289 related articles for article (PubMed ID: 32106411)
21. Chromothripsis in congenital disorders and cancer: similarities and differences.
Kloosterman WP; Cuppen E
Curr Opin Cell Biol; 2013 Jun; 25(3):341-8. PubMed ID: 23478216
[TBL] [Abstract][Full Text] [Related]
22. Impaired nuclear functions in micronuclei results in genome instability and chromothripsis.
Terradas M; Martín M; Genescà A
Arch Toxicol; 2016 Nov; 90(11):2657-2667. PubMed ID: 27542123
[TBL] [Abstract][Full Text] [Related]
23. Mitotic clustering of pulverized chromosomes from micronuclei.
Lin YF; Hu Q; Mazzagatti A; Valle-Inclán JE; Maurais EG; Dahiya R; Guyer A; Sanders JT; Engel JL; Nguyen G; Bronder D; Bakhoum SF; Cortés-Ciriano I; Ly P
Nature; 2023 Jun; 618(7967):1041-1048. PubMed ID: 37165191
[TBL] [Abstract][Full Text] [Related]
24. Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells.
So A; Le Guen T; Lopez BS; Guirouilh-Barbat J
FEBS J; 2017 Aug; 284(15):2324-2344. PubMed ID: 28244221
[TBL] [Abstract][Full Text] [Related]
25. Boveri and beyond: Chromothripsis and genomic instability from mitotic errors.
Mazzagatti A; Engel JL; Ly P
Mol Cell; 2024 Jan; 84(1):55-69. PubMed ID: 38029753
[TBL] [Abstract][Full Text] [Related]
26. Chromosomal Rearrangements and Chromothripsis: The Alternative End Generation Model.
de Groot D; Spanjaard A; Hogenbirk MA; Jacobs H
Int J Mol Sci; 2023 Jan; 24(1):. PubMed ID: 36614236
[TBL] [Abstract][Full Text] [Related]
27. Micronuclei-based model system reveals functional consequences of chromothripsis in human cells.
Kneissig M; Keuper K; de Pagter MS; van Roosmalen MJ; Martin J; Otto H; Passerini V; Campos Sparr A; Renkens I; Kropveld F; Vasudevan A; Sheltzer JM; Kloosterman WP; Storchova Z
Elife; 2019 Nov; 8():. PubMed ID: 31778112
[TBL] [Abstract][Full Text] [Related]
28. Induction of chromosome-specific micronuclei and chromothripsis by centromere inactivation.
Lin YF; Hu Q; Guyer A; Fachinetti D; Ly P
Methods Cell Biol; 2024; 182():1-20. PubMed ID: 38359973
[TBL] [Abstract][Full Text] [Related]
29. DNA breaks and chromosome pulverization from errors in mitosis.
Crasta K; Ganem NJ; Dagher R; Lantermann AB; Ivanova EV; Pan Y; Nezi L; Protopopov A; Chowdhury D; Pellman D
Nature; 2012 Jan; 482(7383):53-8. PubMed ID: 22258507
[TBL] [Abstract][Full Text] [Related]
30. Chromothripsis: an emerging crossroad from aberrant mitosis to therapeutic opportunities.
Ejaz U; Dou Z; Yao PY; Wang Z; Liu X; Yao X
J Mol Cell Biol; 2024 May; ():. PubMed ID: 38710586
[TBL] [Abstract][Full Text] [Related]
31. Copy number variations and constitutional chromothripsis (Review).
Brás A; Rodrigues AS; Rueff J
Biomed Rep; 2020 Sep; 13(3):11. PubMed ID: 32765850
[TBL] [Abstract][Full Text] [Related]
32. Chromothripsis-like chromosomal rearrangements induced by ionizing radiation using proton microbeam irradiation system.
Morishita M; Muramatsu T; Suto Y; Hirai M; Konishi T; Hayashi S; Shigemizu D; Tsunoda T; Moriyama K; Inazawa J
Oncotarget; 2016 Mar; 7(9):10182-92. PubMed ID: 26862731
[TBL] [Abstract][Full Text] [Related]
33. Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells.
Middelkamp S; van Heesch S; Braat AK; de Ligt J; van Iterson M; Simonis M; van Roosmalen MJ; Kelder MJ; Kruisselbrink E; Hochstenbach R; Verbeek NE; Ippel EF; Adolfs Y; Pasterkamp RJ; Kloosterman WP; Kuijk EW; Cuppen E
Genome Med; 2017 Jan; 9(1):9. PubMed ID: 28126037
[TBL] [Abstract][Full Text] [Related]
34. Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization.
Nazaryan-Petersen L; Eisfeldt J; Pettersson M; Lundin J; Nilsson D; Wincent J; Lieden A; Lovmar L; Ottosson J; Gacic J; Mäkitie O; Nordgren A; Vezzi F; Wirta V; Käller M; Hjortshøj TD; Jespersgaard C; Houssari R; Pignata L; Bak M; Tommerup N; Lundberg ES; Tümer Z; Lindstrand A
PLoS Genet; 2018 Nov; 14(11):e1007780. PubMed ID: 30419018
[TBL] [Abstract][Full Text] [Related]
35. Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations.
Suzuki E; Shima H; Toki M; Hanew K; Matsubara K; Kurahashi H; Narumi S; Ogata T; Kamimaki T; Fukami M
Cytogenet Genome Res; 2016; 150(2):86-92. PubMed ID: 28099951
[TBL] [Abstract][Full Text] [Related]
36. Chromothripsis in hematologic malignancies.
Lagunas-Rangel FA
Exp Hematol; 2024 Apr; 132():104172. PubMed ID: 38309572
[TBL] [Abstract][Full Text] [Related]
37. Chromothripsis - Extensive Chromosomal Rearrangements and Their Significance in Cancer.
Závacká K; Plevová K; Jarošová M; Pospíšilová Š
Klin Onkol; 2019; 32(2):101-108. PubMed ID: 30995849
[TBL] [Abstract][Full Text] [Related]
38. Chromothripsis: A New Mechanism for Rapid Karyotype Evolution.
Leibowitz ML; Zhang CZ; Pellman D
Annu Rev Genet; 2015; 49():183-211. PubMed ID: 26442848
[TBL] [Abstract][Full Text] [Related]
39. Established and Novel Mechanisms Leading to de novo Genomic Rearrangements in the Human Germline.
Hattori A; Fukami M
Cytogenet Genome Res; 2020; 160(4):167-176. PubMed ID: 32396893
[TBL] [Abstract][Full Text] [Related]
40. Chromothripsis: breakage-fusion-bridge over and over again.
Sorzano CO; Pascual-Montano A; Sánchez de Diego A; Martínez-A C; van Wely KH
Cell Cycle; 2013 Jul; 12(13):2016-23. PubMed ID: 23759584
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]