(Q28343524)

English

High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss

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scholarly article

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High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss (English)

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1 reference

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author name string

A Maitra

1

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I I Wistuba

2

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C Washington

3

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A K Virmani

4

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R Ashfaq

5

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S Milchgrub

6

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A F Gazdar

7

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J D Minna

8

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language of work or name

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publication date

July 2001

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The American Journal of Pathology

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159

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1

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119-30

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Epigenetic inactivation of RASSF1A in lung and breast cancers and malignant phenotype suppression

1 reference

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20 March 2017

The 630-kb lung cancer homozygous deletion region on human chromosome 3p21.3: identification and evaluation of the resident candidate tumor suppressor genes. The International Lung Cancer Chromosome 3p21.3 Tumor Suppressor Gene Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

20 March 2017

Genetic instabilities in human cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

20 March 2017

Homozygous deletions at 3p12 in breast and lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

20 March 2017

Widely dispersed p53 mutation in respiratory epithelium. A novel mechanism for field carcinogenesis

1 reference

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20 March 2017

Construction of a 600-kilobase cosmid clone contig and generation of a transcriptional map surrounding the lung cancer tumor suppressor gene (TSG) locus on human chromosome 3p21.3: progress toward the isolation of a lung cancer TSG

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

20 March 2017

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

20 March 2017

Molecular origin of cancer: catechol estrogen-3,4-quinones as endogenous tumor initiators

1 reference

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20 March 2017

Identification of the von Hippel-Lindau disease tumor suppressor gene

1 reference

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7 April 2017

Comparative genomic hybridization analysis of 38 breast cancer cell lines: a basis for interpreting complementary DNA microarray data.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Genome-wide search for loss of heterozygosity using laser capture microdissected tissue of breast carcinoma: an implication for mutator phenotype and breast cancer pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Epigenetic inactivation of a RAS association domain family protein from the lung tumour suppressor locus 3p21.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Loss of heterozygosity in fibrocystic change of the breast: genetic relationship between benign proliferative lesions and associated carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Two identical triplet sisters carrying a germline BRCA1 gene mutation acquire very similar breast cancer somatic mutations at multiple other sites throughout the genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Use of archival fine-needle aspirates for the allelotyping of tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

The tumor-suppressor gene FHIT is involved in the regulation of apoptosis and in cell cycle control

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

A novel signature mutation for oxidative damage resembles a mutational pattern found commonly in human cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Loss of heterozygosity at 3p in benign lesions preceding invasive breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Comparison of features of human breast cancer cell lines and their corresponding tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Characterization of paired tumor and non-tumor cell lines established from patients with breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Computerized polymorphic marker identification: experimental validation and a predicted human polymorphism catalog

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Comparison of molecular changes in lung cancers in HIV-positive and HIV-indeterminate subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Analysis of loss of heterozygosity in 399 premalignant breast lesions at 15 genetic loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Laser capture microdissection: molecular analysis of tissue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Human/mouse microcell hybrid based elimination test reduces the putative tumor suppressor region at 3p21.3 to 1.6 cM.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Loss of heterozygosity induced by a chromosomal double-strand break

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Deletions of chromosome 3p are frequent and early events in the pathogenesis of uterine cervical carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Chromosome 3 allelic losses and microsatellite alterations in transitional cell carcinoma of the urinary bladder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Distinct 3p21.3 deletions in lung cancer and identification of a new human semaphorin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Allele-specific chromosome 3p deletions occur at an early stage in the pathogenesis of lung carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Molecular genetic studies of early breast cancer evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p and 17q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

29 September 2017

Deletion of the short arm of chromosome 3 in breast tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

2 June 2018

Loss of heterozygosity in normal tissue adjacent to breast carcinomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

2 June 2018

A homozygous deletion on chromosome 3 in a small cell lung cancer cell line correlates with a region of tumor suppressor activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

2 June 2018

A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

2 June 2018

A central role for chromosome breakage in gene amplification, deletion formation, and amplicon integration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

2 June 2018

Methylation and silencing of the retinoic acid receptor-beta2 gene in breast cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

27 November 2018

Chromosome 3p14 homozygous deletions and sequence analysis of FRA3B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

27 November 2018

Deletion of two separate regions on chromosome 3p in breast cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

27 November 2018

A nonrandom chromosomal abnormality, del 3p(14–23), in human small cell lung cancer (SCLC)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850416

27 November 2018

Risk factors for breast cancer in women with proliferative breast disease

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Specific chromosome defect associated with human small-cell lung cancer; deletion 3p(14-23)

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Chromosome abnormalities in benign hyperproliferative disorders of epithelial and stromal breast tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Karyotypic abnormalities in fibroadenomas of the breast

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

A 3p21.3 region is preferentially eliminated from human chromosome 3/mouse microcell hybrids during tumor growth in SCID mice

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

The expression of Fhit protein is related inversely to disease progression in patients with breast carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Loss of heterozygosity at 3p24-p25 as a prognostic factor in breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Promoter Methylation and Silencing of the Retinoic Acid Receptor- Gene in Lung Carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

Homozygous deletion, rearrangement and hypermethylation implicate chromosome region 3p14.3-3p21.3 in sporadic breast-cancer development

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

In vitro repair of synthetic ionizing radiation-induced multiply damaged DNA sites 1 1Edited by J. H. Miller

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961679-3

7 January 2021

FHIT loss of function in human primary breast cancer correlates with advanced stage of the disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breast cancer risk associated with genotype polymorphism of the estrogen-metabolizing genes CYP17, CYP1A1, and COMT: a multigenic study on cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide map showing common regions of loss of heterozygosity/allelic imbalance in breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accumulation of genetic alterations and progression of primary breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the FHIT gene and FRA3B region in sporadic breast cancer, preneoplastic lesions, and familial breast cancer probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of fragile histidine triad expression in colorectal carcinomas and premalignant lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive evaluation of family history and breast cancer risk. The Utah Population Database

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the FHIT gene in colorectal cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detailed deletion mapping of chromosome arm 3p in breast cancers: a 2-cM region on 3p14.3-21.1 and a 5-cM region on 3p24.3-25.1 commonly deleted in tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Location of several putative genes possibly involved in human breast cancer progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro repair of synthetic ionizing radiation-induced multiply damaged DNA sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/11438460

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)61679-3

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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