Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2 (Q37092814)

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scientific article published on 06 July 2008

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English	Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2	scientific article published on 06 July 2008

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

title

Mouse embryonic stem cell-based functional assay to evaluate mutations in BRCA2 (English)

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Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

author name string

Sergey G Kuznetsov

series ordinal

1

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Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

Pentao Liu

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2

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Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

Shyam K Sharan

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3

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Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

language of work or name

English

0 references

publication date

6 July 2008

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Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

published in

Nature Medicine

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stated in

Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

volume

14

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Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

issue

8

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Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

page(s)

875-881

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Europe PubMed Central

PMC publication ID

2640324

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18 August 2017

cites work

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

RAD51C deficiency in mice results in early prophase I arrest in males and sister chromatid separation at metaphase II in females

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

Functional assays for BRCA1 and BRCA2.

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

Integrated evaluation of DNA sequence variants of unknown clinical significance: application to BRCA1 and BRCA2

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

BRCA2 deficiency in mice leads to meiotic impairment and infertility

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

A full-likelihood method for the evaluation of causality of sequence variants from family data

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29 September 2017

A simple two-step, 'hit and fix' method to generate subtle mutations in BACs using short denatured PCR fragments

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29 September 2017

Deletion of Brca2 exon 27 causes hypersensitivity to DNA crosslinks, chromosomal instability, and reduced life span in mice.

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PubMed Central

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29 September 2017

Interaction between BRCA2 and replication protein A is compromised by a cancer-predisposing mutation in BRCA2

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PubMed Central

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29 September 2017

BRCA2 function in DNA binding and recombination from a BRCA2-DSS1-ssDNA structure

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

BRCA2 T2722R is a deleterious allele that causes exon skipping

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PubMed Central

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29 September 2017

DNA double-strand breaks: signaling, repair and the cancer connection

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29 September 2017

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

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29 September 2017

Cells deleted for Brca2 COOH terminus exhibit hypersensitivity to gamma-radiation and premature senescence

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PubMed Central

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29 September 2017

Involvement of Brca2 in DNA Repair

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

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29 September 2017

Chromosome engineering in mice

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PubMed Central

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29 September 2017

Evaluation of a soluble tetrazolium/formazan assay for cell growth and drug sensitivity in culture using human and other tumor cell lines

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PubMed Central

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29 September 2017

Mini-λ: a tractable system for chromosome and BAC engineering

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

retrieved

3 September 2018

Aberrant splicing induced by missense mutations in BRCA1: clues from a humanized mouse model

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

retrieved

3 September 2018

The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2640324

retrieved

4 December 2018

BRCA2 is required for ionizing radiation-induced assembly of Rad51 complex in vivo

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygous germ line mutation in exon 27 of murine Brca2 disrupts the Fancd2-Brca2 pathway in the homologous recombination-mediated DNA interstrand cross-links' repair but does not affect meiosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Embryonic stem cells deficient for Brca2 or Blm exhibit divergent genotoxic profiles that support opposing activities during homologous recombination

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of Common BRCA1 and BRCA2 Variants

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variation in BRCA2 and breast cancer risk: a haplotype-based analysis in the Multiethnic Cohort

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphic stop codon in BRCA2

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional evaluation and cancer risk assessment of BRCA2 unclassified variants

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/18607349

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1038/NM.1719

1 reference

stated in

Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

PMC publication ID

2640324

1 reference

stated in

Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

PubMed publication ID

18607349

1 reference

stated in

Europe PubMed Central

PMC publication ID

2640324

retrieved

18 August 2017

ResearchGate publication ID

5244269

0 references

 

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