Work

Arrestin-3 interaction with maternal embryonic leucine-zipper kinase

Year: 2019

Type: article

Source: Cellular Signalling

DOI: 10.1016/j.cellsig.2019.109366

Authors: Nicole A. Perry, Kevin P. Fialkowski, Tamer S. Kaoud, Ali I. Kaya, Andrew L. Chen, Juliana M. Taliaferro, Vsevolod V. Gurevich, Kevin N. Dalby, T.M. Iverson

Institutions: Vanderbilt University, The University of Texas at Austin, Minia University

Language: English

Topic: Protein Kinase Regulation and GTPase Signaling

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: green

Funders: Welch Foundation, American Heart Association, Cancer Prevention and Research Institute of Texas, Vanderbilt-Ingram Cancer Center, National Institutes of Health, Vanderbilt Digestive Diseases Research Center, Vanderbilt University Medical Center, National Institute on Drug Abuse, National Cancer Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases

Awards: G1300984159, Targeted Therapeutic Drug Discovery & Development Program, Arrestin-3 scaffolding of the JNK3 activation cascade as a model of arrestin-dependent signaling, G2268269956, G4057519856, G52711424, Arrestin-3 interaction with the ASK1-MKK4/7-JNK3 cascade, G580823730, G725763919, G858087134, G9000003960, G9000071520, G9000191919, Molecular and Cellular Basis for Digestive Diseases, Molecular basis for arrestin-mediated signaling

OpenAlex ID: W2963619906

FWCI: 0.501

Cites: 64

Cited by: 16

Related to: 10