Heterozygous Germ Line hCHK2 Mutations in Li-Fraumeni Syndrome von Bell, Daphne W., Varley, Jennifer M., Szydlo, Tara E., Kang, Deborah H., Doke C. R. Wahrer, Shannon, Kristen E., Lubratovich, Marcie, Verselis, Sigitas J., Isselbacher, Kurt J., Fraumeni, Joseph F., Birch, Jillian M., Li, Frederick P., Garber, Judy E., Haber, Daniel A.

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Laser Diagnostic Development and Measurement and Modeling of Turbulent Flowfields of Jets and Wakes. Part 2. Numerical Predictions of Isothermal Flowfields in a Ducted Centerbody C... von Krishnamurthy,L, Park,S O, Wahrer,D J, Cochran,H S

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Heterozygous Germline ATM Mutations Do Not Contribute to Radiation-Associated Malignancies After Hodgkin's Disease von NICHOLS, K. E, LEVITZ, S, MAUCH, P, ISHIOKA, C, HABER, D. A, DILLER, L, SHANNON, K. E, WAHRER, D. C. R, BELL, D. W, CHANG, G, HEGDE, S, NEUBERG, D, SHAFMAN, T, TARBELL, N. J

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Common nonsense mutations in RAD52 von BELL, D. W, WAHRER, D. C. R, KANG, D. H, MACMAHON, M. S, FITZGERALD, M. G, ISHIOKA, C, ISSELBACHER, K. J, KRAINER, M, HABER, D. A

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ATP-dependent efflux of calcein by the multidrug resistance protein (MRP): no inhibition by intracellular glutathione depletion von Feller, N., Broxterman, H.J., Währer, D.C.R., Pinedo, H.M.

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Quality Control of Multidrug Resistance Assays in Adult Acute Leukemia: Correlation Between Assays for P-Glycoprotein Expression and Activity von Broxterman, H.J., Sonneveld, P., Feller, N., Ossenkoppele, G.J., Währer, D.C.R., Eekman, C.A., Schoester, M., Lankelma, J., Pinedo, H.M., Löwenberg, B., Schuurhuis, G.J.

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Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni syndrome von SEAN BONG LEE, SANG HYON KIM, VARLEY, Jenny M, GODWIN, Andrew K, SHANNON, Kristen M, HARLOW, Ed, HABER, Daniel A, BELL, Daphne W, WAHRER, Doke C. R, SCHIRIPO, Taryn A, JORCZAK, Melissa M, SGROI, Dennis C, GARBER, Judy E, LI, Frederick P, NICHOLS, Kim E

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Theoretical and practical considerations for the measurement of P-glycoprotein function in acute myeloid leukemia von Broxterman, H J, Lankelma, J, Pinedo, H M, Eekman, C A, Währer, D C, Ossenkoppele, G J, Schuurhuis, G J

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Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer von FITZGERALD, M. G, MARSH, D. J, HABER, D. A, WAHRER, D, BELL, D, CARON, S, SHANNON, K. E, ISHIOKA, C, ISSELBACHER, K. J, GARBER, J. E, ENG, C

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Theoretical and practical considerations for the measurement of P-glycoprotein function in acute myeloid leukemia : Phenotypic and genotypic analyses of multidrug resistance (MDR)... von BROXTERMAN, H. J, LANKELMA, J, PINEDO, H. M, EEKMAN, C. A, WÄHRER, D. C. R, OSSENKOPPELE, G. J, SCHUURHUIS, G. J

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