Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci (Q83654351)

From Wikidata

Jump to navigation Jump to search

scientific article published on 01 May 2012

Language	Label	Description	Also known as
English	Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci	scientific article published on 01 May 2012

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Use of multilocus methylation-specific single nucleotide primer extension (MS-SNuPE) technology in diagnostic testing for human imprinted loci (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

DNA methylation

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:22419125

27 December 2024

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:22419125

27 December 2024

author name string

Matthias Begemann

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Isabelle Leisten

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Lukas Soellner

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Klaus Zerres

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Thomas Eggermann

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Sabrina Spengler

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=22419125

27 December 2024

publication date

1 May 2012

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

473-481

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

1

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus

2

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

3

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

4

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

5

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

6

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

7

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci

8

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

An atypical case of hypomethylation at multiple imprinted loci

9

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).

10

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

11

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Hunting for the 5th base: Techniques for analyzing DNA methylation

12

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndrome

13

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Methylation-specific multiplex ligation-dependent probe amplification (MS-MLPA) robustly detects and distinguishes 11p15 abnormalities associated with overgrowth and growth retardation

14

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Profiling epigenetic alterations in disease

15

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Rapid quantitation of methylation differences at specific sites using methylation-sensitive single nucleotide primer extension (Ms-SNuPE)

16

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Quantitative methylation analysis using methylation-sensitive single-nucleotide primer extension (Ms-SNuPE).

17

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Single nucleotide extension technology for quantitative site-specific evaluation of metC/C in GC-rich regions

18

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.

19

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation

20

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

The clinical phenotype of mosaicism for genome-wide paternal uniparental disomy: two new reports

21

1 reference

10.4161/EPI.19719

https://api.crossref.org/works/10.4161/EPI.19719

27 December 2024

Identifiers

10.4161/EPI.19719

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22419125 AND SRC:MED&resulttype=core&format=json

26 January 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q83654351&oldid=2291705924"