Literature DB >> 32404988

Publisher Correction: Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing.

Isidro Cortés-Ciriano1,2,3,4, Jake June-Koo Lee1,2, Ruibin Xi5, Dhawal Jain1, Youngsook L Jung1, Lixing Yang6,7, Dmitry Gordenin8, Leszek J Klimczak9, Cheng-Zhong Zhang1,10, David S Pellman11,12,13, Peter J Park14,15.   

Abstract

Entities:  

Year:  2020        PMID： 32404988     DOI： 10.1038/s41588-020-0634-1

Source DB:  PubMed          Journal:  Nat Genet        ISSN： 1061-4036            Impact factor:   38.330


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  3 in total

Review 1.  Chromosome structural variation in tumorigenesis: mechanisms of formation and carcinogenesis.

Authors:  Wen-Jun Wang; Ling-Yu Li; Jiu-Wei Cui
Journal:  Epigenetics Chromatin       Date:  2020-11-10       Impact factor: 4.954

2.  Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier.

Authors:  Jesper Eisfeldt; Maria Pettersson; Anna Petri; Daniel Nilsson; Lars Feuk; Anna Lindstrand
Journal:  Hum Genet       Date:  2020-12-14       Impact factor: 4.132

3.  Chromosome aberrations induced by the non-mutagenic carcinogen acetamide involve in rat hepatocarcinogenesis through micronucleus formation in hepatocytes.

Authors:  Kenji Nakamura; Yuji Ishii; Shinji Takasu; Takehiko Nohmi; Makoto Shibutani; Kumiko Ogawa
Journal:  Arch Toxicol       Date:  2021-06-23       Impact factor: 5.153
  3 in total

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