Raimondi SC - Search Results

1

Reference alignment of SNP microarray signals for copy number analysis of tumors.

Pounds S, Cheng C, Mullighan C, Raimondi SC, Shurtleff S, Downing JR. Pounds S, et al. Among authors: raimondi sc. Bioinformatics. 2009 Feb 1;25(3):315-21. doi: 10.1093/bioinformatics/btn624. Epub 2008 Dec 3. Bioinformatics. 2009. PMID: 19052058 Free PMC article.

2

Childhood acute lymphoblastic leukemia with equivocal chromosome markers of the t(1;19) translocation.

Filatov LV, Behm FG, Pui CH, Head DR, Downing JR, Raimondi SC. Filatov LV, et al. Among authors: raimondi sc. Genes Chromosomes Cancer. 1995 Jun;13(2):99-103. doi: 10.1002/gcc.2870130205. Genes Chromosomes Cancer. 1995. PMID: 7542913

3

Acute lymphoblastic leukemias with deletion of 11q23 or a novel inversion (11)(p13q23) lack MLL gene rearrangements and have favorable clinical features.

Raimondi SC, Frestedt JL, Pui CH, Downing JR, Head DR, Kersey JH, Behm FG. Raimondi SC, et al. Blood. 1995 Sep 1;86(5):1881-6. Blood. 1995. PMID: 7655016 Free article.

4

Frequent deletion of p16INK4a/MTS1 and p15INK4b/MTS2 in pediatric acute lymphoblastic leukemia.

Okuda T, Shurtleff SA, Valentine MB, Raimondi SC, Head DR, Behm F, Curcio-Brint AM, Liu Q, Pui CH, Sherr CJ, et al. Okuda T, et al. Among authors: raimondi sc. Blood. 1995 May 1;85(9):2321-30. Blood. 1995. PMID: 7727766 Free article.

5

Heterogeneity in CBF beta/MYH11 fusion messages encoded by the inv(16)(p13q22) and the t(16;16)(p13;q22) in acute myelogenous leukemia.

Shurtleff SA, Meyers S, Hiebert SW, Raimondi SC, Head DR, Willman CL, Wolman S, Slovak ML, Carroll AJ, Behm F, et al. Shurtleff SA, et al. Among authors: raimondi sc. Blood. 1995 Jun 15;85(12):3695-703. Blood. 1995. PMID: 7780153 Free article.

6

The der(11)-encoded MLL/AF-4 fusion transcript is consistently detected in t(4;11)(q21;q23)-containing acute lymphoblastic leukemia.

Downing JR, Head DR, Raimondi SC, Carroll AJ, Curcio-Brint AM, Motroni TA, Hulshof MG, Pullen DJ, Domer PH. Downing JR, et al. Among authors: raimondi sc. Blood. 1994 Jan 15;83(2):330-5. Blood. 1994. PMID: 8286732 Free article.

7

Identification of an inversion 16 coexisting with an isochromosome 22q by in situ hybridization in a case of childhood AML M4e.

Gad SG, Callen DF, Kuss B, Downing JR, Behm F, Head D, Ribeiro RC, Raimondi SC. Gad SG, et al. Among authors: raimondi sc. Leukemia. 1993 Oct;7(10):1658-62. Leukemia. 1993. PMID: 8412329

8

An AML1/ETO fusion transcript is consistently detected by RNA-based polymerase chain reaction in acute myelogenous leukemia containing the (8;21)(q22;q22) translocation.

Downing JR, Head DR, Curcio-Brint AM, Hulshof MG, Motroni TA, Raimondi SC, Carroll AJ, Drabkin HA, Willman C, Theil KS, et al. Downing JR, et al. Among authors: raimondi sc. Blood. 1993 Jun 1;81(11):2860-5. Blood. 1993. PMID: 8499624 Free article.

9

TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis.

Shurtleff SA, Buijs A, Behm FG, Rubnitz JE, Raimondi SC, Hancock ML, Chan GC, Pui CH, Grosveld G, Downing JR. Shurtleff SA, et al. Among authors: raimondi sc. Leukemia. 1995 Dec;9(12):1985-9. Leukemia. 1995. PMID: 8609706

10

Molecular analysis of t(11;19) breakpoints in childhood acute leukemias.

Rubnitz JE, Behm FG, Curcio-Brint AM, Pinheiro RP, Carroll AJ, Raimondi SC, Shurtleff SA, Downing JR. Rubnitz JE, et al. Among authors: raimondi sc. Blood. 1996 Jun 1;87(11):4804-8. Blood. 1996. PMID: 8639852 Free article.

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