These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
197 related articles for article (PubMed ID: 17245344)
1. Genome-wide analysis of allelic imbalance in prostate cancer using the Affymetrix 50K SNP mapping array. Tørring N; Borre M; Sørensen KD; Andersen CL; Wiuf C; Ørntoft TF Br J Cancer; 2007 Feb; 96(3):499-506. PubMed ID: 17245344 [TBL] [Abstract][Full Text] [Related]
2. 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; 8():53. PubMed ID: 17311676 [TBL] [Abstract][Full Text] [Related]
3. Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrence. Coenen MJ; Ploeg M; Schijvenaars MM; Cornel EB; Karthaus HF; Scheffer H; Witjes JA; Franke B; Kiemeney LA Clin Cancer Res; 2008 Dec; 14(24):8198-204. PubMed ID: 19088036 [TBL] [Abstract][Full Text] [Related]
4. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays. Carr J; Bown NP; Case MC; Hall AG; Lunec J; Tweddle DA Cancer Genet Cytogenet; 2007 Jan; 172(2):127-38. PubMed ID: 17213021 [TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 16774939 [TBL] [Abstract][Full Text] [Related]
6. [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; 88(37):2636-41. PubMed ID: 19080713 [TBL] [Abstract][Full Text] [Related]
7. A SNP microarray and FISH-based procedure to detect allelic imbalances in multiple myeloma: an integrated genomics approach reveals a wide gene dosage effect. Agnelli L; Mosca L; Fabris S; Lionetti M; Andronache A; Kwee I; Todoerti K; Verdelli D; Battaglia C; Bertoni F; Deliliers GL; Neri A Genes Chromosomes Cancer; 2009 Jul; 48(7):603-14. PubMed ID: 19396863 [TBL] [Abstract][Full Text] [Related]
8. 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; 25(40):5581-90. PubMed ID: 16785998 [TBL] [Abstract][Full Text] [Related]
9. Genome-wide loss of heterozygosity analysis from laser capture microdissected prostate cancer using single nucleotide polymorphic allele (SNP) arrays and a novel bioinformatics platform dChipSNP. Lieberfarb ME; Lin M; Lechpammer M; Li C; Tanenbaum DM; Febbo PG; Wright RL; Shim J; Kantoff PW; Loda M; Meyerson M; Sellers WR Cancer Res; 2003 Aug; 63(16):4781-5. PubMed ID: 12941794 [TBL] [Abstract][Full Text] [Related]
10. High resolution analysis of follicular lymphoma genomes reveals somatic recurrent sites of copy-neutral loss of heterozygosity and copy number alterations that target single genes. Cheung KJ; Delaney A; Ben-Neriah S; Schein J; Lee T; Shah SP; Cheung D; Johnson NA; Mungall AJ; Telenius A; Lai B; Boyle M; Connors JM; Gascoyne RD; Marra MA; Horsman DE Genes Chromosomes Cancer; 2010 Aug; 49(8):669-81. PubMed ID: 20544841 [TBL] [Abstract][Full Text] [Related]
11. Microsatellite analysis of allelic imbalance in tumour and blood from patients with prostate cancer. Schwarzenbach H; Chun FK; Müller I; Seidel C; Urban K; Erbersdobler A; Huland H; Pantel K; Friedrich MG BJU Int; 2008 Jul; 102(2):253-8. PubMed ID: 18336598 [TBL] [Abstract][Full Text] [Related]
12. [Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0]. Ma F; Wu FX; Li N; Liu Q; Yang W; Zhang X; Sun M Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):336-9. PubMed ID: 19504452 [TBL] [Abstract][Full Text] [Related]
13. Identifying allelic loss and homozygous deletions in pancreatic cancer without matched normals using high-density single-nucleotide polymorphism arrays. Calhoun ES; Hucl T; Gallmeier E; West KM; Arking DE; Maitra A; Iacobuzio-Donahue CA; Chakravarti A; Hruban RH; Kern SE Cancer Res; 2006 Aug; 66(16):7920-8. PubMed ID: 16912165 [TBL] [Abstract][Full Text] [Related]
14. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Nannya Y; Sanada M; Nakazaki K; Hosoya N; Wang L; Hangaishi A; Kurokawa M; Chiba S; Bailey DK; Kennedy GC; Ogawa S Cancer Res; 2005 Jul; 65(14):6071-9. PubMed ID: 16024607 [TBL] [Abstract][Full Text] [Related]
15. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray. Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819 [TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 18787345 [TBL] [Abstract][Full Text] [Related]
17. Genome-wide detection of allelic imbalance in renal cell carcinoma using high-density single-nucleotide polymorphism microarrays. Lam CW; To KF; Tong SF Clin Biochem; 2006 Mar; 39(3):187-90. PubMed ID: 16513104 [TBL] [Abstract][Full Text] [Related]
18. Reliable high-throughput genotyping and loss-of-heterozygosity detection in formalin-fixed, paraffin-embedded tumors using single nucleotide polymorphism arrays. Lips EH; Dierssen JW; van Eijk R; Oosting J; Eilers PH; Tollenaar RA; de Graaf EJ; van't Slot R; Wijmenga C; Morreau H; van Wezel T Cancer Res; 2005 Nov; 65(22):10188-91. PubMed ID: 16288005 [TBL] [Abstract][Full Text] [Related]
19. Integrative analysis of genomic aberrations associated with prostate cancer progression. Kim JH; Dhanasekaran SM; Mehra R; Tomlins SA; Gu W; Yu J; Kumar-Sinha C; Cao X; Dash A; Wang L; Ghosh D; Shedden K; Montie JE; Rubin MA; Pienta KJ; Shah RB; Chinnaiyan AM Cancer Res; 2007 Sep; 67(17):8229-39. PubMed ID: 17804737 [TBL] [Abstract][Full Text] [Related]
20. Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays. Wang L; Fidler C; Nadig N; Giagounidis A; Della Porta MG; Malcovati L; Killick S; Gattermann N; Aul C; Boultwood J; Wainscoat JS Haematologica; 2008 Jul; 93(7):994-1000. PubMed ID: 18508791 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]