S. Tumati

发表

Sustained morphine‐mediated pain sensitization and antinociceptive tolerance are blocked by intrathecal treatment with Raf‐1‐selective siRNA

T. Vanderah, E. Varga, W. Roeske, 2010, British journal of pharmacology.

Design of novel neurokinin 1 receptor antagonists based on conformationally constrained aromatic amino acids and discovery of a potent chimeric opioid agonist-neurokinin 1 receptor antagonist.

P. Schiller, J. Vanden Broeck, F. Porreca, 2011, Journal of medicinal chemistry.

Plasmon-waveguide resonance studies of ligand binding to integral proteins in membrane fragments derived from bacterial and mammalian cells.

Z. Salamon, G. Tollin, E. Navratilova, 2009, Analytical biochemistry.

Design, Synthesis, and Biological Evaluation of Novel Bifunctional C-Terminal-Modified Peptides for δ/μ Opioid Receptor Agonists and Neurokinin-1 Receptor Antagonists

V. Hruby, E. Navratilova, H. Yamamura, 2007 .

Repeated morphine treatment-mediated hyperalgesia, allodynia and spinal glial activation are blocked by co-administration of a selective cannabinoid receptor type-2 agonist

T. Vanderah, A. Keresztes, E. Varga, 2012, Journal of Neuroimmunology.

A Structure–Activity Relationship Study and Combinatorial Synthetic Approach of C-Terminal Modified Bifunctional Peptides That Are δ / μ Opioid Receptor Agonists and Neurokinin 1 Receptor Antagonists

V. Hruby, E. Navratilova, T. Vanderah, 2009 .

Sustained Morphine Treatment Augments Capsaicin-Evoked Calcitonin Gene-Related Peptide Release from Primary Sensory Neurons in a Protein Kinase A- and Raf-1-Dependent Manner

H. Yamamura, T. Vanderah, E. Varga, 2009, Journal of Pharmacology and Experimental Therapeutics.

Crystal structure and functional analysis of Dcp 2 p from Schizosaccharomyces pombe

R. Parker, Haiwei Song, N. Chen, 2007 .

Crystal structure and functional analysis of Dcp2p from Schizosaccharomyces pombe

Haiwei Song, Nan Chen, Roy Parker, 2006, Nature Structural &Molecular Biology.

Design, synthesis, and biological evaluation of novel bifunctional C-terminal-modified peptides for delta/mu opioid receptor agonists and neurokinin-1 receptor antagonists.

V. Hruby, E. Navratilova, H. Yamamura, 2007, Journal of medicinal chemistry.

Functional regulation of opioid receptor signaling

S. Tumati, 2009 .

Tachykinin NK₁ receptor antagonist co-administration attenuates opioid withdrawal-mediated spinal microglia and astrocyte activation.

V. Hruby, T. Vanderah, A. Keresztes, 2012, European journal of pharmacology.

Sustained morphine treatment augments basal CGRP release from cultured primary sensory neurons in a Raf-1 dependent manner.

E. Navratilova, H. Yamamura, T. Vanderah, 2008, European journal of pharmacology.

Sustained morphine treatment augments prostaglandin E2-evoked calcitonin gene-related peptide release from primary sensory neurons in a PKA-dependent manner.

T. Vanderah, E. Varga, W. Roeske, 2010, European journal of pharmacology.

Intrathecal PKA-selective siRNA treatment blocks sustained morphine-mediated pain sensitization and antinociceptive tolerance in rats

E. Varga, T. Largent-Milnes, S. Tumati, 2011, Journal of Neuroscience Methods.

Intrathecal Raf-1-selective siRNA attenuates sustained morphine-mediated thermal hyperalgesia.

H. Yamamura, T. Vanderah, E. Varga, 2008, European journal of pharmacology.

Functional selectivity in cannabinoid signaling.

I. Alves, Z. Salamon, G. Tollin, 2008, Current molecular pharmacology.

A structure-activity relationship study and combinatorial synthetic approach of C-terminal modified bifunctional peptides that are delta/mu opioid receptor agonists and neurokinin 1 receptor antagonists.

V. Hruby, E. Navratilova, H. Yamamura, 2008, Journal of medicinal chemistry.

Repeated morphine treatment-mediated hyperalgesia, allodynia and spinal glial activation are blocked by co-administration of a selective cannabinoid receptor type-2 agonist

T. Vanderah, A. Keresztes, E. Varga, 2012, Journal of Neuroimmunology.