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Items: 1 to 20 of 396

1.

High-resolution genomic profiling reveals gain of chromosome 14 as a predictor of poor outcome in ileal carcinoids.

Andersson E, Swärd C, Stenman G, Ahlman H, Nilsson O.

Endocr Relat Cancer. 2009 Sep;16(3):953-66. doi: 10.1677/ERC-09-0052. Epub 2009 May 20.

2.

High-resolution analysis of DNA copy number alterations and gene expression in renal clear cell carcinoma.

Yoshimoto T, Matsuura K, Karnan S, Tagawa H, Nakada C, Tanigawa M, Tsukamoto Y, Uchida T, Kashima K, Akizuki S, Takeuchi I, Sato F, Mimata H, Seto M, Moriyama M.

J Pathol. 2007 Dec;213(4):392-401.

PMID:
17922474
3.

Comparative genomic hybridization identifies loss of 18q22-qter as an early and specific event in tumorigenesis of midgut carcinoids.

Kytölä S, Höög A, Nord B, Cedermark B, Frisk T, Larsson C, Kjellman M.

Am J Pathol. 2001 May;158(5):1803-8.

4.

Profiling of ileal carcinoids.

Nilsson O.

Neuroendocrinology. 2013;97(1):7-18. doi: 10.1159/000343232. Epub 2012 Nov 2. Review.

PMID:
22986706
5.

Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.

Espinosa AB, Mackintosh C, Maíllo A, Gutierrez L, Sousa P, Merino M, Ortiz J, de Alava E, Orfao A, Tabernero MD.

Eur J Hum Genet. 2008 Dec;16(12):1450-8. doi: 10.1038/ejhg.2008.128. Epub 2008 Jul 16.

6.

Common pathogenetic mechanism involving human chromosome 18 in familial and sporadic ileal carcinoid tumors.

Cunningham JL, Díaz de Ståhl T, Sjöblom T, Westin G, Dumanski JP, Janson ET.

Genes Chromosomes Cancer. 2011 Feb;50(2):82-94. doi: 10.1002/gcc.20834.

PMID:
21104784
7.

Copy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridization.

Hashemi J, Fotouhi O, Sulaiman L, Kjellman M, Höög A, Zedenius J, Larsson C.

BMC Cancer. 2013 Oct 29;13:505. doi: 10.1186/1471-2407-13-505.

8.

Genome-wide analysis of DNA copy number alterations and gene expression in gastric cancer.

Tsukamoto Y, Uchida T, Karnan S, Noguchi T, Nguyen LT, Tanigawa M, Takeuchi I, Matsuura K, Hijiya N, Nakada C, Kishida T, Kawahara K, Ito H, Murakami K, Fujioka T, Seto M, Moriyama M.

J Pathol. 2008 Dec;216(4):471-82. doi: 10.1002/path.2424.

PMID:
18798223
9.

Genomic profiling of gastric carcinoma in situ and adenomas by array-based comparative genomic hybridization.

Uchida M, Tsukamoto Y, Uchida T, Ishikawa Y, Nagai T, Hijiya N, Nguyen LT, Nakada C, Kuroda A, Okimoto T, Kodama M, Murakami K, Noguchi T, Matsuura K, Tanigawa M, Seto M, Ito H, Fujioka T, Takeuchi I, Moriyama M.

J Pathol. 2010 May;221(1):96-105. doi: 10.1002/path.2686.

PMID:
20217874
10.

Integrated analysis of copy number alteration and RNA expression profiles of cancer using a high-resolution whole-genome oligonucleotide array.

Jung SH, Shin SH, Yim SH, Choi HS, Lee SH, Chung YJ.

Exp Mol Med. 2009 Jul 31;41(7):462-70. doi: 10.3858/emm.2009.41.7.051.

11.

LSAMP, a novel candidate tumor suppressor gene in human osteosarcomas, identified by array comparative genomic hybridization.

Kresse SH, Ohnstad HO, Paulsen EB, Bjerkehagen B, Szuhai K, Serra M, Schaefer KL, Myklebost O, Meza-Zepeda LA.

Genes Chromosomes Cancer. 2009 Aug;48(8):679-93. doi: 10.1002/gcc.20675.

PMID:
19441093
12.

Patterns of chromosomal imbalances defines subgroups of breast cancer with distinct clinical features and prognosis. A study of 305 tumors by comparative genomic hybridization.

Rennstam K, Ahlstedt-Soini M, Baldetorp B, Bendahl PO, Borg A, Karhu R, Tanner M, Tirkkonen M, Isola J.

Cancer Res. 2003 Dec 15;63(24):8861-8.

13.

DNA copy number changes in high-grade malignant peripheral nerve sheath tumors by array CGH.

Kresse SH, Skårn M, Ohnstad HO, Namløs HM, Bjerkehagen B, Myklebost O, Meza-Zepeda LA.

Mol Cancer. 2008 Jun 3;7:48. doi: 10.1186/1476-4598-7-48.

14.

Mantle-cell lymphoma genotypes identified with CGH to BAC microarrays define a leukemic subgroup of disease and predict patient outcome.

Rubio-Moscardo F, Climent J, Siebert R, Piris MA, Martín-Subero JI, Nieländer I, Garcia-Conde J, Dyer MJ, Terol MJ, Pinkel D, Martinez-Climent JA.

Blood. 2005 Jun 1;105(11):4445-54. Epub 2005 Feb 17.

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Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study.

Petzmann S, Ullmann R, Halbwedl I, Popper HH.

Virchows Arch. 2004 Aug;445(2):151-9. Epub 2004 Jul 3.

PMID:
15235910
18.

Comparative genomic hybridization of postirradiation sarcomas.

Tarkkanen M, Wiklund TA, Virolainen MJ, Larramendy ML, Mandahl N, Mertens F, Blomqvist CP, Tukiainen EJ, Miettinen MM, Elomaa AI, Knuutila YS.

Cancer. 2001 Oct 1;92(7):1992-8.

PMID:
11745275
19.

Gain of 5p15 detected by comparative genomic hybridization as an independent marker of poor prognosis in patients with esophageal squamous cell carcinoma.

Ueno T, Tangoku A, Yoshino S, Abe T, Toshimitsu H, Furuya T, Kawauchi S, Oga A, Oka M, Sasaki K.

Clin Cancer Res. 2002 Feb;8(2):526-33.

20.

Distinct patterns of DNA copy number alteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer.

Bergamaschi A, Kim YH, Wang P, Sørlie T, Hernandez-Boussard T, Lonning PE, Tibshirani R, Børresen-Dale AL, Pollack JR.

Genes Chromosomes Cancer. 2006 Nov;45(11):1033-40.

PMID:
16897746

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