The Berberich
laboratory studies how abnormal levels of the cancer proteins mdm-2
and mdm-X lead to tumor formation in human cells, and how inactivation
of the oncogenes coding for these proteins can be used to inhibit
tumor growth. The Bubulya
research group examines the role of proteins stored in nuclear speckles
in the regulation of transcription, the processing of pre-messenger
RNA, and cell division. Molecular embryology is the focus of the
Kadakia
laboratory, which examines the p63 transcription factor during development,
and uses nanoparticles as sensors of intracellular signaling. The
primary interests of the Leffak
laboratory are in the identification of DNA sequences and proteins
involved in the initiation of DNA replication, and the role of DNA
replication in human diseases. The Liu
laboratory examines the mechanisms by which the replication of repetitive
DNA sequences leads to genome instability and human neuromuscular
diseases. The
Markey laboratory uses DNA microarray technology in genomics-based
approaches to identify target genes regulated by the tumor suppressor
proteins Rb and p53. The fungus N. crassa is the model organism
used in the Paietta
laboratory to characterize the molecular controls over the multi-gene
network responsible for sulfur acquisition and metabolism.
Participating Faculty:
Steven Berberich, Ph.D. Nuclear proteins associated with cellular
proliferation; oncogenes and tumor suppressor genes
[home][e-mail]
Paula Bubulya, Ph.D. Nuclear structure and gene expression, live
cell imaging [bio][e-mail]
Madhavi Kadakia, Ph.D. Transcriptional regulation of p63 and p73
target genes [home][e-mail]
Michael Leffak, Ph.D. DNA sequences and proteins involved in eukaryotic
DNA replication [home][e-mail]
John Paietta, Ph.D. Molecular genetics, gene regulation, and control
of sulfur metabolism [home][e-mail]
Yong-jie Xu, Ph.D. The DNA replication checkpoint [home][e-mail]
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