Publications:
A selected list of publications:
Scoles, D.R., Pavelka, J., Cass, I., Tran, H., Baldwin, R., Armstrong, K., and Karlan, B.Y.
Characterization of CSOC 882, a novel immortalized ovarian cancer cell line expressing EGFR, HER2, and activated AKT,
Gynecologic Oncology,
2007; 104:
120-128.
Scoles, D.R., Das, A., and Pulst, S.M., (eds: Rimoin, D.L., Connor, J.M., Pyeritz, R.E., Korf, B.R.)
Primary Tumors of the Nervous System,
Emory and Rimoin���s Principals and Practice of Medical Genetics,
2007; 5th Edition:
.
Scoles, D.R., Yong, W., Qin, Y., Wawrowsky, K. and Pulst, S.M.
Schwannomin inhibits tumorigenesis through direct interaction with the eukaryotic initiation factor 3 subunit c (eIF3c),
Human Molecular Genetics,
2006; 15:
1059-1070.
Scoles, D.R., Qin, Y., Nguyen, V., Gutmann, D.H., and Pulst
HRS inhibits EGF receptor signaling in the RT4 rat schwannoma cell line,
Biochemical and Biophysical Research Communications,
2005; 335:
385-392.
Scoles, D.R. and Pulst, S.M. (eds: Aminoff, M., and Daroff, R.)
Brain Tumors, Genetics,
Encyclopedia of the Neurological Sciences,
2003; 1:
470-472.
Oh, M.K., Scoles, D.R., Haipek, C., Gutmann, D.H., Pulst, S.M.
Genetic heterogeneity of stably transfected cell lines revealed by expression profiling with oligonucleotides microarrays,
Journal of Cellular Biochemistry,
2003; 90:
1068-78.
Huynh, D.P., Scoles, D.R., Nguyen, D., and Pulst, S.M.
The autosomal recessive juvenile Parkinson disease gene product, parkin, interacts with and ubiquitinates synaptotagmin XI,
Human Molecular Genetics,
2003; 12:
2587-97.
Sun CX, Haipek C, Scoles DR, Pulst SM, Giovannini M, Komada M and Gutmann DH
Functional analysis of the relationship between the neurofibromatosis 2 (NF2) tumor suppressor and its binding partner, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS/HGS),
Human Molecular Genetics,
2002; 11:
3167-3178.
Pulst, S.M. and Scoles, D.R. (eds: Rimoin, D.L., Connor, J.M., Pyeritz, R.E., Korf, B.R.)
Primary Tumors of the Nervous System,
Emory and Rimoins Principals and Practice of Medical Genetics,
2002; 4th Edition(Chapter 121):
3231-3249.