scispace - formally typeset
J

James Gilbert

Researcher at Australian National University

Publications -  152
Citations -  5970

James Gilbert is an academic researcher from Australian National University. The author has contributed to research in topics: Telescope & Spectrograph. The author has an hindex of 29, co-authored 143 publications receiving 5455 citations. Previous affiliations of James Gilbert include University of New South Wales & University of Sussex.

Papers
More filters

An integrated encyclopedia of DNA elements in the human genome

Ian Dunham, +442 more
TL;DR: The Encyclopedia of DNA Elements project provides new insights into the organization and regulation of the authors' genes and genome, and is an expansive resource of functional annotations for biomedical research.
Journal ArticleDOI

Inhibition of the cation channel TRPV4 improves bladder function in mice and rats with cyclophosphamide-induced cystitis

TL;DR: It is shown that the development of cystitis-induced bladder dysfunction is strongly impaired in Trpv4−/− mice, and HC-067047 is described, a previously uncharacterized, potent, and selective TRPV4 antagonist that increases functional bladder capacity and reduces micturition frequency in WT mice and rats with Cystitis.
Journal ArticleDOI

Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity.

TL;DR: This review article focuses on the major genes and signaling pathways implicated in ASD and discusses the cellular, molecular and functional studies that have shed light on common dysregulated pathways using in vitro, in vivo and human evidence.
Journal ArticleDOI

Nedd4-mediated AMPA receptor ubiquitination regulates receptor turnover and trafficking.

TL;DR: In this article, the E3 ubiquitin ligase neural precursor cell (Nedd4) was shown to be responsible for AMPAR ubiquitination, leading to reduced AMPAR surface expression and suppressed excitatory synaptic transmission.
Journal ArticleDOI

Homeostatic Regulation of AMPA Receptor Trafficking and Degradation by Light-Controlled Single-Synaptic Activation

TL;DR: In cultured hippocampal neurons, it is reported that when activity of an individual presynaptic terminal is selectively elevated by light-controlled excitation, AMPAR abundance at the excited synapses is selectively downregulated in an NMDAR-dependent manner, indicating that AMPAR accumulation at individual synapse is subject to autonomous homeostatic regulation in response to synaptic activity.