Collective evidence supports neutrality of BRCA1 V1687I, a novel sequence variant in the conserved THV motif of the first BRCT repeat. (Q44803655)

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29 January 2020

title

Collective evidence supports neutrality of BRCA1 V1687I, a novel sequence variant in the conserved THV motif of the first BRCT repeat (English)

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29 January 2020

4

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29 January 2020

Antonio Rossi

7

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29 January 2020

Daniela Turchetti

5

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29 January 2020

Giulio Rossi

8

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29 January 2020

Massimo Federico

10

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29 January 2020

Massimo Federico

11

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1

Laura Cortesi

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29 January 2020

author name string

Arcangela De Nicolo

2

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29 January 2020

Veronica Medici

3

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29 January 2020

Laura Maria Pradella

6

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29 January 2020

Emilio Parisini

9

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29 January 2020

language of work or name

English

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publication date

22 April 2012

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Breast Cancer Research and Treatment

29 January 2020

published in

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volume

134

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issue

1

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29 January 2020

page(s)

435-441

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Clinical relevance of rare germline sequence variants in cancer genes: evolution and application of classification models

29 January 2020

cites work

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The C-terminal (BRCT) domains of BRCA1 interact in vivo with CtIP, a protein implicated in the CtBP pathway of transcriptional repression

21 January 2018

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Abraxas and RAP80 form a BRCA1 protein complex required for the DNA damage response

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BRCT Repeats As Phosphopeptide-Binding Modules Involved in Protein Targeting

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Multimodal assessment of protein functional deficiency supports pathogenicity of BRCA1 p.V1688del

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A novel breast cancer-associated BRIP1 (FANCJ/BACH1) germ-line mutation impairs protein stability and function

21 January 2018

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Functional impact of missense variants in BRCA1 predicted by supervised learning

21 January 2018

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Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from the California cancer Registry

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ESPript: analysis of multiple sequence alignments in PostScript

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Genetic and Histopathologic Evaluation ofBRCA1andBRCA2DNA Sequence Variants of Unknown Clinical Significance

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