(Q44009195)

28 November 2017

A change in the last base of BRCA1 exon 23, 5586G-->A, results in abnormal RNA splicing (English)

1 reference

28 November 2017

Drakoulis Yannoukakos

9

1 reference

28 November 2017

Irene Konstantopoulou

object named as

Irene Konstantopoulou

2

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author name string

Angela Ladopoulou

1

1 reference

28 November 2017

Sofia Armaou

3

1 reference

28 November 2017

Eleni Efstathiou

4

1 reference

28 November 2017

Markos Mihalatos

5

1 reference

28 November 2017

George Nasioulas

6

1 reference

28 November 2017

Georgia Bardi

7

1 reference

28 November 2017

Nikos Pandis

8

1 reference

28 November 2017

Athens

10

1 reference

28 November 2017

Hellenic Cooperative Oncology Group

11

1 reference

28 November 2017

language of work or name

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1 April 2002

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Cancer Genetics and Cytogenetics

28 November 2017

1 reference

28 November 2017

134

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28 November 2017

2

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28 November 2017

175-177

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

28 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

BRCA1 mutations in primary breast and ovarian carcinomas.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

Detection of germline mutations in the BRCA1 gene by RNA-based sequencing.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

A Finnish BRCA1 exon 12 4216-2nt A to G splice acceptor site mutation causes aberrant splicing and frameshift, leading to protein truncation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

A characterization of genetic variants in BRCA1 intron 8 identifies a mutation and a polymorphism.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

BRCA1 IVS16+6T-->C is a deleterious mutation that creates an aberrant transcript by activating a cryptic splice donor site

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

A BRCA1 variant, IVS23+1G-->A, causes abnormal RNA splicing by deleting exon 23.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

Classification of IVS1-10T-->C as a polymorphism of BRCA1.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

The breast cancer information core: database design, structure, and scope

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

Construction of a novel database containing aberrant splicing mutations of mammalian genes

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

BRCA1 mutation analysis in breast/ovarian cancer families from Greece

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2801%2900623-9

7 January 2021

10.1016/S0165-4608(01)00623-9

Identifiers

DOI

1 reference

28 November 2017

1 reference