Works matching IS 10452257 AND DT 1998 AND VI 21 AND IP 1

Results: 9

Cytogenetic and fluorescence in situ hybridization analyses of chromosome 19 aberrations in pancreatic carcinomas: Frequent loss of 19p13.3 and gain of 19q13.1-13.2.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 8, doi. 10.1002/(SICI)1098-2264(199801)21:1<8::AID-GCC3>3.0.CO;2-5
By:
- Höglund, Mattias;
- Gorunova, Ludmila;
- Andrén-Sandberg, Åke;
- Dawiskiba, Sigmund;
- Mitelman, Felix;
- Johansson, Bertil
Publication type:
Article
Barrett's oesophagus: Microsatellite analysis provides evidence to support the proposed metaplasia-dysplasia-carcinoma sequence.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 49, doi. 10.1002/(SICI)1098-2264(199801)21:1<49::AID-GCC7>3.0.CO;2-8
By:
- Gleeson, Catherine M.;
- Sloan, James M.;
- McGuigan, James A.;
- Ritchie, Andrew J.;
- Weber, James L.;
- Russell, S.E. Hilary
Publication type:
Article
Molecular alterations in the TP53 gene of peripheral blood cells of patients with chronic myeloid leukemia.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 2, doi. 10.1002/(SICI)1098-2264(199801)21:1<2::AID-GCC2>3.0.CO;2-5
By:
- Peller, Shoshana;
- Yona, Rivka;
- Kopilova, Yulia;
- Prokocimer, Miron;
- Goldfinger, Naomi;
- Uysal, Akin;
- Karabulut, Halil G.;
- Tukun, Ajlan;
- Bokesoy, Isik;
- Tuncman, Gurol;
- Rotter, Varda
Publication type:
Article
Minimal deletion of 3p13→14.2 associated with immortalization of human uroepithelial cells.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 39, doi. 10.1002/(SICI)1098-2264(199801)21:1<39::AID-GCC6>3.0.CO;2-9
By:
- Vieten, Lydia;
- Belair, Cassandra D.;
- Savelieva, Lena;
- Jülicher, Knut;
- Bröcker, Frank;
- Bardenheuer, Walter;
- Schütte, Jochen;
- Opalka, Bertram;
- Reznikoff, Catherine A.
Publication type:
Article
Another reason to look for tumor suppressor genes on chromosome 21.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 1, doi. 10.1002/(SICI)1098-2264(199801)21:1<1::AID-GCC1>3.0.CO;2-5
By:
- Satgé, Daniel;
- Sasco, Annie J.;
- Geneix, Aimé;
- Malet, Paul
Publication type:
Article
Chromosome loss with concomitant duplication and recombination both contribute most to loss of heterozygosity in vitro.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 30, doi. 10.1002/(SICI)1098-2264(199801)21:1<30::AID-GCC5>3.0.CO;2-9
By:
- de Nooij-van Dalen, Arnolda G.;
- van Buuren-van Seggelen, Vera H. A.;
- Lohman, Paul H. M.;
- Giphart-Gassler, Micheline
Publication type:
Article
Characterization of a t(8;13)(p11;q11-12) in an atypical myeloproliferative disorder.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 70, doi. 10.1002/(SICI)1098-2264(199801)21:1<70::AID-GCC9>3.0.CO;2-5
By:
- Smedley, Damian;
- Somers, Gino;
- Venter, Deon;
- Chow, Chung Wo;
- Cooper, Colin;
- Shipley, Janet
Publication type:
Article
Refinement of the BCL2/immunoglobulin heavy chain fusion gene in t(14;18)(q32;q21) by polymerase chain reaction amplification for long targets.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 17, doi. 10.1002/(SICI)1098-2264(199801)21:1<17::AID-GCC4>3.0.CO;2-B
By:
- Akasaka, Takashi;
- Akasaka, Hiroshi;
- Yonetani, Noboru;
- Ohno, Hitoshi;
- Yamabe, Hirohiko;
- Fukuhara, Shirou;
- Okuma, Minoru
Publication type:
Article
Allelic imbalance, including deletion of PTEN/MMAC1, at the Cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation.
Published in:
Genes, Chromosomes & Cancer, 1998, v. 21, n. 1, p. 61, doi. 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6
By:
- Marsh, Debbie J.;
- Dahia, Patricia L. M.;
- Coulon, Valérie;
- Zheng, Zimu;
- Dorion-Bonnet, Françoise;
- Call, Katherine M.;
- Little, Randall;
- Lin, Albert Y.;
- Eeles, Rosalind A.;
- Goldstein, Alisa M.;
- Hodgson, Shirley V.;
- Richardson, Anne-Louise;
- Robinson, Bruce G.;
- Weber, H. Christian;
- Longy, Michel;
- Eng, Charis
Publication type:
Article