(Q47864302)

6 November 2019

title

Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

Y J Lee

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

C W Park

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J Park

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J Lee

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J H Yun

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

B Hyun

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J H Chung

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

language of work or name

English

0 references

publication date

1 April 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

472

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

2-3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

230-234

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10788617%20AND%20SRC:MED&resulttype=core&format=json

Imprinting and the initiation of gene silencing in the germ line.

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

The sins of the fathers and mothers: genomic imprinting in mammalian development

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

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

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Human PEG1/MEST, an imprinted gene on chromosome 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Cloning of human neuronatin gene and its localization to chromosome-20q 11.2-12: the deduced protein is a novel "proteolipid'

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Imprinted expression of the Igf2r gene depends on an intronic CpG island.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Maternal uniparental disomy 7 in Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

Identification of the C-->T polymorphism in the +93 position of the apo(a) gene by mismatch PCR-mediated site-directed mutagenesis and restriction enzyme digestion

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2800%2901461-7