Dr. Tony A. Pham

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University of Washington
School of Medicine
Psychiatry and Behavioral Sciences
Assistant ProfessorAppointed: 2000
Professional Headshot of Tony A. Pham

Mailing Address

Department of Psychiatry and Behavioral Sciences
University of Washington School of Medicine
325 Ninth Ave.
Seattle, Washington 98104
United States

Contact Information

Phone: (206) 731-2896
Fax: (206) 731-3236
tonypham@u.washington.edu

Qualifications

M.D., Baylor College of Medicine, 1993.
Ph.D., Baylor College of Medicine, Molecular/Cellular Biology, 1991.
B.A., Rice University, Biochemistry, 1986.

Expertise and Research Interests

Dr. Pham's research interests are in the area of developmental and molecular neurobiology. His laboratory examines the molecular mechanisms that underlie the precise development of neural circuitry in the mammalian forebrain, focusing on the neocortex and thalamus. The two major areas of investigation are outlined below:

A. Experience-dependent plasticity of neocortical circuitry during the developmental critical period.
Early in life, the mammalian brain has tremendous capacity to adapt to the individual's environment. This is accomplished through the plasticity of neural connections of the brain during the postnatal developmental phase. Dr. Pham is interested in understanding the molecular mechanisms that underlie developmental neural plasticity and the critical period, using the central visual system as a model system. Current research examines the function of the intracellular messengers calcium and cyclic AMP in neocortical plasticity.

B. Refinement of neural connections in thalamic and thalamocortical circuitry.
During development, the initial connections of neurons are imprecise, with many inappropriate projections/connections that eventually are eliminated. Because cognitive and sensory processing are dependent on the precision of neural circuitry, neural refinement is a critical step in the maturation of the forebrain. Current research examines the role of calcium and cyclic AMP-mediated gene expression, which is induced within a defined developmental window, on the patterning and refinement of retinothalamic and thalamocortical connections. Key questions that will be addressed include:

(1) What are the signaling systems that contribute to Ca2+/cAMP-mediated gene expression during early postnatal thalamic development?

(2) What are the mechanisms responsible for initiating and terminating Ca2+/cAMP-mediated gene expression in the thalamus during development?

(3) What are the consequences of disrupting components of Ca2+/cAMP signaling, using transgenic mouse models, on the patterning of thalamocortical connections and on the morphology of dendrites and axons of thalamic neurons?

Keywords

COS Keywords:

Brain, Brain Development, Developmental Neurobiology, Neurobiology.

Additional Terms:

Developmental Neurobiology, Developmental Plasticity of Neural Connections.

Publications

  • Pham TA, Impey S, Storm DR, Stryker MP, CRE-mediated gene transcription in neocortical neuronal plasticity during the developmental critical period [published erratum appears in Neuron 1999 Mar, Neuron, 22(1), 63-72, Jan 1999 Abstract
  • Pham TA, Hwung YP, Santiso-Mere D, McDonnell DP, O'Malley BW, Ligand-dependent and -independent function of the transactivation regions of the human estrogen receptor in yeast, Molecular Endocrinology, 6(7), 1043-50, July 1992 Abstract
  • Pham TA, McDonnell DP, Tsai MJ, O'Malley BW, Modulation of progesterone receptor binding to progesterone response elements by positioned nucleosomes, Biochemistry, 31(5), 1570-8, February 1992 Abstract
  • Pham TA, Hwung YP, McDonnell DP, O'Malley BW, Transactivation functions facilitate the disruption of chromatin structure by estrogen receptor derivatives in vivo, Journal of Biological Chemistry, 266(27), 18179-87, September 1991 Abstract
  • McDonnell DP, Nawaz Z, Densmore C, Weigel NL, Pham TA, Clark JH, O'Malley BW, High level expression of biologically active estrogen receptor in Saccharomyces cerevisiae, Journal of Steroid Biochemistry and Molecular Biology, 39(3), 291-7, September 1991 Abstract
  • Pham TA, Elliston JF, Nawaz Z, McDonnell DP, Tsai MJ, O'Malley BW, Antiestrogen can establish nonproductive receptor complexes and alter chromatin structure at target enhancers, Proceedings of the National Academy of Sciences (USA), 88(8), 3125-9, April 1991 Abstract

Profile Details

Last Updated: 9/24/2001

COS Expertise ID #851361
Reference this profile directly: http://myprofile.cos.com/tpham