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Meltem Gürel

Researcher at Johns Hopkins University

Publications -  8
Citations -  1513

Meltem Gürel is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Prostate cancer & Regulation of gene expression. The author has an hindex of 6, co-authored 8 publications receiving 1308 citations. Previous affiliations of Meltem Gürel include Trinity College, Dublin & University of Washington.

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Distinct Transcriptional Programs Mediated by the Ligand-Dependent Full-Length Androgen Receptor and Its Splice Variants in Castration-Resistant Prostate Cancer

TL;DR: These findings support an adaptive shift toward AR-V-mediated signaling in a subset of CRPC tumors as the AR-LBD is rendered inactive, suggesting an important mechanism contributing to drug resistance to CRPC therapy.
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Tracking the clonal origin of lethal prostate cancer.

TL;DR: This case illustrates the potential need in precision medicine to longitudinally sample metastatic lesions to capture the evolving constellation of alterations during progression and highlights the potential importance of developing and implementing molecular prognostic and predictive markers to augment current pathological evaluation and delineate clonal heterogeneity.
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DNA Methylation Alterations Exhibit Intraindividual Stability and Interindividual Heterogeneity in Prostate Cancer Metastases

TL;DR: It is shown that somatic DNA methylation alterations, despite showing marked interindividual heterogeneity among men with lethal metastatic prostate cancer, were maintained across all metastases within the same individual, and the overall extent of maintenance in DNAmethylation changes was comparable to that of genetic copy number alterations.
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Genome-wide comparison of the transcriptomes of highly enriched normal and chronic myeloid leukemia stem and progenitor cell populations.

TL;DR: Governing-wide transcriptome analysis of highly refined CML and normal stem and progenitor cell populations was performed to identify novel targets for the eradication of CML LSCs using exon microarrays, identifying 97 genes that were differentially expressed in CML versus normalstem and progensitor cells.