Barry Ganetzky

Genetic analysis of the mammalian K+ channel beta subunit Kvbeta 2 (Kcnab2).

Segregation distortion induced by wild-type RanGAP in Drosophila.

Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila.

Closing the (Ran)GAP on segregation distortion in Drosophila.

Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants.

Molecular characterization, functional expression, and developmental profile of an ether à-go-go K+ channel in the tobacco hornworm Manduca sexta.

International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels.

Nervous wreck, an SH3 adaptor protein that interacts with Wsp, regulates synaptic growth in Drosophila.

A Drosophila model of early onset torsion dystonia suggests impairment in TGF-beta signaling.

Reduced sleep in Drosophila Shaker mutants.

Neuropathology in Drosophila membrane excitability mutants.

In vivo analysis of a gain-of-function mutation in the Drosophila eag-encoded K+ channel.

Metabolic disruption in Drosophila bang-sensitive seizure mutants.

wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death.

Tributes to Jeff Hall.

Neuropathology in Drosophila mutants with increased seizure susceptibility.

Meeting report: genes, neurons, circuits, and behaviors: highlights of cold spring harbor meeting on Drosophila neurobiology, October 3-7, 2007.

Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and Abeta accumulation.

Nervous wreck interacts with thickveins and the endocytic machinery to attenuate retrograde BMP signaling during synaptic growth.

DeltaFY mutation in human torsin A [corrected] induces locomotor disability and abberant synaptic structures in Drosophila.

Autophagy promotes synapse development in Drosophila.

Nibbling away at synaptic development.

A Drosophila behavioral mutant, down and out (dao), is defective in an essential regulator of Erg potassium channels.

Satellite signaling at synapses.

A neuropeptide signaling pathway regulates synaptic growth in Drosophila.

Extensive morphological divergence and rapid evolution of the larval neuromuscular junction in Drosophila.

A mutation in Drosophila Aldolase causes temperature-sensitive paralysis, shortened lifespan, and neurodegeneration.

Drosulfakinin activates CCKLR-17D1 and promotes larval locomotion and escape response in Drosophila.

Guidelines for the use and interpretation of assays for monitoring autophagy.

Analysis of synaptic growth and function in Drosophila with an extended larval stage.

Dnr1 mutations cause neurodegeneration in Drosophila by activating the innate immune response in the brain.

Identification of Mob2, a novel regulator of larval neuromuscular junction morphology, in natural populations of Drosophila melanogaster.

A Drosophila model of closed head traumatic brain injury.