Works matching IS 10452257 AND DT 1999 AND VI 24 AND IP 3

Results: 18

HMG1 is not rearranged by 13q12 aberrations in lipomas.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 290, doi. 10.1002/(SICI)1098-2264(199903)24:3<290::AID-GCC17>3.0.CO;2-E
By:
- Kazmierczak, Bernd;
- Dal Cin, Paola;
- Meyer-Bolte, Kerstin;
- Berghe, Herman Van den;
- Bullerdiek, Jörn
Publication type:
Article
The genetic background modifies the spontaneous and X-ray-induced tumor spectrum in the Apc1638N mouse model.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 191, doi. 10.1002/(SICI)1098-2264(199903)24:3<191::AID-GCC3>3.0.CO;2-L
By:
- van der Houven van Oordt, C. Willemien;
- Smits, Ron;
- Schouten, Theo G.;
- Houwing-Duistermaat, Jeanine J.;
- Williamson, Sophia L.H.;
- Luz, Arne;
- Khan, P. Meera;
- van der Eb, Alex J.;
- Breuer, Marco L.;
- Fodde, Riccardo
Publication type:
Article
Cytogenetic polyclonality in hematologic malignancies.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 222, doi. 10.1002/(SICI)1098-2264(199903)24:3<222::AID-GCC7>3.0.CO;2-A
By:
- Johansson, Bertil;
- Billström, Rolf;
- Broberg, Karin;
- Fioretos, Thoas;
- Nilsson, Per-Gunnar;
- Ahlgren, Tomas;
- Malm, Claes;
- Samuelsson, Bengt O.;
- Mitelman, Felix
Publication type:
Article
Involvement of the HMGI(Y) gene in a microfollicular adenoma of the thyroid.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 286, doi. 10.1002/(SICI)1098-2264(199903)24:3<286::AID-GCC16>3.0.CO;2-E
By:
- Cin, Paola Dal;
- Fusco, Alfredo;
- Belge, Gazanfer;
- Chiappetta, Gennaro;
- Fedele, Monica;
- Pauwels, Patrick;
- Bullerdiek, Jörn;
- Van den Berghe, Herman
Publication type:
Article
Identification of a 1-cM region of common deletion on 13q14 associated with human prostate cancer.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 183, doi. 10.1002/(SICI)1098-2264(199903)24:3<183::AID-GCC2>3.0.CO;2-J
By:
- Ueda, Takeshi;
- Emi, Mitsuru;
- Suzuki, Hiroyoshi;
- Komiya, Akira;
- Akakura, Koichiro;
- Ichikawa, Tomohiko;
- Watanabe, Masatoshi;
- Shiraishi, Taizo;
- Masai, Motoyuki;
- Igarashi, Tatsuo;
- Ito, Haruo
Publication type:
Article
Allelic imbalance in chromosome band 18q21 and SMAD4 mutations in ovarian cancers.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 264, doi. 10.1002/(SICI)1098-2264(199903)24:3<264::AID-GCC12>3.0.CO;2-Y
By:
- Takakura, Satoshi;
- Okamoto, Aikou;
- Saito, Misato;
- Yasuhara, Takaomi;
- Shinozaki, Hideo;
- Isonishi, Seiji;
- Yoshimura, Tomoaki;
- Ohtake, Yasuyuki;
- Ochiai, Kazunori;
- Tanaka, Tadao
Publication type:
Article
Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 213, doi. 10.1002/(SICI)1098-2264(199903)24:3<213::AID-GCC6>3.0.CO;2-B
By:
- Tosi, Sabrina;
- Giudici, Giovanni;
- Rambaldi, Alessandro;
- Scherer, Stephen W.;
- Bray-Ward, Patricia;
- Dirscherl, Luke;
- Biondi, Andrea;
- Kearney, Lyndal
Publication type:
Article
Deletion mapping of chromosomal region 1p32-pter in primary breast cancer.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 255, doi. 10.1002/(SICI)1098-2264(199903)24:3<255::AID-GCC11>3.0.CO;2-2
By:
- Bièche, Ivan;
- Khodja, Abderrahmane;
- Lidereau, Rosette
Publication type:
Article
Distinct deleted regions on chromosome segment 16q23-24 associated with metastases in prostate cancer.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 175, doi. 10.1002/(SICI)1098-2264(199903)24:3<175::AID-GCC1>3.0.CO;2-H
By:
- Li, Chunde;
- Berx, Geert;
- Larsson, Catharina;
- Auer, Gert;
- Aspenblad, Ulla;
- Pan, Yi;
- Sundelin, Birgitta;
- Ekman, Peter;
- Nordenskjöld, Magnus;
- van Roy, Frans;
- Bergerheim, Ulf S.R.
