(Q33681805)

English

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

inferred from title

8

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15 October 2019

16

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15 October 2019

Andrew P. Feinberg

20

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15 October 2019

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J M Hoovers

1

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15 October 2019

L M Kalikin

2

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15 October 2019

L A Johnson

3

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15 October 2019

M Alders

4

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15 October 2019

B Redeker

5

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15 October 2019

D J Law

6

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15 October 2019

J Bliek

7

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15 October 2019

M Benedict

9

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15 October 2019

J Wiegant

10

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15 October 2019

C Lengauer

11

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15 October 2019

P Taillon-Miller

12

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15 October 2019

D Schlessinger

13

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15 October 2019

M C Edwards

14

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15 October 2019

S J Elledge

15

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15 October 2019

A Westerveld

17

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15 October 2019

P Little

18

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15 October 2019

M Mannens

19

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15 October 2019

language of work or name

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publication date

1 December 1995

1 reference

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15 October 2019

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

1 reference

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15 October 2019

92

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15 October 2019

26

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

12456-12460

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

WAF1, a potential mediator of p53 tumor suppression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Epigenetic effects in eukaryotic gene expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Genomic sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Isolation of single-copy human genes from a library of yeast artificial chromosome clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Beckwith-Wiedemann syndrome, tumourigenesis and imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

21 June 2018

Relaxation of imprinted genes in human cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40376

30 October 2018

The generation of ordered sets of cosmid DNA clones from human chromosome region 11p

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCR buffer optimization with uniform temperature regimen to facilitate automation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of cytogenetic alterations associated with the Beckwith — Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two simple procedures for releasing chromatin from routinely fixed cells for fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic lesions at the H19 locus in Wilms' tumour patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting in hepatoblastoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 11 and Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8618920

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.92.26.12456

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1995PNAS...9212456H

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8618920%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

ResearchGate publication ID

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