(Q44311705)

1 December 2017

title

Identification of high-risk breast cancer patients from genetic changes of their tumors (English)

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1 December 2017

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M Watatani

1

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1 December 2017

H Inui

2

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1 December 2017

K Nagayama

3

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1 December 2017

Y Imanishi

4

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1 December 2017

K Nishimura

5

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1 December 2017

Y Hashimoto

6

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1 December 2017

E Yamauchi

7

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1 December 2017

T Hojo

8

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1 December 2017

Y Kotsuma

9

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1 December 2017

M Yamato

10

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1 December 2017

N Matsunami

11

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1 December 2017

M Yasutomi

12

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1 December 2017

publication date

1 January 2000

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1 December 2017

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1 December 2017

volume

30

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1 December 2017

issue

6

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1 December 2017

page(s)

516-522

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Loss of heterozygosity in normal tissue adjacent to breast carcinomas.

1 December 2017

cites work

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https://api.crossref.org/works/10.1007%2FS005950070118

Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

Loss of heterozygosity on chromosome 1q in human breast cancer

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

Loss of heterozygosity on chromosomes 17 and 18 in breast carcinoma: two additional regions identified

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

Analysis of genetic alterations related to the development and progression of breast carcinoma.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

Linkage of early-onset familial breast cancer to chromosome 17q21

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

The NM23 gene maps to human chromosome band 17q22 and shows a restriction fragment length polymorphism with BglII.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Allelic loss on chromosome 9q is associated with lymph node metastasis of primary breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Association of INT2/HST1 coamplification in primary breast cancer with hormone-dependent phenotype and poor prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Association of genetic alterations on chromosome 17 and loss of hormone receptors in breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

A Hypothesis of the Origin of Human Breast Cancer from the Terminal Ductal Lobular Unit

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

Genetic alterations of the tumour suppressor gene regions 3p, 11p, 13q, 17p, and 17q in human breast carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Prognostic value of erb-B2 and myc amplification in breast cancer imprints

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Allele loss on short arm of chromosome 17 in breast cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Genetic studies of 457 breast cancers. Clinicopathologic parameters compared with genetic alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Genetic alterations on chromosome 17 in human breast cancer: relationships to clinical features and DNA ploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Allelic loss on chromosome 1p is associated with progression and lymph node metastasis of primary breast carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Five distinct deleted regions on chromosome 17 defining different subsets of human primary breast tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

INT2 and ERBB2 amplification and ERBB2 expression in breast tumors from patients with different outcomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

int-2 oncogene amplification and prognosis in node-negative breast carcinoma

21 January 2018

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https://api.crossref.org/works/10.1007%2FS005950070118

A prospective study of the significance of gene and chromosome alterations as prognostic indicators of breast cancer patients with lymph node metastases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

EMS1 amplification can occur independently of CCND1 or INT-2 amplification at 11q13 and may identify different phenotypes in primary breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS005950070118

Identification and cloning of two overexpressed genes, U21B31/PRAD1 and EMS1, within the amplified chromosome 11q13 region in human carcinomas

21 January 2018

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12 December 2020

Accumulation of genetic alterations and progression of primary breast cancer

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12 December 2020

Correlation between long-term survival in breast cancer patients and amplification of two putative oncogene-coamplification units: hst-1/int-2 and c-erbB-2/ear-1

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12 December 2020

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

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12 December 2020

Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas

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12 December 2020

Correlation of loss of alleles on the short arms of chromosomes 11 and 17 with metastasis of primary breast cancer to lymph nodes

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12 December 2020

Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted

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12 December 2020

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

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12 December 2020

Int-2/FGF3 amplification is a better independent predictor of relapse than c-myc and c-erbB-2/neu amplifications in primary human breast cancer

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12 December 2020

Distal deletion of chromosome Ip in ductal carcinoma of the breast

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12 December 2020

Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parameters

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12 December 2020

Somatic mutations that contribute to breast cancer

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12 December 2020

Deletions on chromosome 16 in primary familial breast carcinomas are associated with development of distant metastases

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12 December 2020

c-myc amplification is a better prognostic factor than HER2/neu amplification in primary breast cancer

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12 December 2020

Identifiers

DOI

10.1007/S005950070118

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1 December 2017

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