(Q28589840)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 (English)

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

Potassium voltage-gated channel, subfamily Q, member 1

14 December 2019

main subject

1 reference

GOA release 2020-03-11

author

Paul D. Soloway

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

author name string

Galina V Fitzpatrick

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

Michael J Higgins

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

language of work or name

English

0 references

publication date

9 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

volume

32

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

issue

3

2 references

31 January 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

page(s)

426-431

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

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

14 December 2019

cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

1 reference

7 January 2021

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

7 January 2021

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

1 reference

7 January 2021

Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

1 reference

7 January 2021

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

7 January 2021

Genomic imprinting. Silence across the border.

1 reference

7 January 2021

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

1 reference

7 January 2021

Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

1 reference

7 January 2021

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

1 reference

7 January 2021

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

1 reference

7 January 2021

Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain

1 reference

7 January 2021

Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

1 reference

7 January 2021

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

1 reference

7 January 2021

A mouse model for Prader-Willi syndrome imprinting-centre mutations

1 reference

7 January 2021

Bidirectional action of the Igf2r imprint control element on upstream and downstream imprinted genes

1 reference

7 January 2021

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

7 January 2021

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting

1 reference

7 January 2021

Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome

1 reference

7 January 2021

A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator

1 reference

7 January 2021

The non-coding Air RNA is required for silencing autosomal imprinted genes

1 reference

7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

1 reference

7 January 2021

Dnmt3L and the establishment of maternal genomic imprints.

1 reference

7 January 2021

Zp3-cre, a transgenic mouse line for the activation or inactivation of loxP-flanked target genes specifically in the female germ line

1 reference

7 January 2021

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG988

2 references

Consolidated OpenCitations Corpus – April 2017

3249696

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12410230%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

3249696

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3249696