De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders

A Novel Human CAMK2A Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors

(2017) Jason R. Stephenson et al.   JOURNAL OF NEUROSCIENCE

Long-Term Potentiation: From CaMKII to AMPA Receptor Trafficking

(2016) Bruce E. Herring et al.   Annual Review of Physiology

The Phyre2 web portal for protein modeling, prediction and analysis

(2015) Lawrence A Kelley et al.   Nature Protocols

Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation

(2014) Hane Lee et al.   HUMAN MOLECULAR GENETICS

CaMKII: Claiming Center Stage in Postsynaptic Function and Organization

(2014) Johannes W. Hell   NEURON

Emerging role of CaMKII in neuropsychiatric disease

(2014) A.J. Robison   TRENDS IN NEUROSCIENCES

Structural studies on the regulation of Ca2+/calmodulin dependent protein kinase II

(2013) Margaret M Stratton et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood

(2013) Hirotomo Saitsu et al.   NATURE GENETICS

IA Channels

(2013) Yarimar Carrasquillo et al.   NEUROSCIENTIST

Neuronal excitability and calcium/calmodulin-dependent protein kinase type II: Location, location, location

(2012) Xiao-Bo Liu et al.   EPILEPSIA

A-type K+channels encoded by Kv4.2, Kv4.3 and Kv1.4 differentially regulate intrinsic excitability of cortical pyramidal neurons

(2012) Yarimar Carrasquillo et al.   JOURNAL OF PHYSIOLOGY-LONDON

A Mechanism for Tunable Autoinhibition in the Structure of a Human Ca2+/Calmodulin- Dependent Kinase II Holoenzyme

(2011) Luke H. Chao et al.   CELL

Analysis of CaM-kinase signaling in cells

(2011) Gary A. Wayman et al.   CELL CALCIUM

 CaMKII Plays a Nonenzymatic Role in Hippocampal Synaptic Plasticity and Learning by Targeting  CaMKII to Synapses

(2011) N. Z. Borgesius et al.   JOURNAL OF NEUROSCIENCE

Inactivity-induced increase in nAChRs upregulates Shal K+ channels to stabilize synaptic potentials

(2011) Yong Ping et al.   NATURE NEUROSCIENCE

Dominant-Negative Mutations in α-II Spectrin Cause West Syndrome with Severe Cerebral Hypomyelination, Spastic Quadriplegia, and Developmental Delay

(2010) Hirotomo Saitsu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular Dissection of IA in Cortical Pyramidal Neurons Reveals Three Distinct Components Encoded by Kv4.2, Kv4.3, and Kv1.4  -Subunits

(2010) A. J. Norris et al.   JOURNAL OF NEUROSCIENCE

Structure of the CaMKIIδ/Calmodulin Complex Reveals the Molecular Mechanism of CaMKII Kinase Activation

(2010) Peter Rellos et al.   PLOS BIOLOGY

βCaMKII controls the direction of plasticity at parallel fiber–Purkinje cell synapses

(2009) Geeske M van Woerden et al.   NATURE NEUROSCIENCE

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy

(2008) Hirotomo Saitsu et al.   NATURE GENETICS