Leith CP - Search Results

1

Acute myeloid leukemia in the elderly: assessment of multidrug resistance (MDR1) and cytogenetics distinguishes biologic subgroups with remarkably distinct responses to standard chemotherapy. A Southwest Oncology Group study.

Leith CP, Kopecky KJ, Godwin J, McConnell T, Slovak ML, Chen IM, Head DR, Appelbaum FR, Willman CL. Leith CP, et al. Blood. 1997 May 1;89(9):3323-9. Blood. 1997. PMID: 9129038 Free article. Clinical Trial.

2

Multidrug resistance-1 (MDR1) expression and functional dye/drug efflux is highly correlated with the t(8;21) chromosomal translocation in pediatric acute myeloid leukemia.

Pearson L, Leith CP, Duncan MH, Chen IM, McConnell T, Trinkaus K, Foucar K, Willman CL. Pearson L, et al. Among authors: leith cp. Leukemia. 1996 Aug;10(8):1274-82. Leukemia. 1996. PMID: 8709631

3

Prognostic markers in acute leukemia.

Leith CP, Willman CL. Leith CP, et al. Curr Opin Hematol. 1996 Jul;3(4):329-34. doi: 10.1097/00062752-199603040-00013. Curr Opin Hematol. 1996. PMID: 9372096 Review.

4

A double-blind placebo-controlled trial of granulocyte colony-stimulating factor in elderly patients with previously untreated acute myeloid leukemia: a Southwest oncology group study (9031).

Godwin JE, Kopecky KJ, Head DR, Willman CL, Leith CP, Hynes HE, Balcerzak SP, Appelbaum FR. Godwin JE, et al. Among authors: leith cp. Blood. 1998 May 15;91(10):3607-15. Blood. 1998. PMID: 9572995 Free article. Clinical Trial.

5

Frequency and clinical significance of the expression of the multidrug resistance proteins MDR1/P-glycoprotein, MRP1, and LRP in acute myeloid leukemia: a Southwest Oncology Group Study.

Leith CP, Kopecky KJ, Chen IM, Eijdems L, Slovak ML, McConnell TS, Head DR, Weick J, Grever MR, Appelbaum FR, Willman CL. Leith CP, et al. Blood. 1999 Aug 1;94(3):1086-99. Blood. 1999. PMID: 10419902 Free article. Clinical Trial.

6

Correlation of multidrug resistance (MDR1) protein expression with functional dye/drug efflux in acute myeloid leukemia by multiparameter flow cytometry: identification of discordant MDR-/efflux+ and MDR1+/efflux- cases.

Leith CP, Chen IM, Kopecky KJ, Appelbaum FR, Head DR, Godwin JE, Weick JK, Willman CL. Leith CP, et al. Blood. 1995 Sep 15;86(6):2329-42. Blood. 1995. PMID: 7545025 Free article.

7

The Burkitt-like lymphomas: a Southwest Oncology Group study delineating phenotypic, genotypic, and clinical features.

Braziel RM, Arber DA, Slovak ML, Gulley ML, Spier C, Kjeldsberg C, Unger J, Miller TP, Tubbs R, Leith C, Fisher RI, Grogan TM. Braziel RM, et al. Blood. 2001 Jun 15;97(12):3713-20. doi: 10.1182/blood.v97.12.3713. Blood. 2001. PMID: 11389007 Free article.

8

A phase I study of induction chemotherapy for older patients with newly diagnosed acute myeloid leukemia (AML) using mitoxantrone, etoposide, and the MDR modulator PSC 833: a southwest oncology group study 9617.

Chauncey TR, Rankin C, Anderson JE, Chen I, Kopecky KJ, Godwin JE, Kalaycio ME, Moore DF, Shurafa MS, Petersdorf SH, Kraut EH, Leith CP, Head DR, Luthardt FW, Willman CL, Appelbaum FR. Chauncey TR, et al. Among authors: leith cp. Leuk Res. 2000 Jul;24(7):567-74. doi: 10.1016/s0145-2126(00)00024-2. Leuk Res. 2000. PMID: 10867130 Clinical Trial.

9

Methods to detect P-glycoprotein-associated multidrug resistance in patients' tumors: consensus recommendations.

Beck WT, Grogan TM, Willman CL, Cordon-Cardo C, Parham DM, Kuttesch JF, Andreeff M, Bates SE, Berard CW, Boyett JM, Brophy NA, Broxterman HJ, Chan HS, Dalton WS, Dietel M, Fojo AT, Gascoyne RD, Head D, Houghton PJ, Srivastava DK, Lehnert M, Leith CP, Paietta E, Pavelic ZP, Weinstein R. Beck WT, et al. Among authors: leith cp. Cancer Res. 1996 Jul 1;56(13):3010-20. Cancer Res. 1996. PMID: 8674056 Review.

10

The presence of bcl-1 and bcl-2 gene rearrangements in diffuse small cleaved-cell lymphoma. A disease with diverse molecular and immunophenotypic findings.

Leith CP, Willman CL, Spier CM, Miller TP, Grogan TM. Leith CP, et al. Diagn Mol Pathol. 1994 Sep;3(3):178-83. doi: 10.1097/00019606-199409000-00007. Diagn Mol Pathol. 1994. PMID: 7981893

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