scispace - formally typeset
H

Haluk Resat

Researcher at Pacific Northwest National Laboratory

Publications -  49
Citations -  2820

Haluk Resat is an academic researcher from Pacific Northwest National Laboratory. The author has contributed to research in topics: Signal transduction & Receptor. The author has an hindex of 26, co-authored 48 publications receiving 2618 citations. Previous affiliations of Haluk Resat include Koç University & University of California, San Diego.

Papers
More filters
Journal ArticleDOI

Constitutive activation of STAT3 in breast cancer cells: A review.

TL;DR: This review provides a full spectrum of STAT3's involvement in breast cancers by consolidating the knowledge about its role in breast cancer development at multiple levels: its differential regulation by different receptor signaling pathways, its downstream target genes, and modification of its transcriptional activity by its coregulatory transcription factors.
Journal ArticleDOI

Rapid and sustained nuclear–cytoplasmic ERK oscillations induced by epidermal growth factor

TL;DR: The characterization of single‐cell ERK dynamics provides a quantitative foundation for understanding the regulatory structure of this signaling cascade and revealed that negative feedback from phosphorylated ERK to the cascade input was necessary to match the robustness of the oscillation characteristics observed over a broad range of ligand concentrations.
Journal ArticleDOI

An Integrated Model of Epidermal Growth Factor Receptor Trafficking and Signal Transduction

TL;DR: An integrated model of both the trafficking and signaling pathway of the epidermal growth factor receptor (EGFR) using a probability weighted-dynamic Monte Carlo simulation is presented, suggesting that receptor trafficking controls the compartmental bias of signal transduction, rather than simply modulating signal magnitude.
Journal ArticleDOI

A molecular theory of solvation dynamics

TL;DR: In this article, the dynamic solvation time correlation function Z(t) is formulated in terms of the intermolecular solute-solvent interactions, without recourse to the intrinsically macroscopic concept of a cavity carved out of a dielectric medium.
Journal ArticleDOI

Comparative molecular dynamics simulations of amphotericin B-cholesterol/ergosterol membrane channels.

TL;DR: Simulation data revealed that the sterol type has noticeable effect on the properties of AmB membrane channels, and observed differences suggest that the channel in the ergosterol-containing membrane is more stable and, due to its larger size, would have a higher ion conductance.