scispace - formally typeset
J

Jennifer L. Ariazi

Researcher at GlaxoSmithKline

Publications -  8
Citations -  618

Jennifer L. Ariazi is an academic researcher from GlaxoSmithKline. The author has contributed to research in topics: Hypoxia-inducible factors & Erythropoiesis. The author has an hindex of 5, co-authored 8 publications receiving 527 citations. Previous affiliations of Jennifer L. Ariazi include Fox Chase Cancer Center.

Papers
More filters
OtherDOI

Estrogen Receptors as Therapeutic Targets in Breast Cancer

TL;DR: The development of resistance to endocrine therapy remains a clinically important problem, and laboratory models based on human breast cancer cells grown as tumors in immune-compromised mice have led to important insights into this problem.
Journal ArticleDOI

Tunneling Nanotubes and Gap Junctions-Their Role in Long-Range Intercellular Communication during Development, Health, and Disease Conditions.

TL;DR: The combined data from numerous laboratories indicate that some TNT mediate a long-range gap junctional communication to coordinate metabolism and signaling, in relation to infectious, genetic, metabolic, cancer, and age-related diseases.
Journal ArticleDOI

Chronic inhibition of hypoxia-inducible factor prolyl 4-hydroxylase improves ventricular performance, remodeling, and vascularity after myocardial infarction in the rat.

TL;DR: Chronic post-myocardial infarction treatment with a selective HIF PHD inhibitor (GSK360A) exerts systemic and local effects by stabilizing HIF-1α signaling and improves long-term ventricular function, remodeling, and vascularity in a model of established ventricular dysfunction.
Journal ArticleDOI

Discovery and Preclinical Characterization of GSK1278863 (Daprodustat), a Small Molecule Hypoxia Inducible Factor–Prolyl Hydroxylase Inhibitor for Anemia

TL;DR: GSK1278863 is a pyrimidinetrione-glycinamide low nanomolar inhibitor of PHDs 1–3 that stabilizes HIFα in cell lines, resulting in the production of increased levels of EPO, and is currently in phase 3 clinical trials for treatment of anemia in patients with chronic kidney disease.
Journal ArticleDOI

Rational Design, Synthesis, and SAR of a Novel Thiazolopyrimidinone Series of Selective PI3K-beta Inhibitors

TL;DR: A novel thiazolopyrimidinone series of PI3K-beta selective inhibitors has been identified and provided an excellent tool compound that showed potent growth inhibition in the PTEN-deficient breast cancer cell line MDA-MB-468 under anchorage-independent conditions.