(Q58862231)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454289%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

title

Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas (English)

1 reference

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12 October 2019

1 reference

5

1 reference

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12 October 2019

1

A Lindblom

1 reference

12 October 2019

L Skoog

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454289%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

T I Andersen

series ordinal

3

1 reference

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12 October 2019

S Rotstein

series ordinal

4

1 reference

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12 October 2019

C Larsson

series ordinal

6

1 reference

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12 October 2019

publication date

1 March 1993

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12 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454289%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

volume

91

1 reference

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12 October 2019

page(s)

6-12

1 reference

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12 October 2019

issue

1

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00230213

12 October 2019

exact match

0 references

cites work

Retinoblastoma: a prototypic hereditary neoplasm

1 reference

12 December 2020

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

1 reference

12 December 2020

TP53 tumor suppressor gene: a model for investigating human mutagenesis

1 reference

12 December 2020

Epidemiology and risk factors

1 reference

12 December 2020

Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

1 reference

12 December 2020

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

1 reference

12 December 2020

Somatic mutations in the neurofibromatosis 1 gene in human tumors

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Loss of NF1 alleles in phaeochromocytomas from patients with type I neurofibromatosis

1 reference

12 December 2020

Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer

1 reference

12 December 2020

Allele loss on short arm of chromosome 17 in breast cancers

1 reference

12 December 2020

Evidence implicating at least two genes on chromosome 17p in breast carcinogenesis.

1 reference

12 December 2020

Loss of heterozygosity on 17p in human breast carcinomas: defining the smallest common region of deletion

1 reference

12 December 2020

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

1 reference

12 December 2020

Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms

1 reference

12 December 2020

p53 mutations in human cancers

1 reference

12 December 2020

Inherited p53 gene mutations in breast cancer

1 reference

12 December 2020

Screening for germ line TP53 mutations in breast cancer patients

1 reference

12 December 2020

Closing in on a breast cancer gene on chromosome 17q

1 reference

12 December 2020

Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q

1 reference

12 December 2020

Deletion mapping in human renal cell carcinoma

1 reference

12 December 2020

Amplification and protein over-expression of the neu/HER-2/c-erbB-2 protooncogene in human breast carcinomas: relationship to loss of gene sequences on chromosome 17, family history and prognosis

1 reference

12 December 2020

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

12 December 2020

Mutations in p53 do not account for heritable breast cancer: a study in five affected families

1 reference

12 December 2020

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

1 reference

12 December 2020

Genetic origin of mutations predisposing to retinoblastoma

1 reference

12 December 2020

Constant denaturant gel electrophoresis as a rapid screening technique for p53 mutations

1 reference

12 December 2020

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

1 reference

12 December 2020

Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma

1 reference

12 December 2020

Familial breast-ovarian cancer locus on chromosome 17q12-q23

1 reference

12 December 2020

Genetic alterations during colorectal-tumor development

1 reference

12 December 2020

Suppression of the neoplastic phenotype by replacement of the RB gene in human cancer cells

1 reference

12 December 2020

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

1 reference

12 December 2020

Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome

1 reference

12 December 2020

Genomic alterations in human breast carcinomas

1 reference

12 December 2020

Constitutional p53 mutation in a non-Li-Fraumeni cancer family

1 reference

12 December 2020

p53 gene mRNA expression and chromosome 17p allele loss in breast cancer

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00230213

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8454289%20AND%20SRC:MED&resulttype=core&format=json

12 October 2019

1 reference