191 related articles for article (PubMed ID: 37932252)
21. Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.
Marescalco MS; Capizzi C; Condorelli DF; Barresi V
J Oral Pathol Med; 2014 Jan; 43(1):20-7. PubMed ID: 23750501
[TBL] [Abstract][Full Text] [Related]
22. Identification of Recurrent Chromosome Breaks Underlying Structural Rearrangements in Mammary Cancer Cell Lines.
Senter NC; McCulley A; Kuznetsov VA; Feng W
Genes (Basel); 2022 Jul; 13(7):. PubMed ID: 35886011
[TBL] [Abstract][Full Text] [Related]
23. Copy number neutral loss of heterozygosity at 17p and homozygous mutations of TP53 are associated with complex chromosomal aberrations in patients newly diagnosed with myelodysplastic syndromes.
Svobodova K; Zemanova Z; Lhotska H; Novakova M; Podskalska L; Belickova M; Brezinova J; Sarova I; Izakova S; Lizcova L; Berkova A; Siskova M; Jonasova A; Cermak J; Michalova K
Leuk Res; 2016 Mar; 42():7-12. PubMed ID: 26851439
[TBL] [Abstract][Full Text] [Related]
24. Modelling chromosome structural and copy number changes to understand cancer genomes.
Kneissig M; Bernhard S; Storchova Z
Curr Opin Genet Dev; 2019 Feb; 54():25-32. PubMed ID: 30921673
[TBL] [Abstract][Full Text] [Related]
25. Replication stress generates distinctive landscapes of DNA copy number alterations and chromosome scale losses.
Shaikh N; Mazzagatti A; De Angelis S; Johnson SC; Bakker B; Spierings DCJ; Wardenaar R; Maniati E; Wang J; Boemo MA; Foijer F; McClelland SE
Genome Biol; 2022 Oct; 23(1):223. PubMed ID: 36266663
[TBL] [Abstract][Full Text] [Related]
26. Early contribution of germline and nevi genetic alterations to a rapidly-progressing cutaneous melanoma patient: a case report.
Mordoh A; Triviño Pardo JC; Carri I; Barrio MM; Mordoh J; Aris M
BMC Med Genomics; 2023 Jan; 16(1):1. PubMed ID: 36604730
[TBL] [Abstract][Full Text] [Related]
27. Spectral karyotypic study of the HL-60 cell line: detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1.
Liang JC; Ning Y; Wang RY; Padilla-Nash HM; Schröck E; Soenksen D; Nagarajan L; Ried T
Cancer Genet Cytogenet; 1999 Sep; 113(2):105-9. PubMed ID: 10484974
[TBL] [Abstract][Full Text] [Related]
28. Copy number variation in archival melanoma biopsies versus benign melanocytic lesions.
Mahas A; Potluri K; Kent MN; Naik S; Markey M
Cancer Biomark; 2016 Mar; 16(4):575-97. PubMed ID: 27002761
[TBL] [Abstract][Full Text] [Related]
29. Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial.
Goschzik T; Schwalbe EC; Hicks D; Smith A; Zur Muehlen A; Figarella-Branger D; Doz F; Rutkowski S; Lannering B; Pietsch T; Clifford SC
Lancet Oncol; 2018 Dec; 19(12):1602-1616. PubMed ID: 30392813
[TBL] [Abstract][Full Text] [Related]
30. Single-molecule analysis of genome rearrangements in cancer.
Pole JC; McCaughan F; Newman S; Howarth KD; Dear PH; Edwards PA
Nucleic Acids Res; 2011 Jul; 39(13):e85. PubMed ID: 21525129
[TBL] [Abstract][Full Text] [Related]
31. Multiregional Sequencing Reveals Genomic Alterations and Clonal Dynamics in Primary Malignant Melanoma of the Esophagus.
