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Jane Bayani

Researcher at Ontario Institute for Cancer Research

Publications -  96
Citations -  11254

Jane Bayani is an academic researcher from Ontario Institute for Cancer Research. The author has contributed to research in topics: Comparative genomic hybridization & Cancer. The author has an hindex of 36, co-authored 82 publications receiving 10399 citations. Previous affiliations of Jane Bayani include University of Toronto & Mount Sinai Hospital, Toronto.

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Identification of human brain tumour initiating cells

TL;DR: The development of a xenograft assay that identified human brain tumour initiating cells that initiate tumours in vivo gives strong support for the CSC hypothesis as the basis for many solid tumours, and establishes a previously unidentified cellular target for more effective cancer therapies.
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Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity.

TL;DR: It is predicted that integration of functional and genomic analysis at a clonal level will be essential for understanding evolution and therapeutic resistance of human cancer, and will lead to the discovery of novel driver mechanisms and clone-specific cancer treatment.
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Characterization of male breast cancer: Results of the EORTC 10085/TBCRC/BIG/NABCG International Male Breast Cancer Program

TL;DR: Better overall (OS) and recurrence-free survival (RFS) and a significant improvement over time was observed in age-corrected BC mortality and there was no association between OS/RFS and HER-2 status, Ki67, IHC subtypes nor grade.
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Three-color FISH analysis of TMPRSS2/ERG fusions in prostate cancer indicates that genomic microdeletion of chromosome 21 is associated with rearrangement.

TL;DR: Three-color fluorescence in situ hybridization confirms that TMPRSS2/ERG fusion may be accompanied by a small hemizygous sequence deletion on chromosome 21 between ERG and TMPR SS2 genes.
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Single cell derived clonal analysis of human glioblastoma links functional and genomic heterogeneity.

TL;DR: The results suggest that functional clonal profiling used to identify tumorigenic and drug resistant tumor clones will lead to the discovery of new GBM clone-specific treatment strategies.