(Q28249408)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

main subject

Prader–Willi syndrome

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Rachel Wevrick

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

H R MacDonald

series ordinal

1

0 references

R Wevrick

series ordinal

2

0 references

language of work or name

English

0 references

publication date

1 October 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

1873-1878

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9302265%20AND%20SRC:MED&resulttype=core&format=json

Gametic imprinting in mammals

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

An STS-based map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Assignment of the human aggrecan gene (AGC1) to 15q26 using fluorescence in situ hybridization analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

A Gene Map of the Human Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Isolation and regional mapping of cDNAs expressed during early human development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

A novel brain-specific mRNA encoding nuclear protein (necdin) expressed in neurally differentiated embryonal carcinoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

An imprinted mouse transcript homologous to the human imprinted in Prader-Willi syndrome (IPW) gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Comparative analysis of 1196 orthologous mouse and human full-length mRNA and protein sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873

Mapping the whole human genome by fingerprinting yeast artificial chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1873