Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility (Q57305903)

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English	Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility	article

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instance of

scholarly article

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title

Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility (English)

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main subject

ovarian cancer

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based on heuristic

inferred from title

author

Katri Pylkäs

object named as

Katri Pylkäs

series ordinal

2

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Arto Mannermaa

series ordinal

12

object named as

Arto Mannermaa

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Annika Lindblom

series ordinal

5

object named as

Annika Lindblom

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Jaana M Hartikainen

series ordinal

3

object named as

Jaana M. Hartikainen

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Veli-Matti Kosma

series ordinal

11

object named as

Veli-Matti Kosma

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Robert Winqvist

series ordinal

13

object named as

Robert Winqvist

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author name string

Mikko Vuorela

series ordinal

1

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Karin Sundfeldt

series ordinal

4

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Anna von Wachenfeldt Wäppling

series ordinal

6

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Maria Haanpää

series ordinal

7

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Ulla Puistola

series ordinal

8

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Annika Rosengren

series ordinal

9

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Maarit Anttila

series ordinal

10

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language of work or name

English

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publication date

13 July 2011

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published in

Breast Cancer Research and Treatment

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volume

130

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issue

3

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page(s)

1003-1010

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cites work

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Fanconi anemia and breast cancer susceptibility meet again

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21 January 2018

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

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reference URL

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retrieved

21 January 2018

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene

1 reference

stated in

Crossref

reference URL

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retrieved

21 January 2018

Complex formation by the human RAD51C and XRCC3 recombination repair proteins

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21 January 2018

Identification and purification of two distinct complexes containing the five RAD51 paralogs

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21 January 2018

RAD51C is required for Holliday junction processing in mammalian cells

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21 January 2018

How the fanconi anemia pathway guards the genome

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21 January 2018

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

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Evidence of founder mutations in Finnish BRCA1 and BRCA2 families

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Refinement of the 22q12-q13 breast cancer--associated region: evidence of TMPRSS6 as a candidate gene in an eastern Finnish population

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21 January 2018

RAD51C germline mutations in breast and ovarian cancer patients

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21 January 2018

Mutation screening of RAD51C in male breast cancer patients.

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Identification of functional domains in the RAD51L2 (RAD51C) protein and its requirement for gene conversion

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retrieved

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Identifiers

DOI

10.1007/S10549-011-1677-X

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PubMed publication ID

21750962

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