Coignet LJ - Search Results

1

Molecular cloning of translocation t(1;14)(q21;q32) defines a novel gene (BCL9) at chromosome 1q21.

Willis TG, Zalcberg IR, Coignet LJ, Wlodarska I, Stul M, Jadayel DM, Bastard C, Treleaven JG, Catovsky D, Silva ML, Dyer MJ. Willis TG, et al. Among authors: coignet lj. Blood. 1998 Mar 15;91(6):1873-81. Blood. 1998. PMID: 9490669 Free article.

2

Rapid molecular cloning of rearrangements of the IGHJ locus using long-distance inverse polymerase chain reaction.

Willis TG, Jadayel DM, Coignet LJ, Abdul-Rauf M, Treleaven JG, Catovsky D, Dyer MJ. Willis TG, et al. Among authors: coignet lj. Blood. 1997 Sep 15;90(6):2456-64. Blood. 1997. PMID: 9310498 Free article.

3

The BCL7 gene family: deletion of BCL7B in Williams syndrome.

Jadayel DM, Osborne LR, Coignet LJ, Zani VJ, Tsui LC, Scherer SW, Dyer MJ. Jadayel DM, et al. Among authors: coignet lj. Gene. 1998 Dec 11;224(1-2):35-44. doi: 10.1016/s0378-1119(98)00514-9. Gene. 1998. PMID: 9931421

4

ATM is usually rearranged in T-cell prolymphocytic leukaemia.

Yuille MA, Coignet LJ, Abraham SM, Yaqub F, Luo L, Matutes E, Brito-Babapulle V, Vorechovský I, Dyer MJ, Catovsky D. Yuille MA, et al. Among authors: coignet lj. Oncogene. 1998 Feb 12;16(6):789-96. doi: 10.1038/sj.onc.1201603. Oncogene. 1998. PMID: 9488043

5

B cell prolymphocytic leukaemia (B-PLL) with complex karyotype and concurrent abnormalities of the p53 and c-MYC gene.

Lens D, Coignet LJ, Brito-Babapulle V, Lima CS, Matutes E, Dyer MJ, Catovsky D. Lens D, et al. Among authors: coignet lj. Leukemia. 1999 Jun;13(6):873-6. doi: 10.1038/sj.leu.2401416. Leukemia. 1999. PMID: 10360375

6

Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia.

Coignet LJ, Lima CS, Min T, Streubel B, Swansbury J, Telford N, Swanton S, Bowen A, Nagai M, Catovsky D, Fonatsch C, Dyer MJ. Coignet LJ, et al. Genes Chromosomes Cancer. 1999 Jul;25(3):222-9. doi: 10.1002/(sici)1098-2264(199907)25:3<222::aid-gcc4>3.0.co;2-c. Genes Chromosomes Cancer. 1999. PMID: 10379868

7

Frequent deletions at 11q23 and 13q14 in B cell prolymphocytic leukemia (B-PLL).

Lens D, Matutes E, Catovsky D, Coignet LJ. Lens D, et al. Among authors: coignet lj. Leukemia. 2000 Mar;14(3):427-30. doi: 10.1038/sj.leu.2401644. Leukemia. 2000. PMID: 10720137

8

The impact of molecular cytogenetics on chronic lymphoid leukaemia.

Brito-Babapulle V, Garcia-Marco J, Maljaie SH, Hiorns L, Coignet L, Conchon M, Catovsky D. Brito-Babapulle V, et al. Acta Haematol. 1997;98(4):175-86. doi: 10.1159/000203621. Acta Haematol. 1997. PMID: 9401494 Review.

9

FISH analysis for BCL-1 rearrangements and trisomy 12 helps the diagnosis of atypical B cell leukaemias.

Matutes E, Carrara P, Coignet L, Brito-Babapulle V, Villamor N, Wotherspoon A, Catovsky D. Matutes E, et al. Leukemia. 1999 Nov;13(11):1721-6. doi: 10.1038/sj.leu.2401561. Leukemia. 1999. PMID: 10557044

10

The incidence of trisomy 3 in splenic lymphoma with villous lymphocytes: a study by FISH.

Gruszka-Westwood AM, Matutes E, Coignet LJ, Wotherspoon A, Catovsky D. Gruszka-Westwood AM, et al. Among authors: coignet lj. Br J Haematol. 1999 Mar;104(3):600-4. doi: 10.1046/j.1365-2141.1999.01209.x. Br J Haematol. 1999. PMID: 10086800 Free article.

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