(Q67482957)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

title

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

main subject

Prader–Willi syndrome

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1303278

11 September 2022

Cattanach BM

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Barr JA

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Evans EP

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Burtenshaw M

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Beechey CV

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Leff SE

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Brannan CI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Copeland NG

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Jenkins NA

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

Jones J

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1303278

11 September 2022

publication date

1 December 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

page(s)

270-274

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting

13 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

The association of Angelman's syndrome with deletions within 15q11-13

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

DNA deletion and its parental origin in Angelman syndrome patients

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Parental imprinting of the mouse insulin-like growth factor II gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Parental imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Prader-Willi syndrome: current understanding of cause and diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Noncomplementation phenomena and their bearing on nondisjunctional effects.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Genetic analysis of genomic imprinting: An Imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Genomic imprinting in mammalian development: a parental tug-of-war

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

A fetal skeletal muscle actin mRNA in the mouse and its identity with cardiac actin mRNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

https://api.crossref.org/works/10.1038%2FNG1292-270

1 reference

7 January 2021

Homology of a candidate spermatogenic gene from the mouse Y chromosome to the ubiquitin-activating enzyme El

1 reference

https://api.crossref.org/works/10.1038%2FNG1292-270

7 January 2021

Identifiers

DOI

10.1038/NG1292-270

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1303278%20AND%20SRC:MED&resulttype=core&format=json