Aventín A - Search Results

1

A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemia.

Wlodarska I, Aventín A, Inglés-Esteve J, Falzetti D, Criel A, Cassiman JJ, Mecucci C, Van den Berghe H, Marynen P. Wlodarska I, et al. Among authors: aventin a. Blood. 1997 Mar 1;89(5):1716-22. Blood. 1997. PMID: 9057655 Free article.

2

Philadelphia-positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils.

Mecucci C, Noens L, Aventin A, Testoni N, Van den Berghe H. Mecucci C, et al. Among authors: aventin a. Am J Hematol. 1988 Jan;27(1):69-71. doi: 10.1002/ajh.2830270118. Am J Hematol. 1988. PMID: 3162648

3

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).

Wlodarska I, Mecucci C, Marynen P, Guo C, Franckx D, La Starza R, Aventin A, Bosly A, Martelli MF, Cassiman JJ, et al. Wlodarska I, et al. Among authors: aventin a. Blood. 1995 May 15;85(10):2848-52. Blood. 1995. PMID: 7742547 Free article.

4

Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies.

La Starza R, Wlodarska I, Aventin A, Falzetti D, Crescenzi B, Martelli MF, Van den Berghe H, Mecucci C. La Starza R, et al. Among authors: aventin a. Blood. 1998 Jan 1;91(1):231-7. Blood. 1998. PMID: 9414289 Free article.

5

Variant (3;21) translocation and megakaryocytic involvement in blastic crisis of Philadelphia positive chronic myeloid leukaemia.

Aventin A, Mecucci C, Van Orshoven A, Delannoy A, Van den Berghe H. Aventin A, et al. Br J Haematol. 1989 Apr;71(4):562-4. doi: 10.1111/j.1365-2141.1989.tb06319.x. Br J Haematol. 1989. PMID: 2713276 No abstract available.

6

Blastic phase of Ph1-positive chronic myeloid leukemia and t(3;21).

Aventin A, Mecucci C, van den Berghe H. Aventin A, et al. Blood. 1988 Jul;72(1):369. Blood. 1988. PMID: 3164638 Free article. No abstract available.

7

Burkitt-type ALL with variant t(2;8) and complex additional rearrangements at diagnosis.

Aventin A, Mecucci C, Tricot G, Van den Berghe H. Aventin A, et al. Ann Genet. 1987;30(1):52-5. Ann Genet. 1987. PMID: 3498431

8

Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization.

Aventín A, La Starza R, Martínez C, Wlodarska I, Boogaerts M, Van den Berghe H, Mecucci C. Aventín A, et al. Cancer Genet Cytogenet. 1999 Jan 1;108(1):48-52. doi: 10.1016/s0165-4608(98)00110-1. Cancer Genet Cytogenet. 1999. PMID: 9973924

9

Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemia.

Cools J, Peeters P, Voet T, Aventin A, Mecucci C, Grandchamp B, Marynen P. Cools J, et al. Among authors: aventin a. Cytogenet Cell Genet. 1999;85(3-4):260-6. doi: 10.1159/000015308. Cytogenet Cell Genet. 1999. PMID: 10449913

10

A variant translocation t(2;18) in follicular lymphoma involves the 5' end of bcl-2 and Ig kappa light chain gene.

Hillion J, Mecucci C, Aventin A, Leroux D, Wlodarska I, Van Den Berghe H, Larsen CJ. Hillion J, et al. Among authors: aventin a. Oncogene. 1991 Jan;6(1):169-72. Oncogene. 1991. PMID: 1899478

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