonn Sheridan

series ordinal

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16 February 2018

language of work or name

English

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publication date

1 April 2002

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16 February 2018

published in

Nature

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16 February 2018

volume

416

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16 February 2018

issue

6880

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16 February 2018

page(s)

539-542

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16 February 2018

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

cites work

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A GNAS1 imprinting defect in pseudohypoparathyroidism type IB

21 January 2018

1 reference

Androgenetic origin of hydatidiform mole

21 January 2018

1 reference

Genetic mapping of a maternal locus responsible for familial hydatidiform moles

21 January 2018

1 reference

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

21 January 2018

1 reference

High sensitivity mapping of methylated cytosines

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Imprinting-mutation mechanisms in Prader-Willi syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

An imprinted antisense transcript at the human GNAS1 locus

21 January 2018

1 reference

Identification of a methylation imprint mark within the mouse Gnas locus

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Dnmt3L and the establishment of maternal genomic imprints

21 January 2018

1 reference

A human parthenogenetic chimaera.

21 January 2018

1 reference

An imprinted locus associated with transient neonatal diabetes mellitus

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/416539A

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16 February 2018

Dimensions Publication ID

Altmetric DOI

10.1038/416539A

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1051945129

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16 February 2018