S. Howard

Serum-glucocorticoid-inducible kinase 1 confers protection in cell-based and in in vivo neurotoxin models via the c-Jun N-terminal kinase signaling pathway

P. Lograsso, S. Iqbal, S. Howard, 2015 .

Serum- and Glucocorticoid-Inducible Kinase 1 Confers Protection in Cell-Based and in In Vivo Neurotoxin Models via the c-Jun N-Terminal Kinase Signaling Pathway

P. Lograsso, S. Iqbal, S. Howard, 2015, Molecular and Cellular Biology.

Blocking c-Jun N-terminal Kinase (JNK) Translocation to the Mitochondria Prevents 6-Hydroxydopamine-induced Toxicity in Vitro and in Vivo*

P. Lograsso, J. Chambers, S. Howard, 2012, The Journal of Biological Chemistry.

Inhibition of JNK Mitochondrial Localization and Signaling Is Protective against Ischemia/Reperfusion Injury in Rats*

P. Lograsso, J. Chambers, S. Iqbal, 2012, The Journal of Biological Chemistry.

Bis-aryl urea derivatives as potent and selective LIM kinase (Limk) inhibitors.

Weilin Wu, P. Lograsso, Ji-Hak Jeong, 2015, Journal of medicinal chemistry.

Identification of a highly neurotoxic α-synuclein species inducing mitochondrial damage and mitophagy in Parkinson’s disease

N. Kamasawa, P. Lograsso, L. Volpicelli-Daley, 2018, Proceedings of the National Academy of Sciences.

Small Molecule c-jun-N-terminal Kinase (JNK) Inhibitors Protect Dopaminergic Neurons in a Model of Parkinson's Disease.

Li Lin, P. Lograsso, M. Cameron, 2011, ACS chemical neuroscience.

Pharmacological Inhibition of c-Jun N-terminal Kinase Reduces Food Intake and Sensitizes Leptin’s Anorectic Signaling Actions

P. Lograsso, Su Gao, S. Howard, 2017, Scientific Reports.