(Q41868632)

13 October 2017

Constitutional and somatic methylation status of DMRH19 and KvDMR in Wilms tumor patients (English)

1 reference

13 October 2017

Leila C A Cardoso

1

1 reference

13 October 2017

Jair A Tenorio Castaño

2

1 reference

13 October 2017

Hanna S Pereira

3

1 reference

13 October 2017

Maria Angélica de F D Lima

4

1 reference

13 October 2017

Anna Cláudia E Dos Santos

5

1 reference

13 October 2017

Paulo S de Faria

6

1 reference

13 October 2017

Sima Ferman

7

1 reference

13 October 2017

Héctor N Seuánez

8

1 reference

13 October 2017

Julián B Nevado

9

1 reference

13 October 2017

José Carlos Cabral de Almeida

10

1 reference

13 October 2017

Pablo Lapunzina

11

1 reference

13 October 2017

Fernando R Vargas

12

1 reference

13 October 2017

language of work or name

1 reference

9 November 2012

1 reference

Genetics and Molecular Biology

13 October 2017

1 reference

13 October 2017

35

1 reference

13 October 2017

4

1 reference

13 October 2017

714-724

1 reference

Stratification of Wilms tumor by genetic and epigenetic analysis

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Socioeconomic status and the incidence of non-central nervous system childhood embryonic tumours in Brazil

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Current management of wilms' tumor

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Management of Wilms' tumor: NWTS vs SIOP.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Growth regulation, imprinted genes, and chromosome 11p15.5.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

A simple salting out procedure for extracting DNA from human nucleated cells

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Quantitative 1-step DNA methylation analysis with native genomic DNA as template.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Abnormal methylation at the KvDMR1 imprinting control region in clinically normal children conceived by assisted reproductive technologies.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

Nephrogenic rests and the pathogenesis of Wilms tumor: developmental and clinical considerations

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3526076

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

18 August 2018

1 reference

https://api.crossref.org/works/10.1590%2FS1415-47572012005000073

Frequency and Timing of Loss of Imprinting at 11p13 and 11p15 in Wilms' Tumor Development

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS1415-47572012005000073

Alterations of H19 Imprinting and IGF2 Replication Timing Are Infrequent in Beckwith–Wiedemann Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS1415-47572012005000073

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS1415-47572012005000073

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

21 January 2018

1 reference

PubMed

12 December 2020

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

PubMed

12 December 2020

1 reference

12 December 2020

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment

1 reference

PubMed

12 December 2020

10.1590/S1415-47572012005000073

Identifiers

DOI

1 reference

13 October 2017

1 reference

13 October 2017

PubMed publication ID

23271929

1 reference