8q24 allelic imbalance and MYC gene copy number in primary prostate cancer (Q37658495)

21 August 2017

8q24 allelic imbalance and MYC gene copy number in primary prostate cancer (English)

1 reference

21 August 2017

1 reference

H Chen

1

1 reference

21 August 2017

W Liu

2

1 reference

21 August 2017

W Roberts

3

1 reference

21 August 2017

S Hooker

4

1 reference

21 August 2017

H Fedor

5

1 reference

21 August 2017

A DeMarzo

6

1 reference

21 August 2017

W Isaacs

7

1 reference

21 August 2017

R A Kittles

8

1 reference

21 August 2017

13 July 2010

1 reference

full work available at URL

21 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3963483

0 references

published in

Prostate Cancer and Prostatic Diseases

1 reference

21 August 2017

13

1 reference

21 August 2017

3

1 reference

21 August 2017

238-243

1 reference

Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans

21 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Sequence variant on 8q24 confers susceptibility to urinary bladder cancer

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Homozygous deletions and recurrent amplifications implicate new genes involved in prostate cancer

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Multiple loci with different cancer specificities within the 8q24 gene desert

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Nuclear MYC protein overexpression is an early alteration in human prostate carcinogenesis

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Confirmation study of prostate cancer risk variants at 8q24 in African Americans identifies a novel risk locus.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Human MMS21/NSE2 is a SUMO ligase required for DNA repair

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Multiple regions within 8q24 independently affect risk for prostate cancer

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

A common variant associated with prostate cancer in European and African populations

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.

25 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Genomic profiling reveals alternative genetic pathways of prostate tumorigenesis

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Relative copy number gain of MYC in diagnostic needle biopsies is an independent prognostic factor for prostate cancer patients

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

c-MYC Asn11Ser is associated with increased risk for familial breast cancer

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

Gene copy number for epidermal growth factor receptor (EGFR) and clinical response to antiEGFR treatment in colorectal cancer: a cohort study

1 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3963483

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21

1 September 2018

1 reference

https://api.crossref.org/works/10.1038%2FPCAN.2010.20

Two Common Chromosome 8q24 Variants Are Associated with Increased Risk for Prostate Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPCAN.2010.20

Allelic Imbalance at rs6983267 Suggests Selection of the Risk Allele in Somatic Colorectal Tumor Evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPCAN.2010.20

Multiple prostate cancer risk variants on 8q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPCAN.2010.20

Cumulative association of five genetic variants with prostate cancer

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPCAN.2010.20

Semiautomated assessment of loss of heterozygosity and replication error in tumors

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20634801

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of c-myc oncogene amplification and chromosomal anomalies in metastatic prostatic carcinoma by fluorescence in situ hybridization

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20634801

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Detection of chromosomal anomalies and c-myc gene amplification in the cribriform pattern of prostatic intraepithelial neoplasia and carcinoma by fluorescence in situ hybridization

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20634801

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/PCAN.2010.20

1 reference

Dimensions Publication ID

21 August 2017

0 references

1 reference

21 August 2017

PubMed publication ID

20634801

1 reference