Publication type:
Article
Loss of NF1 allele in schwann cells but not in fibroblasts derived from an NF1-associated neurofibroma.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 283, doi. 10.1002/(SICI)1098-2264(199903)24:3<283::AID-GCC15>3.0.CO;2-K
By:
- Kluwe, Lan;
- Friedrich, Reinhard;
- Mautner, Victor-F.
Publication type:
Article
Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 278, doi. 10.1002/(SICI)1098-2264(199903)24:3<278::AID-GCC14>3.0.CO;2-L
By:
- Broberg, Karin;
- Höglund, Mattias;
- Limon, Janusz;
- Lindstrand, Anders;
- Toksvig-Larsen, Sören;
- Mandahl, Nils;
- Mertens, Fredrik
Publication type:
Article
A somatic BRCA2 mutation in RER<sup>+</sup> endometrial carcinomas that specifically deletes the amino-terminal transactivation domain.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 207, doi. 10.1002/(SICI)1098-2264(199903)24:3<207::AID-GCC5>3.0.CO;2-3
By:
- Koul, Anjila;
- Nilbert, Mef;
- Borg, Åke
Publication type:
Article
Frequent mutations of NF2 and allelic loss from chromosome band 22q12 in malignant mesothelioma: Evidence for a two-hit mechanism of NF2 inactivation.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 238, doi. 10.1002/(SICI)1098-2264(199903)24:3<238::AID-GCC9>3.0.CO;2-M
By:
- Cheng, Jin Quan;
- Lee, Wen-Ching;
- Klein, Matias A.;
- Cheng, George Z.;
- Jhanwar, Suresh C.;
- Testa, Joseph R.
Publication type:
Article
Prognostic impact of deletions at 1p36 and numerical aberrations in Ewing tumors.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 243, doi. 10.1002/(SICI)1098-2264(199903)24:3<243::AID-GCC10>3.0.CO;2-A
By:
- Hattinger, C.M.;
- Rumpler, S.;
- Strehl, S.;
- Ambros, I.M.;
- Zoubek, A.;
- Pötschger, U.;
- Gadner, H.;
- Ambros, P.F.
Publication type:
Article
Consistent aneuploidies in choroid plexus papillomas.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 293, doi. 10.1002/(SICI)1098-2264(199903)24:3<293::AID-GCC18>3.0.CO;2-8
By:
- Punnett, Hope H.;
- Chadarevian, Jean-Pierre de;
- Tomczak, Ewa Z.
Publication type:
Article
Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 199, doi. 10.1002/(SICI)1098-2264(199903)24:3<199::AID-GCC4>3.0.CO;2-V
By:
- Wlodarska, Iwona;
- Selleri, Licia;
- La Starza, Roberta;
- Paternotte, Caroline;
- Evans, Glen A.;
- Boogaerts, Marc;
- Van den Berghe, Herman;
- Mecucci, Cristina
Publication type:
Article
Chromosome arm 6q loss is the most common recurrent autosomal alteration detected in primary pediatric ependymoma.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 230, doi. 10.1002/(SICI)1098-2264(199903)24:3<230::AID-GCC8>3.0.CO;2-C
By:
- Reardon, David A.;
- Entrekin, Ruth E.;
- Sublett, Jack;
- Ragsdale, Susan;
- Li, Hao;
- Boyett, James;
- Kepner, James L.;
- Look, A. Thomas
Publication type:
Article
Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion.
Published in:
Genes, Chromosomes & Cancer, 1999, v. 24, n. 3, p. 272, doi. 10.1002/(SICI)1098-2264(199903)24:3<272::AID-GCC13>3.0.CO;2-U
By:
- Loncarevic, Ivan F.;
- Roitzheim, Barbara;
- Ritterbach, Jutta;
- Viehmann, Susanne;
- Borkhardt, Arndt;
- Lampert, Fritz;
- Harbott, Jochen
Publication type:
Article