scispace - formally typeset
F

Fariba Ghaidi

Researcher at University of British Columbia

Publications -  14
Citations -  354

Fariba Ghaidi is an academic researcher from University of British Columbia. The author has contributed to research in topics: PARP1 & Prostate cancer. The author has an hindex of 7, co-authored 9 publications receiving 307 citations.

Papers
More filters
Journal ArticleDOI

Short Hairpin RNA Knockdown of the Androgen Receptor Attenuates Ligand-Independent Activation and Delays Tumor Progression

TL;DR: By inducibly suppressing AR expression in vivo, there is an extensive delay in progression to androgen independence as well as a dramatic inhibition of tumor growth and decrease in serum PSA, which exceeds that seen with castration alone.
Journal ArticleDOI

Molecular phenotyping of thyroid tumors identifies a marker panel for differentiated thyroid cancer diagnosis.

TL;DR: Evaluation of the molecular phenotype of differentiated thyroid cancer (DTC) and benign thyroid tumor molecular phenotype has allowed for identification of a marker panel, composed of both established and novel markers, useful for thyroid cancer diagnosis.
Journal ArticleDOI

Computer-aided drug discovery of Myc-Max inhibitors as potential therapeutics for prostate cancer.

TL;DR: Among compounds identified that effectively inhibit Myc-Max activity with low to mid-micromolar range potency and no or minimal generic cytotoxicity, VPC-70067, a close analog of the previously identified Myc inhibitor 10058-F4, served as proof-of-concept that the in silico drug discovery strategy performed as expected.
Journal ArticleDOI

Computer-Aided Discovery of Small Molecules Targeting the RNA Splicing Activity of hnRNP A1 in Castration-Resistant Prostate Cancer.

TL;DR: This study reports compound VPC-80051 as the first small molecule inhibitor of hnRNP A1 splicing activity discovered to date by using a computer-aided drug discovery approach and lays the groundwork for future structure-based development of more potent and selective small molecule inhibitors of hmR NP A1–RNA interactions aimed at altering the production of cancer-specific alternative splice isoforms.