THOMAS KING |
Office: Copernicus 204
Lab: Copernicus 429 (Animal Suite)
860-832-2654
kingt@ccsu.edu
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Courses Taught:
- BMS 102 - Introduction to Biomolecular Sciences
- BMS 201 - Principles of Cell and Molecular Biology
- BMS 306 - Principles of Genetics
- BMS 570 - Advanced Genetics
Research Interests:
My research interests concern the genetic analysis of development in mammals,
using mice and rats as model mammalian systems. With the long-term goal of
gaining access to the molecular biology underlying interesting mutant
phenotypes, my laboratory has made progress pursuing four different projects: 1)
We are investigating the molecular genetic basis of a pleiotropic developmental
mutation in the mouse, designated mshi. 2) We are initiating a phenotypic
and genetic characterization of a hairless mutant (called “shorn”) that arose
spontaneously in CCSU’s laboratory rat colony. 3) Another project has suggested
Fgfr2 as a possible gene candidate for the Charles River “hairless”
mutation, which we have shown is an allele of rat fuzzy and a likely
orthologue of mouse frizzy. 4) We are now intensively pursuing a series
of experiments aimed at identifying minor histocompatibility loci on the mouse X
chromosome that might differ between standard inbred mouse strains
Recent Publications:
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Alner, K.A., Loman, J., Hall, E.H., Mutcherson II, R.J. & King, T.R. (2003)
An X-encoded alloantigenicity between BALB/c and C57BL/6 strains of mice. Immunogenetics 55, 87-94.
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R.R. Chrisluis, T. Stoklasek, J. Loman, A. Guariglia & T.R. King
(2002).The rat shorn mutation (shn) maps between D7Got143 and D7Rat94. Molecular
Genetics and Metabolism 76, 335-339.
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K. Ahearn, G. Akkouris, P.R. Berry, R. R. Chrisslius, I. Crooks,
A.K. Dull, S. Grable, J. Jeruzal, J. Lanza, C. Lavoie, R. A. Maloney,
M. Pitruzzello, R. Sharma, T.A. Stoklasek, J. Tweeddale & T.R. King. The
Charles River “hairless” rat mutation: Maps to Chromosome 1, allelic with fuzzy,
and a likely orthologue of mouse frizzy. Journal of Heredity 93, 210-213.
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E.H. Hall, J.A. Lathrop, B. Medina, R.J.
Mutcherson II & T.R. King (2000) The hypotrichosis-generating shorn (shn)
mutation maps to distal Chromosome 7 in the Norway rat. Journal of Heredity
91, 345-347.
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M. C. Rule, R. J. Mutcherson II, A. D. Foss, T.
K.-X. Nguyen, K. A. Myrie & T. R. King (1999) Mouse male
sterility and histocompatibility (mshi) maps between the D10Mit51/168/212
cluster and D10Mit213. Mammalian Genome 10, 447-450.
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A. L. Hildebrandt, A. M. Cantwell, M.C. Rule &
T.R. King (1999) The H-mshi antigen is conserved between standard BALB/cBy,
C57BL/6J, and wild-derived CAST/Ei and SPRET/Ei inbred strains of mice.
Immunogenetics 49, 666-672.
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A. N. Moemeka, A. L. Hildebrandt, P. Radaskiewicz
& T. R. King (1998) Shorn (shn): A new mutation causing hypotrichosis in
the Norway rat. Journal of Heredity89,257-260.
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J. P. Turner, J. E. Carpentino, A. M. Cantwell, A.
L. Hildebrandt, K. A. Myrie & T. R. King (1997) Molecular genetic mapping of the
mouse male sterility and histoincompatibility (mshi) mutation on proximal Chromosome
10.Genomics 39, 1-7.
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Revised
December 08, 2006