What is he best known for?
The fields of study he is best known for:
- Retina
- Neuroscience
- Neurotransmitter
His primary scientific interests are in Retina, Neuroscience, Anatomy, Lucifer yellow and Inner plexiform layer.
His Retina research includes elements of Biophysics and Gap junction.
He has researched Gap junction in several fields, including Biocytin and Cell junction.
Specifically, his work in Anatomy is concerned with the study of Ganglion.
His Lucifer yellow research incorporates themes from Neuropil, Central nervous system and Iontophoresis.
The various areas that he examines in his Amacrine cell study include Cholinergic Fibers and Cholinergic.
His most cited work include:
- Many diverse types of retinal neurons show tracer coupling when injected with biocytin or Neurobiotin. (368 citations)
- Chapter 2 The mosaic of amacrine cells in the mammalian retina (347 citations)
- Dopaminergic modulation of gap junction permeability between amacrine cells in mammalian retina. (290 citations)
What are the main themes of his work throughout his whole career to date?
David I. Vaney mostly deals with Retina, Neuroscience, Anatomy, Gap junction and Biophysics.
The Retina study combines topics in areas such as Cell biology, Retinal and Ganglion.
He integrates Anatomy and Rabbit in his studies.
His Gap junction research incorporates elements of Biocytin, Axon and Cell junction.
His biological study spans a wide range of topics, including Lucifer yellow, Dopamine and Intracellular.
The concepts of his Inner plexiform layer study are interwoven with issues in Dendrite, Ganglion cell layer and Inner nuclear layer.
He most often published in these fields:
- Retina (78.48%)
- Neuroscience (53.16%)
- Anatomy (31.65%)
What were the highlights of his more recent work (between 2005-2020)?
- Neuroscience (53.16%)
- Retina (78.48%)
- Amacrine cell (22.78%)
In recent papers he was focusing on the following fields of study:
His main research concerns Neuroscience, Retina, Amacrine cell, Receptive field and Retinal ganglion.
His study in Neuroscience is interdisciplinary in nature, drawing from both Anatomy and Tetrodotoxin.
He combines subjects such as Stimulus, Glycine receptor, Glycine Agents and Detector with his study of Anatomy.
Intrinsically photosensitive retinal ganglion cells, Giant retinal ganglion cells, Retinal ganglion cell, Bistratified cell and Inner plexiform layer are the primary areas of interest in his Retina study.
His Amacrine cell research is multidisciplinary, relying on both Neuropil, Soma, Synapse and Inner nuclear layer.
David I. Vaney works mostly in the field of Ganglion, limiting it down to topics relating to GABAergic and, in certain cases, Biophysics.
Between 2005 and 2020, his most popular works were:
- Direction selectivity in the retina: symmetry and asymmetry in structure and function (202 citations)
- Local Edge Detectors: A Substrate for Fine Spatial Vision at Low Temporal Frequencies in Rabbit Retina (94 citations)
- Uniformity detector retinal ganglion cells fire complex spikes and receive only light-evoked inhibition. (32 citations)
In his most recent research, the most cited papers focused on:
- Retina
- Neuroscience
- Optics
His primary areas of investigation include Retina, Neuroscience, Retinal ganglion, Receptive field and Inhibitory postsynaptic potential.
In the subject of general Neuroscience, his work in Amacrine cell and Giant retinal ganglion cells is often linked to Photic Stimulation, thereby combining diverse domains of study.
His work deals with themes such as Retinal ganglion cell and Excitatory postsynaptic potential, which intersect with Amacrine cell.
His Giant retinal ganglion cells research integrates issues from Intrinsically photosensitive retinal ganglion cells and Visual system.
He incorporates a variety of subjects into his writings, including Photic Stimulation, Anatomy, Stimulus and Patch clamp.
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