Johansson B - Search Results

1

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia.

Safavi S, Olsson L, Biloglav A, Veerla S, Blendberg M, Tayebwa J, Behrendtz M, Castor A, Hansson M, Johansson B, Paulsson K. Safavi S, et al. Among authors: johansson b. Oncotarget. 2015 Dec 15;6(40):42793-802. doi: 10.18632/oncotarget.6000. Oncotarget. 2015. PMID: 26544893 Free PMC article.

2

Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22).

Panagopoulos I, Aman P, Fioretos T, Höglund M, Johansson B, Mandahl N, Heim S, Behrendtz M, Mitelman F. Panagopoulos I, et al. Among authors: johansson b. Genes Chromosomes Cancer. 1994 Dec;11(4):256-62. doi: 10.1002/gcc.2870110408. Genes Chromosomes Cancer. 1994. PMID: 7533529

3

Emergence of novel transient clonal chromosomal bone marrow changes in remission of acute lymphoblastic leukemia.

Andreasson P, Johansson B, Arheden K, Tedgård U, Ljung R, Heim S, Mitelmann F. Andreasson P, et al. Among authors: johansson b. Leukemia. 1996 Feb;10(2):378-83. Leukemia. 1996. PMID: 8637252 Review. No abstract available.

4

Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes.

Mertens F, Johansson B, Mitelman F. Mertens F, et al. Among authors: johansson b. Cancer Genet Cytogenet. 1996 Nov;92(1):8-10. doi: 10.1016/s0165-4608(96)00124-0. Cancer Genet Cytogenet. 1996. PMID: 8956862 Review.

5

Childhood acute lymphoblastic leukaemia with ider(21)(q10)t(12;21)(p12;q22): a new recurrent abnormality showing ETV6/CBFA2 fusion.

Andreasson P, Johansson B, Strömbeck B, Donnér M, Mitelman F, Höglund M. Andreasson P, et al. Among authors: johansson b. Br J Haematol. 1997 Jul;98(1):216-8. doi: 10.1046/j.1365-2141.1997.1652982.x. Br J Haematol. 1997. PMID: 9233588 Free article.

6

Cytogenetic and FISH studies of a single center consecutive series of 152 childhood acute lymphoblastic leukemias.

Andreasson P, Höglund M, Békássy AN, Garwicz S, Heldrup J, Mitelman F, Johansson B. Andreasson P, et al. Among authors: johansson b. Eur J Haematol. 2000 Jul;65(1):40-51. doi: 10.1034/j.1600-0609.2000.90190.x. Eur J Haematol. 2000. PMID: 10914938

7

The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology.

Paulsson K, Säll T, Fioretos T, Mitelman F, Johansson B. Paulsson K, et al. Among authors: johansson b. Cancer Genet Cytogenet. 2001 Oct 15;130(2):160-5. doi: 10.1016/s0165-4608(01)00486-1. Cancer Genet Cytogenet. 2001. PMID: 11675138

8

Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a multicolor and locus-specific fluorescence in situ hybridization study.

Paulsson K, Fioretos T, Strömbeck B, Mauritzson N, Tanke HJ, Johansson B. Paulsson K, et al. Among authors: johansson b. Cancer Genet Cytogenet. 2003 Jan 1;140(1):66-9. doi: 10.1016/s0165-4608(02)00628-3. Cancer Genet Cytogenet. 2003. PMID: 12550762

9

Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.

Paulsson K, Panagopoulos I, Knuutila S, Jee KJ, Garwicz S, Fioretos T, Mitelman F, Johansson B. Paulsson K, et al. Among authors: johansson b. Blood. 2003 Oct 15;102(8):3010-5. doi: 10.1182/blood-2003-05-1444. Epub 2003 Jun 26. Blood. 2003. PMID: 12829594 Free article.

10

Identification of a commonly amplified 4.3 Mb region with overexpression of C8FW, but not MYC in MYC-containing double minutes in myeloid malignancies.

Storlazzi CT, Fioretos T, Paulsson K, Strömbeck B, Lassen C, Ahlgren T, Juliusson G, Mitelman F, Rocchi M, Johansson B. Storlazzi CT, et al. Among authors: johansson b. Hum Mol Genet. 2004 Jul 15;13(14):1479-85. doi: 10.1093/hmg/ddh164. Epub 2004 May 26. Hum Mol Genet. 2004. PMID: 15163636

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