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Alan Ashworth

Researcher at University of California, San Francisco

Publications -  589
Citations -  82138

Alan Ashworth is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 134, co-authored 578 publications receiving 72089 citations. Previous affiliations of Alan Ashworth include Imperial College London & Papworth Hospital.

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Brca2 and Trp53 Deficiency Cooperate in the Progression of Mouse Prostate Tumourigenesis

TL;DR: Evidence is provided that Brca2 can act as a tumour suppressor in the prostate, and the model it is described should prove useful in the development of new therapeutic approaches.
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Phenotypic effects of heterozygosity for a BRCA2 mutation

TL;DR: It is demonstrated that, in a specific vertebrate cell type, the chicken B cell line DT40, heterozygosity for a BRCA2 mutation has a distinct phenotype, characterized by a reduced growth rate, increased cell death, heightened sensitivity to specific DNA damaging agents and reduced RAD51 focus formation after irradiation.
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Investigation of gene-environment interactions between 47 newly identified breast cancer susceptibility loci and environmental risk factors

Anja Rudolph, +97 more
TL;DR: In conclusion, recently identified BC susceptibility loci are not strongly modified by established risk factors and the observed potential interactions require confirmation in independent studies.
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FXY2/MID2, a Gene Related to the X-Linked Opitz Syndrome Gene FXY/MID1, Maps to Xq22 and Encodes a FNIII Domain-Containing Protein That Associates with Microtubules

TL;DR: It is shown that the FXY2 protein similarly associates with microtubules in a manner that is dependent on the carboxy-terminal B30.2 domain, and this has implications for understanding protein function.
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The threonine residues in MAP kinase kinase 1 phosphorylated by MAP kinase in vitro are also phosphorylated in nerve growth factor-stimulated rat phaeochromocytoma (PC12) cells.

TL;DR: The results establish that MAPKK1 is a physiological substrate for MAP kinase, demonstrating that neither species is the MAPKK2 isoform which lacks Thr‐291.