199 related articles for article (PubMed ID: 32396893)
1. 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]
2. Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cells.
Hattori A; Okamura K; Terada Y; Tanaka R; Katoh-Fukui Y; Matsubara Y; Matsubara K; Kagami M; Horikawa R; Fukami M
BMC Med Genomics; 2019 May; 12(1):77. PubMed ID: 31138192
[TBL] [Abstract][Full Text] [Related]
3. Catastrophic cellular events leading to complex chromosomal rearrangements in the germline.
Fukami M; Shima H; Suzuki E; Ogata T; Matsubara K; Kamimaki T
Clin Genet; 2017 May; 91(5):653-660. PubMed ID: 27888607
[TBL] [Abstract][Full Text] [Related]
4. Genes, Proteins, and Biological Pathways Preventing Chromothripsis.
Poot M
Methods Mol Biol; 2018; 1769():231-251. PubMed ID: 29564828
[TBL] [Abstract][Full Text] [Related]
5. Potential Role of Chromothripsis in the Genesis of Complex Chromosomal Rearrangements in Human Gametes and Preimplantation Embryo.
Pellestor F; Gatinois V
Methods Mol Biol; 2018; 1769():35-41. PubMed ID: 29564816
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis.
Arya P; Hodge JC; Matlock PA; Vance GH; Breman AM
Cytogenet Genome Res; 2020; 160(11-12):671-679. PubMed ID: 33535208
[TBL] [Abstract][Full Text] [Related]
8. Chromoanagenesis: cataclysms behind complex chromosomal rearrangements.
Pellestor F
Mol Cytogenet; 2019; 12():6. PubMed ID: 30805029
[TBL] [Abstract][Full Text] [Related]
9. Clinical Consequences of Chromothripsis and Other Catastrophic Cellular Events.
Fukami M; Kurahashi H
Methods Mol Biol; 2018; 1769():21-33. PubMed ID: 29564815
[TBL] [Abstract][Full Text] [Related]
10. Germline Chromothripsis Driven by L1-Mediated Retrotransposition and Alu/Alu Homologous Recombination.
Nazaryan-Petersen L; Bertelsen B; Bak M; Jønson L; Tommerup N; Hancks DC; Tümer Z
Hum Mutat; 2016 Apr; 37(4):385-95. PubMed ID: 26929209
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. The Iceberg under Water: Unexplored Complexity of Chromoanagenesis in Congenital Disorders.
Zepeda-Mendoza CJ; Morton CC
Am J Hum Genet; 2019 Apr; 104(4):565-577. PubMed ID: 30951674
[TBL] [Abstract][Full Text] [Related]
14. Chromoanasynthesis: another way for the formation of complex chromosomal abnormalities in human reproduction.
Pellestor F; Gatinois V
Hum Reprod; 2018 Aug; 33(8):1381-1387. PubMed ID: 30325427
[TBL] [Abstract][Full Text] [Related]
15. Chromoanagenesis, the mechanisms of a genomic chaos.
Pellestor F; Gaillard JB; Schneider A; Puechberty J; Gatinois V
Semin Cell Dev Biol; 2022 Mar; 123():90-99. PubMed ID: 33608210
[TBL] [Abstract][Full Text] [Related]
16. Chromoanagenesis: a piece of the macroevolution scenario.
Pellestor F; Gatinois V
Mol Cytogenet; 2020; 13():3. PubMed ID: 32010222
[TBL] [Abstract][Full Text] [Related]
17. Insight into the Molecular Basis Underlying Chromothripsis.
Ostapińska K; Styka B; Lejman M
Int J Mol Sci; 2022 Mar; 23(6):. PubMed ID: 35328739
[TBL] [Abstract][Full Text] [Related]
18. Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome.
Collins RL; Brand H; Redin CE; Hanscom C; Antolik C; Stone MR; Glessner JT; Mason T; Pregno G; Dorrani N; Mandrile G; Giachino D; Perrin D; Walsh C; Cipicchio M; Costello M; Stortchevoi A; An JY; Currall BB; Seabra CM; Ragavendran A; Margolin L; Martinez-Agosto JA; Lucente D; Levy B; Sanders SJ; Wapner RJ; Quintero-Rivera F; Kloosterman W; Talkowski ME
Genome Biol; 2017 Mar; 18(1):36. PubMed ID: 28260531
[TBL] [Abstract][Full Text] [Related]
19. Mechanistic origins of diverse genome rearrangements in cancer.
Dahiya R; Hu Q; Ly P
Semin Cell Dev Biol; 2022 Mar; 123():100-109. PubMed ID: 33824062
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
