(Q33507538)

English

Analysis of cancer mutation signatures in blood by a novel ultra-sensitive assay: monitoring of therapy or recurrence in non-metastatic breast cancer

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Analysis of cancer mutation signatures in blood by a novel ultra-sensitive assay: monitoring of therapy or recurrence in non-metastatic breast cancer (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

non-metastatic breast cancer

1 reference

based on heuristic

inferred from title

author name string

Zhenbin Chen

1

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Jinong Feng

2

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Carolyn H Buzin

3

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Qiang Liu

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Lawrence Weiss

5

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Kemp Kernstine

6

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

George Somlo

7

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

Steve S Sommer

8

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

language of work or name

0 references

publication date

28 September 2009

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

e7220

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

copyright license

Creative Commons Attribution 4.0 International

28 September 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Circulating mutant DNA to assess tumor dynamics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Accuracy and quality of massively parallel DNA pyrosequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Evidence for mutation showers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Circulating free DNA in plasma or serum as biomarker of carcinogenesis: practical aspects and biological significance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Circulating nucleic acids (CNAs) and cancer--a survey

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Human cancers express a mutator phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

The population dynamics of cancer: a Darwinian perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Somatic mutations of epidermal growth factor receptor signaling pathway in lung cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

PAP: detection of ultra rare mutations depends on P* oligonucleotides: "sleeping beauties" awakened by the kiss of pyrophosphorolysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Spontaneous tandem-base mutations (TBM) show dramatic tissue, age, pattern and spectrum specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Pyrophosphorolysis-activatable oligonucleotides may facilitate detection of rare alleles, mutation scanning and analysis of chromatin structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Cancer, National Cancer Institute of the United States, National Cancer Institute of Canada

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

The molecular epidemiology of p53 gene mutations in human breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Exclusive paternal origin of new mutations in Apert syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Achondroplasia is defined by recurrent G380R mutations of FGFR3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Avoiding false positives with PCR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

The "megaprimer" method of site-directed mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

Direct sequencing from touch preparations of human carcinomas: analysis of p53 mutations in breast carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

21 June 2018

BEAMing up for detection and quantification of rare sequence variants.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Rapid SNP diagnostics using asymmetric isothermal amplification and a new mismatch-suppression technology.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Detection of ultrarare somatic mutation in the human TP53 gene by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acids

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Fen1 mutations result in autoimmunity, chronic inflammation and cancers

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Multiplex dosage pyrophosphorolysis-activated polymerization: application to the detection of heterozygous deletions

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Tumor Size Predicts Survival Within Stage IA Non-Small Cell Lung Cancer *

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Inherited susceptibility to lung cancer may be associated with the T790M drug resistance mutation in EGFR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

31 October 2018

Survival after pathological stage IA nonsmall cell lung cancer: tumor size matters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

31 October 2018

Detection of extremely rare alleles by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification (Bi-PAP-A): measurement of mutation load in mammalian tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2749210

31 October 2018

Shedding light on PCR contamination

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0007220

21 January 2018

Darwinian medicine: a case for cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19789704

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidermal growth factor receptor mutation testing in lung cancer: searching for the ideal method

1 reference

https://pubmed.ncbi.nlm.nih.gov/19789704

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Does cancer kill the individual and save the species?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19789704

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Incidence of local recurrence and second primary tumors in resected stage I lung cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19789704

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of basepair substitution mutation at a frequency of 1 x 10(-7) by combining two genotypic selection methods, MutEx enrichment and allele-specific competitive blocker PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/19789704

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0007220

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

2009PLoSO...4.7220C

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 July 2017

ResearchGate publication ID

0 references

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