Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method (Q28237886)

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scientific article (publication date: March 1997)

Language	Label	Description	Also known as
English	Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method	scientific article (publication date: March 1997)

Statements

scholarly article

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Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method (English)

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DNA methylation

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author name string

M Zeschnigk

1

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B Schmitz

2

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B Dittrich

3

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K Buiting

4

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B Horsthemke

5

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W Doerfler

6

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language of work or name

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publication date

March 1997

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Human Molecular Genetics

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6

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3

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387-95

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Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Cell biology of the snRNP particles

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

DNA methylation and gene activity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Allele-specific replication timing of imprinted gene regions

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

High sensitivity mapping of methylated cytosines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Reaction of sodium bisulfite with uracil, cytosine, and their derivatives

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Comparison of bisulfite modification of 5-methyldeoxycytidine and deoxycytidine residues

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Characterization of a methylation imprint in the Prader-Willi syndrome chromosome region

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Interindividual concordance of methylation profiles in human genes for tumor necrosis factors alpha and beta

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Genomic imprinting determines methylation of parental alleles in transgenic mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Genotype-phenotype correlation in a series of 167 deletion and non-deletion patients with Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.3.387

21 January 2018

Identifiers

10.1093/HMG/6.3.387

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