(Q28137721)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

5

1 reference

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1 November 2019

author name string

N Blagitko

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

U Schulz

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

A A Schinzel

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

H H Ropers

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

language of work or name

English

0 references

publication date

1 December 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

issue

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

page(s)

2387-2396

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10556286%20AND%20SRC:MED&resulttype=core&format=json

Genomic imprinting: nature and clinical relevance

1 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Parental imprinting and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Genomic imprinting: implications for human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Growth effects of uniparental disomies and the conflict theory of genomic imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Imprinting in Prader-Willi and Angelman syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

An enhancer deletion affects both H19 and Igf2 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Gametic imprinting in mammals

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

UBE3A/E6-AP mutations cause Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Mutation analysis of UBE3A in Angelman syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Maternal uniparental disomy 7 in Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Paternal isodisomy of chromosome 7 associated with complete situs inversus and immotile cilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Gamma-COP, a coat subunit of non-clathrin-coated vesicles with homology to Sec21p

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

COPI in ER/Golgi and intra-Golgi transport: do yeast COPI mutants point the way?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

The PROSITE database, its status in 1997.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Nonclathrin coat protein gamma, a subunit of coatomer, binds to the cytoplasmic dilysine motif of membrane proteins of the early secretory pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

A single binding site for dilysine retrieval motifs and p23 within the gamma subunit of coatomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387

Receptor-induced polymerization of coatomer

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.13.2387