Physician

Psychiatry

Eric Turner works in the field of Psychiatry. He researched medicine at University of Washington School of Medicine. Doctor Eric E. Turner, MD is also published. He has 38 publications published. The lastest publication: "Highly cooperative homodimerization is a conserved property of neural POU proteins.'

Publications

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• Efferent pathways of the mouse lateral habenula.
• Role of the dorsal medial habenula in the regulation of voluntary activity, motor function, hedonic state, and primary reinforcement.
• Bidirectional modulation of deep cerebellar nuclear cells revealed by optogenetic manipulation of inhibitory inputs from Purkinje cells.
• The genetics of auricular development and malformation: New findings in model systems driving future directions for microtia research.
• Medial Habenula Output Circuit Mediated by α5 Nicotinic Receptor-Expressing GABAergic Neurons in the Interpeduncular Nucleus.
• Brn3a and islet1 act epistatically to regulate the gene expression program of sensory differentiation.
• Expression of dopamine pathway genes in the midbrain is independent of known ETS transcription factor activity.
• Brn3a regulates the transition from neurogenesis to terminal differentiation and represses non-neural gene expression in the trigeminal ganglion.
• Brn3a and Nurr1 mediate a gene regulatory pathway for habenula development.
• A central role for Islet1 in sensory neuron development linking sensory and spinal gene regulatory programs.
• Tlx1 and Tlx3 coordinate specification of dorsal horn pain-modulatory peptidergic neurons.
• Regulation of the development of tectal neurons and their projections by transcription factors Brn3a and Pax7.
• Brn3a target gene recognition in embryonic sensory neurons.
• Regulation of FGF10 by POU transcription factor Brn3a in the developing trigeminal ganglion.
• Brn3a-expressing retinal ganglion cells project specifically to thalamocortical and collicular visual pathways.
• Sonic hedgehog regulates the position of the trigeminal ganglia.
• Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation.
• Coordinated regulation of gene expression by Brn3a in developing sensory ganglia.
• Allele specific analysis of the ADRBK2 gene in lymphoblastoid cells from bipolar disorder patients.
• POU-domain factor Brn3a regulates both distinct and common programs of gene expression in the spinal and trigeminal sensory ganglia.
• Direct autoregulation and gene dosage compensation by POU-domain transcription factor Brn3a.
• Unaltered expression of Bcl-2 and TAG-1/axonin-1 precedes sensory apoptosis in Brn3a knockout mice.
• Defects in sensory axon growth precede neuronal death in Brn3a-deficient mice.
• POU-domain factor expression in the trigeminal ganglion and implications for herpes virus regulation.
• Inhibitory effects of ventral signals on the development of Brn-3.0-expressing neurons in the dorsal spinal cord.
• Autoregulatory sequences are revealed by complex stability screening of the mouse brn-3.0 locus.
• Highly cooperative homodimerization is a conserved property of neural POU proteins.
• Signals from the ventral midline and isthmus regulate the development of Brn3.0-expressing neurons in the midbrain.
• Optimal Oct-2 affinity for an extended DNA site and the effect of GST fusion on site preference.
• Brn-3.0 expression identifies early post-mitotic CNS neurons and sensory neural precursors.
• The POU-domain factor Brn-3.0 recognizes characteristic sites in the herpes simplex virus genome.
• Cellular and molecular neuropathology of schizophrenia: new directions from developmental neurobiology.
• Brn-3.2: a Brn-3-related transcription factor with distinctive central nervous system expression and regulation by retinoic acid.
• POU domain factors of the Brn-3 class recognize functional DNA elements which are distinctive, symmetrical, and highly conserved in evolution.
• Twin of I-POU: a two amino acid difference in the I-POU homeodomain distinguishes an activator from an inhibitor of transcription.
• Identification of dividing, determined sensory neuron precursors in the mammalian neural crest.
• Similar DNA recognition properties of alternatively spliced Drosophila POU factors.

Schools

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• Loma Linda University

• University of Washington

• University Ca San Diego Med Center

Doctors Specialties

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• Psychiatry

Accepted Insurances

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Education

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• University of California San Diego
• University of Washington School of Medicine

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