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.
4. 8q24 allelic imbalance and MYC gene copy number in primary prostate cancer. Chen H; Liu W; Roberts W; Hooker S; Fedor H; DeMarzo A; Isaacs W; Kittles RA Prostate Cancer Prostatic Dis; 2010 Sep; 13(3):238-43. PubMed ID: 20634801 [TBL] [Abstract][Full Text] [Related]
5. Multiple copies of mutant BRCA1 and BRCA2 alleles in breast tumors from germ-line mutation carriers. Staff S; Nupponen NN; Borg A; Isola JJ; Tanner MM Genes Chromosomes Cancer; 2000 Aug; 28(4):432-42. PubMed ID: 10862052 [TBL] [Abstract][Full Text] [Related]
6. Allele-specific imbalance mapping at human orthologs of mouse susceptibility to colon cancer (Scc) loci. Gerber MM; Hampel H; Zhou XP; Schulz NP; Suhy A; Deveci M; Çatalyürek ÜV; Ewart Toland A Int J Cancer; 2015 Nov; 137(10):2323-31. PubMed ID: 25973956 [TBL] [Abstract][Full Text] [Related]
7. Allele-specific Hras mutations and genetic alterations at tumor susceptibility loci in skin carcinomas from interspecific hybrid mice. Nagase H; Mao JH; Balmain A Cancer Res; 2003 Aug; 63(16):4849-53. PubMed ID: 12941805 [TBL] [Abstract][Full Text] [Related]
8. Landscape of somatic allelic imbalances and copy number alterations in human lung carcinoma. Staaf J; Isaksson S; Karlsson A; Jönsson M; Johansson L; Jönsson P; Botling J; Micke P; Baldetorp B; Planck M Int J Cancer; 2013 May; 132(9):2020-31. PubMed ID: 23023297 [TBL] [Abstract][Full Text] [Related]
9. Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data. Hu H; Huff CD Pac Symp Biocomput; 2014; ():51-62. PubMed ID: 24297533 [TBL] [Abstract][Full Text] [Related]
10. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas. Buckley AR; Ideker T; Carter H; Harismendy O; Schork NJ Genome Med; 2018 Sep; 10(1):69. PubMed ID: 30217226 [TBL] [Abstract][Full Text] [Related]
11. Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA. de Smith AJ; Walsh KM; Hansen HM; Endicott AA; Wiencke JK; Metayer C; Wiemels JL PLoS One; 2015; 10(11):e0143343. PubMed ID: 26575185 [TBL] [Abstract][Full Text] [Related]
12. Allelic imbalances in human bladder cancer: genome-wide detection with high-density single-nucleotide polymorphism arrays. Primdahl H; Wikman FP; von der Maase H; Zhou XG; Wolf H; Orntoft TF J Natl Cancer Inst; 2002 Feb; 94(3):216-23. PubMed ID: 11830611 [TBL] [Abstract][Full Text] [Related]
13. Allele-specific deletions in mouse tumors identify Fbxw7 as germline modifier of tumor susceptibility. Perez-Losada J; Wu D; DelRosario R; Balmain A; Mao JH PLoS One; 2012; 7(2):e31301. PubMed ID: 22348067 [TBL] [Abstract][Full Text] [Related]
14. Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study. Casula M; Paliogiannis P; Ayala F; De Giorgi V; Stanganelli I; Mandalà M; Colombino M; Manca A; Sini MC; Caracò C; Ascierto PA; Satta RR; ; Lissia A; Cossu A; Palmieri G; BMC Cancer; 2019 Aug; 19(1):772. PubMed ID: 31382929 [TBL] [Abstract][Full Text] [Related]
15. Frequency of germline genomic homozygosity associated with cancer cases. Assié G; LaFramboise T; Platzer P; Eng C JAMA; 2008 Mar; 299(12):1437-45. PubMed ID: 18364486 [TBL] [Abstract][Full Text] [Related]
16. Clinical significance of alterations of chromosome 8 detected by fluorescence in situ hybridization analysis in pathologic organ-confined prostate cancer. Tsuchiya N; Slezak JM; Lieber MM; Bergstralh EJ; Jenkins RB Genes Chromosomes Cancer; 2002 Aug; 34(4):363-71. PubMed ID: 12112525 [TBL] [Abstract][Full Text] [Related]