(Q59548827)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8589723%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

title

Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8589723%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference

1 reference

4

Peter Devilee

Devilee P

1 reference

15 October 2019

9

Douglas F. Easton

Easton DF

1 reference

15 October 2019

8

Stratton MR

1 reference

15 October 2019

14

Narod SA

1 reference

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15 October 2019

1

Phelan CM

1 reference

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15 October 2019

13

Goldgar DE

1 reference

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15 October 2019

11

Cannon-Albright L

1 reference

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15 October 2019

author name string

Rebbeck TR

2

1 reference

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15 October 2019

Weber BL

3

1 reference

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15 October 2019

Ruttledge MH

5

1 reference

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15 October 2019

Lynch HT

6

1 reference

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15 October 2019

Lenoir GM

7

1 reference

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15 October 2019

Ponder BA

10

1 reference

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15 October 2019

Larsson C

12

1 reference

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15 October 2019

language of work or name

English

0 references

publication date

1 March 1996

1 reference

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15 October 2019

1 reference

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15 October 2019

volume

12

1 reference

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15 October 2019

issue

3

1 reference

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15 October 2019

page(s)

309-311

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https://scigraph.springernature.com/pub.10.1038/ng0396-309

15 October 2019

exact match

0 references

cites work

Unusual case of Smith-Lemli-Opitz syndrome "type II"

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

High Frequency of Rare Alleles of the Human c-Ha-ras-1 Proto-oncogene in Breast Cancer Patients2

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

An association between the risk of cancer and mutations in the HRAS1 minisatellite locus.

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Risk modifiers in carriers of brca1 mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

A Collaborative Survey of 80 Mutations in the BRCA1 Breast and Ovarian Cancer Susceptibility Gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Rapid detection of BRCA1 mutations by the protein truncation test

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Complete nucleotide sequences of the T24 human bladder carcinoma oncogene and its normal homologue

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Members of therel/NF-χB family of transcriptional regulatory proteins bind theHRAS1minisatellite DNA sequence

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Allelic variation of reporter gene activation by the HRAS1 minisatellite

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Transcriptional enhancer activity in the variable tandem repeat DNA sequence downstream of the human Ha-ras 1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Rapid detection of hypervariable regions by the polymerase chain reaction technique

1 reference

https://api.crossref.org/works/10.1038%2FNG0396-309

7 January 2021

Identifiers

DOI

10.1038/NG0396-309

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8589723%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference