Squire J - Search Results

1

Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia.

Ma Z, Morris SW, Valentine V, Li M, Herbrick JA, Cui X, Bouman D, Li Y, Mehta PK, Nizetic D, Kaneko Y, Chan GC, Chan LC, Squire J, Scherer SW, Hitzler JK. Ma Z, et al. Among authors: squire j. Nat Genet. 2001 Jul;28(3):220-1. doi: 10.1038/90054. Nat Genet. 2001. PMID: 11431691

2

Overgrowth syndromes and genomic imprinting: from mouse to man.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: squire ja. Clin Genet. 1998 Mar;53(3):165-70. Clin Genet. 1998. PMID: 9630066 Review.

3

Molecular genetics of Beckwith-Wiedemann syndrome.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: squire ja. Curr Opin Pediatr. 1997 Dec;9(6):623-9. doi: 10.1097/00008480-199712000-00012. Curr Opin Pediatr. 1997. PMID: 9425596 Review.

4

Molecular genetics of Wiedemann-Beckwith syndrome.

Li M, Squire JA, Weksberg R. Li M, et al. Among authors: squire ja. Am J Med Genet. 1998 Oct 2;79(4):253-9. Am J Med Genet. 1998. PMID: 9781904 Review.

5

Structural characterization and mapping of the normal epithelial cell-specific 1 gene.

Luo L, Herbrick JA, Scherer SW, Beatty B, Squire J, Diamandis EP. Luo L, et al. Among authors: squire j. Biochem Biophys Res Commun. 1998 Jun 29;247(3):580-6. doi: 10.1006/bbrc.1998.8793. Biochem Biophys Res Commun. 1998. PMID: 9647736

6

Juvenile chronic myelogenous leukemia multilineage CD34+ cells: aberrant growth and differentiation properties.

Freedman MH, Hitzler JK, Bunin N, Grunberger T, Squire J. Freedman MH, et al. Among authors: squire j. Stem Cells. 1996 Nov;14(6):690-701. doi: 10.1002/stem.140690. Stem Cells. 1996. PMID: 8948026

7

Mutations in SUFU predispose to medulloblastoma.

Taylor MD, Liu L, Raffel C, Hui CC, Mainprize TG, Zhang X, Agatep R, Chiappa S, Gao L, Lowrance A, Hao A, Goldstein AM, Stavrou T, Scherer SW, Dura WT, Wainwright B, Squire JA, Rutka JT, Hogg D. Taylor MD, et al. Nat Genet. 2002 Jul;31(3):306-10. doi: 10.1038/ng916. Epub 2002 Jun 17. Nat Genet. 2002. PMID: 12068298

8

Alterations of H19 imprinting and IGF2 replication timing are infrequent in Beckwith-Wiedemann syndrome.

Squire JA, Li M, Perlikowski S, Fei YL, Bayani J, Zhang ZM, Weksberg R. Squire JA, et al. Genomics. 2000 May 1;65(3):234-42. doi: 10.1006/geno.2000.6155. Genomics. 2000. PMID: 10857747

9

Lack of BCR/ABL reciprocal fusion in variant Philadelphia chromosome translocations: a use of double fusion signal FISH and spectral karyotyping.

Markovic VD, Bouman D, Bayani J, Al-Maghrabi J, Kamel-Reid S, Squire JA. Markovic VD, et al. Among authors: squire ja. Leukemia. 2000 Jun;14(6):1157-60. doi: 10.1038/sj.leu.2401718. Leukemia. 2000. PMID: 10865986 No abstract available.

10

Frequent monoallelic loss of D13S319 in multiple myeloma patients shown by interphase fluorescence in situ hybridization.

Chang H, Bouman D, Boerkoel CF, Stewart AK, Squire JA. Chang H, et al. Among authors: squire ja. Leukemia. 1999 Jan;13(1):105-9. doi: 10.1038/sj.leu.2401208. Leukemia. 1999. PMID: 10049044

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