Li J; Yan S; Liu Z; Zhou Y; Pan Y; Yuan W; Liu M; Tan Q; Tian G; Dong B; Cai H; Wu N; Ke Y
Cancer Res; 2018 Jan; 78(2):338-347. PubMed ID: 28972077
[TBL] [Abstract][Full Text] [Related]
32. Hi-C analysis of genomic contacts revealed karyotype abnormalities in chicken HD3 cell line.
Maslova A; Plotnikov V; Nuriddinov M; Gridina M; Fishman V; Krasikova A
BMC Genomics; 2023 Feb; 24(1):66. PubMed ID: 36750787
[TBL] [Abstract][Full Text] [Related]
33. A chromosome-level reference genome of Ensete glaucum gives insight into diversity and chromosomal and repetitive sequence evolution in the Musaceae.
Wang Z; Rouard M; Biswas MK; Droc G; Cui D; Roux N; Baurens FC; Ge XJ; Schwarzacher T; Heslop-Harrison PJS; Liu Q
Gigascience; 2022 Apr; 11():. PubMed ID: 35488861
[TBL] [Abstract][Full Text] [Related]
34. Cytogenetically balanced translocations are associated with focal copy number alterations.
Watson SK; deLeeuw RJ; Horsman DE; Squire JA; Lam WL
Hum Genet; 2007 Feb; 120(6):795-805. PubMed ID: 17051368
[TBL] [Abstract][Full Text] [Related]
35. Cytogenetics of Blastic Plasmacytoid Dendritic Cell Neoplasm: Chromosomal Rearrangements and DNA Copy-Number Alterations.
Sakamoto K; Takeuchi K
Hematol Oncol Clin North Am; 2020 Jun; 34(3):523-538. PubMed ID: 32336417
[TBL] [Abstract][Full Text] [Related]
36. High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas.
Salaverria I; Martin-Guerrero I; Burkhardt B; Kreuz M; Zenz T; Oschlies I; Arnold N; Baudis M; Bens S; García-Orad A; Lisfeld J; Schwaenen C; Szczepanowski M; Wessendorf S; Pfreundschuh M; Trümper L; Klapper W; Siebert R
Genes Chromosomes Cancer; 2013 Feb; 52(2):150-5. PubMed ID: 23073988
[TBL] [Abstract][Full Text] [Related]
37. Chromosomal Instability Estimation Based on Next Generation Sequencing and Single Cell Genome Wide Copy Number Variation Analysis.
Greene SB; Dago AE; Leitz LJ; Wang Y; Lee J; Werner SL; Gendreau S; Patel P; Jia S; Zhang L; Tucker EK; Malchiodi M; Graf RP; Dittamore R; Marrinucci D; Landers M
PLoS One; 2016; 11(11):e0165089. PubMed ID: 27851748
[TBL] [Abstract][Full Text] [Related]
38. Chromosomal gains and losses in primary cutaneous melanomas detected by comparative genomic hybridization.
Bastian BC; LeBoit PE; Hamm H; Bröcker EB; Pinkel D
Cancer Res; 1998 May; 58(10):2170-5. PubMed ID: 9605762
[TBL] [Abstract][Full Text] [Related]
39. High-resolution identification of balanced and complex chromosomal rearrangements by 4C technology.
Simonis M; Klous P; Homminga I; Galjaard RJ; Rijkers EJ; Grosveld F; Meijerink JP; de Laat W
Nat Methods; 2009 Nov; 6(11):837-42. PubMed ID: 19820713
[TBL] [Abstract][Full Text] [Related]
40. Breakpoint features of genomic rearrangements in neuroblastoma with unbalanced translocations and chromothripsis.
Boeva V; Jouannet S; Daveau R; Combaret V; Pierre-Eugène C; Cazes A; Louis-Brennetot C; Schleiermacher G; Ferrand S; Pierron G; Lermine A; Rio Frio T; Raynal V; Vassal G; Barillot E; Delattre O; Janoueix-Lerosey I
PLoS One; 2013; 8(8):e72182. PubMed ID: 23991058
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
