Publications

2012

Demichelis F, Setlur SR, Banerjee S, Chakravarty D, Chen JY, Chen CX, et al. Identification of functionally active, low frequency copy number variants at 15q21.3 and 12q21.31 associated with prostate cancer risk. Proc Natl Acad Sci U S A. 2012;109(17):6686-91.
Habegger KM, Matzke D, Ottaway N, Hembree J, Holland J, Raver C, et al. Role of adipose and hepatic atypical protein kinase C lambda (PKCλ) in the development of obesity and glucose intolerance. Adipocyte. 2012;1(4):203-214.
Geetha T, Zheng C, McGregor WC, B White D, Diaz-Meco MT, Moscat J, et al. TRAF6 and p62 inhibit amyloid β-induced neuronal death through p75 neurotrophin receptor. Neurochem Int. 2012;61(8):1289-93.
Mendillo ML, Santagata S, Koeva M, Bell GW, Hu R, Tamimi RM, et al. HSF1 drives a transcriptional program distinct from heat shock to support highly malignant human cancers. Cell. 2012;150(3):549-62.
Chen H-, Ouseph MM, Li J, Pécot T, Chokshi V, Kent L, et al. Canonical and atypical E2Fs regulate the mammalian endocycle. Nat Cell Biol. 2012;14(11):1192-202.
Solomon JP, Page LJ, Balch WE, Kelly JW. Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention. Crit Rev Biochem Mol Biol. 2012;47(3):282-96.
Anglicheau D, Muthukumar T, Hummel A, Ding R, Sharma VK, Dadhania D, et al. Discovery and validation of a molecular signature for the noninvasive diagnosis of human renal allograft fibrosis. Transplantation. 2012;93(11):1136-46.
Howan K, Smith AJ, Westblade LF, Joly N, Grange W, Zorman S, et al. Initiation of transcription-coupled repair characterized at single-molecule resolution. Nature. 2012;490(7420):431-4.

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