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Items: 1 to 20 of 172

1.

Genome-wide copy number analysis in esophageal adenocarcinoma using high-density single-nucleotide polymorphism arrays.

Nancarrow DJ, Handoko HY, Smithers BM, Gotley DC, Drew PA, Watson DI, Clouston AD, Hayward NK, Whiteman DC.

Cancer Res. 2008 Jun 1;68(11):4163-72. doi: 10.1158/0008-5472.CAN-07-6710.

3.

Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts.

Boonstra JJ, van Marion R, Douben HJ, Lanchbury JS, Timms KM, Abkevich V, Tilanus HW, de Klein A, Dinjens WN.

Genes Chromosomes Cancer. 2012 Mar;51(3):272-82. doi: 10.1002/gcc.20952. Epub 2011 Nov 12.

PMID:
22081516
4.

Are there any more ovarian tumor suppressor genes? A new perspective using ultra high-resolution copy number and loss of heterozygosity analysis.

Gorringe KL, Ramakrishna M, Williams LH, Sridhar A, Boyle SE, Bearfoot JL, Li J, Anglesio MS, Campbell IG.

Genes Chromosomes Cancer. 2009 Oct;48(10):931-42. doi: 10.1002/gcc.20694.

PMID:
19603523
5.

Genome-wide analysis of genetic alterations in Barrett's adenocarcinoma using single nucleotide polymorphism arrays.

Wiech T, Nikolopoulos E, Weis R, Langer R, Bartholomé K, Timmer J, Walch AK, Höfler H, Werner M.

Lab Invest. 2009 Apr;89(4):385-97. doi: 10.1038/labinvest.2008.67. Epub 2008 Jul 28.

6.

Frequent occurrence of uniparental disomy in colorectal cancer.

Andersen CL, Wiuf C, Kruhøffer M, Korsgaard M, Laurberg S, Ørntoft TF.

Carcinogenesis. 2007 Jan;28(1):38-48. Epub 2006 Jun 13.

PMID:
16774939
7.

Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.

Gu J, Ajani JA, Hawk ET, Ye Y, Lee JH, Bhutani MS, Hofstetter WL, Swisher SG, Wang KK, Wu X.

Cancer Prev Res (Phila). 2010 Sep;3(9):1176-86. doi: 10.1158/1940-6207.CAPR-09-0265. Epub 2010 Jul 22.

8.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

BMC Genomics. 2007 Feb 20;8:53.

9.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.

Gaasenbeek M, Howarth K, Rowan AJ, Gorman PA, Jones A, Chaplin T, Liu Y, Bicknell D, Davison EJ, Fiegler H, Carter NP, Roylance RR, Tomlinson IP.

Cancer Res. 2006 Apr 1;66(7):3471-9.

10.
11.

A novel approach to simultaneously scan genes at fragile sites.

Willem P, Brown J, Schouten J.

BMC Cancer. 2006 Aug 8;6:205.

12.

Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma.

Akagi T, Ito T, Kato M, Jin Z, Cheng Y, Kan T, Yamamoto G, Olaru A, Kawamata N, Boult J, Soukiasian HJ, Miller CW, Ogawa S, Meltzer SJ, Koeffler HP.

Int J Cancer. 2009 Nov 15;125(10):2349-59. doi: 10.1002/ijc.24620.

13.

[Analyzing the profile of chromosomal imbalances in esophageal atypical hyperplasia and early stage esophageal squamous cell carcinoma by 250K Snp Array].

Zhang X, Zhu ZH, Lin P, Yang H, Fu JH, Zhang LJ, Long H, Wen J, Huang XP, Fang Y, Rong TH.

Zhonghua Yi Xue Za Zhi. 2008 Oct 14;88(37):2636-41. Chinese.

PMID:
19080713
14.

Chromosome copy number analysis in screening for prognosis-related genomic regions in colorectal carcinoma.

Kurashina K, Yamashita Y, Ueno T, Koinuma K, Ohashi J, Horie H, Miyakura Y, Hamada T, Haruta H, Hatanaka H, Soda M, Choi YL, Takada S, Yasuda Y, Nagai H, Mano H.

Cancer Sci. 2008 Sep;99(9):1835-40. doi: 10.1111/j.1349-7006.2008.00881.x. Epub 2008 Jun 28.

15.

Array-based comparative genomic hybridization for the detection of DNA sequence copy number changes in Barrett's adenocarcinoma.

Albrecht B, Hausmann M, Zitzelsberger H, Stein H, Siewert JR, Hopt U, Langer R, Höfler H, Werner M, Walch A.

J Pathol. 2004 Jul;203(3):780-8.

PMID:
15221937
16.

Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.

Midorikawa Y, Yamamoto S, Ishikawa S, Kamimura N, Igarashi H, Sugimura H, Makuuchi M, Aburatani H.

Oncogene. 2006 Sep 7;25(40):5581-90. Epub 2006 Jun 19.

PMID:
16785998
17.

Allelotype analysis of oesophageal adenocarcinoma: loss of heterozygosity occurs at multiple sites.

Dolan K, Garde J, Gosney J, Sissons M, Wright T, Kingsnorth AN, Walker SJ, Sutton R, Meltzer SJ, Field JK.

Br J Cancer. 1998 Oct;78(7):950-7.

18.

Integrated analysis of copy number alterations and loss of heterozygosity in human pancreatic cancer using a high-resolution, single nucleotide polymorphism array.

Lin LJ, Asaoka Y, Tada M, Sanada M, Nannya Y, Tanaka Y, Tateishi K, Ohta M, Seto M, Sasahira N, Tada M, Kawabe T, Zheng CQ, Kanai F, Ogawa S, Omata M.

Oncology. 2008;75(1-2):102-12. doi: 10.1159/000155813. Epub 2008 Sep 12.

PMID:
18787345
19.

Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.

Langdon JA, Lamont JM, Scott DK, Dyer S, Prebble E, Bown N, Grundy RG, Ellison DW, Clifford SC.

Genes Chromosomes Cancer. 2006 Jan;45(1):47-60.

PMID:
16149064
20.

Genome-wide amplification and allelotyping of sporadic pituitary adenomas identify novel regions of genetic loss.

Simpson DJ, Bicknell EJ, Buch HN, Cutty SJ, Clayton RN, Farrell WE.

Genes Chromosomes Cancer. 2003 Jul;37(3):225-36.

PMID:
12759921

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