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Items: 26

1.

Isodicentric 7p, idic(7)(q11.2), in acute myeloid leukemia associated with older age and favorable response to induction chemotherapy: a new clinical entity?

Johansson B, Axelsson P, Billström R, Strömbeck B, Arheden K, Olofsson T, Cervin A, Adriansson M, Tanke HJ, Mitelman F, Fioretos T.

Genes Chromosomes Cancer. 2001 Mar;30(3):261-6.

PMID:
11170283
2.

Genomic amplification of CCND2 is rare in non-Hodgkin lymphomas.

Andreasson P, Johansson B, Arheden K, Kristoffersson U, Akerman M, Mitelman F, Höglund M.

Cancer Genet Cytogenet. 1998 Apr 1;102(1):81-2.

PMID:
9530346
3.

Unbalanced chromosomal rearrangements in a metastasizing salivary gland tumor with benign histology.

Jin Y, Jin C, Arheden K, Larsson O, Bauer HF, Mandahl N, Mertens F.

Cancer Genet Cytogenet. 1998 Apr 1;102(1):59-64.

PMID:
9530342
4.

Deletions of CDKN1B and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities.

Andreasson P, Johansson B, Arheden K, Billström R, Mitelman F, Höglund M.

Genes Chromosomes Cancer. 1997 Jun;19(2):77-83.

PMID:
9171997
5.

Ring marker containing 17q and chromosome 22 in a case of dermatofibrosarcoma protuberans.

Mandahl N, Limon J, Mertens F, Arheden K, Mitelman F.

Cancer Genet Cytogenet. 1996 Jul 1;89(1):88-91. No abstract available.

PMID:
8689621
6.

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.

Leukemia. 1996 Feb;10(2):378-83. Review. No abstract available.

PMID:
8637252
7.

Fluorescence in situ hybridization analysis of whole-arm 7;12 translocations in hematologic malignancies.

Johansson B, Arheden K, Höglund M, Othzén A, Békássy AN, Turesson I, Heim S, Mitelman F.

Genes Chromosomes Cancer. 1995 Sep;14(1):56-62.

PMID:
8527385
8.

Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses.

Jin Y, Mertens F, Arheden K, Mandahl N, Wennerberg J, Dictor M, Heim S, Mitelman F.

Int J Cancer. 1995 Mar 3;60(5):637-41.

PMID:
7860137
9.

Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11).

Aman P, Ron D, Mandahl N, Fioretos T, Heim S, Arheden K, Willén H, Rydholm A, Mitelman F.

Genes Chromosomes Cancer. 1992 Nov;5(4):278-85.

PMID:
1283316
10.
11.

Involvement of 3p deletions in sporadic and hereditary forms of renal cell carcinoma.

Boldog F, Arheden K, Imreh S, Strömbeck B, Szekely L, Erlandsson R, Marcsek Z, Sumegi J, Mitelman F, Klein G.

Genes Chromosomes Cancer. 1991 Sep;3(5):403-6.

PMID:
1797089
12.

GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity.

Ruppert JM, Vogelstein B, Arheden K, Kinzler KW.

Mol Cell Biol. 1990 Oct;10(10):5408-15.

13.

Chromosomal rearrangements in chondromatous tumors.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F.

Cancer. 1990 Jan 15;65(2):242-8.

PMID:
2295046
14.

The INT1 oncogene is not rearranged or amplified in lipomas with structural chromosomal abnormalities of 12q13-15.

Arheden K, Mandahl N, Heim S, Mitelman F.

Cancer Genet Cytogenet. 1989 Oct 1;42(1):143-6.

PMID:
2790742
15.

The gene for the human putative apoE receptor is on chromosome 12 in the segment q13-14.

Myklebost O, Arheden K, Rogne S, Geurts van Kessel A, Mandahl N, Herz J, Stanley K, Heim S, Mitelman F.

Genomics. 1989 Jul;5(1):65-9.

PMID:
2548950
16.

No amplification or rearrangement of INT1, GLI, or COL2A1 in uterine leiomyomas with t(12;14)(q14-15;q23-24).

Arheden K, Nilbert M, Heim S, Mandahl N, Mitelman F.

Cancer Genet Cytogenet. 1989 Jun;39(2):195-201.

PMID:
2752373
17.

In situ hybridization localizes the human putative oncogene GLI to chromosome subbands 12q13.3-14.1.

Arheden K, Rønne M, Mandahl N, Heim S, Kinzler KW, Vogelstein B, Mitelman F.

Hum Genet. 1989 Apr;82(1):1-2.

PMID:
2497059
18.

Separate karyotypic features in a local recurrence and a metastasis of a fibrosarcoma.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F.

Cancer Genet Cytogenet. 1989 Jan;37(1):139-40. No abstract available.

PMID:
2917329
19.

Localization in man of fifteen DNA sequences within the chromosome segment 13q12-q22.

Arheden K, Tantravahi U, Tommerup N, Tranebjaerg L, Mitelman F.

Hereditas. 1989;110(3):253-65.

20.

In situ hybridization localizes the human type II alpha 1 collagen gene (COL2A1) to 12q13.

Arheden K, Mandahl N, Heim S, Mitelman F.

Hereditas. 1989;110(2):165-7.

21.

Multiple karyotypic abnormalities, including structural rearrangements of 11p, in cell lines from malignant melanomas.

Heim S, Mandahl N, Arheden K, Giovanella BC, Yim SO, Stehlin JS Jr, Mitelman F.

Cancer Genet Cytogenet. 1988 Oct 1;35(1):5-20.

PMID:
3180009
22.

Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F.

Hum Genet. 1988 Jul;79(3):203-8.

PMID:
3402992
23.

Multiple karyotypic rearrangements, including t(X;18)(p11;q11), in a fibrosarcoma.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F.

Cancer Genet Cytogenet. 1988 Feb;30(2):323-7.

PMID:
3342387
24.

Chromosome localization of the human oncogene INT1 to 12q13 by in situ hybridization.

Arheden K, Mandahl N, Strömbeck B, Isaksson M, Mitelman F.

Cytogenet Cell Genet. 1988;47(1-2):86-7.

PMID:
3281802
25.

Amplification of the human putative oncogene INT1 in primary retinoblastoma tumors.

Arheden K, Tommerup N, Mandahl N, Heim S, Winther J, Jensen OA, Prause JU, Mitelman F.

Cytogenet Cell Genet. 1988;48(3):174-7.

PMID:
3069341
26.

Rings, dicentrics, and telomeric association in histiocytomas.

Mandahl N, Heim S, Arheden K, Rydholm A, Willén H, Mitelman F.

Cancer Genet Cytogenet. 1988 Jan;30(1):23-33.

PMID:
2825965

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