Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes (Q35881189)

10 August 2017

Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes (English)

1 reference

10 August 2017

J M LaSalle

1

1 reference

10 August 2017

R J Ritchie

series ordinal

2

1 reference

10 August 2017

H Glatt

series ordinal

3

1 reference

10 August 2017

M Lalande

series ordinal

4

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10 August 2017

language of work or name

English

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publication date

1 February 1998

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Proceedings of the National Academy of Sciences of the United States of America

10 August 2017

1 reference

10 August 2017

95

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10 August 2017

4

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10 August 2017

1675-1680

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Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Parental imprinting and human disease

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Dynamic methylation adjustment and counting as part of imprinting mechanisms

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Heritability of X chromosome--inactivation phenotype in a large family

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Creation of genomic methylation patterns

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

DNA methylation in early development

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Role for DNA methylation in genomic imprinting

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

DNA methylation and genomic imprinting

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Epigenetic effects in eukaryotic gene expression.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Gametic imprinting in mammals

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Interclonal variation in methylation patterns for expressed and non-expressed genes.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Variability of DNA methylation patterns during serial passage of human diploid fibroblasts

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Clonal variation in gene methylation: c-H-ras and alpha-hCG regions vary independently in human fibroblast lineages

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Variation in epigenetic inheritance

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Uniparental paternal disomy in Angelman's syndrome

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

X-chromosome inactivation and cell memory

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

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

11 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=19144

24 September 2018

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Reproducible alterations of DNA methylation at a specific population of CpG islands during blast formation of peripheral blood lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Mosaic methylation in clonal tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Interchromosomal Transfer of Epigenetic States in Ascobolus: Transfer of DNA Methylation Is Mechanistically Related to Homologous Recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

Homologous association of oppositely imprinted chromosomal domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.95.4.1675

21 January 2018

Identifiers

DOI

10.1073/PNAS.95.4.1675

1 reference

10 August 2017

0 references

1 reference

10 August 2017

PubMed publication ID

9465075

1 reference