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Rohitha SriRamaratnam

Researcher at Columbia University

Publications -  5
Citations -  3523

Rohitha SriRamaratnam is an academic researcher from Columbia University. The author has contributed to research in topics: Cell & Programmed cell death. The author has an hindex of 4, co-authored 4 publications receiving 1770 citations. Previous affiliations of Rohitha SriRamaratnam include Howard Hughes Medical Institute.

Papers
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Journal ArticleDOI

Regulation of Ferroptotic Cancer Cell Death by GPX4

TL;DR: Targeted metabolomic profiling and chemoproteomics revealed that GPX4 is an essential regulator of ferroptotic cancer cell death and sensitivity profiling in 177 cancer cell lines revealed that diffuse large B cell lymphomas and renal cell carcinomas are particularly susceptible to GPx4-regulated ferroPTosis.
Patent

Oncogenic-RAS-signal dependent lethal compounds

TL;DR: In this paper, RAS-selective lethal compounds and compositions for cancer cell specific lethality are provided. And methods of screening for such compounds and methods of treating a condition in a mammal, by administering to the mammal a therapeutically effective amount of such compounds or compositions.
Journal ArticleDOI

Covalent Proximity Scanning of a Distal Cysteine to Target PI3Kα

TL;DR: A path to target solvent-exposed cysteines at a distance >10 Å from an ATP-site-directed core module and produce potent covalent phosphoinositide 3-kinase α (PI3Kα) inhibitors is delineated and generally suited to develop covalents tools targeting distal, unexplored Cys residues in biologically active enzymes.
Journal ArticleDOI

Identification of PDE6D as a molecular target of anecortave acetate via a methotrexate-anchored yeast three-hybrid screen.

TL;DR: The identification of PDE6D as the molecular binding partner of AA provides insight into the role of this drug candidate in treating glaucoma.
Journal ArticleDOI

Identification of a small molecule that induces ATG5-and-cathepsin-l-dependent cell death and modulates polyglutamine toxicity

TL;DR: The discovery of NID-1 identifies a previously unexplored cell death pathway, and modulating this pathway may have therapeutic applications, and these findings provide a proof-of-principle for using chemical screening to identify novel cell death paradigms.