(Q48382320)

English

Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3.

scientific article published in December 2000

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: mouse Meg3/Gtl2 and human MEG3. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

author name string

Kobayashi S

1

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Wagatsuma H

2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Ono R

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Ichikawa H

4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Yamazaki M

5

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Tashiro H

6

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Aisaka K

7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Miyoshi N

8

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Kohda T

9

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Ogura A

10

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Ohki M

11

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Kaneko-Ishino T

12

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Ishino F

13

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

publication date

1 December 2000

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

5

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

12

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

1029-1037

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Paternal uniparental disomy for chromosome 14: a case report and review

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Maternal uniparental disomy for chromosome 14.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Assignment1 of DLK1 to human chromosome band 14q32 by in situ hybridization

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Assignment of dlk (Dlk1) to mouse chromosome band 12E-F1 by in situ hybridization

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Cloning of a membrane-spanning protein with epidermal growth factor-like repeat motifs from adrenal glomerulosa cells

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Molecular markers of neuroendocrine development and evidence of environmental regulation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Maintenance of somite borders in mice requires the Delta homologue DII1.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Completion of mouse embryogenesis requires both the maternal and paternal genomes

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Pref-1, a protein containing EGF-like repeats, inhibits adipocyte differentiation

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Maternal uniparental disomy for chromosome 14

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2443.2000.00390.X

21 January 2018

Identifiers

10.1046/J.1365-2443.2000.00390.X

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11168589

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