Detection of recurrent genomic alterations using array-CGH and high resolution-CGH in esophageal squamous cell carcinoma (ESCC)

被引:0
|
作者
Sato-Kuwabara, Yukie [1 ]
Silveira, Cassia G. T. [2 ]
Silveira, Sara M. [1 ]
Marchi, Fabio A. [3 ]
Klock, Clovis [4 ]
Coimbra, Felipe [5 ]
Rogatto, Silvia R. [1 ]
Soares, Fernando A. [1 ]
机构
[1] Hosp AC Camargo Fund Antonio Prudente, CIPE, Sao Paulo, Brazil
[2] Univ Sate Sao Paulo, UNESP, Inst Biosci, Botucatu, SP, Brazil
[3] Univ Sao Paulo, Math & Stat Inst, Sao Paulo, Brazil
[4] Hosp Santa Teresinha, Erechim, Brazil
[5] Hosp AC Camargo Fund Antonio Prudente, Dept Abdominal Surg, Sao Paulo, Brazil
关键词
D O I
10.1158/1538-7445.AM2011-3050
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
3050
引用
收藏
页数:1
相关论文
共 50 条
  • [21] MLPA and array CGH evaluation in Oral Squamous Cell Carcinoma
    Santos, Ana
    Ribeiro, Ilda P.
    Esteves, Luisa
    Marques, Francisco
    Barroso, Leonor
    Juliao, Maria J.
    Baptista, Isabel P.
    Carreira, Isabel M.
    Melo, Joana B.
    MEDICINE, 2020, 99 (09)
  • [22] Identification of novel recurrent genomic aberrations by array-CGH in adult acute lymphoblastic leukemia.
    Viardot, Andreas
    Schwanen, Carsten
    Goekbuget, Nicola
    Hoelzer, Dieter
    Dohner, Hartmut
    Wessendorf, Swen
    Schmid, Mathias
    BLOOD, 2006, 108 (11) : 197B - 197B
  • [23] Chromosomal aberrations in acinic cell carcinomas detected by high-resolution oligonucleotide array-CGH
    Passador-Santos, F.
    Jee, K.
    Hagstron, J.
    Makitie, A.
    Knuutila, S.
    Skalova, A.
    Leivo, I.
    HISTOPATHOLOGY, 2008, 53 : 218 - 218
  • [24] Characterization of genetic rearrangements in esophageal squamous carcinoma cell lines by a combination of M-FISH and array-CGH: further confirmation of some split genomic regions in primary tumors
    Hao, Jia-Jie
    Shi, Zhi-Zhou
    Zhao, Zhi-Xin
    Zhang, Yu
    Gong, Ting
    Li, Chun-Xiang
    Zhan, Ting
    Cai, Yan
    Dong, Jin-Tang
    Fu, Song-Bin
    Zhan, Qi-Min
    Wang, Ming-Rong
    BMC CANCER, 2012, 12
  • [25] Characterization of genetic rearrangements in esophageal squamous carcinoma cell lines by a combination of M-FISH and array-CGH: further confirmation of some split genomic regions in primary tumors
    Jia-Jie Hao
    Zhi-Zhou Shi
    Zhi-Xin Zhao
    Yu Zhang
    Ting Gong
    Chun-Xiang Li
    Ting Zhan
    Yan Cai
    Jin-Tang Dong
    Song-Bin Fu
    Qi-Min Zhan
    Ming-Rong Wang
    BMC Cancer, 12
  • [26] cDNA array-CGH profiling identifies genomic alterations specific to stage and MYCN-amplification in neuroblastoma
    Qing-Rong Chen
    Sven Bilke
    Jun S Wei
    Craig C Whiteford
    Nicola Cenacchi
    Alexei L Krasnoselsky
    Braden T Greer
    Chang-Gue Son
    Frank Westermann
    Frank Berthold
    Manfred Schwab
    Daniel Catchpoole
    Javed Khan
    BMC Genomics, 5
  • [27] Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH
    Blattner, Ariane
    Brunner-Agten, Saskia
    Ludin, Katja
    Hergersberg, Martin
    Herklotz, Roberto
    Huber, Andreas R.
    Roethlisberger, Benno
    BLOOD CELLS MOLECULES AND DISEASES, 2013, 51 (01) : 39 - 47
  • [28] Integrated Cytogenetic and High-Resolution Array CGH Analysis of Genomic Alterations Associated with MYCN Amplification
    Pandita, A.
    Bayani, J.
    Paderova, J.
    Marrano, P.
    Graham, C.
    Barrett, M.
    Prasad, M.
    Zielenska, M.
    Squire, J. A.
    CYTOGENETIC AND GENOME RESEARCH, 2011, 134 (01) : 27 - 39
  • [29] Gene amplification profiling of esophageal squamous cell carcinomas by DNA array CGH
    Ishizuka, T
    Tanabe, C
    Sakamoto, H
    Aoyagi, K
    Maekawa, M
    Matsukura, N
    Tokunaga, A
    Tajiri, T
    Yoshida, T
    Terada, M
    Sasaki, H
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 296 (01) : 152 - 155
  • [30] Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)
    Schoumans, J
    Ruivenkamp, C
    Holmberg, E
    Kyllerman, M
    Anderlid, BM
    Nordenskjöld, M
    JOURNAL OF MEDICAL GENETICS, 2005, 42 (09) : 699 - 705