Works matching IS 10452257 AND DT 2005 AND VI 44 AND IP 3

Results: 13

Molecular genetic evidence supporting a novel human hepatocellular carcinoma tumor suppressor locus at 13q12.11.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 320, doi. 10.1002/gcc.20247
By:
- Chian‐Feng Chen;
- Shiou‐Hwei Yeh;
- Ding‐Shinn Chen;
- Pei‐Jer Chen;
- Yuh‐Shan Jou
Publication type:
Article
BCL6 alternative translocation breakpoint cluster region associated with follicular lymphoma grade 3B.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 301, doi. 10.1002/gcc.20246
By:
- Anneke G. Bosga‐Bouwer;
- Eugenia Haralambieva;
- Marije Booman;
- Ronald Boonstra;
- Anke van den Berg;
- Ed Schuuring;
- Eva van den Berg;
- Philip Kluin;
- Sibrand Poppema
Publication type:
Article
Prevalence of 9p21 deletions in UK melanoma families.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 292, doi. 10.1002/gcc.20238
By:
- Sushila H. Mistry;
- Claire Taylor;
- Juliette A. Randerson‐Moor;
- Mark Harland;
- Faye Turner;
- Jennifer H. Barrett;
- Linda Whitaker;
- Robert B. Jenkins;
- Margaret A. Knowles;
- Julia A. Newton Bishop;
- D. Timothy Bishop
Publication type:
Article
Analysis of chromosome breakpoints in neuroblastoma at sub‐kilobase resolution using fine‐tiling oligonucleotide array CGH.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 305, doi. 10.1002/gcc.20243
By:
- Rebecca R. Selzer;
- Todd A. Richmond;
- Nathan J. Pofahl;
- Roland D. Green;
- Peggy S. Eis;
- Prakash Nair;
- Arthur R. Brothman;
- Raymond L. Stallings
Publication type:
Article
Allelotyping of esophageal squamous‐cell carcinoma on chromosome 13 defines deletions related to family historyThis article is a US Government work and, as such, is in the public domain in the United States of America.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 271, doi. 10.1002/gcc.20242
By:
- Nan Hu;
- Hua Su;
- Wen Jun Li;
- Carol Giffen;
- Alisa M. Goldstein;
- Ying Hu;
- Chaoyu Wang;
- Mark J Roth;
- Guang Li;
- Sanford M. Dawsey;
- Yi Xu;
- Philip R. Taylor;
- Michael R. Emmert‐Buck
Publication type:
Article
Novel RUNX1‐PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22).
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 265, doi. 10.1002/gcc.20241
By:
- Ikuya Sakai;
- Tatsushiro Tamura;
- Hirosi Narumi;
- Naoyuki Uchida;
- Yoshihiro Yakushijin;
- Takaaki Hato;
- Shigeru Fujita;
- Masaki Yasukawa
Publication type:
Article
Profile of differentially expressed genes after transfer of chromosome 17 into the breast cancer cell line CAl51.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 233, doi. 10.1002/gcc.20240
By:
- Christiane Klebig;
- Susanne Seitz;
- Eberhard Korsching;
- Glen Kristiansen;
- Dirk Gustavus;
- Siegfried Scherneck;
- Iver Petersen
Publication type:
Article
Genome‐wide array‐based comparative genomic hybridization of natural killer cell lymphoma/leukemia: Different genomic alteration patterns of aggressive NK‐cell leukemia and extranodal Nk/T‐cell lymphoma, nasal type.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 247, doi. 10.1002/gcc.20245
By:
- Yasuhiro Nakashima;
- Hiroyuki Tagawa;
- Ritsuro Suzuki;
- Sivasundaram Karnan;
- Kennosuke Karube;
- Koichi Ohshima;
- Koichiro Muta;
- Hajime Nawata;
- Yasuo Morishima;
- Shigeo Nakamura;
- Masao Seto
Publication type:
Article
IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylation‐sensitive single‐nucleotide primer extension method reflects the origin of GCTs in different stages of primordial germ cell development.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 256, doi. 10.1002/gcc.20237
By:
- Sonja Sievers;
- Katayoun Alemazkour;
- Susanne Zahn;
- Elizabeth J. Perlman;
- Ad J. M. Gillis;
- Leendert H. J. Looijenga;
- Ulrich Göbel;
- Dominik T. Schneider
Publication type:
Article
Delineation of the minimal commonly deleted segment and identification of candidate tumor‐suppressor genes in del(9q) acute myeloid leukemia.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 279, doi. 10.1002/gcc.20236
By:
- David A. Sweetser;
- Andrew J. Peniket;
- Christina Haaland;
- Adam A. Blomberg;
- Yuntian Zhang;
- Syed Tanweer Zaidi;
- Farshid Dayyani;
- Zheng Zhao;
- Nyla A. Heerema;
- Jacqueline Boultwood;
- Gordon W. Dewald;
- Elisabeth Paietta;
- Marilyn L. Slovak;
- Cheryl L. Willman;
- James S. Wainscoat;
- Irwin D. Bernstein;
- Sarah B. Daly
Publication type:
Article
A BCR–JAK2 fusion gene as the result of a t(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 329, doi. 10.1002/gcc.20235
By:
- Frank Griesinger;
- Heike Hennig;
- Frauke Hillmer;
- Martina Podleschny;
- Rainer Steffens;
- Andreas Pies;
- Bernhard Wörmann;
- Detlef Haase;
- Stefan K. Bohlander
Publication type:
Article
Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 334
By:
- Tatiana Alessandra Gorletta;
- Patrizia Gasparini;
- Mario Milco D'Elios;
- Maurizio Trubia;
- Pier Giuseppe Pelicci;
- Pier Paolo Di Fiore
Publication type:
Article
Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98–C6orf80 fusion in a case of acute megakaryoblastic leukemia.
Published in:
Genes, Chromosomes & Cancer, 2005, v. 44, n. 3, p. 225, doi. 10.1002/gcc.20233
By:
- Sabrina Tosi;
- Erica Ballabio;
- Andrea Teigler‐Schlegel;
- Jackie Boultwood;
- Jochen Bruch;
- Jochen Harbott
Publication type:
Article