H. M. Crane

Selectivity of ceramide-mediated biology. Lack of activity of erythro-dihydroceramide.

A. Bielawska, L. Obeid, Y. Hannun, 1993, The Journal of biological chemistry.

Disruption of sphingolipid metabolism and stimulation of DNA synthesis by fumonisin B1. A molecular mechanism for carcinogenesis associated with Fusarium moniliforme.

A. Merrill, D. Liotta, J. Xia, 1994, The Journal of biological chemistry.

SYNTHESIS OF TWO NEW MAYTANSINOID MODEL COMPOUNDS FROM CARBOHYDRATE PRECURSORS

K. Cousins, T. E. Goodwin, T. E. Freyaldenhoven, 1998 .

Stereoselectivity of induction of the retinoblastoma gene product (pRb) dephosphorylation by D-erythro-sphingosine supports a role for pRb in growth suppression by sphingosine.

A. Bielawska, Y. Hannun, B. Lagu, 1995, Biochemistry.

Fumonisin toxicity and sphingolipid biosynthesis.

T. Vales, D. Liotta, E. Wang, 1996, Advances in experimental medicine and biology.

Increasing the cellular PKC inhibitory activity of balanol: A study of ester analogs

G. E. Jagdmann, James W. Darges, Heidi M. Crane, 1995 .

Synthesis and protein kinase C inhibitory activities of acyclic balanol analogs that are highly selective for protein kinase C over protein kinase A.

J. Mendoza, T. Mitchell, S. Hall, 1996, Journal of medicinal chemistry.

Novel PKC inhibitory analogs of balanol with replacement of the ester functionality

S. Hall, Hong Hu, Y. Lai, 1995 .