Tri-Institutional MD-PhD Program

Alumni Publications

2009

Henikoff S, Henikoff JG, Sakai A, Loeb GB, Ahmad K. 2009. Genome-wide profiling of salt fractions maps physical properties of chromatin.. Genome Res. 19(3):460-9.

Roberts WK, Deluca IJ, Thomas A, Fak J, Williams T, Buckley N, Dousmanis AG, Posner JB, Darnell RB. 2009. Patients with lung cancer and paraneoplastic Hu syndrome harbor HuD-specific type 2 CD8+ T cells.. J Clin Invest. 119(7):2042-51.

Darnell JC, Fraser CE, Mostovetsky O, Darnell RB. 2009. Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs.. Hum Mol Genet. 18(17):3164-77.

Darken RS, Bogitch R, Leonard J, Perry A, McKinstry RC, Gutmann DH, Rubin JB. 2009. Brainstem glioma presenting as pruritus in children with neurofibromatosis-1.. J Pediatr Hematol Oncol. 31(12):972-6.

Kanner EM, Netland PA, Sarkisian SR, Du H. 2009. Ex-PRESS miniature glaucoma device implanted under a scleral flap alone or combined with phacoemulsification cataract surgery.. J Glaucoma. 18(6):488-91.

Gillespie C, Bruno JHyland, Kalet A. 2009. What standardised patients tell us about 'activating' patients.. Med Educ. 43(11):1112-3.

2008

Wang Y, Kissenpfennig A, Mingueneau M, Richelme S, Perrin P, Chevrier S, Genton C, Lucas B, DiSanto JP, Acha-Orbea H et al.. 2008. Th2 lymphoproliferative disorder of LatY136F mutant mice unfolds independently of TCR-MHC engagement and is insensitive to the action of Foxp3+ regulatory T cells.. J Immunol. 180(3):1565-75.

Percy MJ, Furlow PW, Lucas GS, Li X, Lappin TRJ, McMullin MFrances, Lee FS. 2008. A gain-of-function mutation in the HIF2A gene in familial erythrocytosis.. N Engl J Med. 358(2):162-8.

Taveggia C, Thaker P, Petrylak A, Caporaso GL, Toews A, Falls DL, Einheber S, Salzer JL. 2008. Type III neuregulin-1 promotes oligodendrocyte myelination.. Glia. 56(3):284-93.

Dolan CM, Kuz JE, Cottingham SL. 2008. Lymphangioma of the finger in a child: a report of two cases.. J Surg Orthop Adv. 17(2):89-92.