Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Pinna

Showing results (121-130 of 595) with videos related to

Pageof 60
Sort By:
The Biochemical Journal|February 27, 2013
Pyrvinium pamoate does not activate protein kinase CK1, but promotes Akt/PKB down-regulation and GSK3 activationAndrea Venerando, Cristina Girardi, Maria Ruzzene, et al.
Biochemistry|June 10, 1997
Physical dissection of the structural elements responsible for regulatory properties and intersubunit interactions of protein kinase CK2 beta-subunitO Marin, F Meggio, S Sarno, et al.
FEBS Letters|June 11, 1984
Opposite and mutually incompatible structural requirements of type-2 casein kinase and cAMP-dependent protein kinase as visualized with synthetic peptide substratesL A Pinna, F Meggio, F Marchiori, et al.
FEBS Letters|May 6, 1985
Distinct structural requirements of Ca2+/phospholipid-dependent protein kinase (protein kinase C) and cAMP-dependent protein kinase as evidenced by synthetic peptide substratesS Ferrari, F Marchiori, G Borin, et al.
Biochimica Et Biophysica Acta|September 16, 1970
A simple procedure for the purification of rat liver phosvitin kinaseB Baggio, L A Pinna, V Moret, et al.
Neuroscience|July 1, 1995
Adenosine A2 receptors stimulate c-fos expression in striatal neurons of 6-hydroxydopamine-lesioned ratsM Morelli, A Pinna, J Wardas, et al.
Farmaco (Societa Chimica Italiana : 1989)|October 1, 1989
Synthesis and pharmacological study of 4,4a,5,6-tetrahydro-4a-substituted-benzo(h)cinnolin-3(2H)onesD Barlocco, G A Pinna, L Carboni, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1992
Opposite effects of NMDA receptor blockade on dopaminergic D1- and D2-mediated behavior in the 6-hydroxydopamine model of turning: relationship with c-fos expressionM Morelli, S Fenu, A Pinna, et al.
FEBS Letters|October 17, 1983
Polyglutamyl peptides: a new class of inhibitors of type-2 casein kinasesF Meggio, L A Pinna, F Marchiori, et al.
Biochemical and Biophysical Research Communications|June 21, 1976
Preferential dephosphorylation of protein bound phosphorylthreonine and phosphorylserine residues by cytosol and mitochondrial "casein phosphatases"L A Pinna, A Donella, G Clari, et al.
Pageof 60

Showing results (121-130 of 595) with videos related to

Sort By:
Pageof 60
The Biochemical Journal|February 27, 2013
Pyrvinium pamoate does not activate protein kinase CK1, but promotes Akt/PKB down-regulation and GSK3 activationAndrea Venerando, Cristina Girardi, Maria Ruzzene, et al.
Biochemistry|June 10, 1997
Physical dissection of the structural elements responsible for regulatory properties and intersubunit interactions of protein kinase CK2 beta-subunitO Marin, F Meggio, S Sarno, et al.
FEBS Letters|June 11, 1984
Opposite and mutually incompatible structural requirements of type-2 casein kinase and cAMP-dependent protein kinase as visualized with synthetic peptide substratesL A Pinna, F Meggio, F Marchiori, et al.
FEBS Letters|May 6, 1985
Distinct structural requirements of Ca2+/phospholipid-dependent protein kinase (protein kinase C) and cAMP-dependent protein kinase as evidenced by synthetic peptide substratesS Ferrari, F Marchiori, G Borin, et al.
Biochimica Et Biophysica Acta|September 16, 1970
A simple procedure for the purification of rat liver phosvitin kinaseB Baggio, L A Pinna, V Moret, et al.
Neuroscience|July 1, 1995
Adenosine A2 receptors stimulate c-fos expression in striatal neurons of 6-hydroxydopamine-lesioned ratsM Morelli, A Pinna, J Wardas, et al.
Farmaco (Societa Chimica Italiana : 1989)|October 1, 1989
Synthesis and pharmacological study of 4,4a,5,6-tetrahydro-4a-substituted-benzo(h)cinnolin-3(2H)onesD Barlocco, G A Pinna, L Carboni, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1992
Opposite effects of NMDA receptor blockade on dopaminergic D1- and D2-mediated behavior in the 6-hydroxydopamine model of turning: relationship with c-fos expressionM Morelli, S Fenu, A Pinna, et al.
FEBS Letters|October 17, 1983
Polyglutamyl peptides: a new class of inhibitors of type-2 casein kinasesF Meggio, L A Pinna, F Marchiori, et al.
Biochemical and Biophysical Research Communications|June 21, 1976
Preferential dephosphorylation of protein bound phosphorylthreonine and phosphorylserine residues by cytosol and mitochondrial "casein phosphatases"L A Pinna, A Donella, G Clari, et al.
Pageof 60